Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10910 |
|---|---|
| ensemblid | ENSG00000165416.15 |
| hgncid | 16987 |
| symbol | SUGT1 |
| name | SGT1 homolog, MIS12 kinetochore complex assembly cochaperone |
| refseq_nuc | NM_006704.5 |
| refseq_prot | NP_006695.1 |
| ensembl_nuc | ENST00000310528.9 |
| ensembl_prot | ENSP00000308067.7 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 52652836 |
| end | 52700909 |
| strand | + |
| ver | v1.2 |
| region | chr13:52652836-52700909 |
| region5000 | chr13:52647836-52705909 |
| regionname0 | SUGT1_chr13_52652836_52700909 |
| regionname5000 | SUGT1_chr13_52647836_52705909 |
| 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 | 333 | 308 | 84 | 68 | 108 | 14 | 32 | 78 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0002 | 0/0 | 333 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0003 | 0/0 | 333 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| 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 | 1002 | 304 | 81 | 67 | 108 | 14 | 32 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| c0002 | 0/0 | 1002 | 4 | 3 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| c0003 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| c0004 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 13170 | 51 | 3 | 14 | 22 | 5 | 7 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0002 | 0/1 | 13169 | 39 | 6 | 5 | 16 | 3 | 8 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0003 | 0/0 | 13169 | 28 | 0 | 4 | 21 | 0 | 3 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0004 | 0/0 | 13169 | 15 | 9 | 4 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0005 | 0/0 | 13168 | 13 | 1 | 2 | 9 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0006 | 0/0 | 13171 | 9 | 7 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0007 | 0/0 | 13170 | 7 | 1 | 1 | 5 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0008 | 0/0 | 13170 | 6 | 0 | 6 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0009 | 0/0 | 13168 | 5 | 5 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0010 | 0/0 | 13168 | 4 | 3 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0011 | 0/0 | 13169 | 4 | 0 | 0 | 4 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0012 | 0/0 | 13172 | 4 | 3 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0013 | 0/0 | 13169 | 4 | 0 | 4 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0014 | 0/0 | 13169 | 3 | 0 | 2 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0015 | 0/0 | 13159 | 3 | 3 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0016 | 0/0 | 13159 | 3 | 0 | 0 | 3 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0017 | 0/0 | 13169 | 3 | 3 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0018 | 0/0 | 13168 | 3 | 0 | 2 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0019 | 0/0 | 13165 | 3 | 0 | 3 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0020 | 1/0 | 13160 | 3 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0021 | 0/0 | 13168 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0022 | 0/0 | 13169 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0023 | 0/0 | 13157 | 2 | 0 | 0 | 1 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0024 | 0/0 | 13170 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0025 | 0/0 | 13170 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0026 | 0/0 | 13169 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0027 | 0/0 | 13169 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0028 | 0/0 | 13170 | 2 | 0 | 0 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0029 | 0/0 | 13169 | 2 | 0 | 0 | 0 | 0 | 2 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0030 | 0/0 | 13167 | 2 | 1 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0031 | 0/0 | 13171 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0032 | 0/0 | 13168 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0033 | 0/0 | 13168 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0034 | 0/0 | 13160 | 2 | 1 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0035 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0036 | 0/0 | 13169 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0037 | 0/0 | 13170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0038 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0039 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0040 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0041 | 0/0 | 13166 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0042 | 0/0 | 13169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0043 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0044 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0045 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0046 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0047 | 0/0 | 13160 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0048 | 0/0 | 13159 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0049 | 0/0 | 13158 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0050 | 0/0 | 13170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0051 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0052 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0053 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0054 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0055 | 0/0 | 13166 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0056 | 0/0 | 13167 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0057 | 0/0 | 13159 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0058 | 0/0 | 13168 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0059 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0060 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0061 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0062 | 0/0 | 13169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0063 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0064 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0065 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0066 | 0/0 | 13170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0067 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0068 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0069 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0070 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0071 | 0/0 | 13121 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0072 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0073 | 0/0 | 13169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0074 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0075 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0076 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0077 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0078 | 0/0 | 13169 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0079 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0080 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0081 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0082 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0083 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0084 | 0/0 | 13168 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0085 | 0/0 | 13162 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0086 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0087 | 0/0 | 13170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0088 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0089 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0090 | 0/0 | 13171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0091 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0092 | 0/0 | 13169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0093 | 0/0 | 13170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0094 | 0/0 | 13170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0095 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0096 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0097 | 0/0 | 13168 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0098 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0099 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0100 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0101 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0102 | 0/0 | 13168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0103 | 0/0 | 13169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0104 | 0/0 | 13169 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0105 | 0/0 | 13165 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| t0106 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| 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 | 11 | 0 | 1 | 8 | 0 | 2 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0002 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0003 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0005 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0008 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| 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 | 1002 | 304 | 81 | 67 | 108 | 14 | 32 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0002 | 0/0 | 1002 | 4 | 3 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0002c0004 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0003c0003 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 14171 | 51 | 3 | 14 | 22 | 5 | 7 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0002 | 0/1 | 14170 | 39 | 6 | 5 | 16 | 3 | 8 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0003 | 0/0 | 14170 | 28 | 0 | 4 | 21 | 0 | 3 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0004 | 0/0 | 14170 | 15 | 9 | 4 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0005 | 0/0 | 14169 | 13 | 1 | 2 | 9 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0006 | 0/0 | 14172 | 9 | 7 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0007 | 0/0 | 14171 | 7 | 1 | 1 | 5 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0008 | 0/0 | 14171 | 6 | 0 | 6 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0009 | 0/0 | 14169 | 5 | 5 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0010 | 0/0 | 14169 | 4 | 3 