Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79613 |
|---|---|
| ensemblid | ENSG00000103047.8 |
| hgncid | 25749 |
| symbol | TANGO6 |
| name | transport and golgi organization 6 homolog |
| refseq_nuc | NM_024562.2 |
| refseq_prot | NP_078838.1 |
| ensembl_nuc | ENST00000261778.2 |
| ensembl_prot | ENSP00000261778.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 68843531 |
| end | 69085182 |
| strand | + |
| ver | v1.2 |
| region | chr16:68843531-69085182 |
| region5000 | chr16:68838531-69090182 |
| regionname0 | TANGO6_chr16_68843531_69085182 |
| regionname5000 | TANGO6_chr16_68838531_69090182 |
| 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 | 1094 | 194 | 60 | 44 | 62 | 8 | 18 | 46 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0002 | 0/0 | 1094 | 5 | 3 | 0 | 0 | 0 | 2 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0003 | 0/0 | 1094 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0004 | 0/0 | 1094 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0005 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0006 | 0/0 | 1094 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3285 | 144 | 53 | 31 | 39 | 4 | 15 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0002 | 0/0 | 3285 | 28 | 0 | 9 | 18 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0003 | 0/0 | 3285 | 16 | 5 | 4 | 4 | 2 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0004 | 0/0 | 3285 | 5 | 5 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0005 | 0/0 | 3285 | 5 | 3 | 0 | 0 | 0 | 2 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0006 | 0/0 | 3285 | 4 | 4 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0007 | 0/0 | 3285 | 3 | 0 | 0 | 0 | 2 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0008 | 0/0 | 3285 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0009 | 0/0 | 3285 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0010 | 0/0 | 3285 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| c0011 | 0/0 | 3285 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| 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 | 1609 | 195 | 65 | 42 | 59 | 7 | 20 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0002 | 0/0 | 1609 | 4 | 4 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0003 | 0/0 | 1609 | 3 | 0 | 2 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0004 | 0/0 | 1609 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0005 | 0/0 | 1609 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0006 | 0/0 | 1609 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0007 | 0/0 | 1609 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| t0008 | 0/0 | 1609 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3285 | 144 | 53 | 31 | 39 | 4 | 15 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0002 | 0/0 | 3285 | 28 | 0 | 9 | 18 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0003 | 0/0 | 3285 | 16 | 5 | 4 | 4 | 2 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0007 | 0/0 | 3285 | 3 | 0 | 0 | 0 | 2 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0008 | 0/0 | 3285 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0009 | 0/0 | 3285 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0002c0005 | 0/0 | 3285 | 5 | 3 | 0 | 0 | 0 | 2 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0003c0004 | 0/0 | 3285 | 5 | 5 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0004c0006 | 0/0 | 3285 | 4 | 4 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0005c0011 | 0/0 | 3285 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0006c0010 | 0/0 | 3285 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4893 | 138 | 51 | 29 | 37 | 4 | 15 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0001t0002 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0001t0003 | 0/0 | 4893 | 2 | 0 | 2 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0001t0005 | 0/0 | 4893 | 2 | 0 | 0 | 2 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0001t0008 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0002t0001 | 0/0 | 4893 | 28 | 0 | 9 | 18 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0003t0001 | 0/0 | 4893 | 12 | 2 | 4 | 3 | 2 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0003t0002 | 0/0 | 4893 | 3 | 3 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0003t0007 | 0/0 | 4893 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0007t0001 | 0/0 | 4893 | 2 | 0 | 0 | 0 | 1 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0007t0003 | 0/0 | 4893 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0008t0001 | 0/0 | 4893 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0001c0009t0001 | 0/0 | 4893 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0002c0005t0001 | 0/0 | 4893 | 3 | 1 | 0 | 0 | 0 | 2 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0002c0005t0006 | 0/0 | 4893 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0003c0004t0001 | 0/0 | 4893 | 3 | 3 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0003c0004t0004 | 0/0 | 4893 | 2 | 2 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0004c0006t0001 | 0/0 | 4893 | 4 | 4 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0005c0011t0001 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| a0006c0010t0001 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | copy fasta | chr16 | 68838531 | 69090182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0003t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0007t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0007t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0008t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0008t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0001c0009t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0002c0005t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0002c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0002c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0002c0005t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0002c0005t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0003c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0003c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0003c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0003c0004t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0003c0004t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0004c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0004c0006t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0004c0006t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0004c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0005c0011t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| a0006c0010t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0131 | EUR | GBR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0125 | EUR | GBR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | CHS | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0129 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0134 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | CLM | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0130 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0071 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02129 | hp1 | a0001 | c0009 | t0001 | g0133 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | KHV | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02257 | hp1 | a0004 | c0006 | t0001 | g0181 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02258 | hp1 | a0003 | c0004 | t0001 | g0151 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02280 | hp2 | a0004 | c0006 | t0001 | g0180 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02615 | hp1 | a0001 | c0003 | t0002 | g0195 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0194 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02717 | hp1 | a0001 | c0008 | t0001 | g0119 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02922 | hp1 | a0006 | c0010 | t0001 | g0206 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02976 | hp2 | a0002 | c0005 | t0006 | g0137 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03041 | hp1 | a0003 | c0004 | t0004 | g0202 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03225 | hp1 | a0003 | c0004 | t0004 | g0203 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03225 | hp2 | a0005 | c0011 | t0001 | g0148 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03239 | hp2 | a0001 | c0007 | t0001 | g0038 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03516 | hp1 | a0003 | c0004 | t0001 | g0201 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03540 | hp1 | a0001 | c0008 | t0001 | g0112 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03579 | hp1 | a0004 | c0006 | t0001 | g0179 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03834 | hp2 | a0002 | c0005 | t0001 | g0162 | SAS | BEB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03927 | hp2 | a0002 | c0005 | t0001 | g0163 | SAS | BEB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0135 | SAS | STU | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0123 | SAS | STU | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18906 | hp1 | a0002 | c0005 | t0006 | g0138 | AFR | YRI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0136 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0196 | AFR | LWK | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19077 | hp1 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19079 | hp2 | a0001 | c0003 | t0007 | g0127 | EAS | JPT | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA20752 | hp2 | a0001 | c0007 | t0001 | g0036 | EUR | TSI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA20805 | hp1 | a0001 | c0007 | t0003 | g0037 | EUR | TSI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02559 | hp1 | a0003 | c0004 | t0001 | g0164 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| HG06807 | hp2 | a0004 | c0006 | t0001 | g0193 | AFR | USA | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0124 | AFR | LWK | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| NA21309 | hp2 | a0002 | c0005 | t0001 | g0002 | AFR | LWK | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0106 | REF | REF | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0039 | REF | REF | TANGO6_chr16_68838531_69090182 | TANGO6 | chr16 | 68838531 | 69090182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68860361
|
C | G | 1 | a0006 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.572C>G | p.Ala191Gly | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/18 | 659/4893 | 572/3285 | 191/1094 | chr16 | 68860361 | ||
| chr16:68902408
|
C | T | 1 | a0005 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1571C>T | p.Ala524Val | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/18 | 1658/4893 | 1571/3285 | 524/1094 | chr16 | 68902408 | ||
| chr16:68927673
|
C | T | 1 | a0002 | 5 | HG02976.hp2 HG03834.hp2 HG03927.hp2 others(2): Show |
missense_variant | MODERATE | c.2233C>T | p.Arg745Cys | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/18 | 2320/4893 | 2233/3285 | 745/1094 | chr16 | 68927673 | ||
| chr16:68927998
|
C | G | 1 | a0004 | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.2558C>G | p.Thr853Arg | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/18 | 2645/4893 | 2558/3285 | 853/1094 | chr16 | 68927998 | ||
| chr16:69040344
|
G | A | 1 | a0003 | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.3031G>A | p.Gly1011Ser | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/18 | 3118/4893 | 3031/3285 | 1011/1094 | chr16 | 69040344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68843662
|
C | T | 1 | a0005c0011 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.45C>T | p.Cys15Cys | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/18 | 132/4893 | 45/3285 | 15/1094 | chr16 | 68843662 | ||
| chr16:68860050
|
T | C | 2 | a0001c0003a0001c0009 | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
synonymous_variant | LOW | c.261T>C | p.Ser87Ser | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/18 | 348/4893 | 261/3285 | 87/1094 | chr16 | 68860050 | ||
| chr16:68909339
|
C | T | 1 | a0001c0007 | 3 | HG03239.hp2 NA20752.hp2 NA20805.hp1 |
synonymous_variant | LOW | c.1929C>T | p.Val643Val | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/18 | 2016/4893 | 1929/3285 | 643/1094 | chr16 | 68909339 | ||
| chr16:68928011
|
C | T | 1 | a0001c0008 | 2 | HG02717.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.2571C>T | p.Ala857Ala | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/18 | 2658/4893 | 2571/3285 | 857/1094 | chr16 | 68928011 | ||
| chr16:68974134
|
C | T | 2 | a0001c0002a0001c0009 | 29 | HG00408.hp1 HG01099.hp1 HG01255.hp2 others(26): Show |
synonymous_variant | LOW | c.2808C>T | p.Val936Val | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/18 | 2895/4893 | 2808/3285 | 936/1094 | chr16 | 68974134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:69083821
|
T | A | 1 | a0003c0004t0004 | 2 | HG03041.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*160T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 160 | chr16 | 69083821 | |||||
| chr16:69083847
|
G | A | 1 | a0001c0001t0005 | 2 | HG02135.hp2 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 186 | chr16 | 69083847 | |||||
| chr16:69084191
|
G | T | 1 | a0001c0001t0008 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 530 | chr16 | 69084191 | |||||
| chr16:69084554
|
A | T | 2 | a0001c0001t0002a0001c0003t0002 | 4 | HG02615.hp1 HG02895.hp1 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*893A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 893 | chr16 | 69084554 | |||||
| chr16:69084606
|
G | A | 1 | a0002c0005t0006 | 2 | HG02976.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*945G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 945 | chr16 | 69084606 | |||||
| chr16:69084653
|
G | T | 1 | a0001c0003t0007 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*992G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 992 | chr16 | 69084653 | |||||
| chr16:69084848
|
C | T | 2 | a0001c0001t0003a0001c0007t0003 | 3 | HG01346.hp1 HG01361.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1187C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 18/18 | 1187 | chr16 | 69084848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:68843800
|
C | T | 7 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0207others(4): Show | 7 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+89C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68843800 | ||||||
| chr16:68843898
|
G | A | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.94+187G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68843898 | ||||||
| chr16:68844207
|
C | T | 3 | a0003c0004t0001g0201a0003c0004t0004g0202a0003c0004t0004g0203 | 3 | HG03041.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.94+496C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68844207 | ||||||
| chr16:68844441
|
T | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+730T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68844441 | ||||||
| chr16:68844550
|
C | A | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0207others(2): Show | 5 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+839C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68844550 | ||||||
| chr16:68844605
|
G | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02135.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.94+894G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68844605 | ||||||
| chr16:68844818
|
A | G | 27 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(24): Show | 27 | HG00099.hp1 HG00544.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.94+1107A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68844818 | ||||||
| chr16:68844967
|
C | CT | 55 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.94+1274dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68844967 | |||||
| chr16:68844967
|
C | CTT | 28 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(25): Show | 28 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+1273_94+1274dup others(2): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68844967 | |||||
| chr16:68845165
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147 | 3 | HG02040.hp2 NA18983.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.94+1454G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68845165 | ||||||
| chr16:68845233
|
G | C | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+1522G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68845233 | ||||||
| chr16:68845384
|
A | T | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+1673A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68845384 | ||||||
| chr16:68845512
|
A | G | 22 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0175others(19): Show | 22 | HG00099.hp1 HG00544.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+1801A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68845512 | ||||||
| chr16:68845780
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+2069G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68845780 | ||||||
| chr16:68845856
|
T | C | 3 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126 | 3 | HG00140.hp2 HG01099.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94+2145T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68845856 | ||||||
| chr16:68846087
|
G | A | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+2376G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846087 | ||||||
| chr16:68846113
|
C | T | 1 | a0001c0002t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.94+2402C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846113 | ||||||
| chr16:68846143
|
A | G | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+2432A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846143 | ||||||
| chr16:68846296
|
G | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+2585G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846296 | ||||||
| chr16:68846430
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.94+2719T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846430 | ||||||
| chr16:68846461
|
C | A | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+2750C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846461 | ||||||
| chr16:68846502
|
CT | C | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+2803delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68846502 | |||||
| chr16:68846535
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+2824G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846535 | ||||||
| chr16:68846611
|
C | T | 81 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.94+2900C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846611 | ||||||
| chr16:68846667
|
C | CT | 13 | a0001c0001t0001g0116a0001c0001t0001g0200a0001c0001t0001g0205others(10): Show | 13 | HG01433.hp2 HG02055.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+2975dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68846667 | |||||
| chr16:68846667
|
CT | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0149a0001c0001t0001g0172others(17): Show | 20 | HG00544.hp1 HG01891.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.94+2975delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68846667 | |||||
| chr16:68846667
|
CTT | C | 17 | a0001c0001t0001g0178a0001c0003t0001g0124a0001c0003t0001g0125others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+2974_94+2975del others(2): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68846667 | |||||
| chr16:68846764
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.94+3053C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846764 | ||||||
| chr16:68846888
|
A | G | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+3177A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846888 | ||||||
| chr16:68846893
|
CT | C | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+3196delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68846893 | |||||
| chr16:68846960
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+3249G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846960 | ||||||
| chr16:68846972
|
C | A | 49 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(46): Show | 49 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.94+3261C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846972 | ||||||
| chr16:68846993
|
C | T | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+3282C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68846993 | ||||||
| chr16:68847057
|
A | G | 3 | a0003c0004t0001g0201a0003c0004t0004g0202a0003c0004t0004g0203 | 3 | HG03041.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.94+3346A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847057 | ||||||
| chr16:68847092
|
G | A | 10 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0003t0001g0194others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+3381G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847092 | ||||||
| chr16:68847168
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94+3457G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847168 | ||||||
| chr16:68847206
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.94+3495A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847206 | ||||||
| chr16:68847214
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.94+3503G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847214 | ||||||
| chr16:68847236
|
C | A | 19 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(16): Show | 19 | HG00544.hp1 HG01891.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+3525C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847236 | ||||||
| chr16:68847399
|
A | G | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+3688A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847399 | ||||||
| chr16:68847407
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0171 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.94+3696A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847407 | ||||||
| chr16:68847423
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+3712G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847423 | ||||||
| chr16:68847475
|
G | T | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+3764G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847475 | ||||||
| chr16:68847495
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+3784A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847495 | ||||||
| chr16:68847560
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.94+3849G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847560 | ||||||
| chr16:68847563
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+3852G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847563 | ||||||
| chr16:68847592
|
C | T | 145 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0066others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.94+3881C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847592 | ||||||
| chr16:68847805
|
G | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+4094G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847805 | ||||||
| chr16:68847806
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+4095C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847806 | ||||||
| chr16:68847860
|
C | A | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+4149C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847860 | ||||||
| chr16:68847872
|
C | T | 19 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(16): Show | 19 | HG00544.hp1 HG01891.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.94+4161C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847872 | ||||||
| chr16:68847986
|
T | G | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.94+4275T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68847986 | ||||||
| chr16:68847999
|
C | CA | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 23 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+4308dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68847999 | |||||
| chr16:68847999
|
C | CAA | 10 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(7): Show | 10 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+4307_94+4308dup others(2): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68847999 | |||||
| chr16:68847999
|
CA | C | 6 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0002t0001g0113others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+4308delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68847999 | |||||
| chr16:68848013
|
A | C | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.94+4302A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848013 | ||||||
| chr16:68848215
|
T | C | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+4504T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848215 | ||||||
| chr16:68848308
|
A | G | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+4597A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848308 | ||||||
| chr16:68848397
|
G | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+4686G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848397 | ||||||
| chr16:68848425
|
G | A | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+4714G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848425 | ||||||
| chr16:68848529
|
AC | A | 84 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.94+4819delC | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848529 | ||||||
| chr16:68848541
|
A | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+4830A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848541 | ||||||
| chr16:68848642
|
A | G | 16 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0001g0176others(13): Show | 16 | HG00099.hp1 HG00544.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+4931A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848642 | ||||||
| chr16:68848779
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | HG00438.hp2 NA18939.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.94+5068A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848779 | ||||||
| chr16:68848879
|
G | A | 18 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+5168G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68848879 | ||||||
| chr16:68849019
|
C | T | 18 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(15): Show | 18 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+5308C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849019 | ||||||
| chr16:68849212
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.94+5501G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849212 | ||||||
| chr16:68849282
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.94+5571C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849282 | ||||||
| chr16:68849312
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0115 | 2 | HG02300.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.94+5601C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849312 | ||||||
| chr16:68849582
|
C | T | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+5871C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849582 | ||||||
| chr16:68849759
|
A | G | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02040.hp2 HG02135.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+6048A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849759 | ||||||
| chr16:68849822
|
AT | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+6117delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68849822 | |||||
| chr16:68849852
|
G | T | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+6141G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849852 | ||||||
| chr16:68849935
|
T | C | 6 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+6224T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68849935 | ||||||
| chr16:68849971
|
C | CT | 13 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0111others(10): Show | 13 | HG01081.hp1 HG01993.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+6280dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68849971 | |||||
| chr16:68849971
|
CT | C | 52 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.94+6280delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68849971 | |||||
| chr16:68850015
|
C | T | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+6304C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850015 | ||||||
| chr16:68850060
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.94+6349G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850060 | ||||||
| chr16:68850194
|
G | A | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.94+6483G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850194 | ||||||
| chr16:68850399
|
A | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+6688A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850399 | ||||||
| chr16:68850452
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+6741G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850452 | ||||||
| chr16:68850468
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.94+6757A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850468 | ||||||
| chr16:68850745
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+7034G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850745 | ||||||
| chr16:68850979
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94+7268T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68850979 | ||||||
| chr16:68851136
|
T | C | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.94+7425T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851136 | ||||||
| chr16:68851147
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+7436G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851147 | ||||||
| chr16:68851224
|
A | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+7513A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851224 | ||||||
| chr16:68851347
|
A | G | 45 | a0001c0001t0001g0055a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.94+7636A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851347 | ||||||
| chr16:68851453
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+7742C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851453 | ||||||
| chr16:68851490
|
A | G | 86 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.94+7779A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851490 | ||||||
| chr16:68851535
|
T | C | 45 | a0001c0001t0001g0055a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.94+7824T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851535 | ||||||
| chr16:68851672
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+7961G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851672 | ||||||
| chr16:68851858
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.95-8026C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851858 | ||||||
| chr16:68851874
|
A | T | 1 | a0001c0002t0001g0004 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.95-8010A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851874 | ||||||
| chr16:68851965
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-7919T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68851965 | ||||||
| chr16:68852257
|
A | G | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-7627A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68852257 | ||||||
| chr16:68852412
|
TA | T | 20 | a0001c0001t0001g0055a0001c0001t0001g0172a0001c0001t0001g0173others(17): Show | 20 | HG00544.hp1 HG01496.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-7471delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68852412 | ||||||
| chr16:68852455
|
CA | C | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02040.hp2 HG02135.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-7419delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68852455 | |||||
| chr16:68852465
|
A | T | 24 | a0001c0001t0001g0055a0001c0001t0001g0172a0001c0001t0001g0173others(21): Show | 24 | HG00544.hp1 HG01496.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.95-7419A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68852465 | ||||||
| chr16:68852600
|
CGGGA | C | 28 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(25): Show | 28 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-7281_95-7278del others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68852600 | |||||
| chr16:68852827
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.95-7057C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68852827 | ||||||
| chr16:68853120
|
G | C | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-6764G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68853120 | ||||||
| chr16:68853561
|
A | G | 73 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.95-6323A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68853561 | ||||||
| chr16:68853731
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.95-6153C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68853731 | ||||||
| chr16:68853890
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-5994G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68853890 | ||||||
| chr16:68853942
|
T | C | 85 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.95-5942T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68853942 | ||||||
| chr16:68853962
|
T | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-5922T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68853962 | ||||||
| chr16:68854090
|
A | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-5794A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854090 | ||||||
| chr16:68854158
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.95-5726G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854158 | ||||||
| chr16:68854215
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.95-5669A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854215 | ||||||
| chr16:68854408
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.95-5476G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854408 | ||||||
| chr16:68854461
|
C | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0161 | 2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.95-5423C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854461 | ||||||
| chr16:68854539
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-5345A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854539 | ||||||
| chr16:68854618
|
G | GT | 6 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(3): Show | 6 | HG01175.hp1 HG01255.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5249dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68854618 | |||||
| chr16:68854618
|
GT | G | 17 | a0001c0001t0001g0024a0001c0003t0001g0124a0001c0003t0001g0125others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-5249delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68854618 | |||||
| chr16:68854623
|
T | G | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.95-5261T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854623 | ||||||
| chr16:68854625
|
T | G | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-5259T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854625 | ||||||
| chr16:68854635
|
T | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5249T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854635 | ||||||
| chr16:68854661
|
A | C | 17 | a0001c0001t0001g0055a0001c0001t0001g0173a0001c0001t0001g0175others(14): Show | 17 | HG00099.hp1 HG00544.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-5223A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854661 | ||||||
| chr16:68854775
|
C | T | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-5109C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854775 | ||||||
| chr16:68854867
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.95-5017G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854867 | ||||||
| chr16:68854932
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.95-4952C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68854932 | ||||||
| chr16:68855009
|
CT | C | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-4864delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68855009 | |||||
| chr16:68855090
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0050 | 2 | HG02129.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.95-4794C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855090 | ||||||
| chr16:68855201
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-4683C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855201 | ||||||
| chr16:68855206
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.95-4678C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855206 | ||||||
| chr16:68855206
|
C | CA | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-4669dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68855206 | |||||
| chr16:68855469
|
C | G | 1 | a0001c0009t0001g0133 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.95-4415C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855469 | ||||||
| chr16:68855627
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-4257G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855627 | ||||||
| chr16:68855826
|
C | A | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-4058C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855826 | ||||||
| chr16:68855834
|
G | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-4050G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68855834 | ||||||
| chr16:68856028
|
T | C | 1 | a0001c0003t0001g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.95-3856T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856028 | ||||||
| chr16:68856139
|
C | T | 10 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0183others(7): Show | 10 | HG00544.hp1 HG01952.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-3745C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856139 | ||||||
| chr16:68856241
|
C | T | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3643C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856241 | ||||||
| chr16:68856621
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.95-3263A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856621 | ||||||
| chr16:68856843
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02040.hp2 HG02135.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-3041C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856843 | ||||||
| chr16:68856912
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-2972G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856912 | ||||||
| chr16:68856917
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.95-2967G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856917 | ||||||
| chr16:68856937
|
A | G | 28 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(25): Show | 28 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-2947A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68856937 | ||||||
| chr16:68857089
|
A | T | 36 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.95-2795A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857089 | ||||||
| chr16:68857129
|
C | T | 36 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.95-2755C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857129 | ||||||
| chr16:68857368
|
G | A | 4 | a0001c0001t0001g0069a0001c0002t0001g0068a0001c0002t0001g0070others(1): Show | 4 | HG01975.hp2 HG01981.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2516G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857368 | ||||||
| chr16:68857389
|
CT | C | 7 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0001t0001g0209others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-2484delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68857389 | |||||
| chr16:68857415
|
A | C | 36 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(33): Show | 36 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.95-2469A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857415 | ||||||
| chr16:68857422
|
C | T | 37 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.95-2462C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857422 | ||||||
| chr16:68857550
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.95-2334G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857550 | ||||||
| chr16:68857565
|
C | T | 6 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2319C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68857565 | ||||||
| chr16:68858065
|
A | AT | 38 | a0001c0001t0001g0055a0001c0001t0001g0173a0001c0001t0001g0175others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(35): Show |
intron_variant | MODIFIER | c.95-1803dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr16 | 68858065 | |||||
| chr16:68858183
|
C | T | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1701C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858183 | ||||||
| chr16:68858193
|
G | A | 142 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0062others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.95-1691G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858193 | ||||||
| chr16:68858344
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.95-1540G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858344 | ||||||
| chr16:68858356
|
G | A | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-1528G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858356 | ||||||
| chr16:68858433
|
T | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-1451T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858433 | ||||||
| chr16:68858482
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-1402G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858482 | ||||||
| chr16:68858593
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-1291A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858593 | ||||||
| chr16:68858671
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0050 | 2 | HG02129.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.95-1213C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858671 | ||||||
| chr16:68858935
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.95-949G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68858935 | ||||||
| chr16:68859226
|
G | A | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-658G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859226 | ||||||
| chr16:68859404
|
C | T | 61 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(58): Show | 61 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.95-480C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859404 | ||||||
| chr16:68859500
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0026 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.95-384C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859500 | ||||||
| chr16:68859537
|
A | T | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-347A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859537 | ||||||
| chr16:68859558
|
T | A | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-326T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859558 | ||||||
| chr16:68859593
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-291A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859593 | ||||||
| chr16:68859791
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-93C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859791 | ||||||
| chr16:68859878
|
C | T | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.95-6C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 1/17 | chr16 | 68859878 | ||||||
| chr16:68860560
|
G | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.735+36G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68860560 | ||||||
| chr16:68860580
|
A | T | 1 | a0001c0003t0001g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.735+56A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68860580 | ||||||
| chr16:68860794
|
T | C | 17 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.735+270T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68860794 | ||||||
| chr16:68861032
|
A | T | 52 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.735+508A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861032 | ||||||
| chr16:68861197
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+673C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861197 | ||||||
| chr16:68861369
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.735+845G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861369 | ||||||
| chr16:68861388
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0025 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.735+864C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861388 | ||||||
| chr16:68861561
|
G | A | 2 | a0001c0002t0001g0072a0001c0002t0001g0073 | 2 | HG00408.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.735+1037G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861561 | ||||||
| chr16:68861846
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.736-1099C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861846 | ||||||
| chr16:68861851
|
C | G | 23 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(20): Show | 23 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.736-1094C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68861851 | ||||||
| chr16:68862022
|
A | T | 85 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.736-923A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862022 | ||||||
| chr16:68862023
|
A | AT | 9 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(6): Show | 9 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.736-912dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 68862023 | |||||
| chr16:68862027
|
T | A | 10 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0207others(7): Show | 10 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.736-918T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862027 | ||||||
| chr16:68862030
|
T | A | 50 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.736-915T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862030 | ||||||
| chr16:68862162
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.736-783C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862162 | ||||||
| chr16:68862290
|
C | G | 22 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0175others(19): Show | 22 | HG00099.hp1 HG00544.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.736-655C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862290 | ||||||
| chr16:68862307
|
C | T | 3 | a0003c0004t0001g0201a0003c0004t0004g0202a0003c0004t0004g0203 | 3 | HG03041.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.736-638C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862307 | ||||||
| chr16:68862394
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.736-551G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862394 | ||||||
| chr16:68862449
|
G | A | 9 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0150others(6): Show | 9 | HG02055.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.736-496G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862449 | ||||||
| chr16:68862488
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.736-457C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862488 | ||||||
| chr16:68862497
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.736-448G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862497 | ||||||
| chr16:68862529
|
C | T | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.736-416C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862529 | ||||||
| chr16:68862555
|
G | A | 7 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0207others(4): Show | 7 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.736-390G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862555 | ||||||
| chr16:68862719
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.736-226C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862719 | ||||||
| chr16:68862888
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.736-57C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862888 | ||||||
| chr16:68862920
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.736-25A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 2/17 | chr16 | 68862920 | ||||||
| chr16:68863119
|
GTCT | G | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.852+65_852+67delTC others(1): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68863119 | |||||
| chr16:68863293
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.852+232A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863293 | ||||||
| chr16:68863335
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.852+274C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863335 | ||||||
| chr16:68863398
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.852+337G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863398 | ||||||
| chr16:68863445
|
C | A | 82 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.852+384C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863445 | ||||||
| chr16:68863501
|
T | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.852+440T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863501 | ||||||
| chr16:68863558
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.852+497C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863558 | ||||||
| chr16:68863573
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.852+512G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863573 | ||||||
| chr16:68863730
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.852+669G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863730 | ||||||
| chr16:68863982
|
T | G | 28 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(25): Show | 28 | HG00544.hp1 HG01891.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.852+921T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68863982 | ||||||
| chr16:68864045
|
A | G | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.852+984A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864045 | ||||||
| chr16:68864130
|
C | T | 13 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0183others(10): Show | 13 | HG00544.hp1 HG01952.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.852+1069C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864130 | ||||||
| chr16:68864174
|
C | CA | 67 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0140others(64): Show | 67 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.852+1126dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68864174 | |||||
| chr16:68864209
|
T | C | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.852+1148T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864209 | ||||||
| chr16:68864234
|
T | C | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.852+1173T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864234 | ||||||
| chr16:68864258
|
G | T | 1 | a0003c0004t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.852+1197G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864258 | ||||||
| chr16:68864411
|
G | C | 86 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.852+1350G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864411 | ||||||
| chr16:68864522
|
A | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.852+1461A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864522 | ||||||
| chr16:68864607
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.852+1546G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68864607 | ||||||
| chr16:68865137
|
C | T | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-1942C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865137 | ||||||
| chr16:68865232
|
C | T | 6 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.853-1847C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865232 | ||||||
| chr16:68865256
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.853-1823A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865256 | ||||||
| chr16:68865275
|
C | CA | 35 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0055others(32): Show | 35 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.853-1786dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68865275 | |||||
| chr16:68865322
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-1757G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865322 | ||||||
| chr16:68865475
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.853-1604G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865475 | ||||||
| chr16:68865575
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-1504G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865575 | ||||||
| chr16:68865699
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-1380G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865699 | ||||||
| chr16:68865753
|
C | CA | 14 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0109others(11): Show | 14 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.853-1310dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68865753 | |||||
| chr16:68865753
|
C | CAA | 26 | a0001c0001t0001g0120a0001c0001t0001g0122a0001c0001t0001g0149others(23): Show | 26 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.853-1311_853-1310d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68865753 | |||||
| chr16:68865753
|
C | CAAA | 18 | a0001c0001t0001g0121a0001c0001t0001g0140a0001c0001t0001g0141others(15): Show | 18 | HG02040.hp2 HG02486.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.853-1312_853-1310d others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68865753 | |||||
| chr16:68865753
|
C | CAAAA | 11 | a0001c0001t0005g0168a0001c0003t0001g0124a0001c0003t0001g0126others(8): Show | 11 | HG01081.hp2 HG01099.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.853-1313_853-1310d others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68865753 | |||||
| chr16:68865866
|
C | G | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.853-1213C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865866 | ||||||
| chr16:68865917
|
CAA | C | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-1151_853-1150d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68865917 | |||||
| chr16:68865993
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.853-1086G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68865993 | ||||||
| chr16:68866048
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.853-1031C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68866048 | ||||||
| chr16:68866236
|
T | C | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.853-843T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68866236 | ||||||