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0011 | 0/0 | 14170 | 4 | 0 | 0 | 4 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0012 | 0/0 | 14173 | 4 | 3 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0013 | 0/0 | 14170 | 4 | 0 | 4 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0014 | 0/0 | 14170 | 3 | 0 | 2 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0015 | 0/0 | 14160 | 3 | 3 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0016 | 0/0 | 14160 | 3 | 0 | 0 | 3 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0017 | 0/0 | 14170 | 3 | 3 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0018 | 0/0 | 14169 | 3 | 0 | 2 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0019 | 0/0 | 14166 | 3 | 0 | 3 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0020 | 1/0 | 14161 | 3 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0021 | 0/0 | 14169 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0022 | 0/0 | 14170 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0023 | 0/0 | 14158 | 2 | 0 | 0 | 1 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0024 | 0/0 | 14171 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0025 | 0/0 | 14171 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0026 | 0/0 | 14170 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0027 | 0/0 | 14170 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0028 | 0/0 | 14171 | 2 | 0 | 0 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0029 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0030 | 0/0 | 14168 | 2 | 1 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0031 | 0/0 | 14172 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0032 | 0/0 | 14169 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0033 | 0/0 | 14169 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0034 | 0/0 | 14161 | 2 | 1 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0035 | 0/0 | 14171 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0036 | 0/0 | 14170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0037 | 0/0 | 14171 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0038 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0043 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0044 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0045 | 0/0 | 14160 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0046 | 0/0 | 14160 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0047 | 0/0 | 14161 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0048 | 0/0 | 14160 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0049 | 0/0 | 14159 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0050 | 0/0 | 14171 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0051 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0052 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0053 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0054 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0055 | 0/0 | 14167 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0056 | 0/0 | 14168 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0057 | 0/0 | 14160 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0058 | 0/0 | 14169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0059 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0060 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0061 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0062 | 0/0 | 14170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0063 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0064 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0065 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0066 | 0/0 | 14171 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0067 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0068 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0069 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0070 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0071 | 0/0 | 14122 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0072 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0073 | 0/0 | 14170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0074 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0075 | 0/0 | 14171 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0076 | 0/0 | 14172 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0077 | 0/0 | 14170 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0078 | 0/0 | 14170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0079 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0080 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0081 | 0/0 | 14168 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0082 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0083 | 0/0 | 14172 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0084 | 0/0 | 14169 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0085 | 0/0 | 14163 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0086 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0087 | 0/0 | 14171 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0088 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0089 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0090 | 0/0 | 14172 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0091 | 0/0 | 14172 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0092 | 0/0 | 14170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0093 | 0/0 | 14171 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0094 | 0/0 | 14171 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0095 | 0/0 | 14171 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0096 | 0/0 | 14173 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0097 | 0/0 | 14169 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0098 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0100 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0101 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0102 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0103 | 0/0 | 14170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0104 | 0/0 | 14170 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0105 | 0/0 | 14166 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0001t0106 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0002t0039 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0002t0040 | 0/0 | 14169 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0002t0041 | 0/0 | 14167 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0001c0002t0042 | 0/0 | 14170 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0002c0004t0099 | 0/0 | 14171 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| a0003c0003t0029 | 0/0 | 14170 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | copy fasta | chr13 | 52647836 | 52705909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0001 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0007g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0008g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0009g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0010g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0010g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0011g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0011g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0011g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0012g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0012g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0013g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0014g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0014g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0015g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0016g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0016g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0018g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0018g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0019g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0019g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0019g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0020g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0020g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0021g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0021g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0022g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0022g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0023g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0023g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0024g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0024g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0025g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0025g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0026g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0027g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0028g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0028g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0029g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0030g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0030g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0031g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0031g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0032g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0032g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0033g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0034g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0034g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0035g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0036g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0037g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0038g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0043g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0044g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0045g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0046g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0047g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0048g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0049g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0050g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0051g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0052g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0053g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0054g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0055g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0056g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0057g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0058g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0059g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0060g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0061g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0062g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0063g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0064g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0065g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0066g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0067g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0068g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0069g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0070g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0071g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0072g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0073g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0074g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0075g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0076g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0077g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0078g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0079g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0080g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0081g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0082g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0083g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0084g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0085g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0086g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0087g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0088g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0089g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0090g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0091g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0092g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0093g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0094g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0095g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0096g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0097g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0098g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0100g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0101g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0102g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0103g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0104g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0105g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0001t0106g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0002t0039g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0002t0040g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0002t0041g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0001c0002t0042g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0002c0004t0099g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| a0003c0003t0029g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00099 | hp2 | a0001 | c0001 | t0014 | g0117 | EUR | GBR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0020 | EUR | GBR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0164 | EUR | FIN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00323 | hp2 | a0001 | c0001 | t0088 | g0189 | EUR | FIN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00438 | hp1 | a0001 | c0001 | t0072 | g0086 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00544 | hp1 | a0001 | c0001 | t0016 | g0011 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00609 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00621 | hp2 | a0001 | c0001 | t0084 | g0025 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00673 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | CHS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01070 | hp1 | a0001 | c0001 | t0019 | g0206 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01071 | hp2 | a0001 | c0001 | t0019 | g0214 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01074 | hp1 | a0001 | c0001 | t0030 | g0175 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01074 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01081 | hp1 | a0001 | c0001 | t0036 | g0018 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01099 | hp1 | a0001 | c0001 | t0049 | g0152 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01109 | hp1 | a0001 | c0001 | t0037 | g0018 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01109 | hp2 | a0001 | c0001 | t0055 | g0135 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01168 | hp1 | a0001 | c0001 | t0014 | g0121 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01168 | hp2 | a0001 | c0001 | t0066 | g0013 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01169 | hp1 | a0001 | c0001 | t0104 | g0084 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01169 | hp2 | a0001 | c0001 | t0014 | g0124 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01175 | hp1 | a0001 | c0001 | t0019 | g0032 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01175 | hp2 | a0001 | c0001 | t0105 | g0026 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01192 | hp2 | a0001 | c0001 | t0010 | g0076 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01243 | hp1 | a0001 | c0002 | t0041 | g0058 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0071 | AMR | PUR | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0178 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01256 | hp1 | a0001 | c0001 | t0031 | g0232 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0182 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01257 | hp2 | a0001 | c0001 | t0018 | g0174 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01346 | hp1 | a0001 | c0001 | t0018 | g0012 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01358 | hp2 | a0001 | c0001 | t0094 | g0235 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0181 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0176 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0205 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01496 | hp2 | a0001 | c0001 | t0078 | g0004 | AMR | CLM | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01516 | hp1 | a0001 | c0001 | t0098 | g0033 | EUR | IBS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0129 | EUR | IBS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | IBS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | IBS | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01891 | hp1 | a0001 | c0001 | t0030 | g0180 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01891 | hp2 | a0001 | c0001 | t0101 | g0142 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01943 | hp1 | a0001 | c0001 | t0050 | g0162 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01952 | hp1 | a0001 | c0001 | t0008 | g0177 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01952 | hp2 | a0001 | c0001 | t0025 | g0003 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01981 | hp1 | a0001 | c0001 | t0076 | g0097 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG01993 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02004 | hp1 | a0001 | c0001 | t0087 | g0026 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02040 | hp1 | a0001 | c0001 | t0068 | g0065 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02145 | hp2 | a0001 | c0001 | t0091 | g0200 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CDX | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02155 | hp2 | a0001 | c0001 | t0081 | g0154 | EAS | CDX | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | CDX | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CDX | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02257 | hp1 | a0001 | c0001 | t0032 | g0141 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02257 | hp2 | a0001 | c0001 | t0021 | g0078 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02258 | hp1 | a0001 | c0001 | t0056 | g0079 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0179 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02280 | hp2 | a0001 | c0001 | t0092 | g0166 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02293 | hp1 | a0001 | c0001 | t0097 | g0168 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02293 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02300 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0062 | EAS | KHV | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02572 | hp2 | a0001 | c0001 | t0079 | g0111 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02615 | hp1 | a0001 | c0001 | t0046 | g0147 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02622 | hp2 | a0001 | c0001 | t0063 | g0081 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02630 | hp1 | a0001 | c0001 | t0045 | g0148 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0144 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02698 | hp2 | a0001 | c0001 | t0064 | g0115 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02717 | hp1 | a0001 | c0001 | t0033 | g0010 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02717 | hp2 | a0001 | c0001 | t0065 | g0072 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02735 | hp2 | a0001 | c0001 | t0018 | g0012 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02809 | hp1 | a0001 | c0001 | t0062 | g0123 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02886 | hp2 | a0001 | c0002 | t0039 | g0060 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02895 | hp1 | a0001 | c0001 | t0102 | g0137 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02895 | hp2 | a0001 | c0001 | t0026 | g0113 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02896 | hp1 | a0001 | c0001 | t0027 | g0005 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02896 | hp2 | a0001 | c0001 | t0054 | g0034 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02897 | hp1 | a0001 | c0001 | t0103 | g0138 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02897 | hp2 | a0001 | c0001 | t0027 | g0005 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0146 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0070 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0075 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02970 | hp1 | a0001 | c0001 | t0100 | g0134 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02970 | hp2 | a0001 | c0001 | t0073 | g0006 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03017 | hp1 | a0001 | c0001 | t0029 | g0056 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03041 | hp1 | a0001 | c0001 | t0083 | g0198 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03130 | hp2 | a0001 | c0001 | t0047 | g0150 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0022 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03139 | hp2 | a0001 | c0001 | t0052 | g0125 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03209 | hp1 | a0001 | c0001 | t0095 | g0031 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0066 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03225 | hp1 | a0001 | c0001 | t0053 | g0069 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03239 | hp1 | a0001 | c0001 | t0106 | g0136 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03239 | hp2 | a0003 | c0003 | t0029 | g0167 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03453 | hp1 | a0001 | c0001 | t0026 | g0005 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03486 | hp1 | a0001 | c0002 | t0042 | g0059 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | MSL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03492 | hp1 | a0001 | c0001 | t0080 | g0091 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | ESN | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03540 | hp2 | a0001 | c0001 | t0096 | g0197 | AFR | GWD | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03688 | hp2 | a0001 | c0001 | t0023 | g0153 | SAS | STU | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03704 | hp2 | a0001 | c0001 | t0082 | g0003 | SAS | PJL | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03831 | hp1 | a0001 | c0001 | t0038 | g0103 | SAS | BEB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03831 | hp2 | a0001 | c0001 | t0028 | g0233 | SAS | BEB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03834 | hp1 | a0001 | c0001 | t0057 | g0155 | SAS | BEB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03927 | hp1 | a0001 | c0001 | t0075 | g0082 | SAS | BEB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG04115 | hp1 | a0002 | c0004 | t0099 | g0033 | SAS | STU | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | STU | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG04199 | hp2 | a0001 | c0001 | t0035 | g0063 | SAS | STU | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | YRI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18522 | hp2 | a0001 | c0001 | t0020 | g0160 | AFR | YRI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18906 | hp1 | a0001 | c0002 | t0040 | g0057 | AFR | YRI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | YRI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18945 | hp2 | a0001 | c0001 | t0093 | g0030 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18949 | hp1 | a0001 | c0001 | t0090 | g0216 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18949 | hp2 | a0001 | c0001 | t0060 | g0047 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18951 | hp1 | a0001 | c0001 | t0074 | g0038 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18951 | hp2 | a0001 | c0001 | t0011 | g0017 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18959 | hp1 | a0001 | c0001 | t0089 | g0213 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18960 | hp1 | a0001 | c0001 | t0058 | g0049 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18960 | hp2 | a0001 | c0001 | t0022 | g0048 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18965 | hp1 | a0001 | c0001 | t0067 | g0061 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18966 | hp1 | a0001 | c0001 | t0022 | g0087 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18967 | hp1 | a0001 | c0001 | t0061 | g0042 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18967 | hp2 | a0001 | c0001 | t0086 | g0237 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18981 | hp1 | a0001 | c0001 | t0077 | g0120 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18994 | hp1 | a0001 | c0001 | t0016 | g0151 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18997 | hp2 | a0001 | c0001 | t0024 | g0037 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19000 | hp1 | a0001 | c0001 | t0070 | g0095 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19005 | hp2 | a0001 | c0001 | t0085 | g0195 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19007 | hp2 | a0001 | c0001 | t0059 | g0001 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19011 | hp1 | a0001 | c0001 | t0071 | g0002 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0143 | AFR | LWK | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0149 | AFR | LWK | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19043 | hp1 | a0001 | c0001 | t0033 | g0010 | AFR | LWK | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0073 | AFR | LWK | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19055 | hp1 | a0001 | c0001 | t0069 | g0102 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19059 | hp2 | a0001 | c0001 | t0031 | g0218 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19064 | hp2 | a0001 | c0001 | t0044 | g0093 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19072 | hp2 | a0001 | c0001 | t0011 | g0014 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19076 | hp2 | a0001 | c0001 | t0011 | g0039 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19080 | hp2 | a0001 | c0001 | t0023 | g0011 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19082 | hp1 | a0001 | c0001 | t0025 | g0001 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19082 | hp2 | a0001 | c0001 | t0016 | g0011 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19086 | hp2 | a0001 | c0001 | t0043 | g0050 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19091 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | YRI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | YRI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | ASW | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20129 | hp2 | a0001 | c0001 | t0020 | g0158 | AFR | ASW | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | TSI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20805 | hp1 | a0001 | c0001 | t0028 | g0219 | EUR | TSI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | GIH | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20905 | hp2 | a0001 | c0001 | t0034 | g0157 | SAS | GIH | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02109 | hp1 | a0001 | c0001 | t0021 | g0077 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02486 | hp1 | a0001 | c0001 | t0032 | g0139 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG02559 | hp2 | a0001 | c0001 | t0048 | g0023 | AFR | ACB | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | USA | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| HG06807 | hp2 | a0001 | c0001 | t0034 | g0161 | AFR | USA | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0023 | AFR | USA | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA20300 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | USA | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA21309 | hp1 | a0001 | c0001 | t0051 | g0140 | AFR | LWK | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0100 | REF | REF | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0020 | g0159 | REF | REF | SUGT1_chr13_52647836_52705909 | SUGT1 | chr13 | 52647836 | 52705909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52676305
|
A | G | 1 | a0002 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.703A>G | p.Lys235Glu | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/13 | 788/14161 | 703/1002 | 235/333 | chr13 | 52676305 | ||
| chr13:52680061
|
A | C | 1 | a0003 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.806A>C | p.Glu269Ala | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/13 | 891/14161 | 806/1002 | 269/333 | chr13 | 52680061 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52676274
|
G | A | 1 | a0001c0002 | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
synonymous_variant | LOW | c.672G>A | p.Lys224Lys | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/13 | 757/14161 | 672/1002 | 224/333 | chr13 | 52676274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52652844
|
G | C | 2 | a0001c0001t0010a0001c0001t0021 | 6 | HG01192.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 1/13 | 77 | chr13 | 52652844 | |||||
| chr13:52652849
|
C | A | 1 | a0001c0001t0014 | 3 | HG00099.hp2 HG01168.hp1 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-72C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 1/13 | 72 | chr13 | 52652849 | |||||
| chr13:52652879
|
T | G | 1 | a0001c0001t0035 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 1/13 | 42 | chr13 | 52652879 | |||||
| chr13:52652917
|
A | T | 1 | a0001c0001t0106 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-4A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 1/13 | 4 | chr13 | 52652917 | |||||
| chr13:52687866
|
A | G | 1 | a0001c0001t0105 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 31 | chr13 | 52687866 | |||||
| chr13:52687886
|
G | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG01081.hp1 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*51G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 51 | chr13 | 52687886 | |||||
| chr13:52688040
|
G | A | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 205 | chr13 | 52688040 | |||||
| chr13:52688316
|
T | C | 1 | a0001c0001t0038 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*481T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 481 | chr13 | 52688316 | |||||
| chr13:52688482
|
T | C | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*647T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 647 | chr13 | 52688482 | |||||
| chr13:52688745
|
A | G | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG01081.hp1 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*910A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 910 | chr13 | 52688745 | |||||
| chr13:52688853
|
G | A | 1 | a0001c0001t0043 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1018 | chr13 | 52688853 | |||||
| chr13:52688944
|
G | A | 1 | a0001c0001t0044 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1109G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1109 | chr13 | 52688944 | |||||
| chr13:52689131
|
C | T | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*1296C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1296 | chr13 | 52689131 | |||||
| chr13:52689218
|
T | C | 1 | a0001c0001t0050 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1383T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1383 | chr13 | 52689218 | |||||
| chr13:52689315
|
A | G | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0049 | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1480A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1480 | chr13 | 52689315 | |||||
| chr13:52689328
|
G | A | 1 | a0001c0001t0051 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1493 | chr13 | 52689328 | |||||
| chr13:52689644
|
C | T | 1 | a0001c0001t0008 | 6 | HG01255.hp2 HG01256.hp2 HG01361.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1809C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1809 | chr13 | 52689644 | |||||
| chr13:52689670
|
T | A | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0049 | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1835T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1835 | chr13 | 52689670 | |||||
| chr13:52689692
|
G | C | 1 | a0001c0001t0052 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1857G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1857 | chr13 | 52689692 | |||||
| chr13:52689800
|
G | A | 1 | a0001c0001t0053 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1965G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 1965 | chr13 | 52689800 | |||||
| chr13:52689857
|
T | C | 1 | a0001c0001t0010 | 4 | HG01192.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2022T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2022 | chr13 | 52689857 | |||||
| chr13:52689870
|
C | T | 1 | a0001c0001t0104 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2035C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2035 | chr13 | 52689870 | |||||
| chr13:52689947
|
C | T | 1 | a0001c0001t0021 | 2 | HG02109.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2112C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2112 | chr13 | 52689947 | |||||
| chr13:52689958
|
C | CA | 101 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(98): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*2131dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2132 | INFO_REALIGN_3_PRIME | chr13 | 52689958 | ||||
| chr13:52689971
|
T | C | 55 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(52): Show | 163 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*2136T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2136 | chr13 | 52689971 | |||||
| chr13:52690221
|
T | C | 1 | a0001c0001t0083 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2386T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2386 | chr13 | 52690221 | |||||
| chr13:52690295
|
C | G | 3 | a0001c0001t0015a0001c0001t0047a0001c0001t0048 | 5 | HG02559.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2460C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2460 | chr13 | 52690295 | |||||
| chr13:52690322
|
A | G | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*2487A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2487 | chr13 | 52690322 | |||||
| chr13:52690410
|
C | CTT | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*2575_*2576insTT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2576 | chr13 | 52690410 | |||||
| chr13:52690665
|
A | G | 4 | a0001c0001t0032a0001c0001t0051a0001c0001t0102others(1): Show | 5 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2830A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2830 | chr13 | 52690665 | |||||
| chr13:52690763
|
A | G | 1 | a0001c0001t0082 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2928A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2928 | chr13 | 52690763 | |||||
| chr13:52690781
|
A | G | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2946A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 2946 | chr13 | 52690781 | |||||
| chr13:52690898
|
GTCT | G | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0049 | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3070_*3072delTCT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3070 | INFO_REALIGN_3_PRIME | chr13 | 52690898 | ||||
| chr13:52690935
|
G | A | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3100G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3100 | chr13 | 52690935 | |||||
| chr13:52690947
|
C | T | 1 | a0001c0001t0053 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3112C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3112 | chr13 | 52690947 | |||||
| chr13:52690988
|
C | T | 51 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(48): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3153C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3153 | chr13 | 52690988 | |||||
| chr13:52691063
|
G | A | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3228G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3228 | chr13 | 52691063 | |||||
| chr13:52691209
|
C | T | 6 | a0001c0001t0032a0001c0001t0051a0001c0001t0100others(3): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3374C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3374 | chr13 | 52691209 | |||||
| chr13:52691283
|
T | C | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3448T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3448 | chr13 | 52691283 | |||||
| chr13:52691375
|
A | AT | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3541dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3542 | INFO_REALIGN_3_PRIME | chr13 | 52691375 | ||||
| chr13:52691434
|
A | G | 1 | a0001c0001t0048 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3599A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3599 | chr13 | 52691434 | |||||
| chr13:52691723
|
A | G | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*3888A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 3888 | chr13 | 52691723 | |||||
| chr13:52691908
|
G | T | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0049 | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4073G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4073 | chr13 | 52691908 | |||||
| chr13:52692075
|
G | A | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*4240G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4240 | chr13 | 52692075 | |||||
| chr13:52692150
|
A | C | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*4315A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4315 | chr13 | 52692150 | |||||
| chr13:52692162
|
A | G | 29 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(26): Show | 85 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4327A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4327 | chr13 | 52692162 | |||||
| chr13:52692276
|
A | G | 2 | a0001c0001t0098a0002c0004t0099 | 2 | HG01516.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4441A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4441 | chr13 | 52692276 | |||||
| chr13:52692412
|
CT | C | 92 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(89): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*4594delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4594 | INFO_REALIGN_3_PRIME | chr13 | 52692412 | ||||
| chr13:52692429
|
T | G | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*4594T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4594 | chr13 | 52692429 | |||||
| chr13:52692453
|
AG | A | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*4621delG | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4621 | INFO_REALIGN_3_PRIME | chr13 | 52692453 | ||||
| chr13:52692457
|
A | C | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*4622A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4622 | chr13 | 52692457 | |||||
| chr13:52692458
|
A | T | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*4623A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4623 | chr13 | 52692458 | |||||
| chr13:52692513
|
T | C | 1 | a0001c0002t0039 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4678T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4678 | chr13 | 52692513 | |||||
| chr13:52692538
|
G | A | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4703G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4703 | chr13 | 52692538 | |||||
| chr13:52692652
|
G | A | 12 | a0001c0001t0003a0001c0001t0011a0001c0001t0024others(9): Show | 44 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4817G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 4817 | chr13 | 52692652 | |||||
| chr13:52692937
|
C | T | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5102C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5102 | chr13 | 52692937 | |||||
| chr13:52693071
|
T | C | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*5236T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5236 | chr13 | 52693071 | |||||
| chr13:52693118
|