| chr16:68866480
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0025 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.853-599G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68866480 | ||||||
| chr16:68866547
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.853-532C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68866547 | ||||||
| chr16:68866629
|
C | CA | 27 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0055others(24): Show | 27 | HG00099.hp1 HG00544.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.853-434dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68866629 | |||||
| chr16:68866629
|
CA | C | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-434delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68866629 | |||||
| chr16:68866740
|
C | T | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.853-339C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68866740 | ||||||
| chr16:68866885
|
C | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.853-194C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68866885 | ||||||
| chr16:68866975
|
C | CT | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 42 | HG00099.hp1 HG00544.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.853-79dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68866975 | |||||
| chr16:68866975
|
C | CTT | 14 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0176others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-80_853-79dupTT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68866975 | |||||
| chr16:68866975
|
CT | C | 14 | a0001c0001t0001g0056a0001c0001t0001g0140a0001c0001t0001g0141others(11): Show | 14 | HG01433.hp2 HG01884.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.853-79delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr16 | 68866975 | |||||
| chr16:68867019
|
G | A | 1 | a0004c0006t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.853-60G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68867019 | ||||||
| chr16:68867021
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.853-58C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 3/17 | chr16 | 68867021 | ||||||
| chr16:68867381
|
C | T | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+161C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867381 | ||||||
| chr16:68867512
|
A | G | 86 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(83): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.994+292A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867512 | ||||||
| chr16:68867753
|
T | C | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+533T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867753 | ||||||
| chr16:68867792
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+572G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867792 | ||||||
| chr16:68867869
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0011others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.994+649T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867869 | ||||||
| chr16:68867878
|
A | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0182a0004c0006t0001g0179others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.994+658A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867878 | ||||||
| chr16:68867978
|
C | CA | 33 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.994+775dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68867978 | |||||
| chr16:68867996
|
T | C | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+776T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68867996 | ||||||
| chr16:68868144
|
CA | C | 17 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0008g0030others(14): Show | 17 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.994+941delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68868144 | |||||
| chr16:68868174
|
A | G | 6 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02717.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.994+954A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68868174 | ||||||
| chr16:68868313
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+1093A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68868313 | ||||||
| chr16:68868403
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+1183G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68868403 | ||||||
| chr16:68868492
|
A | AT | 21 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0023others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.994+1295dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68868492 | |||||
| chr16:68868492
|
A | ATTTTT | 9 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.994+1291_994+1295d others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68868492 | |||||
| chr16:68868492
|
A | T | 2 | a0001c0001t0001g0192a0001c0002t0001g0065 | 2 | NA19009.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.994+1272A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68868492 | ||||||
| chr16:68868492
|
AT | A | 35 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(32): Show | 35 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.994+1295delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68868492 | |||||
| chr16:68868492
|
ATT | A | 19 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.994+1294_994+1295d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68868492 | |||||
| chr16:68868492
|
ATTT | A | 10 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG02040.hp2 HG02135.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.994+1293_994+1295d others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68868492 | |||||
| chr16:68868945
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.994+1725G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68868945 | ||||||
| chr16:68868974
|
G | C | 51 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.994+1754G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68868974 | ||||||
| chr16:68869088
|
T | G | 23 | a0001c0001t0001g0055a0001c0001t0001g0172a0001c0001t0001g0173others(20): Show | 23 | HG00099.hp1 HG00544.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.994+1868T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68869088 | ||||||
| chr16:68869370
|
G | C | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.994+2150G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68869370 | ||||||
| chr16:68869768
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0171 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.994+2548G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68869768 | ||||||
| chr16:68869895
|
G | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+2675G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68869895 | ||||||
| chr16:68869987
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.994+2767G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68869987 | ||||||
| chr16:68870008
|
G | A | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.994+2788G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870008 | ||||||
| chr16:68870398
|
G | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+3178G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870398 | ||||||
| chr16:68870478
|
T | C | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.994+3258T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870478 | ||||||
| chr16:68870602
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.994+3382T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870602 | ||||||
| chr16:68870627
|
A | C | 23 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178others(20): Show | 23 | HG00544.hp1 HG01891.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.994+3407A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870627 | ||||||
| chr16:68870802
|
C | CT | 44 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.994+3595dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68870802 | |||||
| chr16:68870885
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.994+3665A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870885 | ||||||
| chr16:68870937
|
C | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0078a0001c0002t0001g0079 | 3 | NA18982.hp2 NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.994+3717C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68870937 | ||||||
| chr16:68870947
|
AT | A | 58 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(55): Show | 58 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.994+3742delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68870947 | |||||
| chr16:68871126
|
A | C | 1 | a0001c0001t0001g0006 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.994+3906A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871126 | ||||||
| chr16:68871133
|
G | C | 83 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.994+3913G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871133 | ||||||
| chr16:68871254
|
A | G | 82 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.995-3900A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871254 | ||||||
| chr16:68871532
|
T | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.995-3622T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871532 | ||||||
| chr16:68871541
|
C | A | 84 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.995-3613C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871541 | ||||||
| chr16:68871704
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00099.hp1 HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.995-3450C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871704 | ||||||
| chr16:68871705
|
T | C | 73 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.995-3449T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871705 | ||||||
| chr16:68871817
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.995-3337G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871817 | ||||||
| chr16:68871958
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.995-3196G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68871958 | ||||||
| chr16:68872001
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-3153G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872001 | ||||||
| chr16:68872200
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0104 | 2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.995-2954G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872200 | ||||||
| chr16:68872271
|
C | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.995-2883C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872271 | ||||||
| chr16:68872297
|
T | C | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.995-2857T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872297 | ||||||
| chr16:68872309
|
C | CT | 9 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(6): Show | 9 | HG01433.hp2 HG02922.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.995-2835dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68872309 | |||||
| chr16:68872323
|
G | A | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.995-2831G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872323 | ||||||
| chr16:68872619
|
T | A | 3 | a0001c0003t0001g0130a0001c0003t0001g0134a0001c0003t0007g0127 | 3 | HG01346.hp2 HG01975.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.995-2535T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872619 | ||||||
| chr16:68872666
|
AT | A | 58 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(55): Show |
intron_variant | MODIFIER | c.995-2472delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68872666 | |||||
| chr16:68872666
|
ATT | A | 14 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(11): Show | 14 | HG02040.hp2 HG02135.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.995-2473_995-2472d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68872666 | |||||
| chr16:68872782
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-2372C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872782 | ||||||
| chr16:68872874
|
T | A | 33 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(30): Show | 33 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.995-2280T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872874 | ||||||
| chr16:68872918
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.995-2236G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68872918 | ||||||
| chr16:68873068
|
G | A | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.995-2086G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68873068 | ||||||
| chr16:68873416
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.995-1738C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68873416 | ||||||
| chr16:68873511
|
A | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.995-1643A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68873511 | ||||||
| chr16:68873533
|
C | CA | 55 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0032others(52): Show | 55 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.995-1618dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr16 | 68873533 | |||||
| chr16:68874184
|
A | G | 14 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.995-970A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68874184 | ||||||
| chr16:68874371
|
G | A | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-783G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68874371 | ||||||
| chr16:68874569
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.995-585G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68874569 | ||||||
| chr16:68874776
|
T | C | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.995-378T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 4/17 | chr16 | 68874776 | ||||||
| chr16:68875329
|
C | T | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1131+39C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68875329 | ||||||
| chr16:68875385
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1131+95G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68875385 | ||||||
| chr16:68875392
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1131+102A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68875392 | ||||||
| chr16:68875718
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1131+428G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68875718 | ||||||
| chr16:68875769
|
C | CA | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1131+494dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 68875769 | |||||
| chr16:68875769
|
C | CAA | 20 | a0001c0001t0001g0055a0001c0001t0001g0172a0001c0001t0001g0173others(17): Show | 20 | HG00544.hp1 HG01496.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1131+493_1131+494d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 68875769 | |||||
| chr16:68875840
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1131+550G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68875840 | ||||||
| chr16:68876152
|
C | A | 81 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1131+862C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68876152 | ||||||
| chr16:68876164
|
AT | A | 35 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(32): Show | 35 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1131+888delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 68876164 | |||||
| chr16:68876231
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1131+941G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68876231 | ||||||
| chr16:68876322
|
C | G | 1 | a0001c0003t0002g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1131+1032C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68876322 | ||||||
| chr16:68876711
|
C | T | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1132-1407C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68876711 | ||||||
| chr16:68876753
|
A | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(2): Show | 5 | HG02040.hp2 HG02135.hp2 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-1365A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68876753 | ||||||
| chr16:68876934
|
T | C | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1132-1184T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68876934 | ||||||
| chr16:68877338
|
T | C | 81 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1132-780T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877338 | ||||||
| chr16:68877446
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1132-672C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877446 | ||||||
| chr16:68877467
|
CA | C | 81 | a0001c0001t0001g0043a0001c0001t0001g0098a0001c0001t0001g0120others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1132-635delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 68877467 | |||||
| chr16:68877587
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1132-531T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877587 | ||||||
| chr16:68877647
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1132-471G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877647 | ||||||
| chr16:68877669
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG01433.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-449G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877669 | ||||||
| chr16:68877678
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1132-440G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877678 | ||||||
| chr16:68877768
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1132-350C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877768 | ||||||
| chr16:68877859
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0023 | 2 | HG02738.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1132-259C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877859 | ||||||
| chr16:68877860
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1132-258G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877860 | ||||||
| chr16:68877903
|
C | T | 1 | a0003c0004t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1132-215C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877903 | ||||||
| chr16:68877914
|
T | A | 74 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0121others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1132-204T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877914 | ||||||
| chr16:68877921
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1132-197A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 5/17 | chr16 | 68877921 | ||||||
| chr16:68878618
|
GA | G | 29 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(26): Show | 29 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1294+343delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr16 | 68878618 | |||||
| chr16:68878674
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1294+394A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68878674 | ||||||
| chr16:68878802
|
G | T | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294+522G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68878802 | ||||||
| chr16:68878867
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1294+587G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68878867 | ||||||
| chr16:68878918
|
G | A | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1294+638G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68878918 | ||||||
| chr16:68879073
|
C | A | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1294+793C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879073 | ||||||
| chr16:68879156
|
T | A | 14 | a0001c0001t0001g0109a0001c0003t0001g0124a0001c0003t0001g0125others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.1294+876T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879156 | ||||||
| chr16:68879323
|
A | C | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294+1043A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879323 | ||||||
| chr16:68879343
|
C | T | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1294+1063C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879343 | ||||||
| chr16:68879430
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1295-1118C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879430 | ||||||
| chr16:68879619
|
C | CT | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0003t0001g0194others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1295-913dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr16 | 68879619 | |||||
| chr16:68879619
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1295-929C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879619 | ||||||
| chr16:68879619
|
CTT | C | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1295-914_1295-913d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr16 | 68879619 | |||||
| chr16:68879678
|
A | C | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1295-870A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879678 | ||||||
| chr16:68879752
|
G | T | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1295-796G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879752 | ||||||
| chr16:68879773
|
CG | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1295-774delG | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879773 | ||||||
| chr16:68879839
|
G | A | 74 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0055others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1295-709G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879839 | ||||||
| chr16:68879959
|
A | G | 6 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295-589A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68879959 | ||||||
| chr16:68880176
|
A | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0055others(20): Show | 23 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.1295-372A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68880176 | ||||||
| chr16:68880250
|
T | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1295-298T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | chr16 | 68880250 | ||||||
| chr16:68880341
|
C | CATAAA | 17 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0055others(14): Show | 17 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1295-202_1295-198d others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr16 | 68880341 | |||||
| chr16:68880762
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1377+132C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68880762 | ||||||
| chr16:68880812
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+182G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68880812 | ||||||
| chr16:68880866
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1377+236G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68880866 | ||||||
| chr16:68881018
|
G | A | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377+388G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881018 | ||||||
| chr16:68881240
|
A | G | 13 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(10): Show | 13 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377+610A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881240 | ||||||
| chr16:68881369
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1377+739C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881369 | ||||||
| chr16:68881396
|
C | T | 29 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(26): Show | 29 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1377+766C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881396 | ||||||
| chr16:68881420
|
A | T | 29 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(26): Show | 29 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1377+790A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881420 | ||||||
| chr16:68881492
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1377+862G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881492 | ||||||
| chr16:68881513
|
CCAAA | C | 9 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(6): Show | 9 | HG02040.hp2 HG02135.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1377+896_1377+899d others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68881513 | |||||
| chr16:68881600
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+970A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881600 | ||||||
| chr16:68881799
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+1169G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881799 | ||||||
| chr16:68881863
|
T | G | 1 | a0001c0003t0001g0131 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1377+1233T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881863 | ||||||
| chr16:68881889
|
A | C | 1 | a0001c0002t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1377+1259A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881889 | ||||||
| chr16:68881921
|
A | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0198a0001c0001t0001g0200 | 3 | HG02027.hp1 NA18612.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1377+1291A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881921 | ||||||
| chr16:68881938
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+1308G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68881938 | ||||||
| chr16:68882178
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+1548G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882178 | ||||||
| chr16:68882214
|
A | G | 4 | a0001c0003t0001g0194a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377+1584A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882214 | ||||||
| chr16:68882215
|
G | C | 44 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0120others(41): Show | 44 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1377+1585G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882215 | ||||||
| chr16:68882278
|
C | T | 17 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0173others(14): Show | 17 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1377+1648C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882278 | ||||||
| chr16:68882366
|
A | G | 24 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0001g0098others(21): Show | 24 | HG00408.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1377+1736A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882366 | ||||||
| chr16:68882429
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1377+1799A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882429 | ||||||
| chr16:68882463
|
C | G | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1377+1833C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882463 | ||||||
| chr16:68882496
|
C | CA | 13 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0183others(10): Show | 13 | HG00544.hp1 HG01952.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.1377+1879dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68882496 | |||||
| chr16:68882506
|
A | G | 1 | a0001c0002t0001g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1377+1876A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882506 | ||||||
| chr16:68882597
|
C | T | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1377+1967C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882597 | ||||||
| chr16:68882725
|
T | TA | 45 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0049others(42): Show | 45 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1377+2106dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68882725 | |||||
| chr16:68882725
|
TA | T | 10 | a0001c0003t0001g0124a0001c0003t0001g0125a0001c0003t0001g0126others(7): Show | 10 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.1377+2106delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68882725 | |||||
| chr16:68882879
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+2249G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882879 | ||||||
| chr16:68882882
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1377+2252G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68882882 | ||||||
| chr16:68883542
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(2): Show | 5 | HG01433.hp2 HG02922.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+2912G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68883542 | ||||||
| chr16:68883752
|
C | T | 27 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(24): Show | 27 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1377+3122C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68883752 | ||||||
| chr16:68883762
|
T | A | 30 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 30 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1377+3132T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68883762 | ||||||
| chr16:68884159
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+3529C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68884159 | ||||||
| chr16:68884331
|
A | G | 27 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(24): Show | 27 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.1377+3701A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68884331 | ||||||
| chr16:68884501
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+3871G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68884501 | ||||||
| chr16:68884562
|
T | C | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+3932T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68884562 | ||||||
| chr16:68884564
|
G | A | 9 | a0001c0003t0001g0124a0001c0003t0001g0126a0001c0003t0001g0128others(6): Show | 9 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377+3934G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68884564 | ||||||
| chr16:68884656
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1377+4026T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68884656 | ||||||
| chr16:68885094
|
T | C | 32 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1377+4464T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68885094 | ||||||
| chr16:68885379
|
T | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+4749T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68885379 | ||||||
| chr16:68885425
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1377+4795G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68885425 | ||||||
| chr16:68885656
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1377+5026T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68885656 | ||||||
| chr16:68885927
|
T | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377+5297T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68885927 | ||||||
| chr16:68886313
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1377+5683G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68886313 | ||||||
| chr16:68886377
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1377+5747C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68886377 | ||||||
| chr16:68886408
|
GT | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1377+5781delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68886408 | |||||
| chr16:68886699
|
C | T | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1377+6069C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68886699 | ||||||
| chr16:68886878
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1377+6248G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68886878 | ||||||
| chr16:68887043
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0198a0001c0001t0001g0200 | 3 | HG02027.hp1 NA18612.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1377+6413G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68887043 | ||||||
| chr16:68887500
|
T | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+6870T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68887500 | ||||||
| chr16:68887572
|
A | G | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0153others(2): Show | 5 | HG00099.hp2 HG00738.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+6942A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68887572 | ||||||
| chr16:68887902
|
C | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1377+7272C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68887902 | ||||||
| chr16:68887983
|
G | A | 1 | a0001c0003t0001g0126 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1377+7353G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68887983 | ||||||
| chr16:68888218
|
A | G | 2 | a0003c0004t0001g0151a0003c0004t0001g0164 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1377+7588A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68888218 | ||||||
| chr16:68888317
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01255.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1377+7687G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68888317 | ||||||
| chr16:68888570
|
A | G | 5 | a0002c0005t0001g0162a0002c0005t0001g0163a0002c0005t0006g0137others(2): Show | 5 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+7940A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68888570 | ||||||
| chr16:68888869
|
G | C | 5 | a0002c0005t0001g0162a0002c0005t0001g0163a0002c0005t0006g0137others(2): Show | 5 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+8239G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68888869 | ||||||
| chr16:68888873
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1377+8243C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68888873 | ||||||
| chr16:68889038
|
G | T | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1377+8408G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68889038 | ||||||
| chr16:68889129
|
CTT | C | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1377+8501_1377+850 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68889129 | |||||
| chr16:68889272
|
C | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1377+8642C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68889272 | ||||||
| chr16:68889273
|
G | A | 6 | a0001c0001t0001g0114a0002c0005t0001g0162a0002c0005t0001g0163others(3): Show | 6 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+8643G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68889273 | ||||||
| chr16:68889297
|
T | C | 7 | a0001c0001t0001g0114a0002c0005t0001g0002a0002c0005t0001g0162others(4): Show | 7 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377+8667T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68889297 | ||||||
| chr16:68889470
|
A | G | 6 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0088others(3): Show | 6 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+8840A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68889470 | ||||||
| chr16:68889628
|
C | T | 22 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(19): Show | 22 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1377+8998C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68889628 | ||||||
| chr16:68890299
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1377+9669G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890299 | ||||||
| chr16:68890406
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1377+9776C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890406 | ||||||
| chr16:68890424
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1377+9794C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890424 | ||||||
| chr16:68890442
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1377+9812G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890442 | ||||||
| chr16:68890598
|
T | C | 86 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(83): Show | 86 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1378-9836T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890598 | ||||||
| chr16:68890653
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1378-9781G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890653 | ||||||
| chr16:68890778
|
T | C | 27 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(24): Show | 27 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.1378-9656T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890778 | ||||||
| chr16:68890956
|
C | T | 7 | a0001c0001t0001g0114a0002c0005t0001g0002a0002c0005t0001g0162others(4): Show | 7 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378-9478C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68890956 | ||||||
| chr16:68891189
|
A | G | 86 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(83): Show | 86 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1378-9245A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891189 | ||||||
| chr16:68891261
|
C | G | 5 | a0002c0005t0001g0162a0002c0005t0001g0163a0002c0005t0006g0137others(2): Show | 5 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-9173C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891261 | ||||||
| chr16:68891292
|
C | CA | 39 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0040others(36): Show | 39 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1378-9125dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68891292 | |||||
| chr16:68891292
|
C | CAA | 33 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0154others(30): Show | 33 | HG00738.hp2 HG01081.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1378-9126_1378-912 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68891292 | |||||
| chr16:68891349
|
A | C | 27 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(24): Show | 27 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.1378-9085A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891349 | ||||||
| chr16:68891350
|
C | T | 27 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(24): Show | 27 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.1378-9084C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891350 | ||||||
| chr16:68891352
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1378-9082C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891352 | ||||||
| chr16:68891409
|
A | G | 86 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(83): Show | 86 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1378-9025A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891409 | ||||||
| chr16:68891472
|
AAAAG | A | 5 | a0002c0005t0001g0162a0002c0005t0001g0163a0002c0005t0006g0137others(2): Show | 5 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-8950_1378-894 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68891472 | |||||
| chr16:68891503
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0095 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1378-8931C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891503 | ||||||
| chr16:68891668
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1378-8766C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891668 | ||||||
| chr16:68891706
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1378-8728C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891706 | ||||||
| chr16:68891800
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1378-8634A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891800 | ||||||
| chr16:68891817
|
C | G | 7 | a0001c0001t0001g0114a0002c0005t0001g0002a0002c0005t0001g0162others(4): Show | 7 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378-8617C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891817 | ||||||
| chr16:68891833
|
G | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1378-8601G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891833 | ||||||
| chr16:68891837
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1378-8597A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891837 | ||||||
| chr16:68891879
|
AGAGGGAG others(5): Show |
A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1378-8544_1378-853 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68891879 | |||||
| chr16:68891914
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-8520G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68891914 | ||||||
| chr16:68892320
|
T | C | 8 | a0001c0001t0001g0114a0001c0001t0001g0165a0002c0005t0001g0002others(5): Show | 8 | HG02486.hp1 HG02976.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378-8114T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68892320 | ||||||
| chr16:68892511
|
C | CT | 18 | a0001c0001t0001g0045a0001c0001t0001g0140a0001c0001t0001g0141others(15): Show | 18 | HG01891.hp2 HG01928.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1378-7907dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68892511 | |||||
| chr16:68892511
|
C | CTT | 19 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(16): Show | 19 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1378-7908_1378-790 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68892511 | |||||
| chr16:68892601
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(58): Show | 61 | HG00140.hp2 HG00438.hp2 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.1378-7833G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68892601 | ||||||
| chr16:68892806
|
C | T | 6 | a0001c0001t0001g0165a0002c0005t0001g0162a0002c0005t0001g0163others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378-7628C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68892806 | ||||||
| chr16:68893564
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1378-6870C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68893564 | ||||||
| chr16:68893715
|
G | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1378-6719G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68893715 | ||||||
| chr16:68893728
|
T | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1378-6706T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68893728 | ||||||
| chr16:68893735
|
C | CA | 79 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(76): Show | 79 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.1378-6687dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68893735 | |||||
| chr16:68893735
|
C | CAA | 5 | a0001c0001t0001g0198a0003c0004t0001g0151a0003c0004t0001g0164others(2): Show | 5 | HG02027.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-6688_1378-668 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68893735 | |||||
| chr16:68893757
|
C | CAA | 5 | a0001c0001t0001g0165a0002c0005t0001g0162a0002c0005t0001g0163others(2): Show | 5 | HG02486.hp1 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-6661_1378-666 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68893757 | |||||
| chr16:68893779
|
A | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1378-6655A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68893779 | ||||||
| chr16:68893802
|
T | C | 9 | a0001c0003t0001g0124a0001c0003t0001g0126a0001c0003t0001g0128others(6): Show | 9 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378-6632T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68893802 | ||||||
| chr16:68893978
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0034 | 2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1378-6456T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68893978 | ||||||
| chr16:68894201
|
C | G | 7 | a0001c0001t0001g0114a0001c0001t0001g0165a0002c0005t0001g0162others(4): Show | 7 | HG02486.hp1 HG02976.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378-6233C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68894201 | ||||||
| chr16:68894249
|
G | A | 19 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(16): Show | 19 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1378-6185G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68894249 | ||||||
| chr16:68894572
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1378-5862G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68894572 | ||||||
| chr16:68894665
|
G | A | 8 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(5): Show | 8 | HG01891.hp2 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378-5769G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68894665 | ||||||
| chr16:68894696
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1378-5738G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68894696 | ||||||
| chr16:68895106
|
T | G | 27 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(24): Show | 27 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.1378-5328T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895106 | ||||||
| chr16:68895139
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1378-5295T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895139 | ||||||
| chr16:68895156
|
G | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1378-5278G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895156 | ||||||
| chr16:68895242
|
G | A | 51 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(48): Show | 51 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.1378-5192G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895242 | ||||||
| chr16:68895276
|
A | G | 86 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(83): Show | 86 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(83): Show |
intron_variant | MODIFIER | c.1378-5158A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895276 | ||||||
| chr16:68895361
|
T | C | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1378-5073T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895361 | ||||||
| chr16:68895495
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1378-4939T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895495 | ||||||
| chr16:68895620
|
T | G | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1378-4814T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895620 | ||||||
| chr16:68895646
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG02486.hp2 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-4788A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895646 | ||||||
| chr16:68895687
|
G | A | 24 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(21): Show | 24 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1378-4747G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895687 | ||||||
| chr16:68895823
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1378-4611A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895823 | ||||||
| chr16:68895917
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1378-4517T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895917 | ||||||
| chr16:68895939
|
A | T | 7 | a0001c0001t0001g0114a0002c0005t0001g0002a0002c0005t0001g0162others(4): Show | 7 | HG02976.hp2 HG03225.hp2 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1378-4495A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895939 | ||||||
| chr16:68895944
|
T | A | 3 | a0001c0002t0001g0074a0001c0008t0001g0112a0001c0008t0001g0119 | 3 | HG02717.hp1 HG03540.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1378-4490T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895944 | ||||||
| chr16:68895949
|
T | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1378-4485T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68895949 | ||||||
| chr16:68895971
|
C | CAGTGTCT others(20): Show |
13 | a0001c0001t0001g0059a0001c0002t0001g0118a0001c0003t0001g0124others(10): Show | 13 | HG00438.hp2 HG01081.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378-4404_1378-437 others(31): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68895971 | |||||
| chr16:68895971
|
CAGTGTCT others(20): Show |
C | 1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1378-4404_1378-437 others(31): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68895971 | |||||
| chr16:68896340
|
TA | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1378-4093delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68896340 | ||||||
| chr16:68896577
|
G | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG01433.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-3857G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68896577 | ||||||
| chr16:68896685
|
A | G | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-3749A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68896685 | ||||||
| chr16:68896972
|
C | T | 6 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(3): Show | 6 | HG01433.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378-3462C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68896972 | ||||||
| chr16:68897147
|
C | T | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1378-3287C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897147 | ||||||
| chr16:68897519
|
C | T | 13 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378-2915C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897519 | ||||||
| chr16:68897574
|
A | G | 1 | a0001c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1378-2860A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897574 | ||||||
| chr16:68897806
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1378-2628A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897806 | ||||||
| chr16:68897824
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1378-2610C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897824 | ||||||
| chr16:68897856
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0049 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1378-2578G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897856 | ||||||
| chr16:68897947
|
T | G | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1378-2487T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897947 | ||||||
| chr16:68897953
|
G | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1378-2481G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68897953 | ||||||
| chr16:68898065
|
T | A | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1378-2369T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898065 | ||||||
| chr16:68898083
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1378-2351C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898083 | ||||||
| chr16:68898194
|
A | G | 87 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(84): Show | 87 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.1378-2240A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898194 | ||||||
| chr16:68898210
|
C | T | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1378-2224C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898210 | ||||||
| chr16:68898372
|
A | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(63): Show | 66 | HG00140.hp2 HG00438.hp2 HG01081.hp1 others(63): Show |
intron_variant | MODIFIER | c.1378-2062A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898372 | ||||||
| chr16:68898384
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1378-2050A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898384 | ||||||
| chr16:68898639
|
C | T | 15 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(12): Show | 15 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1378-1795C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68898639 | ||||||
| chr16:68898946
|
C | CTTA | 69 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 69 | HG00140.hp2 HG00438.hp2 HG01192.hp1 others(66): Show |
intron_variant | MODIFIER | c.1378-1455_1378-145 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68898946 | |||||
| chr16:68898946
|
C | CTTATTA | 24 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0049others(21): Show | 24 | HG01081.hp1 HG01192.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1378-1458_1378-145 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68898946 | |||||
| chr16:68898946
|
CTTA | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1378-1455_1378-145 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68898946 | |||||
| chr16:68898946
|
CTTATTA | C | 46 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(43): Show | 46 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1378-1458_1378-145 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68898946 | |||||
| chr16:68898946
|
CTTATTAT others(5): Show |
C | 19 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1378-1464_1378-145 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68898946 | |||||
| chr16:68899033
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-1401G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899033 | ||||||
| chr16:68899379
|
G | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1378-1055G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899379 | ||||||
| chr16:68899422
|
A | G | 21 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0121others(18): Show | 21 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1378-1012A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899422 | ||||||
| chr16:68899426
|
G | A | 1 | a0001c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1378-1008G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899426 | ||||||
| chr16:68899505
|
C | CT | 9 | a0001c0001t0001g0011a0001c0001t0001g0121a0001c0001t0001g0122others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1378-915dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68899505 | |||||
| chr16:68899505
|
CT | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0034others(2): Show | 5 | HG02615.hp2 NA18939.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-915delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 68899505 | |||||
| chr16:68899513
|
T | C | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1378-921T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899513 | ||||||
| chr16:68899632
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0008g0030 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1378-802C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899632 | ||||||
| chr16:68899655
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1378-779A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899655 | ||||||
| chr16:68899671
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1378-763C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899671 | ||||||
| chr16:68899727
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-707G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899727 | ||||||
| chr16:68899731
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1378-703T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 7/17 | chr16 | 68899731 | ||||||
| chr16:68900634
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1490+88C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68900634 | ||||||
| chr16:68900710
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1490+164C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68900710 | ||||||
| chr16:68900735
|
T | C | 8 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0153others(5): Show | 8 | HG00099.hp2 HG00738.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1490+189T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68900735 | ||||||
| chr16:68900805
|