G | GTA | 50 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(47): Show | 155 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*5297_*5298dupAT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5299 | INFO_REALIGN_3_PRIME | chr13 | 52693118 | ||||
| chr13:52693118
|
G | GTATA | 6 | a0001c0001t0012a0001c0001t0054a0001c0002t0039others(3): Show | 9 | HG01243.hp1 HG01243.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5295_*5298dupATAT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5299 | INFO_REALIGN_3_PRIME | chr13 | 52693118 | ||||
| chr13:52693121
|
T | A | 1 | a0001c0001t0084 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5286T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5286 | chr13 | 52693121 | |||||
| chr13:52693124
|
A | G | 1 | a0001c0001t0081 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5289A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5289 | chr13 | 52693124 | |||||
| chr13:52693376
|
A | C | 1 | a0001c0001t0027 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5541A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5541 | chr13 | 52693376 | |||||
| chr13:52693386
|
A | G | 3 | a0001c0001t0012a0001c0001t0053a0001c0001t0065 | 6 | HG01243.hp2 HG02717.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5551A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5551 | chr13 | 52693386 | |||||
| chr13:52693493
|
A | G | 1 | a0001c0001t0080 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5658A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5658 | chr13 | 52693493 | |||||
| chr13:52693532
|
G | T | 1 | a0001c0001t0084 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5697G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5697 | chr13 | 52693532 | |||||
| chr13:52693607
|
G | A | 1 | a0001c0001t0053 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5772G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5772 | chr13 | 52693607 | |||||
| chr13:52693645
|
C | CTT | 3 | a0001c0001t0006a0001c0001t0095a0001c0001t0096 | 11 | HG01106.hp1 HG01496.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5811_*5812dupTT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5813 | INFO_REALIGN_3_PRIME | chr13 | 52693645 | ||||
| chr13:52693676
|
G | T | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*5841G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5841 | chr13 | 52693676 | |||||
| chr13:52693711
|
T | TTG | 12 | a0001c0001t0015a0001c0001t0016a0001c0001t0032others(9): Show | 17 | HG00544.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5895_*5896dupTG | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5897 | INFO_REALIGN_3_PRIME | chr13 | 52693711 | ||||
| chr13:52693763
|
C | T | 5 | a0001c0001t0032a0001c0001t0051a0001c0001t0101others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5928C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 5928 | chr13 | 52693763 | |||||
| chr13:52694092
|
A | G | 1 | a0001c0001t0034 | 2 | HG06807.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6257A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6257 | chr13 | 52694092 | |||||
| chr13:52694114
|
C | G | 1 | a0001c0001t0064 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6279C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6279 | chr13 | 52694114 | |||||
| chr13:52694266
|
A | T | 1 | a0001c0001t0084 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6431A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6431 | chr13 | 52694266 | |||||
| chr13:52694291
|
G | T | 1 | a0001c0001t0061 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6456G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6456 | chr13 | 52694291 | |||||
| chr13:52694313
|
T | G | 1 | a0001c0001t0067 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6478T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6478 | chr13 | 52694313 | |||||
| chr13:52694383
|
T | G | 1 | a0001c0001t0026 | 2 | HG02895.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6548T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6548 | chr13 | 52694383 | |||||
| chr13:52694391
|
A | T | 1 | a0001c0001t0094 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6556A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6556 | chr13 | 52694391 | |||||
| chr13:52694400
|
C | A | 1 | a0001c0001t0062 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6565C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6565 | chr13 | 52694400 | |||||
| chr13:52694553
|
C | A | 1 | a0001c0001t0018 | 3 | HG01257.hp2 HG01346.hp1 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6718C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6718 | chr13 | 52694553 | |||||
| chr13:52694563
|
G | T | 1 | a0001c0001t0079 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6728G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6728 | chr13 | 52694563 | |||||
| chr13:52694620
|
C | T | 1 | a0001c0001t0060 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6785C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6785 | chr13 | 52694620 | |||||
| chr13:52694621
|
G | A | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6786G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6786 | chr13 | 52694621 | |||||
| chr13:52694720
|
T | C | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*6885T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6885 | chr13 | 52694720 | |||||
| chr13:52694820
|
C | G | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6985C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 6985 | chr13 | 52694820 | |||||
| chr13:52694879
|
A | C | 1 | a0001c0001t0065 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7044A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7044 | chr13 | 52694879 | |||||
| chr13:52694968
|
G | A | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7133G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7133 | chr13 | 52694968 | |||||
| chr13:52694993
|
G | A | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*7158G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7158 | chr13 | 52694993 | |||||
| chr13:52695188
|
A | T | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7353A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7353 | chr13 | 52695188 | |||||
| chr13:52695363
|
C | T | 1 | a0001c0001t0017 | 3 | HG02647.hp2 HG03139.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7528C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7528 | chr13 | 52695363 | |||||
| chr13:52695586
|
T | G | 1 | a0001c0001t0086 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7751T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7751 | chr13 | 52695586 | |||||
| chr13:52695607
|
G | A | 1 | a0001c0001t0068 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7772G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7772 | chr13 | 52695607 | |||||
| chr13:52695797
|
G | A | 1 | a0001c0001t0012 | 4 | HG01243.hp2 HG02965.hp1 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7962G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 7962 | chr13 | 52695797 | |||||
| chr13:52696056
|
G | A | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8221G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8221 | chr13 | 52696056 | |||||
| chr13:52696159
|
A | G | 1 | a0001c0001t0093 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8324A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8324 | chr13 | 52696159 | |||||
| chr13:52696177
|
A | G | 1 | a0001c0001t0078 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8342A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8342 | chr13 | 52696177 | |||||
| chr13:52696358
|
C | T | 6 | a0001c0001t0005a0001c0001t0018a0001c0001t0029others(3): Show | 20 | HG00323.hp1 HG00408.hp1 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*8523C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8523 | chr13 | 52696358 | |||||
| chr13:52696567
|
G | T | 1 | a0001c0001t0077 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8732G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8732 | chr13 | 52696567 | |||||
| chr13:52696575
|
A | C | 2 | a0001c0001t0013a0001c0001t0078 | 5 | HG01074.hp2 HG01496.hp2 HG01993.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8740A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8740 | chr13 | 52696575 | |||||
| chr13:52696590
|
T | C | 4 | a0001c0002t0039a0001c0002t0040a0001c0002t0041others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*8755T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8755 | chr13 | 52696590 | |||||
| chr13:52696627
|
G | C | 93 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(90): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*8792G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8792 | chr13 | 52696627 | |||||
| chr13:52696697
|
G | A | 2 | a0001c0001t0011a0001c0001t0061 | 5 | NA18951.hp2 NA18967.hp1 NA19003.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8862G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8862 | chr13 | 52696697 | |||||
| chr13:52696734
|
C | T | 1 | a0001c0002t0039 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8899C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 8899 | chr13 | 52696734 | |||||
| chr13:52696880
|
T | C | 1 | a0001c0001t0087 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9045T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9045 | chr13 | 52696880 | |||||
| chr13:52696914
|
C | CT | 20 | a0001c0001t0007a0001c0001t0025a0001c0001t0035others(17): Show | 27 | HG00609.hp1 HG00642.hp2 HG00673.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*9099dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9100 | INFO_REALIGN_3_PRIME | chr13 | 52696914 | ||||
| chr13:52696914
|
CT | C | 39 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(36): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*9099delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9099 | INFO_REALIGN_3_PRIME | chr13 | 52696914 | ||||
| chr13:52696955
|
C | T | 2 | a0001c0001t0052a0001c0001t0063 | 2 | HG02622.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9120C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9120 | chr13 | 52696955 | |||||
| chr13:52696956
|