A | G | 9 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0001g0208others(6): Show | 9 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1490+259A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68900805 | ||||||
| chr16:68901254
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.1490+708C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68901254 | ||||||
| chr16:68901500
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1491-828T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68901500 | ||||||
| chr16:68901557
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1491-771C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68901557 | ||||||
| chr16:68901574
|
T | C | 73 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(70): Show | 73 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.1491-754T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68901574 | ||||||
| chr16:68901629
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1491-699T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68901629 | ||||||
| chr16:68901650
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1491-678G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68901650 | ||||||
| chr16:68902049
|
C | CA | 10 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0105others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1491-259dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr16 | 68902049 | |||||
| chr16:68902049
|
CA | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0173others(2): Show | 5 | HG02572.hp2 HG02615.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491-259delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr16 | 68902049 | |||||
| chr16:68902079
|
G | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1491-249G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68902079 | ||||||
| chr16:68902180
|
T | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1491-148T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68902180 | ||||||
| chr16:68902266
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1491-62G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 8/17 | chr16 | 68902266 | ||||||
| chr16:68903238
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1667+734C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68903238 | ||||||
| chr16:68903615
|
C | CA | 28 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0121others(25): Show | 28 | HG01891.hp2 HG02055.hp1 HG02257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1667+1131dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68903615 | |||||
| chr16:68903615
|
C | CAA | 38 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(35): Show | 38 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.1667+1130_1667+113 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68903615 | |||||
| chr16:68903703
|
C | T | 66 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(63): Show | 66 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(63): Show |
intron_variant | MODIFIER | c.1667+1199C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68903703 | ||||||
| chr16:68903881
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1667+1377C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68903881 | ||||||
| chr16:68904077
|
T | C | 1 | a0001c0002t0001g0004 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1667+1573T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904077 | ||||||
| chr16:68904164
|
T | A | 3 | a0001c0001t0001g0114a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02976.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1667+1660T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904164 | ||||||
| chr16:68904278
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0111 | 2 | HG03927.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1667+1774G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904278 | ||||||
| chr16:68904402
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1667+1898A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904402 | ||||||
| chr16:68904447
|
A | C | 15 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0140others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1667+1943A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904447 | ||||||
| chr16:68904613
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1667+2109C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904613 | ||||||
| chr16:68904989
|
G | A | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1668-2454G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68904989 | ||||||
| chr16:68905007
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1668-2436G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905007 | ||||||
| chr16:68905066
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1668-2377T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905066 | ||||||
| chr16:68905079
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1668-2364G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905079 | ||||||
| chr16:68905144
|
T | C | 78 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(75): Show | 78 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.1668-2299T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905144 | ||||||
| chr16:68905169
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1668-2274G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905169 | ||||||
| chr16:68905212
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1668-2231A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905212 | ||||||
| chr16:68905261
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1668-2182C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905261 | ||||||
| chr16:68905343
|
C | G | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1668-2100C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905343 | ||||||
| chr16:68905495
|
C | T | 1 | a0001c0003t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1668-1948C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905495 | ||||||
| chr16:68905602
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1668-1841C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905602 | ||||||
| chr16:68905604
|
T | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1668-1839T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905604 | ||||||
| chr16:68905947
|
G | A | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1668-1496G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68905947 | ||||||
| chr16:68906043
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1668-1400G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906043 | ||||||
| chr16:68906053
|
G | A | 4 | a0001c0002t0001g0065a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | HG00408.hp1 NA18939.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668-1390G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906053 | ||||||
| chr16:68906097
|
T | C | 5 | a0001c0001t0001g0165a0002c0005t0001g0162a0002c0005t0001g0163others(2): Show | 5 | HG02486.hp1 HG02976.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-1346T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906097 | ||||||
| chr16:68906330
|
A | G | 1 | a0001c0002t0001g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1668-1113A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906330 | ||||||
| chr16:68906398
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1668-1045A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906398 | ||||||
| chr16:68906781
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1668-662A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906781 | ||||||
| chr16:68906792
|
C | CT | 7 | a0001c0001t0001g0023a0001c0001t0001g0082a0001c0001t0001g0110others(4): Show | 7 | HG01192.hp2 HG01496.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668-633dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68906792 | |||||
| chr16:68906792
|
CT | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0029others(66): Show | 69 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.1668-633delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68906792 | |||||
| chr16:68906795
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1668-648T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906795 | ||||||
| chr16:68906984
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1668-459G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68906984 | ||||||
| chr16:68907099
|
A | AT | 46 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(43): Show | 46 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1668-323dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68907099 | |||||
| chr16:68907099
|
A | ATT | 22 | a0001c0001t0001g0121a0001c0001t0001g0153a0001c0001t0001g0156others(19): Show | 22 | HG00099.hp2 HG00738.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1668-324_1668-323d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68907099 | |||||
| chr16:68907099
|
A | ATTTT | 19 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0040others(16): Show | 19 | HG00544.hp1 HG00741.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.1668-326_1668-323d others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68907099 | |||||
| chr16:68907099
|
AT | A | 5 | a0001c0001t0001g0165a0002c0005t0001g0162a0002c0005t0001g0163others(2): Show | 5 | HG02486.hp1 HG02976.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668-323delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr16 | 68907099 | |||||
| chr16:68907156
|
C | T | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0161others(7): Show | 10 | HG02055.hp1 HG02486.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1668-287C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68907156 | ||||||
| chr16:68907296
|
C | T | 6 | a0001c0001t0001g0165a0002c0005t0001g0002a0002c0005t0001g0162others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.1668-147C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68907296 | ||||||
| chr16:68907370
|
A | C | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1668-73A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 9/17 | chr16 | 68907370 | ||||||
| chr16:68907747
|
A | C | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1800+172A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68907747 | ||||||
| chr16:68908081
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1800+506T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68908081 | ||||||
| chr16:68908156
|
G | C | 4 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0008t0001g0112others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1800+581G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68908156 | ||||||
| chr16:68908208
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1800+633G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68908208 | ||||||
| chr16:68908520
|
CA | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1801-681delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr16 | 68908520 | |||||
| chr16:68908687
|
A | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG03654.hp2 HG03704.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1801-524A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68908687 | ||||||
| chr16:68908967
|
A | T | 1 | a0001c0002t0001g0079 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1801-244A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68908967 | ||||||
| chr16:68909066
|
A | G | 5 | a0002c0005t0001g0002a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1801-145A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 10/17 | chr16 | 68909066 | ||||||
| chr16:68909767
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1992+365A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68909767 | ||||||
| chr16:68909787
|
G | A | 1 | a0003c0004t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1992+385G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68909787 | ||||||
| chr16:68909807
|
A | G | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1992+405A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68909807 | ||||||
| chr16:68909968
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1992+566A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68909968 | ||||||
| chr16:68910716
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1992+1314G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68910716 | ||||||
| chr16:68910738
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1992+1336G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68910738 | ||||||
| chr16:68910741
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1992+1339G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68910741 | ||||||
| chr16:68910743
|
C | G | 32 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.1992+1341C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68910743 | ||||||
| chr16:68910864
|
A | G | 24 | a0001c0001t0001g0008a0001c0001t0001g0204a0001c0001t0001g0207others(21): Show | 24 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1992+1462A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68910864 | ||||||
| chr16:68910942
|
G | T | 31 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(28): Show | 31 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1992+1540G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68910942 | ||||||
| chr16:68911266
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1992+1864A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68911266 | ||||||
| chr16:68911415
|
C | CT | 5 | a0001c0008t0001g0112a0001c0008t0001g0119a0002c0005t0001g0162others(2): Show | 5 | HG02717.hp1 HG03540.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1992+2031dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68911415 | |||||
| chr16:68911415
|
CT | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0149a0001c0001t0001g0154others(3): Show | 6 | HG00738.hp2 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1992+2031delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68911415 | |||||
| chr16:68911416
|
T | C | 22 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(19): Show | 22 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1992+2014T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68911416 | ||||||
| chr16:68911422
|
T | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1992+2020T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68911422 | ||||||
| chr16:68911455
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1992+2053G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68911455 | ||||||
| chr16:68911783
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1992+2381C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68911783 | ||||||
| chr16:68912211
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1992+2809G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912211 | ||||||
| chr16:68912236
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1992+2834G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912236 | ||||||
| chr16:68912276
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1992+2874T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912276 | ||||||
| chr16:68912311
|
A | T | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1992+2909A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912311 | ||||||
| chr16:68912314
|
A | G | 9 | a0001c0001t0001g0008a0001c0003t0001g0124a0001c0003t0001g0128others(6): Show | 9 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1992+2912A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912314 | ||||||
| chr16:68912506
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01975.hp2 HG02040.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1992+3104G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912506 | ||||||
| chr16:68912634
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1992+3232C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912634 | ||||||
| chr16:68912794
|
G | A | 9 | a0001c0001t0001g0008a0001c0003t0001g0124a0001c0003t0001g0128others(6): Show | 9 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1992+3392G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912794 | ||||||
| chr16:68912852
|
G | A | 1 | a0001c0002t0001g0089 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1992+3450G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912852 | ||||||
| chr16:68912911
|
C | CA | 6 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0045others(3): Show | 6 | HG01884.hp2 HG01928.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1992+3528dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68912911 | |||||
| chr16:68912911
|
CA | C | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(4): Show | 7 | HG02486.hp2 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1992+3528delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68912911 | |||||
| chr16:68912954
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0104 | 3 | HG02735.hp1 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1992+3552C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68912954 | ||||||
| chr16:68913035
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1992+3633G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913035 | ||||||
| chr16:68913040
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1992+3638A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913040 | ||||||
| chr16:68913073
|
C | CA | 7 | a0001c0001t0001g0040a0001c0001t0001g0063a0001c0001t0001g0085others(4): Show | 7 | HG01361.hp1 HG01981.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1992+3689dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68913073 | |||||
| chr16:68913089
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1992+3687A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913089 | ||||||
| chr16:68913091
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1992+3689A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913091 | ||||||
| chr16:68913157
|
A | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1992+3755A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913157 | ||||||
| chr16:68913262
|
T | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1992+3860T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913262 | ||||||
| chr16:68913404
|
A | AT | 15 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0023others(12): Show | 15 | HG00438.hp1 HG01099.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1992+4024dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68913404 | |||||
| chr16:68913404
|
AT | A | 51 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0024others(48): Show | 51 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.1992+4024delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68913404 | |||||
| chr16:68913404
|
ATT | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01975.hp1 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1992+4023_1992+402 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68913404 | |||||
| chr16:68913405
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1992+4003T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913405 | ||||||
| chr16:68913436
|
T | A | 1 | a0001c0001t0001g0007 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1992+4034T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913436 | ||||||
| chr16:68913465
|
G | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1992+4063G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913465 | ||||||
| chr16:68913470
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1992+4068G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913470 | ||||||
| chr16:68913479
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1992+4077G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913479 | ||||||
| chr16:68913531
|
C | A | 6 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0088others(3): Show | 6 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1992+4129C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913531 | ||||||
| chr16:68913686
|
G | C | 7 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1992+4284G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68913686 | ||||||
| chr16:68914191
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(202): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1992+4789T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914191 | ||||||
| chr16:68914305
|
G | A | 3 | a0001c0003t0001g0130a0001c0003t0001g0134a0001c0003t0007g0127 | 3 | HG01346.hp2 HG01975.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1993-4780G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914305 | ||||||
| chr16:68914318
|
T | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1993-4767T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914318 | ||||||
| chr16:68914353
|
T | G | 66 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(63): Show | 66 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(63): Show |
intron_variant | MODIFIER | c.1993-4732T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914353 | ||||||
| chr16:68914593
|
T | C | 9 | a0001c0001t0001g0008a0001c0003t0001g0124a0001c0003t0001g0128others(6): Show | 9 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993-4492T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914593 | ||||||
| chr16:68914748
|
A | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1993-4337A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914748 | ||||||
| chr16:68914878
|
G | GT | 57 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(54): Show | 57 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.1993-4194dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914878 | |||||
| chr16:68914879
|
T | G | 4 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0008t0001g0112others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1993-4206T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914879 | ||||||
| chr16:68914950
|
T | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1993-4135T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914950 | ||||||
| chr16:68914958
|
T | TAC | 24 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(21): Show | 24 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1993-4085_1993-408 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
T | TACAC | 16 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00408.hp2 HG01255.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1993-4087_1993-408 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
T | TACACAC | 4 | a0001c0001t0001g0005a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | HG00408.hp1 HG01192.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1993-4089_1993-408 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
T | TACACACA others(1): Show |
2 | a0001c0002t0001g0065a0001c0002t0001g0095 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1993-4091_1993-408 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
TAC | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0043others(27): Show | 30 | HG00140.hp2 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1993-4085_1993-408 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
TACAC | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0082others(4): Show | 7 | HG00438.hp2 HG01192.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1993-4087_1993-408 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
TACACAC | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0052 | 2 | HG03490.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1993-4089_1993-408 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
TACACACA others(3): Show |
T | 9 | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0141others(6): Show | 9 | HG02486.hp2 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993-4093_1993-408 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914958
|
TACACACA others(5): Show |
T | 46 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(43): Show | 46 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.1993-4095_1993-408 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68914958 | |||||
| chr16:68914994
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1993-4091C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68914994 | ||||||
| chr16:68915002
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1993-4083T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915002 | ||||||
| chr16:68915049
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1993-4036C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915049 | ||||||
| chr16:68915080
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0161 | 3 | HG02055.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1993-4005A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915080 | ||||||
| chr16:68915085
|
T | A | 58 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 58 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(55): Show |
intron_variant | MODIFIER | c.1993-4000T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915085 | ||||||
| chr16:68915099
|
G | A | 4 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0004g0202others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1993-3986G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915099 | ||||||
| chr16:68915173
|
C | CA | 9 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0121others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993-3893dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68915173 | |||||
| chr16:68915173
|
CA | C | 59 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(56): Show | 59 | HG00544.hp1 HG00741.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1993-3893delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68915173 | |||||
| chr16:68915236
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0047 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1993-3849G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915236 | ||||||
| chr16:68915834
|
C | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0094 | 2 | HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1993-3251C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915834 | ||||||
| chr16:68915994
|
G | T | 2 | a0003c0004t0001g0151a0003c0004t0001g0164 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1993-3091G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68915994 | ||||||
| chr16:68916245
|
C | T | 35 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(32): Show | 35 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.1993-2840C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68916245 | ||||||
| chr16:68916420
|
A | G | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1993-2665A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68916420 | ||||||
| chr16:68916484
|
G | A | 2 | a0001c0003t0001g0128a0001c0003t0001g0132 | 2 | NA18968.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1993-2601G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68916484 | ||||||
| chr16:68916857
|
C | G | 40 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(37): Show | 40 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-2228C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68916857 | ||||||
| chr16:68917147
|
G | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(37): Show | 40 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-1938G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68917147 | ||||||
| chr16:68917205
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1993-1880T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68917205 | ||||||
| chr16:68917238
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993-1847T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68917238 | ||||||
| chr16:68917919
|
A | AT | 17 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0045others(14): Show | 17 | HG01081.hp2 HG01346.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.1993-1148dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68917919 | |||||
| chr16:68917919
|
A | ATT | 49 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(46): Show | 49 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.1993-1149_1993-114 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68917919 | |||||
| chr16:68918188
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1993-897G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918188 | ||||||
| chr16:68918365
|
G | A | 40 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(37): Show | 40 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-720G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918365 | ||||||
| chr16:68918395
|
G | A | 1 | a0004c0006t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1993-690G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918395 | ||||||
| chr16:68918506
|
G | A | 1 | a0001c0002t0001g0090 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1993-579G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918506 | ||||||
| chr16:68918660
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1993-425A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918660 | ||||||
| chr16:68918697
|
GATA | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1993-384_1993-382d others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68918697 | |||||
| chr16:68918731
|
A | C | 1 | a0001c0003t0002g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1993-354A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918731 | ||||||
| chr16:68918805
|
G | C | 1 | a0001c0003t0002g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1993-280G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68918805 | ||||||
| chr16:68919036
|
A | AT | 40 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(37): Show | 40 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.1993-38dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr16 | 68919036 | |||||
| chr16:68919081
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.1993-4G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 11/17 | chr16 | 68919081 | ||||||
| chr16:68919267
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2127+48G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919267 | ||||||
| chr16:68919290
|
A | G | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2127+71A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919290 | ||||||
| chr16:68919338
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2127+119A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919338 | ||||||
| chr16:68919406
|
C | T | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2127+187C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919406 | ||||||
| chr16:68919464
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2127+245A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919464 | ||||||
| chr16:68919486
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2127+267C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919486 | ||||||
| chr16:68919508
|
G | A | 5 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163others(2): Show | 5 | HG02976.hp2 HG03834.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2127+289G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919508 | ||||||
| chr16:68919760
|
C | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2127+541C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919760 | ||||||
| chr16:68919763
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2127+544G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919763 | ||||||
| chr16:68919889
|
T | TA | 20 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(17): Show | 20 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.2127+678dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68919889 | |||||
| chr16:68919890
|
A | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2127+671A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919890 | ||||||
| chr16:68919916
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG00438.hp2 HG02027.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.2127+697G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919916 | ||||||
| chr16:68919940
|
G | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2127+721G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68919940 | ||||||
| chr16:68920018
|
G | A | 1 | a0006c0010t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2127+799G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920018 | ||||||
| chr16:68920075
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2127+856A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920075 | ||||||
| chr16:68920532
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2127+1313G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920532 | ||||||
| chr16:68920619
|
C | A | 1 | a0006c0010t0001g0206 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2127+1400C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920619 | ||||||
| chr16:68920620
|
C | T | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2127+1401C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920620 | ||||||
| chr16:68920672
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2127+1453G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920672 | ||||||
| chr16:68920891
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2127+1672A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68920891 | ||||||
| chr16:68921049
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2127+1830G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921049 | ||||||
| chr16:68921051
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2127+1832G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921051 | ||||||
| chr16:68921074
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2127+1855G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921074 | ||||||
| chr16:68921118
|
C | CA | 23 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(20): Show | 23 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(20): Show |
intron_variant | MODIFIER | c.2127+1919dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68921118 | |||||
| chr16:68921118
|
C | CAA | 27 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(24): Show | 27 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2127+1918_2127+191 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68921118 | |||||
| chr16:68921118
|
C | CAAA | 5 | a0001c0001t0001g0100a0001c0001t0001g0140a0001c0001t0001g0198others(2): Show | 5 | HG01361.hp2 HG02027.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2127+1917_2127+191 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68921118 | |||||
| chr16:68921430
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2127+2211C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921430 | ||||||
| chr16:68921545
|
GTTTTGTT others(3): Show |
G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2127+2332_2127+234 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68921545 | |||||
| chr16:68921550
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2127+2331G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921550 | ||||||
| chr16:68921555
|
T | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2127+2336T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921555 | ||||||
| chr16:68921607
|
C | CT | 48 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(45): Show | 48 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.2127+2410dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68921607 | |||||
| chr16:68921607
|
C | CTT | 14 | a0001c0001t0001g0029a0001c0001t0001g0158a0001c0001t0001g0167others(11): Show | 14 | HG01175.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2127+2409_2127+241 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68921607 | |||||
| chr16:68921651
|
T | C | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2127+2432T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68921651 | ||||||
| chr16:68922405
|
G | A | 2 | a0001c0001t0001g0114a0005c0011t0001g0148 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2127+3186G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68922405 | ||||||
| chr16:68922561
|
TA | T | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2127+3353delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68922561 | |||||
| chr16:68922722
|
A | G | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2127+3503A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68922722 | ||||||
| chr16:68922818
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2127+3599C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68922818 | ||||||
| chr16:68922831
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2127+3612C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68922831 | ||||||
| chr16:68922939
|
G | GT | 22 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0021others(19): Show | 22 | HG00438.hp2 HG01891.hp1 HG01981.hp1 others(19): Show |
intron_variant | MODIFIER | c.2127+3747dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68922939 | |||||
| chr16:68922939
|
G | GTT | 27 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0040others(24): Show | 27 | HG00741.hp1 HG01081.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2127+3746_2127+374 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68922939 | |||||
| chr16:68922939
|
G | GTTT | 22 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0029others(19): Show | 22 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2127+3745_2127+374 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68922939 | |||||
| chr16:68922939
|
G | GTTTT | 6 | a0001c0001t0001g0122a0001c0001t0001g0141a0001c0001t0001g0167others(3): Show | 6 | HG02280.hp1 HG02965.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2127+3744_2127+374 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68922939 | |||||
| chr16:68922950
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2127+3731T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68922950 | ||||||
| chr16:68923121
|
AT | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2127+3916delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68923121 | |||||
| chr16:68923381
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2127+4162A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68923381 | ||||||
| chr16:68923537
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG01975.hp2 HG02040.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2128-4031G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68923537 | ||||||
| chr16:68923800
|
A | ATTTGT | 16 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0015others(13): Show | 16 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(13): Show |
intron_variant | MODIFIER | c.2128-3729_2128-372 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68923800 | |||||
| chr16:68923800
|
A | ATTTGTTT others(3): Show |
5 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0101others(2): Show | 5 | HG02735.hp1 HG03239.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2128-3734_2128-372 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68923800 | |||||
| chr16:68923800
|
ATTTGT | A | 14 | a0001c0001t0001g0027a0001c0001t0001g0056a0001c0001t0001g0057others(11): Show | 14 | HG00140.hp1 HG00741.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2128-3729_2128-372 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68923800 | |||||
| chr16:68923800
|
ATTTGTTT others(8): Show |
A | 64 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(61): Show | 64 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2128-3739_2128-372 others(19): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68923800 | |||||
| chr16:68923834
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2128-3734G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68923834 | ||||||
| chr16:68924193
|
C | CT | 66 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(63): Show | 66 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.2128-3371dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68924193 | |||||
| chr16:68924273
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2128-3295G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924273 | ||||||
| chr16:68924301
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2128-3267G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924301 | ||||||
| chr16:68924332
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2128-3236G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924332 | ||||||
| chr16:68924505
|
C | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2128-3063C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924505 | ||||||
| chr16:68924524
|
A | G | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2128-3044A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924524 | ||||||
| chr16:68924620
|
T | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2128-2948T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924620 | ||||||
| chr16:68924705
|
G | A | 4 | a0001c0001t0001g0115a0001c0007t0001g0036a0001c0007t0001g0038others(1): Show | 4 | HG02300.hp1 HG03239.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.2128-2863G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924705 | ||||||
| chr16:68924799
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2128-2769G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924799 | ||||||
| chr16:68924810
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2128-2758C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924810 | ||||||
| chr16:68924811
|
A | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2128-2757A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924811 | ||||||
| chr16:68924827
|
T | C | 1 | a0001c0007t0001g0036 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2128-2741T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68924827 | ||||||
| chr16:68925048
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2128-2520C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925048 | ||||||
| chr16:68925056
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2128-2512A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925056 | ||||||
| chr16:68925068
|
T | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2128-2500T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925068 | ||||||
| chr16:68925086
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(2): Show | 5 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2128-2482G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925086 | ||||||
| chr16:68925120
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2128-2448C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925120 | ||||||
| chr16:68925175
|
G | C | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2128-2393G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925175 | ||||||
| chr16:68925241
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.2128-2327T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925241 | ||||||
| chr16:68925380
|
A | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2128-2188A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925380 | ||||||
| chr16:68925570
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2128-1998A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925570 | ||||||
| chr16:68925676
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2128-1892G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925676 | ||||||
| chr16:68925677
|
G | T | 6 | a0001c0001t0001g0165a0002c0005t0001g0002a0002c0005t0001g0162others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.2128-1891G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68925677 | ||||||
| chr16:68925867
|
G | GTCTT | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(153): Show | 156 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.2128-1699_2128-169 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68925867 | |||||
| chr16:68925894
|
T | TA | 10 | a0001c0001t0001g0015a0001c0001t0001g0120a0001c0001t0001g0149others(7): Show | 10 | HG00738.hp2 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2128-1660dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68925894 | |||||
| chr16:68926076
|
AT | A | 53 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 53 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.2128-1490delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr16 | 68926076 | |||||
| chr16:68926078
|
T | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2128-1490T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926078 | ||||||
| chr16:68926079
|
A | G | 53 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 53 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.2128-1489A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926079 | ||||||
| chr16:68926124
|
A | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2128-1444A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926124 | ||||||
| chr16:68926151
|
C | A | 53 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 53 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.2128-1417C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926151 | ||||||
| chr16:68926160
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2128-1408G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926160 | ||||||
| chr16:68926322
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2128-1246C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926322 | ||||||
| chr16:68926430
|
G | A | 1 | a0004c0006t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2128-1138G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926430 | ||||||
| chr16:68926589
|
G | A | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2128-979G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926589 | ||||||
| chr16:68926603
|
C | T | 1 | a0001c0002t0001g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2128-965C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926603 | ||||||
| chr16:68926631
|
G | A | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2128-937G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926631 | ||||||
| chr16:68926659
|
C | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2128-909C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926659 | ||||||
| chr16:68926751
|
A | G | 1 | a0001c0003t0007g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2128-817A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926751 | ||||||
| chr16:68926861
|
C | G | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2128-707C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926861 | ||||||
| chr16:68926944
|
G | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2128-624G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68926944 | ||||||
| chr16:68927001
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2128-567A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927001 | ||||||
| chr16:68927079
|
T | C | 53 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 53 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.2128-489T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927079 | ||||||
| chr16:68927105
|
A | C | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2128-463A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927105 | ||||||
| chr16:68927122
|
C | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2128-446C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927122 | ||||||
| chr16:68927293
|
T | A | 1 | a0001c0003t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2128-275T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927293 | ||||||
| chr16:68927333
|
T | A | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2128-235T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927333 | ||||||
| chr16:68927433
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2128-135A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927433 | ||||||
| chr16:68927443
|
C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2128-125C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 12/17 | chr16 | 68927443 | ||||||
| chr16:68928298
|
A | AT | 29 | a0001c0001t0001g0049a0001c0001t0001g0106a0001c0001t0001g0107others(26): Show | 29 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.2643+239dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 68928298 | |||||
| chr16:68928298
|
A | ATT | 22 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 22 | HG01258.hp2 HG01884.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.2643+238_2643+239d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 68928298 | |||||
| chr16:68928298
|
A | ATTT | 64 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.2643+237_2643+239d others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 68928298 | |||||
| chr16:68928298
|
A | ATTTT | 5 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0053others(2): Show | 5 | HG01099.hp2 HG01928.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2643+236_2643+239d others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 68928298 | |||||
| chr16:68928298
|
AT | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2643+239delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr16 | 68928298 | |||||
| chr16:68928353
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2643+270G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928353 | ||||||
| chr16:68928596
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.2643+513A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928596 | ||||||
| chr16:68928607
|
T | C | 1 | a0003c0004t0004g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2643+524T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928607 | ||||||
| chr16:68928644
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2643+561A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928644 | ||||||
| chr16:68928920
|
T | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.2643+837T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928920 | ||||||
| chr16:68928982
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0048others(2): Show | 5 | HG01081.hp1 HG01257.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2643+899G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928982 | ||||||
| chr16:68928999
|
A | C | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2643+916A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68928999 | ||||||
| chr16:68929846
|
A | G | 14 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(11): Show | 14 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2644-392A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68929846 | ||||||
| chr16:68929957
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2644-281T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68929957 | ||||||
| chr16:68929985
|
G | C | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2644-253G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 13/17 | chr16 | 68929985 | ||||||
| chr16:68930542
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2701+247G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930542 | ||||||
| chr16:68930570
|
G | A | 1 | a0001c0002t0001g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2701+275G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930570 | ||||||
| chr16:68930581
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2701+286T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930581 | ||||||
| chr16:68930635
|
C | CT | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(15): Show | 18 | HG00738.hp2 HG01891.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.2701+358dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68930635 | |||||
| chr16:68930635
|
CT | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0077a0001c0001t0001g0141others(2): Show | 5 | HG02723.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2701+358delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68930635 | |||||
| chr16:68930717
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2701+422C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930717 | ||||||
| chr16:68930785
|
G | A | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2701+490G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930785 | ||||||
| chr16:68930792
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2701+497C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930792 | ||||||
| chr16:68930856
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2701+561C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930856 | ||||||
| chr16:68930904
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0001t0008g0030 | 3 | HG01884.hp2 HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+609T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930904 | ||||||
| chr16:68930905
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+610G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68930905 | ||||||
| chr16:68931010
|
C | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(80): Show | 83 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2701+715C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68931010 | ||||||
| chr16:68931206
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2701+911A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68931206 | ||||||
| chr16:68931335
|
C | A | 53 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(50): Show | 53 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(50): Show |
intron_variant | MODIFIER | c.2701+1040C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68931335 | ||||||
| chr16:68931399
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2701+1104C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68931399 | ||||||
| chr16:68931894
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2701+1599G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68931894 | ||||||
| chr16:68931916
|
A | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.2701+1621A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68931916 | ||||||
| chr16:68932095
|
A | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG00140.hp1 HG02486.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2701+1800A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932095 | ||||||
| chr16:68932125
|
T | G | 23 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(20): Show | 23 | HG01081.hp2 HG01346.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.2701+1830T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932125 | ||||||
| chr16:68932155
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2701+1860A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932155 | ||||||
| chr16:68932184
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2701+1889G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932184 | ||||||
| chr16:68932215
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2701+1920C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932215 | ||||||
| chr16:68932219
|
T | G | 3 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2701+1924T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932219 | ||||||
| chr16:68932343
|
G | GGCCT | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2701+2049_2701+205 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68932343 | |||||
| chr16:68932503
|
A | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(57): Show | 60 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.2701+2208A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932503 | ||||||
| chr16:68932505
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(2): Show | 5 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2701+2210C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932505 | ||||||
| chr16:68932785
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0034 | 2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2701+2490G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932785 | ||||||
| chr16:68932991
|
T | G | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2701+2696T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68932991 | ||||||
| chr16:68933041
|
C | T | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2701+2746C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68933041 | ||||||
| chr16:68933188
|
T | G | 58 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(55): Show | 58 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.2701+2893T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68933188 | ||||||
| chr16:68933387
|
C | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2701+3092C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68933387 | ||||||
| chr16:68933722
|
T | C | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2701+3427T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68933722 | ||||||
| chr16:68934005
|
G | A | 2 | a0001c0003t0001g0128a0001c0003t0001g0132 | 2 | NA18968.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2701+3710G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68934005 | ||||||
| chr16:68934041
|
A | AT | 10 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0121others(7): Show | 10 | HG01361.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2701+3764dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68934041 | |||||
| chr16:68934041
|
AT | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG00099.hp2 HG00738.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.2701+3764delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68934041 | |||||
| chr16:68934093
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2701+3798A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68934093 | ||||||
| chr16:68934138
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+3843G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68934138 | ||||||
| chr16:68934157
|
G | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2701+3862G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68934157 | ||||||
| chr16:68934447
|
A | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.2701+4152A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68934447 | ||||||
| chr16:68934567
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0098 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2701+4272G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68934567 | ||||||
| chr16:68935009
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2701+4714G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68935009 | ||||||
| chr16:68935511
|
C | T | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2701+5216C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68935511 | ||||||
| chr16:68935657
|
T | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(42): Show | 45 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.2701+5362T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68935657 | ||||||
| chr16:68936771
|
T | G | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2701+6476T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68936771 | ||||||
| chr16:68936810
|
T | TA | 27 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(24): Show | 27 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2701+6527dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68936810 | |||||
| chr16:68936810
|
TA | T | 8 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2701+6527delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68936810 | |||||
| chr16:68937072
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.2701+6777T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937072 | ||||||
| chr16:68937156
|
G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(42): Show | 45 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.2701+6861G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937156 | ||||||
| chr16:68937396
|
T | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2701+7101T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937396 | ||||||
| chr16:68937671
|
T | G | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2701+7376T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937671 | ||||||
| chr16:68937839
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2701+7544G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937839 | ||||||
| chr16:68937841
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+7546A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937841 | ||||||
| chr16:68937884
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2701+7589T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937884 | ||||||
| chr16:68937912
|
G | C | 1 | a0001c0001t0001g0209 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2701+7617G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937912 | ||||||
| chr16:68937961
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2701+7666G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937961 | ||||||
| chr16:68937990
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+7695A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68937990 | ||||||
| chr16:68938107
|
TTGTC | T | 11 | a0001c0001t0001g0010a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2701+7818_2701+782 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68938107 | |||||
| chr16:68938825
|
G | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2701+8530G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68938825 | ||||||
| chr16:68939072
|
C | CA | 11 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0031others(8): Show | 11 | HG01192.hp1 HG01884.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.2701+8796dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68939072 | |||||
| chr16:68939577
|
A | AT | 11 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0063others(8): Show | 11 | HG01255.hp1 HG01361.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.2701+9300dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68939577 | |||||
| chr16:68939577
|
AT | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.2701+9300delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68939577 | |||||
| chr16:68939577
|
ATT | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0141others(8): Show | 11 | HG02055.hp1 HG02630.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2701+9299_2701+930 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68939577 | |||||
| chr16:68939577
|
ATTT | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(11): Show | 14 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2701+9298_2701+930 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68939577 | |||||
| chr16:68939599
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2701+9304A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68939599 | ||||||
| chr16:68939604
|
G | A | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2701+9309G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68939604 | ||||||
| chr16:68939615
|
T | C | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2701+9320T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68939615 | ||||||
| chr16:68939813
|
T | G | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2701+9518T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68939813 | ||||||
| chr16:68940004
|
A | AT | 26 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(23): Show | 26 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.2701+9716dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940004 | |||||
| chr16:68940011
|
T | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2701+9716T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68940011 | ||||||
| chr16:68940080
|
T | TTC | 3 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156 | 3 | HG00099.hp2 HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2701+9798_2701+979 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940080 | |||||
| chr16:68940090
|
C | T | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2701+9795C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68940090 | ||||||
| chr16:68940166
|
T | C | 3 | a0001c0002t0001g0068a0001c0002t0001g0070a0001c0002t0001g0071 | 3 | HG01981.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2701+9871T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68940166 | ||||||
| chr16:68940166
|
TCTTC | T | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2701+9888_2701+989 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940166 | |||||
| chr16:68940586
|
T | TTGGTGAA others(307): Show |
1 | a0003c0004t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2701+10304_2701+10 others(320): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(310): Show |
3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2701+10304_2701+10 others(323): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(314): Show |
3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2701+10304_2701+10 others(327): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(317): Show |
2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2701+10304_2701+10 others(330): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(319): Show |
5 | a0003c0004t0004g0202a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2701+10304_2701+10 others(332): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(320): Show |
1 | a0003c0004t0004g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2701+10304_2701+10 others(333): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(339): Show |
1 | a0003c0004t0001g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2701+10304_2701+10 others(352): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940586
|
T | TTGGTGAA others(340): Show |
1 | a0003c0004t0001g0164 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2701+10304_2701+10 others(353): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68940586 | |||||
| chr16:68940698
|
T | C | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2701+10403T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68940698 | ||||||
| chr16:68941081
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+10786G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68941081 | ||||||
| chr16:68941196
|
G | T | 1 | a0001c0002t0001g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2701+10901G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68941196 | ||||||
| chr16:68941714
|
A | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2701+11419A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68941714 | ||||||
| chr16:68941824
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+11529A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68941824 | ||||||
| chr16:68942015
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+11720C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942015 | ||||||
| chr16:68942562
|
A | G | 6 | a0001c0001t0001g0165a0002c0005t0001g0002a0002c0005t0001g0162others(3): Show | 6 | HG02486.hp1 HG02976.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.2701+12267A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942562 | ||||||
| chr16:68942612
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2701+12317G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942612 | ||||||
| chr16:68942686
|
C | A | 1 | a0001c0002t0001g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2701+12391C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942686 | ||||||
| chr16:68942770
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2701+12475A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942770 | ||||||
| chr16:68942902
|
AT | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0032others(26): Show | 29 | HG00741.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.2701+12624delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68942902 | |||||
| chr16:68942902
|
ATT | A | 16 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(13): Show | 16 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2701+12623_2701+12 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68942902 | |||||
| chr16:68942911
|
T | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2701+12616T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942911 | ||||||
| chr16:68942912
|
T | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2701+12617T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942912 | ||||||
| chr16:68942935
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2701+12640T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68942935 | ||||||
| chr16:68943020
|
A | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(42): Show | 45 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.2701+12725A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943020 | ||||||
| chr16:68943264
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2701+12969T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943264 | ||||||
| chr16:68943363
|
A | AT | 6 | a0001c0001t0001g0023a0001c0001t0001g0094a0001c0001t0001g0116others(3): Show | 6 | HG02040.hp2 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2701+13086dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68943363 | |||||
| chr16:68943363
|
AT | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0032others(20): Show | 23 | HG00741.hp2 HG01346.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.2701+13086delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68943363 | |||||
| chr16:68943378
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+13083T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943378 | ||||||
| chr16:68943488
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2701+13193C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943488 | ||||||
| chr16:68943512
|
T | C | 1 | a0001c0003t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2701+13217T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943512 | ||||||
| chr16:68943513
|
G | A | 1 | a0001c0003t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2701+13218G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943513 | ||||||
| chr16:68943703
|
C | T | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2701+13408C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943703 | ||||||
| chr16:68943739
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2701+13444T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943739 | ||||||
| chr16:68943812
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2701+13517G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943812 | ||||||
| chr16:68943855
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2701+13560G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68943855 | ||||||
| chr16:68944403
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2701+14108C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68944403 | ||||||
| chr16:68944523
|
C | T | 17 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(14): Show | 17 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2701+14228C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68944523 | ||||||
| chr16:68944786
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+14491C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68944786 | ||||||
| chr16:68945108
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(85): Show | 88 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.2701+14813T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945108 | ||||||
| chr16:68945278
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2701+14983G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945278 | ||||||
| chr16:68945327
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+15032G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945327 | ||||||
| chr16:68945494
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2701+15199A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945494 | ||||||
| chr16:68945515
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(25): Show | 28 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.2701+15220A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945515 | ||||||
| chr16:68945625
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2701+15330T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945625 | ||||||
| chr16:68945660
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2701+15365C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945660 | ||||||
| chr16:68945667
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2701+15372G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945667 | ||||||
| chr16:68945906
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+15611G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945906 | ||||||
| chr16:68945938
|
G | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2701+15643G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945938 | ||||||
| chr16:68945977
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2701+15682G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68945977 | ||||||
| chr16:68946196
|
CT | C | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2701+15914delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68946196 | |||||
| chr16:68946254
|
C | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2701+15959C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946254 | ||||||
| chr16:68946278
|
G | A | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2701+15983G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946278 | ||||||
| chr16:68946316
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2701+16021C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946316 | ||||||
| chr16:68946320
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2701+16025T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946320 | ||||||
| chr16:68946474
|
G | A | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2701+16179G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946474 | ||||||
| chr16:68946516
|
G | C | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2701+16221G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946516 | ||||||
| chr16:68946721
|
G | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2701+16426G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946721 | ||||||
| chr16:68946724
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2701+16429A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946724 | ||||||
| chr16:68946967
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0094 | 2 | HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2701+16672G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68946967 | ||||||
| chr16:68947166
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2701+16871A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947166 | ||||||
| chr16:68947196
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2701+16901G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947196 | ||||||
| chr16:68947311
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0047 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2701+17016A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947311 | ||||||
| chr16:68947507
|
A | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2701+17212A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947507 | ||||||
| chr16:68947582
|
C | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2701+17287C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947582 | ||||||
| chr16:68947587
|
C | CT | 19 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.2701+17314dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68947587 | |||||
| chr16:68947587
|
CT | C | 21 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0051others(18): Show | 21 | HG01099.hp2 HG01255.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2701+17314delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68947587 | |||||
| chr16:68947608
|
T | C | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2701+17313T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947608 | ||||||
| chr16:68947623
|
C | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2701+17328C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947623 | ||||||
| chr16:68947673
|
G | A | 1 | a0004c0006t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2701+17378G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947673 | ||||||
| chr16:68947887
|
C | G | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2701+17592C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947887 | ||||||
| chr16:68947949
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2701+17654G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68947949 | ||||||
| chr16:68948024
|
G | GAT | 22 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0034others(19): Show | 22 | HG01258.hp2 HG01433.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.2701+17746_2701+17 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948024
|
G | GATAT | 11 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0121others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2701+17744_2701+17 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948024
|
G | GATATAT | 5 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2701+17742_2701+17 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948024
|
G | GATATATA others(1): Show |
6 | a0001c0001t0001g0029a0001c0001t0001g0047a0001c0001t0001g0141others(3): Show | 6 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2701+17740_2701+17 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948024
|
G | GATATATA others(3): Show |
4 | a0001c0001t0001g0024a0001c0001t0001g0186a0001c0001t0001g0198others(1): Show | 4 | HG02027.hp1 HG02040.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+17738_2701+17 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948024
|
G | GATATATA others(5): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | NA18957.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2701+17736_2701+17 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948024
|
G | GATATATA others(7): Show |
1 | a0001c0001t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2701+17734_2701+17 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68948024 | |||||
| chr16:68948155
|
C | G | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2701+17860C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68948155 | ||||||
| chr16:68948542
|
C | G | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2701+18247C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68948542 | ||||||
| chr16:68949106
|
A | C | 3 | a0001c0002t0001g0068a0001c0002t0001g0070a0001c0002t0001g0071 | 3 | HG01981.hp2 HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2701+18811A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68949106 | ||||||
| chr16:68949274
|
A | G | 12 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2701+18979A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68949274 | ||||||
| chr16:68949546
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(78): Show | 81 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.2701+19251G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68949546 | ||||||
| chr16:68949685
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2701+19390G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68949685 | ||||||
| chr16:68949833
|
T | TTA | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2701+19551_2701+19 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68949833 | |||||
| chr16:68949889
|
A | G | 3 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2701+19594A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68949889 | ||||||
| chr16:68949902
|
G | A | 25 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(22): Show | 25 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.2701+19607G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68949902 | ||||||
| chr16:68950513
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0008t0001g0112others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+20218C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68950513 | ||||||
| chr16:68950588
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0045 | 2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2701+20293C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68950588 | ||||||
| chr16:68950701
|
G | A | 36 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(33): Show | 36 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.2701+20406G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68950701 | ||||||
| chr16:68950791
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2701+20496G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68950791 | ||||||
| chr16:68950794
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2701+20499G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68950794 | ||||||
| chr16:68950983
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2701+20688G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68950983 | ||||||
| chr16:68951156
|
C | A | 1 | a0001c0001t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2701+20861C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951156 | ||||||
| chr16:68951242
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2701+20947G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951242 | ||||||
| chr16:68951254
|
T | C | 3 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2701+20959T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951254 | ||||||
| chr16:68951337
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2701+21042G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951337 | ||||||
| chr16:68951344
|
T | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(22): Show | 25 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.2701+21049T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951344 | ||||||
| chr16:68951517
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(50): Show | 53 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.2701+21222C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951517 | ||||||
| chr16:68951612
|
C | CT | 14 | a0001c0001t0001g0082a0001c0001t0001g0107a0001c0001t0001g0120others(11): Show | 14 | HG00738.hp1 HG01192.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2701+21335dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68951612 | |||||
| chr16:68951612
|
CT | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2701+21335delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68951612 | |||||
| chr16:68951927
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+21632G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951927 | ||||||
| chr16:68951976
|
A | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2701+21681A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68951976 | ||||||
| chr16:68952542
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2702-21486A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68952542 | ||||||
| chr16:68952601
|
A | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-21427A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68952601 | ||||||
| chr16:68952686
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2702-21342T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68952686 | ||||||
| chr16:68952975
|
T | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(34): Show | 37 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2702-21053T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68952975 | ||||||
| chr16:68952978
|
T | A | 3 | a0001c0002t0001g0076a0001c0002t0001g0078a0001c0002t0001g0079 | 3 | NA18982.hp2 NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2702-21050T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68952978 | ||||||
| chr16:68953050
|
T | TTTA | 11 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0045others(8): Show | 11 | HG01496.hp1 HG01928.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.2702-20939_2702-20 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTATTA | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.2702-20942_2702-20 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTATTAT others(2): Show |
38 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0021others(35): Show | 38 | HG00438.hp2 HG00738.hp2 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.2702-20945_2702-20 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTATTAT others(5): Show |
6 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0002t0001g0108others(3): Show | 6 | HG02004.hp1 HG02738.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.2702-20948_2702-20 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTATTAT others(8): Show |
1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2702-20951_2702-20 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTTTTA | 5 | a0001c0001t0001g0048a0001c0003t0001g0124a0001c0003t0001g0130others(2): Show | 5 | HG01346.hp2 HG01975.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2702-20976_2702-20 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTTTTAT others(2): Show |
7 | a0001c0001t0001g0190a0001c0003t0001g0128a0001c0003t0001g0132others(4): Show | 7 | HG03041.hp1 HG03225.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2702-20976_2702-20 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
T | TTTTTTAT others(11): Show |
1 | a0001c0003t0001g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2702-20976_2702-20 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
TTTA | T | 57 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0032others(54): Show | 57 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.2702-20939_2702-20 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
TTTATTA | T | 8 | a0001c0001t0001g0047a0001c0001t0001g0114a0001c0001t0001g0161others(5): Show | 8 | HG00741.hp2 HG01891.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2702-20942_2702-20 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
TTTATTAT others(2): Show |
T | 17 | a0001c0001t0001g0010a0001c0001t0001g0105a0001c0001t0001g0121others(14): Show | 17 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2702-20945_2702-20 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953050
|
TTTATTAT others(5): Show |
T | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2702-20948_2702-20 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68953050 | |||||
| chr16:68953056
|
A | T | 1 | a0003c0004t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2702-20972A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68953056 | ||||||
| chr16:68953279
|
C | A | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2702-20749C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68953279 | ||||||
| chr16:68953865
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2702-20163G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68953865 | ||||||
| chr16:68953885
|
A | G | 41 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(38): Show | 41 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2702-20143A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68953885 | ||||||
| chr16:68954092
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2702-19936A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954092 | ||||||
| chr16:68954107
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-19921G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954107 | ||||||
| chr16:68954120
|
T | C | 52 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(49): Show | 52 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.2702-19908T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954120 | ||||||
| chr16:68954249
|
C | CA | 22 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(19): Show | 22 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2702-19760dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68954249 | |||||
| chr16:68954249
|
C | CAA | 12 | a0001c0001t0001g0208a0001c0001t0008g0030a0001c0003t0002g0195others(9): Show | 12 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-19761_2702-19 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68954249 | |||||
| chr16:68954249
|
C | CAAA | 15 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2702-19762_2702-19 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68954249 | |||||
| chr16:68954515
|
GA | G | 25 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(22): Show | 25 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.2702-19504delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68954515 | |||||
| chr16:68954571
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2702-19457T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954571 | ||||||
| chr16:68954588
|
T | C | 1 | a0001c0002t0001g0004 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2702-19440T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954588 | ||||||
| chr16:68954601
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2702-19427A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954601 | ||||||
| chr16:68954647
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2702-19381T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954647 | ||||||
| chr16:68954683
|
T | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-19345T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954683 | ||||||
| chr16:68954776
|
A | G | 12 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-19252A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954776 | ||||||
| chr16:68954806
|
T | C | 12 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-19222T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954806 | ||||||
| chr16:68954938
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2702-19090C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68954938 | ||||||
| chr16:68955002
|
T | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(22): Show | 25 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.2702-19026T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68955002 | ||||||
| chr16:68955014
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2702-19014A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68955014 | ||||||
| chr16:68955337
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2702-18691A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68955337 | ||||||
| chr16:68955443
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | NA18957.hp1 NA18960.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2702-18585G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68955443 | ||||||
| chr16:68955530
|
G | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2702-18498G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68955530 | ||||||
| chr16:68955569
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2702-18459G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68955569 | ||||||
| chr16:68956157
|
AC | A | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2702-17870delC | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68956157 | ||||||
| chr16:68956186
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-17842A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68956186 | ||||||
| chr16:68956746
|
G | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-17282G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68956746 | ||||||
| chr16:68956908
|
G | A | 2 | a0001c0003t0001g0128a0001c0003t0001g0132 | 2 | NA18968.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2702-17120G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68956908 | ||||||
| chr16:68956918
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156 | 3 | HG00099.hp2 HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2702-17110T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68956918 | ||||||
| chr16:68957397
|
A | AT | 65 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0023others(62): Show | 65 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.2702-16613dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68957397 | |||||
| chr16:68957397
|
AT | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(43): Show | 46 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.2702-16613delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68957397 | |||||
| chr16:68957415
|
TG | T | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2702-16612delG | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68957415 | ||||||
| chr16:68957529
|
C | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0094 | 2 | HG01361.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2702-16499C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68957529 | ||||||
| chr16:68957819
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2702-16209A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68957819 | ||||||
| chr16:68957987
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2702-16041C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68957987 | ||||||
| chr16:68958171
|
C | CA | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2702-15845dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68958171 | |||||
| chr16:68958350
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2702-15678G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68958350 | ||||||
| chr16:68958454
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2702-15574A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68958454 | ||||||
| chr16:68958505
|
A | AAG | 43 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(40): Show | 43 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(40): Show |
intron_variant | MODIFIER | c.2702-15516_2702-15 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68958505 | |||||
| chr16:68958590
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2702-15438A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68958590 | ||||||
| chr16:68958877
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2702-15151G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68958877 | ||||||
| chr16:68959156
|
G | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-14872G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68959156 | ||||||
| chr16:68959244
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-14784A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68959244 | ||||||
| chr16:68959312
|
A | G | 49 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(46): Show | 49 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.2702-14716A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68959312 | ||||||
| chr16:68959444
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0048others(2): Show | 5 | HG01081.hp1 HG01257.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2702-14584G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68959444 | ||||||
| chr16:68959969
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2702-14059G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68959969 | ||||||
| chr16:68960009
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2702-14019G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960009 | ||||||
| chr16:68960154
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-13874C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960154 | ||||||
| chr16:68960161
|
C | T | 2 | a0001c0003t0001g0128a0001c0003t0001g0132 | 2 | NA18968.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2702-13867C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960161 | ||||||
| chr16:68960297
|
C | CT | 11 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(8): Show | 11 | HG01175.hp1 HG01175.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2702-13714dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68960297 | |||||
| chr16:68960297
|
CT | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0083a0001c0001t0001g0172others(3): Show | 6 | HG01891.hp2 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2702-13714delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68960297 | |||||
| chr16:68960324
|
C | T | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2702-13704C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960324 | ||||||
| chr16:68960411
|
C | T | 10 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(7): Show | 10 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2702-13617C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960411 | ||||||
| chr16:68960650
|
G | A | 1 | a0004c0006t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2702-13378G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960650 | ||||||
| chr16:68960854
|
G | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-13174G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68960854 | ||||||
| chr16:68961332
|
T | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-12696T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68961332 | ||||||
| chr16:68961334
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-12694C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68961334 | ||||||
| chr16:68961661
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2702-12367G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68961661 | ||||||
| chr16:68961725
|
A | G | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2702-12303A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68961725 | ||||||
| chr16:68961726
|
T | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2702-12302T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68961726 | ||||||
| chr16:68961807
|
C | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2702-12221C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68961807 | ||||||
| chr16:68962045
|
G | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2702-11983G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962045 | ||||||
| chr16:68962319
|
G | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(11): Show | 14 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2702-11709G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962319 | ||||||
| chr16:68962320
|
A | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(11): Show | 14 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2702-11708A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962320 | ||||||
| chr16:68962597
|
A | T | 1 | a0001c0003t0001g0126 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2702-11431A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962597 | ||||||
| chr16:68962728
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2702-11300A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962728 | ||||||
| chr16:68962803
|
C | T | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2702-11225C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962803 | ||||||
| chr16:68962804
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0034 | 2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2702-11224G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962804 | ||||||
| chr16:68962907
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2702-11121A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962907 | ||||||
| chr16:68962929
|
G | GA | 12 | a0001c0001t0001g0198a0001c0001t0003g0044a0001c0001t0008g0030others(9): Show | 12 | HG01361.hp2 HG01884.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-11084dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68962929 | |||||
| chr16:68962929
|
GA | G | 6 | a0001c0001t0001g0034a0001c0001t0001g0172a0001c0001t0001g0182others(3): Show | 6 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2702-11084delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68962929 | |||||
| chr16:68962967
|
G | T | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2702-11061G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68962967 | ||||||
| chr16:68963006
|
A | G | 1 | a0003c0004t0004g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2702-11022A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963006 | ||||||
| chr16:68963073
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2702-10955G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963073 | ||||||
| chr16:68963091
|
C | CA | 14 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0023others(11): Show | 14 | HG01192.hp1 HG01192.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.2702-10921dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68963091 | |||||
| chr16:68963091
|
C | CAA | 17 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0121others(14): Show | 17 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2702-10922_2702-10 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68963091 | |||||
| chr16:68963091
|
C | CAAA | 10 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(7): Show | 10 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.2702-10923_2702-10 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68963091 | |||||
| chr16:68963225
|
G | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-10803G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963225 | ||||||
| chr16:68963371
|
C | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2702-10657C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963371 | ||||||
| chr16:68963397
|
G | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2702-10631G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963397 | ||||||
| chr16:68963510
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2702-10518C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963510 | ||||||
| chr16:68963748
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2702-10280C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963748 | ||||||
| chr16:68963783
|
C | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(46): Show | 49 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.2702-10245C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963783 | ||||||
| chr16:68963788
|
A | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(46): Show | 49 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.2702-10240A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963788 | ||||||
| chr16:68963860
|
A | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-10168A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68963860 | ||||||
| chr16:68964201
|
T | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-9827T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68964201 | ||||||
| chr16:68964508
|
TA | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2702-9519delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68964508 | ||||||
| chr16:68964563
|
A | AT | 12 | a0001c0001t0001g0094a0001c0001t0001g0177a0001c0001t0001g0188others(9): Show | 12 | HG01346.hp2 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.2702-9444dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68964563 | |||||
| chr16:68964563
|
AT | A | 10 | a0001c0001t0001g0077a0001c0001t0001g0173a0001c0001t0001g0187others(7): Show | 10 | HG01433.hp2 HG01884.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2702-9444delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68964563 | |||||
| chr16:68964563
|
ATT | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-9445_2702-944 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68964563 | |||||
| chr16:68964591
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2702-9437G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68964591 | ||||||
| chr16:68964722
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2702-9306G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68964722 | ||||||
| chr16:68965154
|
T | TTTTG | 52 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(49): Show | 52 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.2702-8866_2702-886 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68965154 | |||||
| chr16:68965159
|
T | TTTGTTTT others(13): Show |
1 | a0001c0001t0001g0012 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2702-8868_2702-884 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68965159 | |||||
| chr16:68965418
|
G | A | 1 | a0001c0002t0001g0067 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2702-8610G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68965418 | ||||||
| chr16:68965420
|
A | T | 1 | a0001c0002t0001g0067 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2702-8608A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68965420 | ||||||
| chr16:68965711
|
A | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-8317A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68965711 | ||||||
| chr16:68965878
|
GTTTC | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-8147_2702-814 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68965878 | |||||
| chr16:68965950
|
G | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2702-8078G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68965950 | ||||||
| chr16:68965956
|
G | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0008t0001g0112others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-8072G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68965956 | ||||||
| chr16:68966028
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2702-8000T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966028 | ||||||
| chr16:68966204
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(16): Show | 19 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.2702-7824C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966204 | ||||||
| chr16:68966278
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2702-7750C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966278 | ||||||
| chr16:68966306
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-7722C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966306 | ||||||
| chr16:68966375
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0198a0001c0001t0001g0200 | 3 | HG02027.hp1 NA18612.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2702-7653G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966375 | ||||||
| chr16:68966381
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2702-7647A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966381 | ||||||
| chr16:68966513
|
T | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(42): Show | 45 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.2702-7515T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966513 | ||||||
| chr16:68966517
|
A | T | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2702-7511A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966517 | ||||||
| chr16:68966518
|
T | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2702-7510T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966518 | ||||||
| chr16:68966518
|
T | TA | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2702-7506dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68966518 | |||||
| chr16:68966685
|
C | T | 60 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0077others(57): Show | 60 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.2702-7343C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966685 | ||||||
| chr16:68966692
|
T | C | 3 | a0001c0001t0001g0165a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02486.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2702-7336T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966692 | ||||||
| chr16:68966770
|
A | AT | 20 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0023others(17): Show | 20 | HG00408.hp1 HG01099.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2702-7237dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68966770 | |||||
| chr16:68966770
|
A | ATT | 5 | a0001c0003t0002g0195a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2702-7238_2702-723 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68966770 | |||||
| chr16:68966770
|
AT | A | 39 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0025others(36): Show | 39 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.2702-7237delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68966770 | |||||
| chr16:68966770
|
ATT | A | 9 | a0001c0001t0001g0142a0001c0003t0001g0124a0001c0003t0001g0128others(6): Show | 9 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2702-7238_2702-723 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68966770 | |||||
| chr16:68966803
|
G | A | 1 | a0001c0003t0007g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2702-7225G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966803 | ||||||
| chr16:68966841
|
AGCTCACT others(8): Show |
A | 3 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0113 | 3 | NA18957.hp2 NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2702-7186_2702-717 others(19): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966841 | ||||||
| chr16:68966848
|
T | C | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2702-7180T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68966848 | ||||||
| chr16:68967223
|
C | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2702-6805C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68967223 | ||||||
| chr16:68967328
|
G | T | 4 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0008t0001g0112others(1): Show | 4 | HG01891.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-6700G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68967328 | ||||||
| chr16:68967722
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2702-6306T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68967722 | ||||||
| chr16:68967754
|
C | T | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2702-6274C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68967754 | ||||||
| chr16:68967818