A | G | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*9121A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9121 | chr13 | 52696956 | |||||
| chr13:52697236
|
T | C | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*9401T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9401 | chr13 | 52697236 | |||||
| chr13:52697466
|
A | G | 1 | a0001c0001t0046 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9631A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9631 | chr13 | 52697466 | |||||
| chr13:52697508
|
C | T | 3 | a0001c0001t0016a0001c0001t0023a0001c0001t0049 | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*9673C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9673 | chr13 | 52697508 | |||||
| chr13:52697614
|
G | C | 51 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(48): Show | 159 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*9779G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9779 | chr13 | 52697614 | |||||
| chr13:52697731
|
G | A | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*9896G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9896 | chr13 | 52697731 | |||||
| chr13:52697796
|
T | C | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*9961T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 9961 | chr13 | 52697796 | |||||
| chr13:52697979
|
T | C | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01109.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10144T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10144 | chr13 | 52697979 | |||||
| chr13:52697994
|
T | G | 3 | a0001c0001t0012a0001c0001t0053a0001c0001t0065 | 6 | HG01243.hp2 HG02717.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10159T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10159 | chr13 | 52697994 | |||||
| chr13:52698448
|
C | CT | 9 | a0001c0001t0009a0001c0001t0032a0001c0001t0036others(6): Show | 14 | HG01081.hp1 HG01099.hp1 HG01891.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*10633dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10634 | INFO_REALIGN_3_PRIME | chr13 | 52698448 | ||||
| chr13:52698448
|
C | CTT | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(45): Show | 149 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*10632_*10633dupTT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10634 | INFO_REALIGN_3_PRIME | chr13 | 52698448 | ||||
| chr13:52698448
|
C | CTTT | 11 | a0001c0001t0005a0001c0001t0012a0001c0001t0018others(8): Show | 29 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*10631_*10633dupTT others(1): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10634 | INFO_REALIGN_3_PRIME | chr13 | 52698448 | ||||
| chr13:52698448
|
C | CTTTT | 8 | a0001c0001t0006a0001c0001t0010a0001c0001t0021others(5): Show | 20 | HG00323.hp2 HG01106.hp1 HG01192.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*10630_*10633dupTT others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10634 | INFO_REALIGN_3_PRIME | chr13 | 52698448 | ||||
| chr13:52698448
|
C | CTTTTT | 15 | a0001c0001t0001a0001c0001t0008a0001c0001t0028others(12): Show | 72 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*10629_*10633dupTT others(3): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10634 | INFO_REALIGN_3_PRIME | chr13 | 52698448 | ||||
| chr13:52698448
|
CTTTTTTT | C | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*10627_*10633delTT others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10627 | INFO_REALIGN_3_PRIME | chr13 | 52698448 | ||||
| chr13:52698494
|
C | CCAGG | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*10662_*10665dupGG others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10666 | INFO_REALIGN_3_PRIME | chr13 | 52698494 | ||||
| chr13:52698604
|
T | TA | 29 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(26): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*10772dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10773 | INFO_REALIGN_3_PRIME | chr13 | 52698604 | ||||
| chr13:52698608
|
T | A | 1 | a0001c0001t0084 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10773T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10773 | chr13 | 52698608 | |||||
| chr13:52698624
|
A | G | 1 | a0001c0001t0075 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10789A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10789 | chr13 | 52698624 | |||||
| chr13:52698713
|
G | A | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*10878G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10878 | chr13 | 52698713 | |||||
| chr13:52698769
|
T | C | 2 | a0001c0001t0069a0001c0001t0070 | 2 | NA19000.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10934T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10934 | chr13 | 52698769 | |||||
| chr13:52698771
|
G | A | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(99): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*10936G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 10936 | chr13 | 52698771 | |||||
| chr13:52698908
|
TTTTGAAT others(7): Show |
T | 1 | a0001c0001t0057 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11079_*11092delAT others(12): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11079 | INFO_REALIGN_3_PRIME | chr13 | 52698908 | ||||
| chr13:52699047
|
A | G | 1 | a0001c0001t0070 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11212A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11212 | chr13 | 52699047 | |||||
| chr13:52699078
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11243G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11243 | chr13 | 52699078 | |||||
| chr13:52699079
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11244T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11244 | chr13 | 52699079 | |||||
| chr13:52699080
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11245A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11245 | chr13 | 52699080 | |||||
| chr13:52699084
|
T | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11249T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11249 | chr13 | 52699084 | |||||
| chr13:52699086
|
T | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11251T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11251 | chr13 | 52699086 | |||||
| chr13:52699092
|
A | T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11257A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11257 | chr13 | 52699092 | |||||
| chr13:52699094
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11259A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11259 | chr13 | 52699094 | |||||
| chr13:52699095
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11260G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11260 | chr13 | 52699095 | |||||
| chr13:52699096
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11261G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11261 | chr13 | 52699096 | |||||
| chr13:52699098
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11263A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11263 | chr13 | 52699098 | |||||
| chr13:52699100
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11265A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11265 | chr13 | 52699100 | |||||
| chr13:52699103
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11268T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11268 | chr13 | 52699103 | |||||
| chr13:52699106
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11271T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11271 | chr13 | 52699106 | |||||
| chr13:52699107
|
T | TCCTCAAC others(48): Show |
1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11272_*11273insCC others(53): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11273 | chr13 | 52699107 | |||||
| chr13:52699109
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11274G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11274 | chr13 | 52699109 | |||||
| chr13:52699122
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11287A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11287 | chr13 | 52699122 | |||||
| chr13:52699124
|
G | A | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11289G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11289 | chr13 | 52699124 | |||||
| chr13:52699128
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11293T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11293 | chr13 | 52699128 | |||||
| chr13:52699130
|
G | A | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11295G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11295 | chr13 | 52699130 | |||||
| chr13:52699132
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11297T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11297 | chr13 | 52699132 | |||||
| chr13:52699135
|
C | T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11300C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11300 | chr13 | 52699135 | |||||
| chr13:52699138
|
C | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11303C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11303 | chr13 | 52699138 | |||||
| chr13:52699141
|
A | T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11306A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11306 | chr13 | 52699141 | |||||
| chr13:52699142
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11307A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11307 | chr13 | 52699142 | |||||
| chr13:52699144
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11309A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11309 | chr13 | 52699144 | |||||
| chr13:52699150
|
A | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11315A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11315 | chr13 | 52699150 | |||||
| chr13:52699151
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11316T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11316 | chr13 | 52699151 | |||||
| chr13:52699153
|
A | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11318A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11318 | chr13 | 52699153 | |||||
| chr13:52699154
|
A | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11319A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11319 | chr13 | 52699154 | |||||