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2702-6210C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68967818 | ||||||
| chr16:68968072
|
A | T | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2702-5956A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968072 | ||||||
| chr16:68968354
|
G | A | 4 | a0001c0003t0001g0130a0001c0003t0001g0134a0001c0003t0001g0136others(1): Show | 4 | HG01346.hp2 HG01975.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-5674G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968354 | ||||||
| chr16:68968616
|
C | G | 2 | a0001c0001t0001g0114a0005c0011t0001g0148 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2702-5412C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968616 | ||||||
| chr16:68968617
|
G | A | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2702-5411G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968617 | ||||||
| chr16:68968658
|
C | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00099.hp1 HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2702-5370C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968658 | ||||||
| chr16:68968669
|
A | AT | 23 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0045others(20): Show | 23 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2702-5340dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68968669 | |||||
| chr16:68968669
|
A | ATT | 9 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.2702-5341_2702-534 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68968669 | |||||
| chr16:68968669
|
A | ATTT | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2702-5342_2702-534 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68968669 | |||||
| chr16:68968669
|
AT | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0020others(3): Show | 6 | HG01257.hp1 HG01891.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.2702-5340delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68968669 | |||||
| chr16:68968860
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-5168C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968860 | ||||||
| chr16:68968871
|
T | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2702-5157T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968871 | ||||||
| chr16:68968873
|
G | T | 6 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(3): Show | 6 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2702-5155G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68968873 | ||||||
| chr16:68969074
|
T | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-4954T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969074 | ||||||
| chr16:68969084
|
A | G | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2702-4944A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969084 | ||||||
| chr16:68969146
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-4882A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969146 | ||||||
| chr16:68969302
|
C | T | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-4726C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969302 | ||||||
| chr16:68969363
|
C | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-4665C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969363 | ||||||
| chr16:68969389
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2702-4639A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969389 | ||||||
| chr16:68969689
|
CA | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2702-4325delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68969689 | |||||
| chr16:68969845
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2702-4183G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969845 | ||||||
| chr16:68969916
|
T | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2702-4112T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68969916 | ||||||
| chr16:68970663
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2702-3365G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68970663 | ||||||
| chr16:68970667
|
C | CA | 5 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(2): Show | 5 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.2702-3343dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68970667 | |||||
| chr16:68970667
|
CA | C | 162 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0010others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2702-3343delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr16 | 68970667 | |||||
| chr16:68970818
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2702-3210A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68970818 | ||||||
| chr16:68970867
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0111 | 2 | HG03927.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2702-3161G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68970867 | ||||||
| chr16:68970879
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2702-3149C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68970879 | ||||||
| chr16:68971057
|
G | A | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2702-2971G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68971057 | ||||||
| chr16:68971359
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2702-2669C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68971359 | ||||||
| chr16:68971444
|
A | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.2702-2584A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68971444 | ||||||
| chr16:68971553
|
G | T | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2702-2475G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68971553 | ||||||
| chr16:68971624
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2702-2404A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68971624 | ||||||
| chr16:68971967
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2702-2061A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68971967 | ||||||
| chr16:68972287
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-1741C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972287 | ||||||
| chr16:68972324
|
C | G | 2 | a0001c0001t0001g0114a0005c0011t0001g0148 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2702-1704C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972324 | ||||||
| chr16:68972447
|
T | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(48): Show | 51 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.2702-1581T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972447 | ||||||
| chr16:68972479
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2702-1549C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972479 | ||||||
| chr16:68972894
|
A | G | 65 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(62): Show | 65 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.2702-1134A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972894 | ||||||
| chr16:68972925
|
C | T | 1 | a0001c0002t0001g0065 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2702-1103C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972925 | ||||||
| chr16:68972926
|
G | A | 3 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2702-1102G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68972926 | ||||||
| chr16:68973085
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2702-943A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68973085 | ||||||
| chr16:68973943
|
C | T | 47 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(44): Show | 47 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.2702-85C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 14/17 | chr16 | 68973943 | ||||||
| chr16:68974328
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2842+160A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68974328 | ||||||
| chr16:68974427
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2842+259C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68974427 | ||||||
| chr16:68974523
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2842+355G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68974523 | ||||||
| chr16:68974828
|
G | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842+660G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68974828 | ||||||
| chr16:68975200
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2842+1032A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68975200 | ||||||
| chr16:68975503
|
G | A | 3 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2842+1335G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68975503 | ||||||
| chr16:68975616
|
G | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2842+1448G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68975616 | ||||||
| chr16:68975689
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2842+1521C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68975689 | ||||||
| chr16:68975705
|
A | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(33): Show | 36 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.2842+1537A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68975705 | ||||||
| chr16:68975821
|
T | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+1653T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68975821 | ||||||
| chr16:68976351
|
C | T | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2842+2183C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68976351 | ||||||
| chr16:68976752
|
G | A | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842+2584G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68976752 | ||||||
| chr16:68976878
|
AC | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2842+2711delC | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68976878 | ||||||
| chr16:68977140
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2842+2972A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68977140 | ||||||
| chr16:68977312
|
GT | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2842+3155delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68977312 | |||||
| chr16:68977482
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2842+3314G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68977482 | ||||||
| chr16:68977804
|
G | A | 1 | a0001c0003t0007g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2842+3636G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68977804 | ||||||
| chr16:68978131
|
A | G | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842+3963A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68978131 | ||||||
| chr16:68978205
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2842+4037G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68978205 | ||||||
| chr16:68978748
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0111 | 2 | HG03927.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2842+4580C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68978748 | ||||||
| chr16:68978817
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2842+4649G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68978817 | ||||||
| chr16:68978925
|
A | AT | 110 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.2842+4774dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68978925 | |||||
| chr16:68979074
|
C | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2842+4906C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979074 | ||||||
| chr16:68979113
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2842+4945G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979113 | ||||||
| chr16:68979215
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2842+5047C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979215 | ||||||
| chr16:68979778
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0111 | 2 | HG03927.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2842+5610A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979778 | ||||||
| chr16:68979831
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+5663A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979831 | ||||||
| chr16:68979846
|
C | CT | 11 | a0001c0001t0001g0023a0001c0001t0001g0145a0001c0001t0001g0192others(8): Show | 11 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+5694dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68979846 | |||||
| chr16:68979846
|
CT | C | 15 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(12): Show | 15 | HG01433.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2842+5694delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68979846 | |||||
| chr16:68979861
|
T | G | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2842+5693T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979861 | ||||||
| chr16:68979863
|
G | A | 66 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0062others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2842+5695G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979863 | ||||||
| chr16:68979875
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2842+5707C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979875 | ||||||
| chr16:68979931
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0045 | 2 | HG01928.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2842+5763G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68979931 | ||||||
| chr16:68980382
|
AT | A | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2842+6216delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980382 | |||||
| chr16:68980383
|
T | TC | 3 | a0001c0001t0001g0120a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG01433.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTC | 4 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTC | 5 | a0003c0004t0004g0202a0003c0004t0004g0203a0004c0006t0001g0179others(2): Show | 5 | HG02257.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(2): Show |
6 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0001g0161others(3): Show | 6 | HG02027.hp1 HG02965.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(13): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(4): Show |
8 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG02280.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(6): Show |
2 | a0001c0001t0001g0182a0001c0003t0001g0194 | 2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(17): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(8): Show |
2 | a0001c0001t0001g0140a0001c0001t0001g0157 | 2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(19): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(10): Show |
3 | a0001c0001t0001g0141a0001c0001t0001g0153a0001c0001t0001g0158 | 3 | HG00099.hp2 HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(12): Show |
2 | a0001c0001t0001g0156a0001c0001t0001g0160 | 2 | HG00738.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(23): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(14): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0142 | 2 | HG01192.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2842+6215_2842+621 others(25): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TCTCTCTC others(16): Show |
1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2842+6215_2842+621 others(27): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980383 | ||||||
| chr16:68980383
|
T | TTC | 6 | a0001c0001t0001g0052a0001c0001t0001g0054a0001c0001t0001g0058others(3): Show | 6 | HG00544.hp1 HG01928.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+6241_2842+624 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(3): Show |
6 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0097others(3): Show | 6 | HG00438.hp1 HG00544.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.2842+6233_2842+624 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(5): Show |
1 | a0001c0003t0001g0132 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2842+6231_2842+624 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(7): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0003t0001g0128others(1): Show | 4 | HG01081.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+6229_2842+624 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(9): Show |
8 | a0001c0001t0001g0063a0001c0002t0001g0072a0001c0002t0001g0089others(5): Show | 8 | HG01346.hp2 HG01361.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2842+6227_2842+624 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(11): Show |
3 | a0001c0001t0001g0094a0001c0002t0001g0073a0001c0003t0001g0131 | 3 | HG00140.hp1 HG00408.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2842+6225_2842+624 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(13): Show |
6 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0001t0001g0175others(3): Show | 6 | HG00099.hp1 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+6223_2842+624 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(15): Show |
7 | a0001c0001t0001g0012a0001c0001t0001g0066a0001c0001t0001g0083others(4): Show | 7 | HG00408.hp2 HG00741.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.2842+6221_2842+624 others(26): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(17): Show |
5 | a0001c0001t0001g0085a0001c0001t0001g0109a0001c0002t0001g0067others(2): Show | 5 | HG01099.hp1 HG01175.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+6219_2842+624 others(28): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(19): Show |
6 | a0001c0001t0001g0084a0001c0001t0001g0091a0001c0001t0001g0104others(3): Show | 6 | HG01496.hp2 HG01952.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+6217_2842+624 others(30): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(21): Show |
4 | a0001c0002t0001g0004a0001c0002t0001g0068a0001c0002t0001g0079others(1): Show | 4 | HG02129.hp1 HG02273.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(23): Show |
2 | a0001c0002t0001g0070a0001c0002t0001g0078 | 2 | HG02004.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(34): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(27): Show |
2 | a0001c0002t0001g0074a0001c0002t0001g0075 | 2 | NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(38): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(29): Show |
1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(40): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
T | TTCTCTCT others(33): Show |
1 | a0001c0002t0001g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(44): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980383
|
TTCTC | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0154a0001c0001t0001g0205others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+6239_2842+624 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980383 | |||||
| chr16:68980387
|
C | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2842+6219C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980387 | ||||||
| chr16:68980407
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2842+6239C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980407 | ||||||
| chr16:68980407
|
CTCTA | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(2): Show | 5 | HG02723.hp2 HG02895.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+6241_2842+624 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980407 | |||||
| chr16:68980409
|
C | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0017others(9): Show | 12 | HG01257.hp2 HG02300.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.2842+6241C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980409 | ||||||
| chr16:68980409
|
C | CTCTCTCT others(3): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0165 | 2 | HG02486.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(5): Show |
1 | a0001c0001t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(7): Show |
1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(9): Show |
1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(13): Show |
2 | a0001c0002t0001g0093a0002c0005t0001g0162 | 2 | HG03834.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(17): Show |
1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(28): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(19): Show |
1 | a0001c0001t0001g0077 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(30): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(21): Show |
1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0080a0001c0002t0001g0123 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(30): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(21): Show |
1 | a0001c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(23): Show |
1 | a0001c0001t0003g0044 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(34): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(21): Show |
1 | a0002c0005t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(23): Show |
2 | a0001c0002t0001g0071a0001c0002t0001g0076 | 2 | HG01981.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.2842+6242_2842+624 others(34): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
C | CTCTCTCT others(25): Show |
1 | a0001c0002t0001g0113 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2842+6242_2842+624 others(36): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980409
|
CTATA | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0020 | 2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2842+6265_2842+626 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980409 | |||||
| chr16:68980411
|
A | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.2842+6243A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980411 | ||||||
| chr16:68980412
|
T | TCTCTCTC others(18): Show |
1 | a0001c0001t0001g0190 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2842+6244_2842+624 others(29): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980412 | ||||||
| chr16:68980413
|
A | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0021others(31): Show | 34 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.2842+6245A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980413 | ||||||
| chr16:68980415
|
A | C | 12 | a0001c0001t0001g0083a0001c0001t0001g0087a0001c0001t0001g0097others(9): Show | 12 | HG00544.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.2842+6247A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980415 | ||||||
| chr16:68980417
|
A | C | 2 | a0003c0004t0001g0164a0003c0004t0001g0201 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2842+6249A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980417 | ||||||
| chr16:68980428
|
TATATATA | T | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2842+6261_2842+626 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980428 | ||||||
| chr16:68980431
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2842+6263A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980431 | ||||||
| chr16:68980433
|
A | AT | 3 | a0001c0001t0001g0100a0001c0001t0001g0122a0001c0003t0001g0194 | 3 | HG02280.hp1 HG02622.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2842+6266dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980433 | |||||
| chr16:68980433
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2842+6265A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980433 | ||||||
| chr16:68980434
|
TA | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0110a0001c0001t0001g0154others(5): Show | 8 | HG00738.hp2 HG02148.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2842+6267delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980434 | ||||||
| chr16:68980435
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2842+6268_2842+626 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980435 | |||||
| chr16:68980435
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2842+6268_2842+626 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980435 | |||||
| chr16:68980435
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2842+6268_2842+626 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980435 | |||||
| chr16:68980435
|
A | ATATTTTT others(3): Show |
1 | a0001c0008t0001g0112 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2842+6268_2842+626 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980435 | |||||
| chr16:68980435
|
A | T | 16 | a0001c0001t0001g0054a0001c0001t0001g0063a0001c0001t0001g0082others(13): Show | 16 | HG00140.hp2 HG01192.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.2842+6267A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980435 | ||||||
| chr16:68980435
|
AT | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0024others(21): Show | 24 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2842+6284delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68980435 | |||||
| chr16:68980436
|
T | TA | 9 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0115others(6): Show | 9 | HG00741.hp1 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2842+6268_2842+626 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980436 | ||||||
| chr16:68980436
|
T | TATA | 3 | a0001c0001t0001g0141a0001c0001t0001g0157a0001c0001t0008g0030 | 3 | HG01884.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2842+6268_2842+626 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980436 | ||||||
| chr16:68980436
|
T | TATATATA | 4 | a0001c0001t0001g0143a0001c0001t0001g0152a0001c0001t0001g0160others(1): Show | 4 | HG02818.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2842+6268_2842+626 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980436 | ||||||
| chr16:68980437
|
T | A | 49 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0021others(46): Show | 49 | HG00438.hp2 HG00544.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.2842+6269T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980437 | ||||||
| chr16:68980438
|
T | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0053others(9): Show | 12 | HG01884.hp2 HG01975.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2842+6270T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980438 | ||||||
| chr16:68980439
|
T | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0165 | 2 | HG02486.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2842+6271T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980439 | ||||||
| chr16:68980440
|
T | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0157 | 2 | HG02735.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2842+6272T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980440 | ||||||
| chr16:68980554
|
C | T | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2842+6386C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980554 | ||||||
| chr16:68980969
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+6801G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980969 | ||||||
| chr16:68980995
|
A | G | 3 | a0001c0003t0002g0195a0001c0003t0002g0196a0001c0003t0002g0197 | 3 | HG02615.hp1 HG03041.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2842+6827A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68980995 | ||||||
| chr16:68981210
|
C | CT | 41 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0010others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.2842+7063dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68981210 | |||||
| chr16:68981210
|
C | CTT | 7 | a0001c0001t0001g0021a0001c0001t0001g0166a0001c0001t0001g0172others(4): Show | 7 | HG02027.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2842+7062_2842+706 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68981210 | |||||
| chr16:68981310
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2842+7142A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68981310 | ||||||
| chr16:68981663
|
T | A | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2842+7495T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68981663 | ||||||
| chr16:68981824
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0047 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2842+7656G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68981824 | ||||||
| chr16:68981850
|
G | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2842+7682G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68981850 | ||||||
| chr16:68982046
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2842+7878C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982046 | ||||||
| chr16:68982157
|
C | T | 3 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0113 | 3 | NA18957.hp2 NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2842+7989C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982157 | ||||||
| chr16:68982169
|
TTC | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | HG00438.hp2 HG02027.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+8003_2842+800 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982169 | |||||
| chr16:68982182
|
A | C | 2 | a0001c0001t0003g0042a0001c0001t0003g0044 | 2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2842+8014A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982182 | ||||||
| chr16:68982544
|
G | T | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2842+8376G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982544 | ||||||
| chr16:68982550
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2842+8382G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982550 | ||||||
| chr16:68982629
|
C | CATTTTTT others(21): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2842+8461_2842+846 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982629 | ||||||
| chr16:68982630
|
C | CT | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(18): Show | 21 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.2842+8484dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0047 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2842+8471_2842+848 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2842+8470_2842+848 others(19): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0153a0001c0001t0001g0156a0001c0001t0001g0160others(1): Show | 4 | HG00099.hp2 HG00738.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+8469_2842+848 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(10): Show |
5 | a0001c0001t0001g0005a0001c0001t0001g0152a0001c0001t0001g0157others(2): Show | 5 | HG01192.hp1 HG01891.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+8468_2842+848 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(11): Show |
3 | a0001c0003t0002g0196a0001c0003t0002g0197a0005c0011t0001g0148 | 3 | HG03041.hp2 HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2842+8467_2842+848 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(12): Show |
6 | a0001c0001t0001g0114a0001c0001t0001g0120a0001c0001t0001g0207others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2842+8466_2842+848 others(23): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(16): Show |
5 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(2): Show | 5 | HG02486.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+8484_2842+848 others(27): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(19): Show |
12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG01346.hp1 HG02027.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2842+8484_2842+848 others(30): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(20): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0040 | 2 | NA18957.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.2842+8484_2842+848 others(31): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0003t0001g0194 | 3 | HG02040.hp1 HG02622.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2842+8484_2842+848 others(32): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(75): Show |
3 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0193 | 3 | HG02280.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2842+8484_2842+848 others(86): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(77): Show |
1 | a0004c0006t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2842+8484_2842+848 others(88): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2842+8484_2842+848 others(35): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68982630 | |||||
| chr16:68982630
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2842+8462C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982630 | ||||||
| chr16:68982711
|
A | G | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+8543A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982711 | ||||||
| chr16:68982815
|
C | G | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+8647C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68982815 | ||||||
| chr16:68983310
|
A | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0094others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+9142A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983310 | ||||||
| chr16:68983574
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2842+9406G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983574 | ||||||
| chr16:68983695
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2842+9527G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983695 | ||||||
| chr16:68983727
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2842+9559G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983727 | ||||||
| chr16:68983778
|
A | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2842+9610A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983778 | ||||||
| chr16:68983905
|
T | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(41): Show | 44 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2842+9737T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983905 | ||||||
| chr16:68983925
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2842+9757C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983925 | ||||||
| chr16:68983965
|
A | G | 67 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(64): Show | 67 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(64): Show |
intron_variant | MODIFIER | c.2842+9797A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68983965 | ||||||
| chr16:68984034
|
A | C | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2842+9866A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984034 | ||||||
| chr16:68984038
|
G | GA | 10 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0116others(7): Show | 10 | HG00544.hp1 HG01361.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.2842+9886dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68984038 | |||||
| chr16:68984507
|
CTTATA | C | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2842+10343_2842+10 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68984507 | |||||
| chr16:68984522
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2842+10354T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984522 | ||||||
| chr16:68984758
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2842+10590G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984758 | ||||||
| chr16:68984765
|
G | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+10597G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984765 | ||||||
| chr16:68984766
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+10598C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984766 | ||||||
| chr16:68984811
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+10643C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984811 | ||||||
| chr16:68984998
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0103 | 2 | HG02027.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2842+10830G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68984998 | ||||||
| chr16:68985217
|
G | A | 126 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2842+11049G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985217 | ||||||
| chr16:68985376
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0110 | 2 | HG01192.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2842+11208G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985376 | ||||||
| chr16:68985610
|
G | C | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2842+11442G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985610 | ||||||
| chr16:68985728
|
T | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2842+11560T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985728 | ||||||
| chr16:68985817
|
T | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0084others(2): Show | 5 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(2): Show |
intron_variant | MODIFIER | c.2842+11649T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985817 | ||||||
| chr16:68985858
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(25): Show | 28 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.2842+11690G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985858 | ||||||
| chr16:68985941
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156 | 3 | HG00099.hp2 HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2842+11773T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68985941 | ||||||
| chr16:68986093
|
A | G | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+11925A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986093 | ||||||
| chr16:68986250
|
G | T | 1 | a0001c0002t0001g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2842+12082G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986250 | ||||||
| chr16:68986370
|
T | G | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+12202T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986370 | ||||||
| chr16:68986602
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2842+12434A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986602 | ||||||
| chr16:68986726
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2842+12558G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986726 | ||||||
| chr16:68986892
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+12724A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986892 | ||||||
| chr16:68986902
|
A | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(66): Show | 69 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.2842+12734A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68986902 | ||||||
| chr16:68987112
|
T | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2842+12944T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987112 | ||||||
| chr16:68987165
|
T | TC | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2842+12997_2842+12 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987165 | ||||||
| chr16:68987166
|
T | C | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2842+12998T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987166 | ||||||
| chr16:68987166
|
T | TC | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.2842+12999dupC | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68987166 | |||||
| chr16:68987261
|
A | G | 7 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2842+13093A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987261 | ||||||
| chr16:68987268
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2842+13100T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987268 | ||||||
| chr16:68987498
|
G | A | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2842+13330G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987498 | ||||||
| chr16:68987611
|
T | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2842+13443T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987611 | ||||||
| chr16:68987645
|
T | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2842+13477T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987645 | ||||||
| chr16:68987758
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2842+13590T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987758 | ||||||
| chr16:68987824
|
T | C | 1 | a0001c0003t0001g0194 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2842+13656T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68987824 | ||||||
| chr16:68988000
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(52): Show | 55 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.2842+13832A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988000 | ||||||
| chr16:68988561
|
ACCCATTT others(3): Show |
A | 3 | a0002c0005t0001g0002a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2842+14402_2842+14 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988561 | |||||
| chr16:68988565
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2842+14397A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988565 | ||||||
| chr16:68988636
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2842+14468A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988636 | ||||||
| chr16:68988667
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2842+14499T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988667 | ||||||
| chr16:68988692
|
C | CT | 28 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0024others(25): Show | 28 | HG01081.hp1 HG01346.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.2842+14545dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988692 | |||||
| chr16:68988692
|
C | CTT | 11 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0040others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+14544_2842+14 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988692 | |||||
| chr16:68988692
|
C | CTTT | 12 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(9): Show | 12 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2842+14543_2842+14 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988692 | |||||
| chr16:68988692
|
C | CTTTT | 7 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0157others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2842+14542_2842+14 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988692 | |||||
| chr16:68988692
|
CT | C | 5 | a0001c0001t0001g0043a0001c0001t0001g0150a0001c0001t0001g0174others(2): Show | 5 | HG01257.hp2 HG02572.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2842+14545delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988692 | |||||
| chr16:68988692
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+14537_2842+14 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68988692 | |||||
| chr16:68988693
|
T | TC | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2842+14525_2842+14 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988693 | ||||||
| chr16:68988748
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2842+14580G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988748 | ||||||
| chr16:68988768
|
C | T | 11 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+14600C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68988768 | ||||||
| chr16:68989296
|
AT | A | 68 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(65): Show | 68 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.2842+15139delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68989296 | |||||
| chr16:68989552
|
T | C | 3 | a0001c0001t0001g0165a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02486.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2842+15384T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68989552 | ||||||
| chr16:68989722
|
T | C | 1 | a0001c0007t0001g0036 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2842+15554T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68989722 | ||||||
| chr16:68989964
|
G | C | 2 | a0001c0001t0001g0109a0001c0003t0001g0131 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2842+15796G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68989964 | ||||||
| chr16:68989993
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2842+15825T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68989993 | ||||||
| chr16:68990322
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2842+16154C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990322 | ||||||
| chr16:68990467
|
A | T | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+16299A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990467 | ||||||
| chr16:68990487
|
A | G | 130 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.2842+16319A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990487 | ||||||
| chr16:68990536
|
G | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2842+16368G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990536 | ||||||
| chr16:68990573
|
T | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+16405T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990573 | ||||||
| chr16:68990680
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2842+16512T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990680 | ||||||
| chr16:68990808
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+16640G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68990808 | ||||||
| chr16:68991200
|
G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0058 | 2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2842+17032G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68991200 | ||||||
| chr16:68991480
|
G | A | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+17312G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68991480 | ||||||
| chr16:68991519
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0154a0001c0001t0001g0205others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+17351T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68991519 | ||||||
| chr16:68991621
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2842+17453C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68991621 | ||||||
| chr16:68991694
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2842+17526T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68991694 | ||||||
| chr16:68991910
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2842+17742A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68991910 | ||||||
| chr16:68991999
|
C | CT | 8 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0152others(5): Show | 8 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2842+17841dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68991999 | |||||
| chr16:68992051
|
A | G | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2842+17883A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992051 | ||||||
| chr16:68992134
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2842+17966T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992134 | ||||||
| chr16:68992350
|
G | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2842+18182G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992350 | ||||||
| chr16:68992410
|
T | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(48): Show | 51 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.2842+18242T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992410 | ||||||
| chr16:68992507
|
T | C | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2842+18339T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992507 | ||||||
| chr16:68992568
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156 | 3 | HG00099.hp2 HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2842+18400C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992568 | ||||||
| chr16:68992606
|
C | T | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+18438C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992606 | ||||||
| chr16:68992790
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2842+18622C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68992790 | ||||||
| chr16:68993586
|
T | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG03654.hp2 HG03704.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.2842+19418T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68993586 | ||||||
| chr16:68993697
|
A | G | 3 | a0001c0001t0001g0165a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02486.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2842+19529A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68993697 | ||||||
| chr16:68993726
|
T | G | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+19558T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68993726 | ||||||
| chr16:68993780
|
C | G | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2842+19612C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68993780 | ||||||
| chr16:68994505
|
A | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2842+20337A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994505 | ||||||
| chr16:68994576
|
AT | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0175others(2): Show | 5 | HG00099.hp1 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2842+20423delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68994576 | |||||
| chr16:68994609
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2842+20441C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994609 | ||||||
| chr16:68994639
|
A | G | 12 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(9): Show | 12 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2842+20471A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994639 | ||||||
| chr16:68994756
|
T | A | 36 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(33): Show | 36 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.2842+20588T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994756 | ||||||
| chr16:68994796
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2842+20628G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994796 | ||||||
| chr16:68994796
|
G | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0157others(1): Show | 4 | HG02818.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2842+20628G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994796 | ||||||
| chr16:68994890
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2842+20722T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68994890 | ||||||
| chr16:68995056
|
A | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2842+20888A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68995056 | ||||||
| chr16:68995219
|
C | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2842+21051C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68995219 | ||||||
| chr16:68995424
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2842+21256C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68995424 | ||||||
| chr16:68995593
|
A | G | 35 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(32): Show | 35 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.2842+21425A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68995593 | ||||||
| chr16:68995971
|
A | G | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2842+21803A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68995971 | ||||||
| chr16:68996031
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2842+21863A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996031 | ||||||
| chr16:68996249
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2842+22081T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996249 | ||||||
| chr16:68996477
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2842+22309G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996477 | ||||||
| chr16:68996741
|
C | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0062others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2842+22573C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996741 | ||||||
| chr16:68996746
|
T | A | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2842+22578T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996746 | ||||||
| chr16:68996789
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0110 | 2 | HG01192.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2842+22621C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996789 | ||||||
| chr16:68996907
|
C | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2842+22739C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68996907 | ||||||
| chr16:68996965
|
GGAAAT | G | 31 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2842+22803_2842+22 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68996965 | |||||
| chr16:68997169
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2842+23001T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68997169 | ||||||
| chr16:68997341
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2842+23173C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68997341 | ||||||
| chr16:68998459
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2842+24291C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998459 | ||||||
| chr16:68998514
|
A | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156 | 3 | HG00099.hp2 HG00738.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.2843-24314A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998514 | ||||||
| chr16:68998605
|
A | C | 55 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(52): Show | 55 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.2843-24223A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998605 | ||||||
| chr16:68998639
|
GA | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-24188delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998639 | ||||||
| chr16:68998695
|
C | A | 2 | a0001c0003t0001g0128a0001c0003t0001g0132 | 2 | NA18968.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2843-24133C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998695 | ||||||
| chr16:68998696
|
G | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-24132G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998696 | ||||||
| chr16:68998730
|
C | CA | 10 | a0001c0001t0001g0010a0001c0001t0001g0141a0001c0001t0001g0166others(7): Show | 10 | HG01346.hp1 HG01361.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.2843-24083dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68998730 | |||||
| chr16:68998730
|
CA | C | 9 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0094others(6): Show | 9 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.2843-24083delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 68998730 | |||||
| chr16:68998794
|
C | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-24034C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68998794 | ||||||
| chr16:68999135
|
G | T | 8 | a0001c0003t0001g0124a0001c0003t0001g0128a0001c0003t0001g0129others(5): Show | 8 | HG01081.hp2 HG01346.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2843-23693G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68999135 | ||||||
| chr16:68999258
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-23570A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68999258 | ||||||
| chr16:68999326
|
C | T | 2 | a0001c0002t0001g0065a0001c0002t0001g0095 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2843-23502C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68999326 | ||||||
| chr16:68999754
|
T | G | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.2843-23074T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68999754 | ||||||
| chr16:68999953
|
T | A | 7 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2843-22875T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 68999953 | ||||||
| chr16:69000331
|
A | G | 10 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0152others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.2843-22497A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69000331 | ||||||
| chr16:69000580
|
A | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2843-22248A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69000580 | ||||||
| chr16:69000689
|
T | C | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2843-22139T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69000689 | ||||||
| chr16:69000707
|
T | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-22121T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69000707 | ||||||
| chr16:69001404
|
G | A | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2843-21424G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69001404 | ||||||
| chr16:69001454
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(66): Show | 69 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.2843-21374T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69001454 | ||||||
| chr16:69001483
|
GCT | G | 7 | a0001c0001t0001g0069a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG01975.hp2 HG02040.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2843-21342_2843-21 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69001483 | |||||
| chr16:69001801
|
C | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(9): Show | 12 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2843-21027C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69001801 | ||||||
| chr16:69001801
|
C | T | 5 | a0001c0007t0001g0038a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-21027C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69001801 | ||||||
| chr16:69002030
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2843-20798G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002030 | ||||||
| chr16:69002220
|
G | A | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2843-20608G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002220 | ||||||
| chr16:69002222
|
A | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2843-20606A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002222 | ||||||
| chr16:69002224
|
A | T | 64 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2843-20604A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002224 | ||||||
| chr16:69002388
|
G | A | 5 | a0001c0001t0001g0066a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG00741.hp1 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-20440G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002388 | ||||||
| chr16:69002484
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(25): Show | 28 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.2843-20344G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002484 | ||||||
| chr16:69002609
|
C | T | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2843-20219C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002609 | ||||||
| chr16:69002679
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-20149A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002679 | ||||||
| chr16:69002789
|
C | T | 8 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2843-20039C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002789 | ||||||
| chr16:69002986
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2843-19842G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69002986 | ||||||
| chr16:69003055
|
A | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0152others(5): Show | 8 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2843-19773A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69003055 | ||||||
| chr16:69003254
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0120a0001c0001t0001g0152others(11): Show | 14 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2843-19574A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69003254 | ||||||
| chr16:69003861
|
C | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2843-18967C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69003861 | ||||||
| chr16:69004018
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2843-18810A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69004018 | ||||||
| chr16:69004153
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2843-18675A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69004153 | ||||||
| chr16:69004168
|
C | T | 1 | a0001c0002t0001g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2843-18660C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69004168 | ||||||
| chr16:69004355
|
C | CT | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843-18461dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69004355 | |||||
| chr16:69004448
|
T | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(43): Show | 46 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.2843-18380T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69004448 | ||||||
| chr16:69004510
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2843-18318C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69004510 | ||||||
| chr16:69004832
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-17996C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69004832 | ||||||
| chr16:69005197
|
C | T | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2843-17631C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005197 | ||||||
| chr16:69005269
|
TTG | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2843-17558_2843-17 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005269 | ||||||
| chr16:69005284
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2843-17544G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005284 | ||||||
| chr16:69005395
|
C | T | 6 | a0001c0001t0001g0165a0001c0002t0001g0086a0001c0002t0001g0093others(3): Show | 6 | HG02129.hp1 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2843-17433C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005395 | ||||||
| chr16:69005439
|
T | A | 13 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0173others(10): Show | 13 | HG00544.hp1 HG01099.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.2843-17389T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005439 | ||||||
| chr16:69005519
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-17309C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005519 | ||||||
| chr16:69005558
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2843-17270G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005558 | ||||||
| chr16:69005627
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2843-17201C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69005627 | ||||||
| chr16:69005788
|
CA | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(48): Show | 51 | HG00741.hp2 HG01099.hp1 HG01175.hp2 others(48): Show |
intron_variant | MODIFIER | c.2843-17023delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69005788 | |||||
| chr16:69005788
|
CAA | C | 5 | a0001c0001t0001g0182a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-17024_2843-17 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69005788 | |||||
| chr16:69006045
|
A | G | 3 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0113 | 3 | NA18957.hp2 NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2843-16783A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006045 | ||||||
| chr16:69006181
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-16647A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006181 | ||||||
| chr16:69006186
|
C | T | 17 | a0001c0001t0001g0010a0001c0001t0001g0114a0001c0001t0001g0121others(14): Show | 17 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.2843-16642C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006186 | ||||||
| chr16:69006477
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2843-16351C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006477 | ||||||
| chr16:69006512
|
G | A | 7 | a0001c0001t0001g0035a0001c0001t0001g0069a0001c0001t0001g0145others(4): Show | 7 | HG01258.hp2 HG01975.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.2843-16316G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006512 | ||||||
| chr16:69006846
|
T | G | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2843-15982T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006846 | ||||||
| chr16:69006847
|
A | G | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-15981A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006847 | ||||||
| chr16:69006926
|
C | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-15902C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006926 | ||||||
| chr16:69006952
|
T | G | 4 | a0001c0001t0001g0152a0001c0001t0001g0157a0001c0001t0001g0160others(1): Show | 4 | HG02486.hp1 HG02818.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-15876T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69006952 | ||||||
| chr16:69007269
|
CT | C | 48 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0024others(45): Show | 48 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.2843-15542delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69007269 | |||||
| chr16:69007332
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2843-15496C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69007332 | ||||||
| chr16:69007584
|
A | G | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2843-15244A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69007584 | ||||||
| chr16:69007637
|
T | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-15191T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69007637 | ||||||
| chr16:69007746
|
A | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2843-15082A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69007746 | ||||||
| chr16:69007856
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2843-14972A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69007856 | ||||||
| chr16:69007936
|
G | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(12): Show | 15 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2843-14892G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69007936 | ||||||
| chr16:69008103
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2843-14725T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008103 | ||||||
| chr16:69008142
|
CT | C | 6 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0088others(3): Show | 6 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.2843-14677delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69008142 | |||||
| chr16:69008411
|
T | C | 1 | a0001c0002t0001g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2843-14417T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008411 | ||||||
| chr16:69008434
|
G | A | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2843-14394G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008434 | ||||||
| chr16:69008651
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2843-14177T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008651 | ||||||
| chr16:69008789
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2843-14039C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008789 | ||||||
| chr16:69008897
|
T | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(43): Show | 46 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.2843-13931T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008897 | ||||||
| chr16:69008958
|
A | G | 133 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2843-13870A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69008958 | ||||||
| chr16:69009046
|
T | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-13782T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009046 | ||||||
| chr16:69009072
|
C | CT | 26 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0047others(23): Show | 26 | HG00438.hp1 HG00741.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.2843-13730dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69009072 | |||||
| chr16:69009072
|
CT | C | 22 | a0001c0001t0001g0043a0001c0001t0001g0085a0001c0001t0001g0149others(19): Show | 22 | HG01081.hp2 HG01257.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.2843-13730delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69009072 | |||||
| chr16:69009072
|
CTTTTTT | C | 5 | a0001c0001t0001g0077a0001c0001t0001g0105a0001c0001t0001g0175others(2): Show | 5 | HG00099.hp1 HG01433.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-13735_2843-13 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69009072 | |||||
| chr16:69009072
|
CTTTTTTT | C | 9 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0183others(6): Show | 9 | HG00544.hp1 HG01952.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.2843-13736_2843-13 others(13): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69009072 | |||||
| chr16:69009142
|
C | T | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2843-13686C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009142 | ||||||
| chr16:69009185
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2843-13643G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009185 | ||||||
| chr16:69009214
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2843-13614T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009214 | ||||||
| chr16:69009382
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2843-13446G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009382 | ||||||
| chr16:69009499
|
C | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-13329C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009499 | ||||||
| chr16:69009561
|
C | T | 31 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2843-13267C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009561 | ||||||
| chr16:69009976
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2843-12852C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009976 | ||||||
| chr16:69009992
|
C | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2843-12836C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009992 | ||||||
| chr16:69009993
|
G | A | 3 | a0001c0008t0001g0112a0001c0008t0001g0119a0002c0005t0001g0002 | 3 | HG02717.hp1 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2843-12835G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69009993 | ||||||
| chr16:69010243
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2843-12585G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69010243 | ||||||
| chr16:69010427
|
C | G | 1 | a0001c0002t0001g0064 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2843-12401C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69010427 | ||||||
| chr16:69010819
|
A | G | 7 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0157others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2843-12009A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69010819 | ||||||
| chr16:69011125
|
C | T | 11 | a0001c0002t0001g0068a0001c0002t0001g0070a0001c0002t0001g0071others(8): Show | 11 | HG01981.hp2 HG01993.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.2843-11703C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011125 | ||||||
| chr16:69011217
|
T | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2843-11611T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011217 | ||||||
| chr16:69011259
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2843-11569C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011259 | ||||||
| chr16:69011388
|
G | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2843-11440G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011388 | ||||||
| chr16:69011455
|
C | CT | 6 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(3): Show | 6 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-11358dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69011455 | |||||
| chr16:69011455
|
CT | C | 19 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0001g0124others(16): Show | 19 | HG01081.hp2 HG01099.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.2843-11358delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69011455 | |||||
| chr16:69011482
|
C | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-11346C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011482 | ||||||
| chr16:69011593
|
T | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-11235T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011593 | ||||||
| chr16:69011660
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0199 | 2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2843-11168A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011660 | ||||||
| chr16:69011666
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2843-11162C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011666 | ||||||
| chr16:69011959
|
T | G | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843-10869T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69011959 | ||||||
| chr16:69012210
|
T | C | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2843-10618T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012210 | ||||||
| chr16:69012277
|
T | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.2843-10551T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012277 | ||||||
| chr16:69012295
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-10533G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012295 | ||||||
| chr16:69012354
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2843-10474C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012354 | ||||||
| chr16:69012373
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0205 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2843-10455G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012373 | ||||||
| chr16:69012515
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2843-10313C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012515 | ||||||
| chr16:69012544
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2843-10284G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012544 | ||||||
| chr16:69012556
|
C | CA | 10 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0082others(7): Show | 10 | HG01175.hp1 HG01192.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.2843-10250dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012556
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0041others(3): Show | 6 | HG01175.hp2 HG03225.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-10257_2843-10 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012556
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0114others(8): Show | 11 | HG02027.hp1 HG02040.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843-10258_2843-10 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012556
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0140others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-10259_2843-10 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012556
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0159 | 2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2843-10260_2843-10 others(17): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012556
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0171a0001c0003t0001g0194 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2843-10261_2843-10 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012556
|
CA | C | 27 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0116others(24): Show | 27 | HG00099.hp2 HG00738.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2843-10250delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012556 | |||||
| chr16:69012563
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0003g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2843-10250_2843-10 others(23): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69012563 | |||||
| chr16:69012569
|
AAAAAAAA others(3): Show |
A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2843-10258_2843-10 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012569 | ||||||
| chr16:69012579
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0032others(25): Show | 28 | HG00741.hp2 HG01175.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.2843-10249G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012579 | ||||||
| chr16:69012581
|
A | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0032others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.2843-10247A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012581 | ||||||
| chr16:69012842
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(25): Show | 28 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.2843-9986G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012842 | ||||||
| chr16:69012923
|
G | A | 46 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(43): Show | 46 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.2843-9905G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012923 | ||||||
| chr16:69012936
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2843-9892C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69012936 | ||||||
| chr16:69013118
|
C | CT | 14 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(11): Show | 14 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2843-9698dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69013118 | |||||
| chr16:69013318
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2843-9510C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013318 | ||||||
| chr16:69013479
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(62): Show | 65 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.2843-9349T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013479 | ||||||
| chr16:69013526
|
A | C | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2843-9302A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013526 | ||||||
| chr16:69013553
|
T | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.2843-9275T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013553 | ||||||
| chr16:69013617
|
C | CA | 10 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0091others(7): Show | 10 | HG01952.hp1 HG02135.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2843-9195dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69013617 | |||||
| chr16:69013636
|
CG | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00099.hp1 HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2843-9188delG | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69013636 | |||||
| chr16:69013654
|
C | CT | 58 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0018others(55): Show | 58 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2843-9156dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69013654 | |||||
| chr16:69013654
|
C | CTT | 19 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0029others(16): Show | 19 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.2843-9157_2843-915 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69013654 | |||||
| chr16:69013673
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-9155C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013673 | ||||||
| chr16:69013766
|
C | T | 1 | a0001c0002t0001g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2843-9062C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013766 | ||||||
| chr16:69013777
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2843-9051C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013777 | ||||||
| chr16:69013938
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-8890G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69013938 | ||||||
| chr16:69014341
|
T | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843-8487T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014341 | ||||||
| chr16:69014342
|
C | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843-8486C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014342 | ||||||
| chr16:69014357
|
CA | C | 31 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2843-8470delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014357 | ||||||
| chr16:69014364
|
T | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0006c0010t0001g0206 | 3 | HG01433.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2843-8464T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014364 | ||||||
| chr16:69014442
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-8386G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014442 | ||||||
| chr16:69014457
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2843-8371A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014457 | ||||||
| chr16:69014813
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2843-8015T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69014813 | ||||||
| chr16:69014895
|
C | CA | 31 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0024others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.2843-7917dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69014895 | |||||
| chr16:69015126
|
A | G | 7 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0157others(4): Show | 7 | HG02486.hp1 HG02818.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2843-7702A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015126 | ||||||
| chr16:69015257
|
G | C | 2 | a0001c0001t0001g0114a0005c0011t0001g0148 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2843-7571G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015257 | ||||||
| chr16:69015267
|
A | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2843-7561A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015267 | ||||||
| chr16:69015311
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2843-7517A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015311 | ||||||
| chr16:69015390
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177 | 3 | HG00099.hp1 HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2843-7438C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015390 | ||||||
| chr16:69015464
|
T | TTTTA | 34 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0024others(31): Show | 34 | HG00738.hp1 HG00741.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.2843-7332_2843-732 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69015464 | |||||
| chr16:69015464
|
T | TTTTATTT others(1): Show |
10 | a0001c0001t0001g0142a0001c0001t0003g0042a0001c0003t0001g0129others(7): Show | 10 | HG01081.hp2 HG01346.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.2843-7336_2843-732 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69015464 | |||||
| chr16:69015464
|
T | TTTTATTT others(5): Show |
11 | a0001c0001t0001g0082a0001c0001t0001g0110a0001c0003t0001g0128others(8): Show | 11 | HG01192.hp2 HG02148.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2843-7340_2843-732 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69015464 | |||||
| chr16:69015464
|
T | TTTTATTT others(9): Show |
66 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2843-7344_2843-732 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69015464 | |||||
| chr16:69015464
|
T | TTTTATTT others(13): Show |
2 | a0001c0002t0001g0072a0001c0002t0001g0139 | 2 | HG01993.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.2843-7348_2843-732 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69015464 | |||||
| chr16:69015634
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2843-7194A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015634 | ||||||
| chr16:69015656
|
T | A | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2843-7172T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015656 | ||||||
| chr16:69015844
|
C | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2843-6984C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69015844 | ||||||
| chr16:69016136
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-6692G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69016136 | ||||||
| chr16:69016435
|
G | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-6393G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69016435 | ||||||
| chr16:69016509
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2843-6319T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69016509 | ||||||
| chr16:69016567
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02055.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2843-6261C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69016567 | ||||||
| chr16:69016735
|
C | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2843-6093C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69016735 | ||||||
| chr16:69016843
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2843-5985G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69016843 | ||||||
| chr16:69017305
|
T | C | 125 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.2843-5523T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017305 | ||||||
| chr16:69017394
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2843-5434T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017394 | ||||||
| chr16:69017450
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2843-5378C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017450 | ||||||
| chr16:69017526
|
G | A | 3 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0113 | 3 | NA18957.hp2 NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2843-5302G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017526 | ||||||
| chr16:69017649
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-5179C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017649 | ||||||
| chr16:69017778
|
C | T | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2843-5050C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017778 | ||||||
| chr16:69017901
|
C | CT | 8 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG01257.hp2 HG02027.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.2843-4910dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69017901 | |||||
| chr16:69017918
|
T | G | 1 | a0001c0001t0005g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2843-4910T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017918 | ||||||
| chr16:69017936
|
C | G | 1 | a0001c0002t0001g0108 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2843-4892C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69017936 | ||||||
| chr16:69018028
|
C | CA | 32 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(29): Show | 32 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.2843-4798dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018028 | |||||
| chr16:69018054
|
C | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0094others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-4774C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018054 | ||||||
| chr16:69018139
|
C | CT | 67 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0054others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.2843-4667dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTCTTTTT others(10): Show |
1 | a0001c0008t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2843-4688_2843-468 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTCTTTTT others(11): Show |
1 | a0001c0008t0001g0112 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2843-4688_2843-468 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(3): Show |
9 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(6): Show | 9 | HG01346.hp1 HG01361.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2843-4676_2843-466 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2843-4677_2843-466 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2843-4679_2843-466 others(17): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2843-4680_2843-466 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0143others(2): Show | 5 | HG02486.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-4681_2843-466 others(19): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0167others(1): Show | 4 | HG02055.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-4682_2843-466 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
C | CTTTTTTT others(10): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-4683_2843-466 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
CT | C | 5 | a0001c0001t0001g0034a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-4667delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018139
|
CTTT | C | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-4669_2843-466 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69018139 | |||||
| chr16:69018145
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-4683T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018145 | ||||||
| chr16:69018248
|
A | G | 1 | a0004c0006t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2843-4580A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018248 | ||||||
| chr16:69018265
|
A | C | 63 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.2843-4563A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018265 | ||||||
| chr16:69018435
|
A | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-4393A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018435 | ||||||
| chr16:69018455
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2843-4373T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018455 | ||||||
| chr16:69018746
|
C | A | 1 | a0001c0002t0001g0072 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2843-4082C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018746 | ||||||
| chr16:69018866
|
C | A | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-3962C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69018866 | ||||||
| chr16:69019295
|
A | G | 36 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(33): Show | 36 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.2843-3533A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69019295 | ||||||
| chr16:69019449
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-3379C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69019449 | ||||||
| chr16:69020071
|
T | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-2757T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020071 | ||||||
| chr16:69020502
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2843-2326G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020502 | ||||||
| chr16:69020550
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2843-2278A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020550 | ||||||
| chr16:69020630
|
G | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0198 | 2 | HG02027.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2843-2198G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020630 | ||||||
| chr16:69020716
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2843-2112A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020716 | ||||||
| chr16:69020809
|
A | T | 84 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2843-2019A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020809 | ||||||
| chr16:69020886
|
C | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-1942C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020886 | ||||||
| chr16:69020896
|
ATGTATGT others(19): Show |
A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2843-1928_2843-190 others(30): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020896 | |||||
| chr16:69020900
|
A | ATGTGTGT others(3): Show |
1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2843-1925_2843-192 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020900 | |||||
| chr16:69020900
|
ATGTATGT others(1): Show |
A | 3 | a0001c0001t0001g0101a0001c0001t0001g0111a0001c0002t0001g0117 | 3 | HG03927.hp1 NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2843-1924_2843-191 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020900 | |||||
| chr16:69020900
|
ATGTATGT others(3): Show |
A | 4 | a0001c0001t0001g0077a0001c0002t0001g0065a0001c0002t0001g0073others(1): Show | 4 | HG00408.hp1 NA18960.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843-1924_2843-191 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020900 | |||||
| chr16:69020900
|
ATGTATGT others(5): Show |
A | 52 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.2843-1924_2843-191 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020900 | |||||
| chr16:69020900
|
ATGTATGT others(7): Show |
A | 2 | a0001c0001t0001g0082a0001c0001t0001g0109 | 2 | HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2843-1924_2843-191 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020900 | |||||
| chr16:69020904
|
A | ATG | 18 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0035others(15): Show | 18 | HG00544.hp1 HG01255.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.2843-1887_2843-188 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTG | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0050others(10): Show | 13 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.2843-1889_2843-188 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTG | 5 | a0001c0001t0001g0121a0001c0003t0001g0128a0001c0003t0001g0132others(2): Show | 5 | HG01346.hp2 HG02886.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-1891_2843-188 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0001g0171a0001c0003t0007g0127a0002c0005t0001g0002 | 3 | HG02965.hp2 NA19079.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2843-1893_2843-188 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0166 | 3 | HG00741.hp2 HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2843-1895_2843-188 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTGT others(5): Show |
14 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0140others(11): Show | 14 | HG02040.hp1 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2843-1897_2843-188 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTGT others(9): Show |
1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2843-1911_2843-191 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTGT others(7): Show |
5 | a0001c0001t0001g0114a0001c0001t0001g0158a0001c0001t0003g0042others(2): Show | 5 | HG01346.hp1 HG01361.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-1899_2843-188 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0001g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2843-1901_2843-188 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
A | G | 3 | a0001c0001t0001g0165a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02486.hp1 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2843-1924A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020904 | ||||||
| chr16:69020904
|
ATG | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0026others(3): Show | 6 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2843-1887_2843-188 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
ATGTG | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(12): Show | 15 | HG00738.hp2 HG01433.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2843-1889_2843-188 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020904
|
ATGTGTG | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0001g0204others(2): Show | 5 | HG01884.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2843-1891_2843-188 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69020904 | |||||
| chr16:69020908
|
G | A | 3 | a0001c0007t0001g0036a0001c0007t0001g0038a0001c0007t0003g0037 | 3 | HG03239.hp2 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2843-1920G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020908 | ||||||
| chr16:69020942
|
G | GT | 2 | a0001c0001t0001g0003a0001c0001t0001g0034 | 2 | HG03139.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2843-1886_2843-188 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020942 | ||||||
| chr16:69020942
|
G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2843-1886_2843-188 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69020942 | ||||||
| chr16:69021128
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843-1700G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69021128 | ||||||
| chr16:69021263
|
G | T | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2843-1565G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69021263 | ||||||
| chr16:69021772
|
C | A | 61 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.2843-1056C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69021772 | ||||||
| chr16:69021790
|
A | T | 47 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(44): Show | 47 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.2843-1038A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69021790 | ||||||
| chr16:69021886
|
C | CT | 9 | a0001c0001t0001g0023a0001c0001t0001g0109a0001c0001t0001g0122others(6): Show | 9 | HG01175.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2843-925dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69021886 | |||||
| chr16:69021886
|
CT | C | 5 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0172others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2843-925delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69021886 | |||||
| chr16:69021907
|
A | G | 1 | a0001c0003t0001g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2843-921A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69021907 | ||||||
| chr16:69022232
|
A | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0174 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2843-596A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69022232 | ||||||
| chr16:69022423
|
G | T | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2843-405G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69022423 | ||||||
| chr16:69022455
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0209a0001c0001t0001g0210 | 3 | HG01884.hp1 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2843-373G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69022455 | ||||||
| chr16:69022621
|
C | T | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2843-207C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | chr16 | 69022621 | ||||||
| chr16:69022703
|
C | CA | 61 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.2843-115dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 69022703 | |||||
| chr16:69023016
|
T | C | 5 | a0001c0001t0001g0120a0001c0001t0001g0152a0001c0001t0001g0157others(2): Show | 5 | HG02486.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2994+37T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69023016 | ||||||
| chr16:69023466
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2994+487A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69023466 | ||||||
| chr16:69023513
|
A | G | 52 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(49): Show |
intron_variant | MODIFIER | c.2994+534A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69023513 | ||||||
| chr16:69023556
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2994+577A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69023556 | ||||||
| chr16:69023740
|
C | CA | 16 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0023others(13): Show | 16 | HG00438.hp2 HG01175.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2994+770dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69023740 | |||||
| chr16:69024154
|
A | G | 10 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(7): Show | 10 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2994+1175A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024154 | ||||||
| chr16:69024297
|
C | T | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+1318C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024297 | ||||||
| chr16:69024329
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2994+1350C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024329 | ||||||
| chr16:69024359
|
C | T | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+1380C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024359 | ||||||
| chr16:69024457
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2994+1478C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024457 | ||||||
| chr16:69024513
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2994+1534C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024513 | ||||||
| chr16:69024526
|
C | G | 1 | a0001c0001t0001g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2994+1547C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024526 | ||||||
| chr16:69024536
|
G | C | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2994+1557G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024536 | ||||||
| chr16:69024710
|
A | G | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2994+1731A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024710 | ||||||
| chr16:69024883
|
CT | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+1905delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024883 | ||||||
| chr16:69024999
|
T | C | 4 | a0001c0002t0001g0065a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | HG00408.hp1 NA18939.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2994+2020T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69024999 | ||||||
| chr16:69025313
|
A | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2994+2334A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69025313 | ||||||
| chr16:69025452
|
T | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+2473T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69025452 | ||||||
| chr16:69025466
|
T | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2994+2487T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69025466 | ||||||
| chr16:69025578
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0001g0199 | 2 | HG02135.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2994+2599G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69025578 | ||||||
| chr16:69025679
|
T | G | 10 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(7): Show | 10 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2994+2700T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69025679 | ||||||
| chr16:69026002
|
CT | C | 11 | a0001c0001t0001g0032a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2994+3037delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69026002 | |||||
| chr16:69026153
|
C | T | 3 | a0001c0001t0001g0155a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2994+3174C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69026153 | ||||||
| chr16:69026212
|
G | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(27): Show | 30 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2994+3233G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69026212 | ||||||
| chr16:69026220
|
T | TC | 52 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(49): Show |
intron_variant | MODIFIER | c.2994+3241_2994+324 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69026220 | ||||||
| chr16:69026360
|
T | C | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+3381T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69026360 | ||||||
| chr16:69026534
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2994+3555G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69026534 | ||||||
| chr16:69026707
|
CTGTTTGT others(1): Show |
C | 6 | a0001c0003t0001g0128a0001c0003t0001g0130a0001c0003t0001g0132others(3): Show | 6 | HG01346.hp2 HG01975.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2994+3744_2994+375 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69026707 | |||||
| chr16:69026769
|
G | A | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2994+3790G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69026769 | ||||||
| chr16:69027107
|
G | A | 70 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2994+4128G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027107 | ||||||
| chr16:69027141
|
C | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+4162C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027141 | ||||||
| chr16:69027151
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2994+4172C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027151 | ||||||
| chr16:69027191
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2994+4212A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027191 | ||||||
| chr16:69027285
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2994+4306T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027285 | ||||||
| chr16:69027601
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2994+4622G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027601 | ||||||
| chr16:69027637
|
G | C | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2994+4658G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027637 | ||||||
| chr16:69027755
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2994+4776G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027755 | ||||||
| chr16:69027782
|
A | AT | 9 | a0001c0001t0001g0152a0001c0001t0001g0172a0001c0001t0001g0182others(6): Show | 9 | HG01433.hp2 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.2994+4819dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69027782 | |||||
| chr16:69027993
|
A | G | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+5014A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69027993 | ||||||
| chr16:69028023
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+5044G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028023 | ||||||
| chr16:69028050
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2994+5071G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028050 | ||||||
| chr16:69028367
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2994+5388C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028367 | ||||||
| chr16:69028384
|
C | T | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+5405C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028384 | ||||||
| chr16:69028393
|
G | T | 5 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0094others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+5414G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028393 | ||||||
| chr16:69028547
|
C | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2994+5568C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028547 | ||||||
| chr16:69028557
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2994+5578C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028557 | ||||||
| chr16:69028571
|
T | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2994+5592T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028571 | ||||||
| chr16:69028589
|
C | T | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2994+5610C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028589 | ||||||
| chr16:69028617
|
C | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(49): Show | 52 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(49): Show |
intron_variant | MODIFIER | c.2994+5638C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028617 | ||||||
| chr16:69028856
|
C | CA | 17 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0029others(14): Show | 17 | HG00741.hp2 HG01175.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2994+5895dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69028856 | |||||
| chr16:69028856
|
CAAAAAAA | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(3): Show | 6 | HG01433.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2994+5889_2994+589 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69028856 | |||||
| chr16:69028870
|
A | AG | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.2994+5891_2994+589 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028870 | ||||||
| chr16:69028871
|
A | AG | 5 | a0001c0001t0001g0152a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+5892_2994+589 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028871 | ||||||
| chr16:69028976
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0047 | 2 | HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.2994+5997A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69028976 | ||||||
| chr16:69029369
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2994+6390A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69029369 | ||||||
| chr16:69029378
|
A | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2994+6399A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69029378 | ||||||
| chr16:69029466
|
A | T | 6 | a0001c0003t0001g0128a0001c0003t0001g0130a0001c0003t0001g0132others(3): Show | 6 | HG01346.hp2 HG01975.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2994+6487A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69029466 | ||||||
| chr16:69029528
|
A | G | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+6549A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69029528 | ||||||
| chr16:69029861
|
ACTTTGGG others(2764): Show |
A | 4 | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0033others(1): Show | 4 | HG02004.hp1 NA18952.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+6911_2995-764 others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69029861 | |||||
| chr16:69029895
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2994+6916G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69029895 | ||||||
| chr16:69029939
|
C | G | 64 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2994+6960C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69029939 | ||||||
| chr16:69030044
|
G | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2994+7065G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69030044 | ||||||
| chr16:69030091
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2994+7112G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69030091 | ||||||
| chr16:69030107
|
C | CA | 14 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0054others(11): Show | 14 | HG00099.hp2 HG01192.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.2994+7148dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69030107 | |||||
| chr16:69030107
|
C | CAA | 11 | a0001c0001t0001g0156a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | HG00738.hp1 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2994+7147_2994+714 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69030107 | |||||
| chr16:69030107
|
CA | C | 5 | a0001c0001t0001g0173a0001c0002t0001g0092a0003c0004t0001g0151others(2): Show | 5 | HG01099.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+7148delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69030107 | |||||
| chr16:69030790
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0188 | 2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2994+7811G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69030790 | ||||||
| chr16:69030818
|
G | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0154a0001c0001t0001g0205others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+7839G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69030818 | ||||||
| chr16:69030887
|
T | TA | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2994+7919dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69030887 | |||||
| chr16:69030922
|
G | A | 4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2994+7943G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69030922 | ||||||
| chr16:69031010
|
C | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2994+8031C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031010 | ||||||
| chr16:69031038
|
G | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2994+8059G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031038 | ||||||
| chr16:69031049
|
G | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2994+8070G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031049 | ||||||
| chr16:69031067
|
T | A | 1 | a0001c0001t0001g0011 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2994+8088T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031067 | ||||||
| chr16:69031206
|
C | T | 1 | a0001c0007t0003g0037 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2994+8227C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031206 | ||||||
| chr16:69031285
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2994+8306C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031285 | ||||||
| chr16:69031321
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2994+8342A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031321 | ||||||
| chr16:69031751
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2995-8557G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031751 | ||||||
| chr16:69031895
|
T | TCATGCAA others(1): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0110 | 2 | HG02148.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2995-8411_2995-840 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69031895 | |||||
| chr16:69031955
|
G | A | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2995-8353G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69031955 | ||||||
| chr16:69032058
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2995-8250A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69032058 | ||||||
| chr16:69032066
|
C | T | 6 | a0001c0003t0001g0128a0001c0003t0001g0130a0001c0003t0001g0132others(3): Show | 6 | HG01346.hp2 HG01975.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.2995-8242C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69032066 | ||||||
| chr16:69032245
|
G | GTTCATTC others(5): Show |
4 | a0004c0006t0001g0179a0004c0006t0001g0180a0004c0006t0001g0181others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2995-8056_2995-804 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69032245 | |||||
| chr16:69032298
|
C | T | 1 | a0001c0002t0001g0071 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2995-8010C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69032298 | ||||||
| chr16:69032875
|
CA | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(144): Show | 147 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.2995-7417delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69032875 | |||||
| chr16:69033144
|
C | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-7164C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69033144 | ||||||
| chr16:69033635
|
T | C | 59 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.2995-6673T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69033635 | ||||||
| chr16:69033889
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-6419G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69033889 | ||||||
| chr16:69033913
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-6395C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69033913 | ||||||
| chr16:69033962
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2995-6346G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69033962 | ||||||
| chr16:69034437
|
C | A | 59 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.2995-5871C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69034437 | ||||||
| chr16:69034665
|
A | G | 3 | a0001c0007t0001g0036a0001c0007t0001g0038a0001c0007t0003g0037 | 3 | HG03239.hp2 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2995-5643A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69034665 | ||||||
| chr16:69034719
|
G | A | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2995-5589G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69034719 | ||||||
| chr16:69034867
|
CT | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0156others(3): Show | 6 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.2995-5427delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69034867 | |||||
| chr16:69034891
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-5417C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69034891 | ||||||
| chr16:69034894
|
GT | G | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2995-5412delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69034894 | |||||
| chr16:69034906
|
G | A | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2995-5402G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69034906 | ||||||
| chr16:69035402
|
G | A | 2 | a0001c0001t0001g0114a0005c0011t0001g0148 | 2 | HG03225.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2995-4906G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69035402 | ||||||
| chr16:69035880
|
A | C | 13 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(10): Show | 13 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.2995-4428A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69035880 | ||||||
| chr16:69036042
|
C | CA | 20 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0028others(17): Show | 20 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2995-4246dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69036042 | |||||
| chr16:69036529
|
G | A | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2995-3779G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69036529 | ||||||
| chr16:69036777
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2995-3531A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69036777 | ||||||
| chr16:69036864
|
G | A | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.2995-3444G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69036864 | ||||||
| chr16:69037117
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2995-3191C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037117 | ||||||
| chr16:69037127
|
G | T | 11 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(8): Show | 11 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(8): Show |
intron_variant | MODIFIER | c.2995-3181G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037127 | ||||||
| chr16:69037135
|
C | CA | 9 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0047others(6): Show | 9 | HG00741.hp2 HG01175.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-3152dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69037135 | |||||
| chr16:69037351
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0170 | 2 | NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2995-2957A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037351 | ||||||
| chr16:69037452
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2995-2856G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037452 | ||||||
| chr16:69037583
|
A | G | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2995-2725A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037583 | ||||||
| chr16:69037637
|
G | A | 3 | a0001c0003t0001g0130a0001c0003t0001g0134a0001c0003t0007g0127 | 3 | HG01346.hp2 HG01975.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2995-2671G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037637 | ||||||
| chr16:69037641
|
G | A | 1 | a0001c0003t0001g0124 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2995-2667G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037641 | ||||||
| chr16:69037832
|
C | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-2476C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69037832 | ||||||
| chr16:69038148
|
G | A | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2995-2160G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038148 | ||||||
| chr16:69038225
|
T | C | 57 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(54): Show | 57 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(54): Show |
intron_variant | MODIFIER | c.2995-2083T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038225 | ||||||
| chr16:69038226
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-2082G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038226 | ||||||
| chr16:69038500
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2995-1808G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038500 | ||||||
| chr16:69038614
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2995-1694C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038614 | ||||||
| chr16:69038638
|
G | T | 1 | a0001c0003t0001g0135 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2995-1670G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038638 | ||||||
| chr16:69038795
|
C | T | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2995-1513C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038795 | ||||||
| chr16:69038864
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2995-1444G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038864 | ||||||
| chr16:69038885
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2995-1423A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038885 | ||||||
| chr16:69038904
|
C | T | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2995-1404C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69038904 | ||||||
| chr16:69039000
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2995-1308G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039000 | ||||||
| chr16:69039327
|
C | CA | 16 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0028others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.2995-964dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69039327 | |||||
| chr16:69039327
|
CA | C | 36 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(33): Show | 36 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.2995-964delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69039327 | |||||
| chr16:69039344
|
A | T | 1 | a0001c0002t0001g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2995-964A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039344 | ||||||
| chr16:69039485
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2995-823A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039485 | ||||||
| chr16:69039504
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2995-804C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039504 | ||||||
| chr16:69039506
|
C | G | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2995-802C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039506 | ||||||
| chr16:69039635
|
C | CAAACA | 35 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(32): Show | 35 | HG00438.hp2 HG00741.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.2995-657_2995-653d others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69039635 | |||||
| chr16:69039635
|
C | CAAACAAA others(3): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | NA18957.hp1 NA18960.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2995-662_2995-653d others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 69039635 | |||||
| chr16:69039661
|
A | G | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.2995-647A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039661 | ||||||
| chr16:69039665
|
C | T | 2 | a0001c0003t0002g0195a0001c0003t0002g0197 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2995-643C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 16/17 | chr16 | 69039665 | ||||||
| chr16:69040600
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3108+179C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69040600 | ||||||
| chr16:69040860
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0154a0001c0001t0001g0205others(1): Show | 4 | HG00738.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+439G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69040860 | ||||||
| chr16:69040965
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3108+544A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69040965 | ||||||
| chr16:69041091
|
C | T | 6 | a0001c0003t0001g0128a0001c0003t0001g0130a0001c0003t0001g0132others(3): Show | 6 | HG01346.hp2 HG01975.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+670C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69041091 | ||||||
| chr16:69041315
|
G | A | 4 | a0001c0002t0001g0065a0001c0002t0001g0072a0001c0002t0001g0073others(1): Show | 4 | HG00408.hp1 NA18939.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.3108+894G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69041315 | ||||||
| chr16:69041446
|
CA | C | 14 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(11): Show | 14 | HG02257.hp1 HG02280.hp2 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.3108+1040delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69041446 | |||||
| chr16:69041500
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3108+1079T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69041500 | ||||||
| chr16:69041521
|
A | G | 37 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.3108+1100A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69041521 | ||||||
| chr16:69041700
|
C | G | 10 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0183others(7): Show | 10 | HG00544.hp1 HG01952.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.3108+1279C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69041700 | ||||||
| chr16:69041846
|
G | A | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3108+1425G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69041846 | ||||||
| chr16:69042337
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3108+1916G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69042337 | ||||||
| chr16:69042624
|
C | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0111 | 2 | HG03927.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.3108+2203C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69042624 | ||||||
| chr16:69042718
|
T | C | 116 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.3108+2297T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69042718 | ||||||
| chr16:69042733
|
T | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+2312T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69042733 | ||||||
| chr16:69043023
|
G | A | 11 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0003t0002g0195others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3108+2602G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69043023 | ||||||
| chr16:69043027
|
G | A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3108+2606G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69043027 | ||||||
| chr16:69043262
|
G | C | 1 | a0001c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3108+2841G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69043262 | ||||||
| chr16:69043283
|
A | AGT | 13 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0116others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.3108+2901_3108+290 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
A | AGTGT | 8 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0046others(5): Show | 8 | HG01192.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.3108+2899_3108+290 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
A | AGTGTGT | 3 | a0001c0001t0001g0031a0001c0001t0001g0152a0001c0003t0001g0126 | 3 | HG01099.hp2 HG02148.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3108+2897_3108+290 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
AGT | A | 32 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0032others(29): Show | 32 | HG00140.hp1 HG00741.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.3108+2901_3108+290 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
AGTGT | A | 34 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(31): Show | 34 | HG00738.hp2 HG01257.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.3108+2899_3108+290 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
AGTGTGT | A | 50 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0062others(47): Show | 50 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.3108+2897_3108+290 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3108+2893_3108+290 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043283
|
AGTGTGTG others(11): Show |
A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+2885_3108+290 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69043283 | |||||
| chr16:69043691
|
T | G | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3108+3270T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69043691 | ||||||
| chr16:69044020
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+3599G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044020 | ||||||
| chr16:69044157
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0171others(1): Show | 4 | HG02280.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+3736C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044157 | ||||||
| chr16:69044400
|
C | A | 6 | a0001c0003t0001g0128a0001c0003t0001g0130a0001c0003t0001g0132others(3): Show | 6 | HG01346.hp2 HG01975.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+3979C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044400 | ||||||
| chr16:69044572
|
T | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+4151T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044572 | ||||||
| chr16:69044589
|
C | T | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3108+4168C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044589 | ||||||
| chr16:69044615
|
A | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG02055.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3108+4194A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044615 | ||||||
| chr16:69044889
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3108+4468C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044889 | ||||||
| chr16:69044898
|
A | G | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3108+4477A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69044898 | ||||||
| chr16:69045032
|
C | T | 31 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.3108+4611C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045032 | ||||||
| chr16:69045049
|
C | T | 59 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.3108+4628C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045049 | ||||||
| chr16:69045156
|
C | CA | 12 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0035others(9): Show | 12 | HG01192.hp1 HG01258.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+4752dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69045156 | |||||
| chr16:69045156
|
C | CAA | 58 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0063others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.3108+4751_3108+475 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69045156 | |||||
| chr16:69045331
|
C | G | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+4910C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045331 | ||||||
| chr16:69045332
|
T | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3108+4911T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045332 | ||||||
| chr16:69045443
|
C | CA | 28 | a0001c0001t0001g0010a0001c0001t0001g0034a0001c0001t0001g0040others(25): Show | 28 | HG00544.hp1 HG01952.hp2 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.3108+5040dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69045443 | |||||
| chr16:69045443
|
C | CAA | 13 | a0001c0001t0001g0005a0001c0001t0001g0101a0001c0001t0001g0120others(10): Show | 13 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.3108+5039_3108+504 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69045443 | |||||
| chr16:69045496
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3108+5075C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045496 | ||||||
| chr16:69045658
|
G | A | 9 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(6): Show | 9 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.3108+5237G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045658 | ||||||
| chr16:69045945
|
T | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3108+5524T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69045945 | ||||||
| chr16:69046055
|
C | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3108+5634C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69046055 | ||||||
| chr16:69046063
|
C | CA | 21 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0055others(18): Show | 21 | HG00438.hp2 HG01433.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.3108+5661dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046063 | |||||
| chr16:69046063
|
C | CAA | 56 | a0001c0001t0001g0011a0001c0001t0001g0063a0001c0001t0001g0066others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.3108+5660_3108+566 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046063 | |||||
| chr16:69046063
|
CA | C | 29 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(26): Show | 29 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.3108+5661delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046063 | |||||
| chr16:69046321
|
A | AT | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG03516.hp1 HG03579.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.3108+5916dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046321 | |||||
| chr16:69046321
|
A | ATT | 15 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0040others(12): Show | 15 | HG00741.hp2 HG01081.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.3108+5915_3108+591 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046321 | |||||
| chr16:69046321
|
A | ATTT | 12 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0121others(9): Show | 12 | HG01175.hp2 HG02055.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3108+5914_3108+591 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046321 | |||||
| chr16:69046321
|
AT | A | 6 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0001t0001g0199others(3): Show | 6 | HG01891.hp2 HG02135.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3108+5916delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046321 | |||||
| chr16:69046414
|
A | G | 50 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00741.hp2 HG01081.hp1 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.3108+5993A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69046414 | ||||||
| chr16:69046451
|
T | G | 1 | a0001c0001t0001g0001 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3108+6030T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69046451 | ||||||
| chr16:69046468
|
G | A | 1 | a0001c0001t0005g0169 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3108+6047G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69046468 | ||||||
| chr16:69046478
|
G | A | 1 | a0001c0002t0001g0079 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3108+6057G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69046478 | ||||||
| chr16:69046694
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3108+6273A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69046694 | ||||||
| chr16:69046767
|
T | TA | 5 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3108+6355dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69046767 | |||||
| chr16:69047039
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3108+6618G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047039 | ||||||
| chr16:69047175
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3108+6754T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047175 | ||||||
| chr16:69047180
|
C | CA | 58 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0045others(55): Show | 58 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.3108+6776dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69047180 | |||||
| chr16:69047180
|
CA | C | 22 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(19): Show | 22 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.3108+6776delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69047180 | |||||
| chr16:69047321
|
C | T | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3108+6900C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047321 | ||||||
| chr16:69047330
|
A | G | 1 | a0001c0002t0001g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3108+6909A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047330 | ||||||
| chr16:69047530
|
G | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3108+7109G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047530 | ||||||
| chr16:69047579
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3108+7158A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047579 | ||||||
| chr16:69047884
|
T | C | 34 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(31): Show | 34 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3108+7463T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047884 | ||||||
| chr16:69047968
|
A | G | 34 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(31): Show | 34 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3108+7547A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69047968 | ||||||
| chr16:69048258
|
A | AT | 31 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0012others(28): Show | 31 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.3108+7861dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69048258 | |||||
| chr16:69048258
|
AT | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0041others(13): Show | 16 | HG01099.hp2 HG01175.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.3108+7861delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69048258 | |||||
| chr16:69048258
|
ATT | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0040others(13): Show | 16 | HG00741.hp2 HG01346.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.3108+7860_3108+786 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69048258 | |||||
| chr16:69048258
|
ATTT | A | 13 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(10): Show | 13 | HG00544.hp1 HG01433.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3108+7859_3108+786 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69048258 | |||||
| chr16:69048258
|
ATTTTTTT others(2): Show |
A | 56 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0045others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.3108+7853_3108+786 others(13): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69048258 | |||||
| chr16:69048258
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3108+7852_3108+786 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69048258 | |||||
| chr16:69048341
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3108+7920A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048341 | ||||||
| chr16:69048383
|
T | C | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3108+7962T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048383 | ||||||
| chr16:69048557
|
T | C | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3108+8136T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048557 | ||||||
| chr16:69048649
|
G | A | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3108+8228G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048649 | ||||||
| chr16:69048686
|
A | G | 3 | a0001c0002t0001g0074a0001c0002t0001g0075a0001c0002t0001g0113 | 3 | NA18957.hp2 NA18975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3108+8265A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048686 | ||||||
| chr16:69048898
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3108+8477C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048898 | ||||||
| chr16:69048914
|
C | T | 103 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(100): Show | 103 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.3108+8493C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69048914 | ||||||
| chr16:69049232
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3108+8811A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69049232 | ||||||
| chr16:69049695
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0110a0001c0003t0001g0125others(1): Show | 4 | HG00140.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+9274C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69049695 | ||||||
| chr16:69050010
|
G | C | 34 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(31): Show | 34 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3108+9589G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050010 | ||||||
| chr16:69050080
|
C | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019 | 3 | HG02559.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3108+9659C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050080 | ||||||
| chr16:69050130
|
G | GT | 5 | a0001c0003t0001g0128a0001c0003t0001g0132a0001c0003t0001g0134others(2): Show | 5 | HG01346.hp2 NA18964.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.3108+9712dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69050130 | |||||
| chr16:69050176
|
G | C | 1 | a0001c0007t0003g0037 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3108+9755G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050176 | ||||||
| chr16:69050275
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0120others(13): Show | 16 | HG00099.hp2 HG00738.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3108+9854A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050275 | ||||||
| chr16:69050417
|
G | A | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3108+9996G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050417 | ||||||
| chr16:69050491
|
A | AT | 7 | a0001c0001t0001g0035a0001c0001t0001g0069a0001c0001t0001g0145others(4): Show | 7 | HG00408.hp1 HG01258.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3108+10086dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69050491 | |||||
| chr16:69050582
|
C | T | 1 | a0001c0003t0001g0126 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3108+10161C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050582 | ||||||
| chr16:69050777
|
C | T | 6 | a0001c0002t0001g0064a0001c0002t0001g0071a0001c0002t0001g0088others(3): Show | 6 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.3108+10356C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050777 | ||||||
| chr16:69050851
|
G | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3108+10430G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050851 | ||||||
| chr16:69050883
|
C | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(20): Show | 23 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.3108+10462C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050883 | ||||||
| chr16:69050893
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3108+10472G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050893 | ||||||
| chr16:69050959
|
A | G | 10 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG00544.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3108+10538A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69050959 | ||||||
| chr16:69051008
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3108+10587A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69051008 | ||||||
| chr16:69051459
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3108+11038T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69051459 | ||||||
| chr16:69051857
|
T | A | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3108+11436T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69051857 | ||||||
| chr16:69051868
|
A | T | 32 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(29): Show | 32 | HG00408.hp1 HG00544.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.3108+11447A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69051868 | ||||||
| chr16:69052269
|
C | CT | 36 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0054others(33): Show | 36 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.3108+11864dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69052269 | |||||
| chr16:69052269
|
CT | C | 69 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0029others(66): Show | 69 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.3108+11864delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69052269 | |||||
| chr16:69052311
|
C | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3108+11890C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69052311 | ||||||
| chr16:69052429
|
C | T | 57 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0045others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.3108+12008C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69052429 | ||||||
| chr16:69052532
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3108+12111A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69052532 | ||||||
| chr16:69052834
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3108+12413C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69052834 | ||||||
| chr16:69052924
|
C | T | 1 | a0001c0003t0001g0130 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3108+12503C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69052924 | ||||||
| chr16:69053098
|
G | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(20): Show | 23 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.3108+12677G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69053098 | ||||||
| chr16:69053261
|
C | T | 14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3108+12840C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69053261 | ||||||
| chr16:69053469
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3108+13048G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69053469 | ||||||
| chr16:69053496
|
G | C | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3108+13075G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69053496 | ||||||
| chr16:69053588
|
T | G | 33 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(30): Show | 33 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.3108+13167T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69053588 | ||||||
| chr16:69054056
|
C | G | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3108+13635C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054056 | ||||||
| chr16:69054190
|
T | A | 12 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0069others(9): Show | 12 | HG00408.hp1 HG01258.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+13769T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054190 | ||||||
| chr16:69054206
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3108+13785G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054206 | ||||||
| chr16:69054278
|
A | G | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3108+13857A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054278 | ||||||
| chr16:69054303
|
G | A | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3108+13882G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054303 | ||||||
| chr16:69054749
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3108+14328C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054749 | ||||||
| chr16:69054758
|
A | C | 2 | a0001c0002t0001g0086a0001c0009t0001g0133 | 2 | HG02129.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.3108+14337A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054758 | ||||||
| chr16:69054758
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3108+14337A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054758 | ||||||
| chr16:69054777
|
CA | C | 113 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3108+14370delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69054777 | |||||
| chr16:69054802
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3108+14381G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054802 | ||||||
| chr16:69054866
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+14445G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054866 | ||||||
| chr16:69054880
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3108+14459G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054880 | ||||||
| chr16:69054882
|
A | C | 1 | a0003c0004t0004g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3108+14461A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69054882 | ||||||
| chr16:69054940
|
C | CA | 21 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0023others(18): Show | 21 | HG01175.hp2 HG01346.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+14543dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69054940 | |||||
| chr16:69054940
|
CA | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0045others(28): Show | 31 | HG00408.hp2 HG00544.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.3108+14543delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69054940 | |||||
| chr16:69054940
|
CAA | C | 65 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0056others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.3108+14542_3108+14 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69054940 | |||||
| chr16:69055020
|
AT | A | 26 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(23): Show | 26 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.3108+14611delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69055020 | |||||
| chr16:69055020
|
ATT | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3108+14610_3108+14 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69055020 | |||||
| chr16:69055702
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3108+15281A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69055702 | ||||||
| chr16:69055760
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+15339G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69055760 | ||||||
| chr16:69055844
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3108+15423C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69055844 | ||||||
| chr16:69055952
|
T | C | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3108+15531T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69055952 | ||||||
| chr16:69056123
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0154a0001c0001t0001g0205 | 3 | HG00738.hp2 HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3108+15702G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69056123 | ||||||
| chr16:69056203
|
C | G | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3108+15782C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69056203 | ||||||
| chr16:69056256
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3108+15835C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69056256 | ||||||
| chr16:69056429
|
C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3108+16008C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69056429 | ||||||
| chr16:69056576
|
C | CA | 14 | a0001c0001t0001g0012a0001c0001t0001g0094a0001c0001t0001g0105others(11): Show | 14 | HG01361.hp2 HG01891.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.3108+16168dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69056576 | |||||
| chr16:69056997
|
C | CT | 34 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0019others(31): Show | 34 | HG00438.hp2 HG01192.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.3108+16605dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69056997 | |||||
| chr16:69056997
|
C | CTT | 11 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0100others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3108+16604_3108+16 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69056997 | |||||
| chr16:69056997
|
CT | C | 67 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0029others(64): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.3108+16605delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69056997 | |||||
| chr16:69057269
|
G | A | 11 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(8): Show | 11 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.3108+16848G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057269 | ||||||
| chr16:69057305
|
G | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0104 | 3 | HG02735.hp1 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3108+16884G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057305 | ||||||
| chr16:69057315
|
C | T | 123 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.3108+16894C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057315 | ||||||
| chr16:69057383
|
CA | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+16963delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057383 | ||||||
| chr16:69057457
|
G | A | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+17036G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057457 | ||||||
| chr16:69057533
|
C | G | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+17112C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057533 | ||||||
| chr16:69057538
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3108+17117A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057538 | ||||||
| chr16:69057748
|
G | A | 10 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG00544.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3108+17327G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057748 | ||||||
| chr16:69057920
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+17499C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69057920 | ||||||
| chr16:69058199
|
G | C | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3108+17778G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058199 | ||||||
| chr16:69058332
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3108+17911A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058332 | ||||||
| chr16:69058556
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+18135G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058556 | ||||||
| chr16:69058676
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0116 | 2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3108+18255T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058676 | ||||||
| chr16:69058712
|
C | T | 1 | a0001c0002t0001g0067 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3108+18291C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058712 | ||||||
| chr16:69058760
|
T | G | 44 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(41): Show | 44 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.3108+18339T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058760 | ||||||
| chr16:69058868
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3108+18447G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058868 | ||||||
| chr16:69058909
|
C | CT | 6 | a0001c0001t0001g0028a0001c0001t0001g0049a0003c0004t0001g0151others(3): Show | 6 | HG02258.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3108+18503dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69058909 | |||||
| chr16:69058922
|
T | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0058 | 2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3108+18501T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69058922 | ||||||
| chr16:69059098
|
G | A | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3108+18677G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69059098 | ||||||
| chr16:69059105
|
T | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3108+18684T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69059105 | ||||||
| chr16:69059167
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+18746C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69059167 | ||||||
| chr16:69059658
|
T | C | 1 | a0001c0002t0001g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3108+19237T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69059658 | ||||||
| chr16:69059729
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3108+19308C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69059729 | ||||||
| chr16:69059893
|
G | A | 125 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(122): Show | 125 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.3108+19472G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69059893 | ||||||
| chr16:69060519
|
C | T | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+20098C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69060519 | ||||||
| chr16:69060549
|
T | C | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3108+20128T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69060549 | ||||||
| chr16:69060618
|
A | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3108+20197A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69060618 | ||||||
| chr16:69060907
|
A | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.3108+20486A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69060907 | ||||||
| chr16:69060989
|
T | TA | 16 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0057others(13): Show | 16 | HG01081.hp1 HG01192.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.3108+20578dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69060989 | |||||
| chr16:69061000
|
C | A | 1 | a0001c0001t0001g0140 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3108+20579C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061000 | ||||||
| chr16:69061022
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3108+20601G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061022 | ||||||
| chr16:69061085
|
A | G | 4 | a0001c0001t0001g0027a0001c0002t0001g0076a0001c0002t0001g0078others(1): Show | 4 | NA18952.hp2 NA18982.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.3108+20664A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061085 | ||||||
| chr16:69061135
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3108+20714G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061135 | ||||||
| chr16:69061182
|
G | C | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3108+20761G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061182 | ||||||
| chr16:69061259
|
T | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3108+20838T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061259 | ||||||
| chr16:69061674
|
T | C | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3108+21253T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061674 | ||||||
| chr16:69061752
|
G | A | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3108+21331G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061752 | ||||||
| chr16:69061793
|
G | T | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3108+21372G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061793 | ||||||
| chr16:69061880
|
A | G | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3108+21459A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69061880 | ||||||
| chr16:69062067
|
A | G | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3109-21418A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062067 | ||||||
| chr16:69062095
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3109-21390T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062095 | ||||||
| chr16:69062486
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3109-20999T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062486 | ||||||
| chr16:69062519
|
C | T | 10 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(7): Show | 10 | HG00544.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3109-20966C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062519 | ||||||
| chr16:69062621
|
T | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.3109-20864T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062621 | ||||||
| chr16:69062687
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0204a0001c0001t0001g0209others(1): Show | 4 | HG01884.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-20798G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062687 | ||||||
| chr16:69062786
|
T | TA | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-20699_3109-20 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062786 | ||||||
| chr16:69062787
|
T | A | 9 | a0001c0001t0001g0054a0001c0001t0001g0152a0001c0001t0001g0207others(6): Show | 9 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.3109-20698T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062787 | ||||||
| chr16:69062787
|
T | TA | 83 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0029others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.3109-20677dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69062787 | |||||
| chr16:69062787
|
TAAAAA | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-20681_3109-20 others(11): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69062787 | |||||
| chr16:69062788
|
A | T | 1 | a0001c0001t0001g0017 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3109-20697A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062788 | ||||||
| chr16:69062891
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3109-20594G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69062891 | ||||||
| chr16:69063104
|
T | C | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-20381T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063104 | ||||||
| chr16:69063222
|
G | GA | 8 | a0001c0001t0001g0053a0001c0001t0001g0082a0001c0001t0001g0160others(5): Show | 8 | HG01192.hp2 HG02818.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-20248dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063222 | |||||
| chr16:69063222
|
GA | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.3109-20248delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063222 | |||||
| chr16:69063562
|
T | G | 2 | a0001c0008t0001g0112a0001c0008t0001g0119 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3109-19923T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063562 | ||||||
| chr16:69063643
|
C | CA | 72 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.3109-19815dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063643 | |||||
| chr16:69063643
|
C | CAA | 23 | a0001c0001t0001g0062a0001c0001t0001g0083a0001c0001t0001g0091others(20): Show | 23 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.3109-19816_3109-19 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063643 | |||||
| chr16:69063643
|
C | CAAA | 5 | a0001c0001t0001g0005a0001c0002t0001g0004a0001c0002t0001g0090others(2): Show | 5 | HG01192.hp1 HG01928.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3109-19817_3109-19 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063643 | |||||
| chr16:69063643
|
CA | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0122others(17): Show | 20 | HG01433.hp2 HG02055.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.3109-19815delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063643 | |||||
| chr16:69063660
|
A | C | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-19825A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063660 | ||||||
| chr16:69063668
|
A | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0121others(20): Show | 23 | HG01433.hp2 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.3109-19817A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063668 | ||||||
| chr16:69063672
|
A | G | 7 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0071others(4): Show | 7 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-19813A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063672 | ||||||
| chr16:69063758
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3109-19727A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063758 | ||||||
| chr16:69063781
|
T | TTTC | 44 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 44 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.3109-19677_3109-19 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTC | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0040others(30): Show | 33 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.3109-19680_3109-19 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(2): Show |
19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0021others(16): Show | 19 | HG00738.hp2 HG01081.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.3109-19683_3109-19 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(5): Show |
18 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0015others(15): Show | 18 | HG00741.hp1 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.3109-19686_3109-19 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(8): Show |
9 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0100others(6): Show | 9 | HG02559.hp2 HG02615.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.3109-19689_3109-19 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(11): Show |
7 | a0001c0001t0001g0018a0001c0001t0001g0049a0001c0001t0001g0143others(4): Show | 7 | HG02486.hp1 HG02572.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-19692_3109-19 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(14): Show |
7 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0114others(4): Show | 7 | HG01891.hp1 HG02886.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-19695_3109-19 others(27): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(17): Show |
2 | a0001c0001t0001g0025a0001c0001t0001g0111 | 2 | HG01884.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3109-19698_3109-19 others(30): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(20): Show |
1 | a0001c0001t0001g0101 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3109-19701_3109-19 others(33): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
T | TTTCTTCT others(23): Show |
1 | a0001c0001t0001g0204 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3109-19675_3109-19 others(36): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
TTTC | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0026others(15): Show | 18 | HG00738.hp1 HG02027.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.3109-19677_3109-19 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
TTTCTTC | T | 6 | a0001c0001t0001g0141a0001c0002t0001g0067a0001c0002t0001g0068others(3): Show | 6 | HG01255.hp2 HG02273.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-19680_3109-19 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063781
|
TTTCTTCT others(5): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3109-19686_3109-19 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063781 | |||||
| chr16:69063808
|
C | CTTA | 34 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(31): Show | 34 | HG00438.hp1 HG01255.hp1 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.3109-19642_3109-19 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
C | CTTATTA | 29 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0013others(26): Show | 29 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.3109-19645_3109-19 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
C | CTTATTAT others(2): Show |
7 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0026others(4): Show | 7 | HG00544.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-19648_3109-19 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
C | CTTATTAT others(5): Show |
1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3109-19651_3109-19 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTA | C | 32 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(29): Show | 32 | HG01081.hp1 HG01081.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.3109-19642_3109-19 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTATTA | C | 15 | a0001c0001t0001g0056a0001c0001t0001g0063a0001c0001t0001g0077others(12): Show | 15 | HG01361.hp1 HG01496.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.3109-19645_3109-19 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTATTAT others(2): Show |
C | 21 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0087others(18): Show | 21 | HG01257.hp1 HG01258.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.3109-19648_3109-19 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTATTAT others(5): Show |
C | 4 | a0001c0001t0001g0025a0001c0001t0001g0122a0001c0001t0001g0204others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-19651_3109-19 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTATTAT others(8): Show |
C | 6 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0208others(3): Show | 6 | HG02818.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-19654_3109-19 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTATTAT others(11): Show |
C | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0166others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-19657_3109-19 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063808
|
CTTATTAT others(14): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3109-19660_3109-19 others(27): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69063808 | |||||
| chr16:69063811
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19674A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063811 | ||||||
| chr16:69063814
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19671A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063814 | ||||||
| chr16:69063817
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19668A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063817 | ||||||
| chr16:69063820
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19665A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063820 | ||||||
| chr16:69063823
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19662A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063823 | ||||||
| chr16:69063826
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19659A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063826 | ||||||
| chr16:69063829
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19656A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063829 | ||||||
| chr16:69063832
|
A | C | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-19653A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063832 | ||||||
| chr16:69063962
|
G | A | 2 | a0001c0007t0001g0036a0001c0007t0001g0038 | 2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3109-19523G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063962 | ||||||
| chr16:69063967
|
G | C | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3109-19518G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69063967 | ||||||
| chr16:69064161
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3109-19324G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064161 | ||||||
| chr16:69064211
|
A | G | 1 | a0001c0003t0002g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3109-19274A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064211 | ||||||
| chr16:69064379
|
C | G | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3109-19106C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064379 | ||||||
| chr16:69064546
|
G | A | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3109-18939G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064546 | ||||||
| chr16:69064884
|
A | G | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3109-18601A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064884 | ||||||
| chr16:69064918
|
C | T | 3 | a0001c0001t0001g0106a0002c0005t0001g0162a0002c0005t0001g0163 | 3 | HG03834.hp2 HG03927.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3109-18567C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064918 | ||||||
| chr16:69064963
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-18522C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69064963 | ||||||
| chr16:69065023
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3109-18462C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065023 | ||||||
| chr16:69065095
|
T | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-18390T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065095 | ||||||
| chr16:69065131
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3109-18354G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065131 | ||||||
| chr16:69065191
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3109-18294C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065191 | ||||||
| chr16:69065510
|
T | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-17975T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065510 | ||||||
| chr16:69065551
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3109-17934C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065551 | ||||||
| chr16:69065765
|
T | C | 106 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.3109-17720T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065765 | ||||||
| chr16:69065987
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-17498A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69065987 | ||||||
| chr16:69066153
|
G | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-17332G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066153 | ||||||
| chr16:69066287
|
CATTT | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG02486.hp2 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3109-17197_3109-17 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066287 | ||||||
| chr16:69066321
|
G | A | 1 | a0004c0006t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3109-17164G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066321 | ||||||
| chr16:69066356
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3109-17129G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066356 | ||||||
| chr16:69066588
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3109-16897C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066588 | ||||||
| chr16:69066745
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3109-16740G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066745 | ||||||
| chr16:69066856
|
A | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-16629A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066856 | ||||||
| chr16:69066965
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0001t0008g0030 | 3 | HG01884.hp2 HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3109-16520C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69066965 | ||||||
| chr16:69067039
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-16446A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067039 | ||||||
| chr16:69067382
|
T | C | 113 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0024others(110): Show | 113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.3109-16103T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067382 | ||||||
| chr16:69067518
|
C | CA | 67 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(64): Show | 67 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3109-15948dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(3): Show |
10 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG02280.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-15957_3109-15 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(4): Show |
11 | a0001c0001t0001g0054a0001c0001t0001g0140a0001c0001t0001g0158others(8): Show | 11 | HG01433.hp2 HG02055.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.3109-15958_3109-15 others(17): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0182a0001c0007t0003g0037a0003c0004t0001g0151others(4): Show | 7 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3109-15959_3109-15 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(6): Show |
18 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0040others(15): Show | 18 | HG00544.hp1 HG00741.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.3109-15960_3109-15 others(19): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0008t0001g0112others(1): Show | 4 | HG01175.hp2 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-15961_3109-15 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0150a0001c0001t0001g0174others(1): Show | 4 | HG02572.hp1 HG03486.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-15962_3109-15 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(9): Show |
1 | a0002c0005t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3109-15963_3109-15 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(10): Show |
2 | a0002c0005t0006g0138a0005c0011t0001g0148 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3109-15964_3109-15 others(23): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067518
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3109-15965_3109-15 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067518 | |||||
| chr16:69067538
|
C | A | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-15947C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067538 | ||||||
| chr16:69067546
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3109-15939G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067546 | ||||||
| chr16:69067548
|
C | T | 1 | a0001c0002t0001g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3109-15937C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067548 | ||||||
| chr16:69067573
|
A | G | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-15912A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067573 | ||||||
| chr16:69067627
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3109-15858G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067627 | ||||||
| chr16:69067708
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3109-15777C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067708 | ||||||
| chr16:69067713
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3109-15772G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067713 | ||||||
| chr16:69067937
|
C | CA | 12 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0150others(9): Show | 12 | HG01346.hp2 HG02135.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.3109-15529dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067937 | |||||
| chr16:69067937
|
CA | C | 31 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0122others(28): Show | 31 | HG01433.hp2 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.3109-15529delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067937 | |||||
| chr16:69067937
|
CAA | C | 21 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(18): Show | 21 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.3109-15530_3109-15 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69067937 | |||||
| chr16:69067938
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3109-15547A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69067938 | ||||||
| chr16:69068071
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-15414G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068071 | ||||||
| chr16:69068357
|
T | C | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-15128T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068357 | ||||||
| chr16:69068537
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3109-14948G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068537 | ||||||
| chr16:69068578
|
G | C | 1 | a0001c0002t0001g0113 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3109-14907G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068578 | ||||||
| chr16:69068651
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3109-14834T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068651 | ||||||
| chr16:69068743
|
C | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3109-14742C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068743 | ||||||
| chr16:69068774
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-14711C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068774 | ||||||
| chr16:69068871
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-14614G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69068871 | ||||||
| chr16:69069086
|
T | C | 58 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(55): Show | 58 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(55): Show |
intron_variant | MODIFIER | c.3109-14399T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069086 | ||||||
| chr16:69069096
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-14389C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069096 | ||||||
| chr16:69069192
|
A | G | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-14293A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069192 | ||||||
| chr16:69069288
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-14197A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069288 | ||||||
| chr16:69069498
|
C | T | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-13987C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069498 | ||||||
| chr16:69069595
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.3109-13890T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069595 | ||||||
| chr16:69069596
|
G | C | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3109-13889G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069596 | ||||||
| chr16:69069857
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-13628C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069857 | ||||||
| chr16:69069883
|
A | G | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-13602A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69069883 | ||||||
| chr16:69070044
|
T | TA | 11 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0077others(8): Show | 11 | HG01081.hp1 HG01175.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.3109-13421dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070044 | |||||
| chr16:69070185
|
G | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3109-13300G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070185 | ||||||
| chr16:69070191
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-13294G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070191 | ||||||
| chr16:69070194
|
C | G | 2 | a0001c0002t0001g0065a0001c0002t0001g0095 | 2 | NA18960.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.3109-13291C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070194 | ||||||
| chr16:69070266
|
G | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-13219G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070266 | ||||||
| chr16:69070360
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-13125C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070360 | ||||||
| chr16:69070364
|
G | A | 12 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0067others(9): Show | 12 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-13121G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070364 | ||||||
| chr16:69070478
|
C | T | 11 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(8): Show | 11 | HG01433.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.3109-13007C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070478 | ||||||
| chr16:69070597
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-12888C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070597 | ||||||
| chr16:69070632
|
C | CA | 12 | a0001c0001t0001g0066a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG00544.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-12839dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070632 | |||||
| chr16:69070632
|
C | CAA | 10 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(7): Show | 10 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-12840_3109-12 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070632 | |||||
| chr16:69070647
|
C | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0183a0003c0004t0001g0151others(2): Show | 5 | HG00544.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3109-12838C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070647 | ||||||
| chr16:69070656
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3109-12829A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070656 | ||||||
| chr16:69070746
|
A | ATAT | 11 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0034others(8): Show | 11 | HG01192.hp1 HG01433.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.3109-12701_3109-12 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
A | ATATTAT | 12 | a0001c0001t0001g0099a0001c0001t0001g0107a0001c0001t0001g0114others(9): Show | 12 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.3109-12704_3109-12 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
A | ATATTATT others(2): Show |
2 | a0001c0001t0001g0100a0001c0003t0002g0197 | 2 | HG03041.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3109-12707_3109-12 others(15): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
A | ATATTATT others(5): Show |
1 | a0001c0003t0002g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3109-12710_3109-12 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
ATAT | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(114): Show | 117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.3109-12701_3109-12 others(9): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
ATATTAT | A | 4 | a0001c0001t0001g0204a0001c0001t0003g0042a0001c0001t0003g0044others(1): Show | 4 | HG01346.hp1 HG01361.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-12704_3109-12 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
ATATTATT others(5): Show |
A | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3109-12710_3109-12 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070746
|
ATATTATT others(14): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3109-12719_3109-12 others(27): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69070746 | |||||
| chr16:69070758
|
T | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0161 | 2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3109-12727T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070758 | ||||||
| chr16:69070963
|
G | A | 1 | a0001c0003t0007g0127 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3109-12522G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69070963 | ||||||
| chr16:69071397
|
G | A | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-12088G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69071397 | ||||||
| chr16:69071782
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3109-11703A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69071782 | ||||||
| chr16:69071801
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3109-11684A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69071801 | ||||||
| chr16:69071982
|
C | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-11503C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69071982 | ||||||
| chr16:69071990
|
C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | NA18957.hp1 NA18960.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.3109-11495C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69071990 | ||||||
| chr16:69072026
|
C | CGT | 61 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0028others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3109-11418_3109-11 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGT | 22 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0015others(19): Show | 22 | HG00741.hp1 HG01255.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.3109-11420_3109-11 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGT | 11 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0121others(8): Show | 11 | HG00544.hp1 HG00741.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.3109-11422_3109-11 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(1): Show |
19 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0107others(16): Show | 19 | HG00738.hp1 HG01175.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.3109-11424_3109-11 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(3): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0099others(3): Show | 6 | HG01192.hp1 HG02040.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-11426_3109-11 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(5): Show |
6 | a0001c0001t0001g0101a0001c0001t0001g0141a0001c0001t0008g0030others(3): Show | 6 | HG01884.hp2 HG02717.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3109-11428_3109-11 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(7): Show |
5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0140others(2): Show | 5 | HG00099.hp2 HG02486.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.3109-11430_3109-11 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(9): Show |
1 | a0001c0001t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3109-11432_3109-11 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(11): Show |
1 | a0001c0001t0001g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3109-11434_3109-11 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(13): Show |
1 | a0001c0001t0001g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3109-11436_3109-11 others(26): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
C | CGTGTGTG others(15): Show |
1 | a0001c0001t0001g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3109-11438_3109-11 others(28): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
CGT | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0023others(16): Show | 19 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.3109-11418_3109-11 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
CGTGTGT | C | 2 | a0001c0001t0001g0021a0001c0007t0001g0036 | 2 | HG02630.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3109-11422_3109-11 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072026
|
CGTGTGTG others(11): Show |
C | 2 | a0001c0001t0001g0172a0001c0001t0001g0182 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3109-11434_3109-11 others(24): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072026 | |||||
| chr16:69072028
|
T | TGTGTGTG others(105): Show |
1 | a0001c0003t0002g0195 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3109-11417_3109-11 others(118): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072028 | |||||
| chr16:69072034
|
T | TGTGTGTG others(199): Show |
1 | a0001c0001t0001g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3109-11417_3109-11 others(212): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072034 | |||||
| chr16:69072049
|
G | GTGTGTT | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0167 | 3 | HG03098.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3109-11431_3109-11 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072049 | |||||
| chr16:69072064
|
TGTGTAGA others(12): Show |
T | 2 | a0003c0004t0001g0164a0003c0004t0001g0201 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-11416_3109-11 others(25): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072064 | |||||
| chr16:69072068
|
TAGAGAGA others(8): Show |
T | 1 | a0003c0004t0001g0151 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3109-11416_3109-11 others(21): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072068 | ||||||
| chr16:69072083
|
C | CGTGTGT | 27 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(24): Show | 27 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.3109-11391_3109-11 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072083
|
C | CGTGTGTG others(1): Show |
12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-11393_3109-11 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072083
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0054a0001c0003t0002g0195 | 2 | HG02615.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3109-11395_3109-11 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072083
|
C | CGTGTGTG others(101): Show |
2 | a0001c0001t0001g0208a0006c0010t0001g0206 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3109-11386_3109-11 others(114): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072083
|
C | CGTGTGTG others(103): Show |
2 | a0001c0001t0001g0207a0001c0003t0002g0196 | 2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3109-11386_3109-11 others(116): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072083
|
C | CGTGTGTG others(109): Show |
1 | a0001c0001t0002g0022 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3109-11386_3109-11 others(122): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072083
|
C | CGTGTGTG others(111): Show |
1 | a0001c0003t0002g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3109-11386_3109-11 others(124): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072083 | |||||
| chr16:69072084
|
G | A | 14 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3109-11401G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072084 | ||||||
| chr16:69072122
|
C | CGT | 33 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0035others(30): Show | 33 | HG01081.hp2 HG01257.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.3109-11332_3109-11 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
C | CGTGT | 37 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0029others(34): Show | 37 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.3109-11334_3109-11 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
C | CGTGTGT | 7 | a0001c0001t0001g0024a0001c0001t0001g0183a0001c0001t0001g0207others(4): Show | 7 | HG00544.hp1 HG01433.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.3109-11336_3109-11 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
C | CGTGTGTG others(1): Show |
5 | a0001c0003t0001g0134a0004c0006t0001g0179a0004c0006t0001g0180others(2): Show | 5 | HG01346.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-11338_3109-11 others(14): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
C | CGTGTGTG others(3): Show |
1 | a0003c0004t0004g0203 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3109-11340_3109-11 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
C | CGTGTGTG others(7): Show |
1 | a0003c0004t0004g0202 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3109-11344_3109-11 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
CGT | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0199others(1): Show | 4 | HG01884.hp2 HG02129.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-11332_3109-11 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072122
|
CGTGTGTG others(5): Show |
C | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-11342_3109-11 others(18): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69072122 | |||||
| chr16:69072203
|
C | A | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-11282C>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072203 | ||||||
| chr16:69072378
|
T | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-11107T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072378 | ||||||
| chr16:69072394
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3109-11091G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072394 | ||||||
| chr16:69072476
|
G | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0024others(65): Show | 68 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.3109-11009G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072476 | ||||||
| chr16:69072549
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-10936T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072549 | ||||||
| chr16:69072725
|
C | T | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3109-10760C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072725 | ||||||
| chr16:69072945
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3109-10540G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69072945 | ||||||
| chr16:69073212
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-10273A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073212 | ||||||
| chr16:69073301
|
A | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG01081.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.3109-10184A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073301 | ||||||
| chr16:69073338
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0182a0001c0001t0008g0030 | 3 | HG01884.hp2 HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3109-10147C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073338 | ||||||
| chr16:69073541
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3109-9944T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073541 | ||||||
| chr16:69073604
|
C | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-9881C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073604 | ||||||
| chr16:69073682
|
C | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3109-9803C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073682 | ||||||
| chr16:69073729
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-9756G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073729 | ||||||
| chr16:69073778
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-9707A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073778 | ||||||
| chr16:69073812
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-9673C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073812 | ||||||
| chr16:69073891
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-9594G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69073891 | ||||||
| chr16:69073960
|
T | TA | 30 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(27): Show | 30 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.3109-9509dupA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69073960 | |||||
| chr16:69073960
|
TA | T | 13 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0106others(10): Show | 13 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.3109-9509delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69073960 | |||||
| chr16:69074009
|
C | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(46): Show | 49 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.3109-9476C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074009 | ||||||
| chr16:69074173
|
C | T | 13 | a0001c0001t0001g0106a0001c0001t0001g0155a0001c0001t0001g0172others(10): Show | 13 | HG01346.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3109-9312C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074173 | ||||||
| chr16:69074265
|
C | CTG | 3 | a0001c0001t0001g0152a0001c0001t0001g0172a0001c0001t0001g0182 | 3 | HG01891.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3109-9206_3109-920 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074265 | |||||
| chr16:69074269
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3109-9216G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074269 | ||||||
| chr16:69074279
|
G | GTA | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-9192_3109-919 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074279 | |||||
| chr16:69074306
|
A | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-9179A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074306 | ||||||
| chr16:69074312
|
G | A | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-9173G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074312 | ||||||
| chr16:69074453
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0104 | 3 | HG02735.hp1 HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3109-9032C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074453 | ||||||
| chr16:69074484
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0105 | 2 | HG03490.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3109-9001C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074484 | ||||||
| chr16:69074536
|
G | C | 9 | a0001c0001t0001g0173a0001c0001t0001g0178a0001c0001t0001g0184others(6): Show | 9 | HG01952.hp2 HG01981.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.3109-8949G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074536 | ||||||
| chr16:69074798
|
C | CTG | 34 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0033others(31): Show | 34 | HG00140.hp2 HG00544.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.3109-8647_3109-864 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
C | CTGTG | 34 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0045others(31): Show | 34 | HG00408.hp2 HG00438.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.3109-8649_3109-864 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
C | CTGTGTG | 10 | a0001c0001t0001g0066a0001c0002t0001g0064a0001c0002t0001g0088others(7): Show | 10 | HG00140.hp1 HG00741.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.3109-8651_3109-864 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTG | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0023others(13): Show | 16 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3109-8647_3109-864 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTGTG | C | 14 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0054others(11): Show | 14 | HG00544.hp1 HG00741.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.3109-8649_3109-864 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTGTGTG | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(18): Show | 21 | HG01175.hp2 HG02040.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.3109-8651_3109-864 others(10): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTGTGTGT others(1): Show |
C | 6 | a0001c0001t0001g0101a0001c0001t0001g0111a0004c0006t0001g0179others(3): Show | 6 | HG02257.hp1 HG02280.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.3109-8653_3109-864 others(12): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0003g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3109-8657_3109-864 others(16): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTGTGTGT others(9): Show |
C | 3 | a0001c0001t0001g0155a0002c0005t0006g0137a0002c0005t0006g0138 | 3 | HG02976.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3109-8661_3109-864 others(20): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074798
|
CTGTGTGT others(11): Show |
C | 1 | a0001c0002t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3109-8663_3109-864 others(22): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074798 | |||||
| chr16:69074840
|
A | G | 3 | a0001c0001t0001g0174a0001c0008t0001g0112a0001c0008t0001g0119 | 3 | HG02717.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3109-8645A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074840 | ||||||
| chr16:69074852
|
A | AT | 3 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0007t0003g0037 | 3 | HG01346.hp1 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3109-8631dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69074852 | |||||
| chr16:69074855
|
A | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0024a0001c0001t0001g0029others(20): Show | 23 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.3109-8630A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074855 | ||||||
| chr16:69074902
|
A | C | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-8583A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074902 | ||||||
| chr16:69074909
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3109-8576G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69074909 | ||||||
| chr16:69075174
|
CT | C | 25 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0040others(22): Show | 25 | HG00544.hp1 HG01346.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.3109-8295delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69075174 | |||||
| chr16:69075267
|
T | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-8218T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075267 | ||||||
| chr16:69075286
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3109-8199T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075286 | ||||||
| chr16:69075455
|
AT | A | 27 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(24): Show | 27 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.3109-8014delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69075455 | |||||
| chr16:69075460
|
T | A | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3109-8025T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075460 | ||||||
| chr16:69075488
|
C | T | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-7997C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075488 | ||||||
| chr16:69075540
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-7945G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075540 | ||||||
| chr16:69075677
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3109-7808C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075677 | ||||||
| chr16:69075762
|
CT | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(10): Show | 13 | HG01993.hp1 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3109-7703delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69075762 | |||||
| chr16:69075869
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-7616C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075869 | ||||||
| chr16:69075919
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3109-7566C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075919 | ||||||
| chr16:69075948
|
A | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-7537A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69075948 | ||||||
| chr16:69076042
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0110a0001c0003t0001g0125others(1): Show | 4 | HG00140.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.3109-7443C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69076042 | ||||||
| chr16:69076043
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3109-7442G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69076043 | ||||||
| chr16:69076055
|
G | A | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-7430G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69076055 | ||||||
| chr16:69076088
|
C | CT | 89 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.3109-7376dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69076088 | |||||
| chr16:69076088
|
C | CTT | 17 | a0001c0001t0001g0010a0001c0001t0001g0063a0001c0001t0001g0107others(14): Show | 17 | HG01361.hp1 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.3109-7377_3109-737 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69076088 | |||||
| chr16:69076088
|
C | CTTT | 25 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(22): Show | 25 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.3109-7378_3109-737 others(7): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69076088 | |||||
| chr16:69076335
|
G | A | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3109-7150G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69076335 | ||||||
| chr16:69076372
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3109-7113G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69076372 | ||||||
| chr16:69076531
|
G | A | 22 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(19): Show | 22 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3109-6954G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69076531 | ||||||
| chr16:69077031
|
T | C | 1 | a0002c0005t0006g0138 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3109-6454T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077031 | ||||||
| chr16:69077045
|
A | AT | 17 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(14): Show | 17 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.3109-6427dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69077045 | |||||
| chr16:69077090
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3109-6395A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077090 | ||||||
| chr16:69077098
|
G | C | 2 | a0002c0005t0001g0162a0002c0005t0001g0163 | 2 | HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3109-6387G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077098 | ||||||
| chr16:69077226
|
A | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0114others(16): Show | 19 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.3109-6259A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077226 | ||||||
| chr16:69077256
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-6229A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077256 | ||||||
| chr16:69077343
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 12 | HG02055.hp1 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3109-6142G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077343 | ||||||
| chr16:69077690
|
G | A | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3109-5795G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69077690 | ||||||
| chr16:69078064
|
A | G | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-5421A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078064 | ||||||
| chr16:69078086
|
TAA | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3109-5398_3109-539 others(6): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078086 | ||||||
| chr16:69078125
|
C | T | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-5360C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078125 | ||||||
| chr16:69078249
|
G | A | 14 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(11): Show | 14 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.3109-5236G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078249 | ||||||
| chr16:69078362
|
T | C | 1 | a0005c0011t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3109-5123T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078362 | ||||||
| chr16:69078495
|
A | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0010others(79): Show | 82 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.3109-4990A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078495 | ||||||
| chr16:69078504
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0165a0001c0001t0008g0030 | 3 | HG01884.hp2 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3109-4981A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078504 | ||||||
| chr16:69078581
|
A | G | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(36): Show | 39 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.3109-4904A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69078581 | ||||||
| chr16:69078683
|
T | TTACA | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-4801_3109-479 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69078683 | |||||
| chr16:69079092
|
A | G | 7 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0071others(4): Show | 7 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-4393A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69079092 | ||||||
| chr16:69079094
|
G | A | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-4391G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69079094 | ||||||
| chr16:69079261
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(25): Show | 28 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.3109-4224C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69079261 | ||||||
| chr16:69079333
|
C | CAAAT | 16 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0032others(13): Show | 16 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.3109-4130_3109-412 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69079333 | |||||
| chr16:69079337
|
T | C | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-4148T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69079337 | ||||||
| chr16:69079466
|
T | A | 28 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(25): Show | 28 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.3109-4019T>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69079466 | ||||||
| chr16:69079575
|
TA | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0024a0001c0001t0001g0029others(37): Show | 40 | HG00544.hp1 HG00741.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.3109-3901delA | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69079575 | |||||
| chr16:69079956
|
T | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-3529T>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69079956 | ||||||
| chr16:69080165
|
G | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0188 | 2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.3109-3320G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080165 | ||||||
| chr16:69080227
|
A | C | 1 | a0001c0001t0008g0030 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3109-3258A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080227 | ||||||
| chr16:69080241
|
T | TC | 84 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(81): Show | 84 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(81): Show |
intron_variant | MODIFIER | c.3109-3244_3109-324 others(5): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080241 | ||||||
| chr16:69080258
|
C | T | 1 | a0002c0005t0001g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3109-3227C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080258 | ||||||
| chr16:69080287
|
G | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-3198G>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080287 | ||||||
| chr16:69080494
|
G | A | 1 | a0001c0001t0001g0106 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3109-2991G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080494 | ||||||
| chr16:69080674
|
A | G | 1 | a0002c0005t0006g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3109-2811A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080674 | ||||||
| chr16:69080713
|
A | G | 5 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0094others(2): Show | 5 | HG01257.hp1 HG01258.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.3109-2772A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080713 | ||||||
| chr16:69080731
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0175a0001c0001t0001g0176others(2): Show | 5 | HG00099.hp1 HG01081.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.3109-2754A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080731 | ||||||
| chr16:69080910
|
G | A | 1 | a0001c0003t0001g0136 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3109-2575G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080910 | ||||||
| chr16:69080919
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-2566A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080919 | ||||||
| chr16:69080920
|
T | C | 3 | a0001c0003t0001g0134a0001c0003t0001g0136a0001c0003t0007g0127 | 3 | HG01346.hp2 NA18964.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-2565T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080920 | ||||||
| chr16:69080993
|
C | T | 4 | a0001c0001t0002g0022a0001c0003t0002g0195a0001c0003t0002g0196others(1): Show | 4 | HG02615.hp1 HG02895.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-2492C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69080993 | ||||||
| chr16:69081221
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3109-2264G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081221 | ||||||
| chr16:69081312
|
C | CT | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-2172dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69081312 | |||||
| chr16:69081329
|
C | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-2156C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081329 | ||||||
| chr16:69081345
|
C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-2140C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081345 | ||||||
| chr16:69081399
|
G | A | 57 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(54): Show | 57 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3109-2086G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081399 | ||||||
| chr16:69081582
|
C | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0107others(2): Show | 5 | HG00544.hp1 HG03654.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-1903C>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081582 | ||||||
| chr16:69081593
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(5): Show | 8 | HG01891.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3109-1892G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081593 | ||||||
| chr16:69081746
|
G | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 77 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.3109-1739G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081746 | ||||||
| chr16:69081832
|
C | CT | 25 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0018others(22): Show | 25 | HG01346.hp2 HG01884.hp1 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.3109-1638dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69081832 | |||||
| chr16:69081857
|
TCTCA | T | 3 | a0003c0004t0001g0151a0003c0004t0001g0164a0003c0004t0001g0201 | 3 | HG02258.hp1 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3109-1620_3109-161 others(8): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69081857 | |||||
| chr16:69081867
|
TC | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.3109-1617delC | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081867 | ||||||
| chr16:69081873
|
G | T | 4 | a0001c0001t0001g0150a0001c0001t0001g0174a0001c0008t0001g0112others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3109-1612G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081873 | ||||||
| chr16:69081945
|
A | T | 77 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(74): Show | 77 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.3109-1540A>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081945 | ||||||
| chr16:69081947
|
C | T | 7 | a0001c0001t0001g0091a0001c0002t0001g0064a0001c0002t0001g0071others(4): Show | 7 | HG01099.hp1 HG01255.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.3109-1538C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69081947 | ||||||
| chr16:69082069
|
C | T | 1 | a0001c0002t0001g0081 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3109-1416C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69082069 | ||||||
| chr16:69082141
|
G | A | 55 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(52): Show | 55 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.3109-1344G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69082141 | ||||||
| chr16:69082488
|
T | C | 2 | a0003c0004t0004g0202a0003c0004t0004g0203 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3109-997T>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69082488 | ||||||
| chr16:69082778
|
A | G | 80 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(77): Show | 80 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.3109-707A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69082778 | ||||||
| chr16:69082838
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0034 | 2 | NA18968.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.3109-647G>A | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69082838 | ||||||
| chr16:69083095
|
C | CT | 11 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0066others(8): Show | 11 | HG00741.hp1 HG02258.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.3109-369dupT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69083095 | |||||
| chr16:69083095
|
CT | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(40): Show | 43 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.3109-369delT | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69083095 | |||||
| chr16:69083095
|
CTT | C | 37 | a0001c0001t0001g0010a0001c0001t0001g0029a0001c0001t0001g0032others(34): Show | 37 | HG00741.hp2 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.3109-370_3109-369d others(4): Show |
TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr16 | 69083095 | |||||
| chr16:69083139
|
A | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0198 | 2 | HG02027.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.3109-346A>C | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69083139 | ||||||
| chr16:69083253
|
G | T | 2 | a0001c0003t0001g0134a0001c0003t0007g0127 | 2 | HG01346.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.3109-232G>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69083253 | ||||||
| chr16:69083260
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0156 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.3109-225C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69083260 | ||||||
| chr16:69083373
|
A | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0107others(2): Show | 5 | HG00544.hp1 HG03654.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3109-112A>G | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69083373 | ||||||
| chr16:69083442
|
C | T | 2 | a0002c0005t0006g0137a0002c0005t0006g0138 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3109-43C>T | TANGO6 | ENSG00000103047.8 | transcript | ENST00000261778.2 | protein_coding | 17/17 | chr16 | 69083442 |