| chr13:52699158
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11323G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11323 | chr13 | 52699158 | |||||
| chr13:52699160
|
A | T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11325A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11325 | chr13 | 52699160 | |||||
| chr13:52699163
|
G | A | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11328G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11328 | chr13 | 52699163 | |||||
| chr13:52699165
|
A | G | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11330A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11330 | chr13 | 52699165 | |||||
| chr13:52699166
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11331G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11331 | chr13 | 52699166 | |||||
| chr13:52699171
|
G | T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11336G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11336 | chr13 | 52699171 | |||||
| chr13:52699174
|
G | T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11339G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11339 | chr13 | 52699174 | |||||
| chr13:52699181
|
G | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11346G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11346 | chr13 | 52699181 | |||||
| chr13:52699188
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11353T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11353 | chr13 | 52699188 | |||||
| chr13:52699191
|
T | A | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11356T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11356 | chr13 | 52699191 | |||||
| chr13:52699195
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11360T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11360 | chr13 | 52699195 | |||||
| chr13:52699196
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11361A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11361 | chr13 | 52699196 | |||||
| chr13:52699198
|
T | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11363T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11363 | chr13 | 52699198 | |||||
| chr13:52699199
|
C | A | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11364C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11364 | chr13 | 52699199 | |||||
| chr13:52699201
|
TGGGGGGT others(56): Show |
T | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11367_*11429delGG others(61): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11367 | chr13 | 52699201 | |||||
| chr13:52699250
|
C | G | 1 | a0001c0001t0091 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11415C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11415 | chr13 | 52699250 | |||||
| chr13:52699265
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11430A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11430 | chr13 | 52699265 | |||||
| chr13:52699266
|
A | C | 1 | a0001c0001t0085 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11431A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11431 | chr13 | 52699266 | |||||
| chr13:52699270
|
A | G | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*11435A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11435 | chr13 | 52699270 | |||||
| chr13:52699282
|
A | T | 1 | a0001c0001t0098 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11447A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11447 | chr13 | 52699282 | |||||
| chr13:52699295
|
C | A | 1 | a0001c0002t0040 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11460C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11460 | chr13 | 52699295 | |||||
| chr13:52699345
|
T | C | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*11510T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11510 | chr13 | 52699345 | |||||
| chr13:52699435
|
C | T | 87 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*11600C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11600 | chr13 | 52699435 | |||||
| chr13:52699456
|
C | T | 98 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*11621C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11621 | chr13 | 52699456 | |||||
| chr13:52699474
|
T | C | 1 | a0001c0001t0092 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11639T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11639 | chr13 | 52699474 | |||||
| chr13:52699499
|
G | A | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*11664G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11664 | chr13 | 52699499 | |||||
| chr13:52699515
|
T | A | 1 | a0001c0002t0040 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11680T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11680 | chr13 | 52699515 | |||||
| chr13:52699616
|
A | G | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11781A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11781 | chr13 | 52699616 | |||||
| chr13:52699782
|
A | C | 1 | a0001c0001t0074 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11947A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 11947 | chr13 | 52699782 | |||||
| chr13:52699979
|
A | T | 1 | a0001c0001t0089 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12144A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12144 | chr13 | 52699979 | |||||
| chr13:52700126
|
T | G | 5 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(2): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12291T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12291 | chr13 | 52700126 | |||||
| chr13:52700328
|
ACCTGCAT others(41): Show |
A | 1 | a0001c0001t0071 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12494_*12541delCC others(46): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12494 | chr13 | 52700328 | |||||
| chr13:52700492
|
T | C | 93 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(90): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*12657T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12657 | chr13 | 52700492 | |||||
| chr13:52700529
|
C | A | 1 | a0001c0001t0012 | 4 | HG01243.hp2 HG02965.hp1 NA19240.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*12694C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12694 | chr13 | 52700529 | |||||
| chr13:52700548
|
T | C | 105 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(102): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*12713T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12713 | chr13 | 52700548 | |||||
| chr13:52700602
|
ACT | A | 6 | a0001c0001t0015a0001c0001t0045a0001c0001t0046others(3): Show | 8 | HG01243.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12772_*12773delCT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12772 | INFO_REALIGN_3_PRIME | chr13 | 52700602 | ||||
| chr13:52700696
|
G | A | 1 | a0001c0001t0028 | 2 | HG03831.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12861G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12861 | chr13 | 52700696 | |||||
| chr13:52700801
|
A | G | 1 | a0001c0001t0021 | 2 | HG02109.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12966A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 12966 | chr13 | 52700801 | |||||
| chr13:52700902
|
G | C | 1 | a0001c0001t0059 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13067G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 13/13 | 13067 | chr13 | 52700902 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:52653166
|
C | T | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(95): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.96+63C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653166 | ||||||
| chr13:52653208
|
G | A | 1 | a0001c0001t0050g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.96+105G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653208 | ||||||
| chr13:52653327
|
G | A | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.96+224G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653327 | ||||||
| chr13:52653386
|
AT | A | 226 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(223): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.96+293delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 52653386 | |||||
| chr13:52653386
|
ATT | A | 33 | a0001c0001t0002g0003a0001c0001t0002g0041a0001c0001t0003g0001others(30): Show | 44 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.96+292_96+293delTT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 52653386 | |||||
| chr13:52653595
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.96+492A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653595 | ||||||
| chr13:52653699
|
A | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(71): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.96+596A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653699 | ||||||
| chr13:52653705
|
G | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.96+602G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653705 | ||||||
| chr13:52653763
|
A | C | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+660A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653763 | ||||||
| chr13:52653850
|
G | GA | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(97): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.96+750dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 52653850 | |||||
| chr13:52653984
|
C | T | 250 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(247): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.96+881C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52653984 | ||||||
| chr13:52654107
|
A | G | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1004A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654107 | ||||||
| chr13:52654316
|
C | G | 5 | a0001c0001t0002g0022a0001c0001t0002g0145a0001c0001t0017g0022others(2): Show | 5 | HG02109.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+1213C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654316 | ||||||
| chr13:52654325
|
T | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.96+1222T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654325 | ||||||
| chr13:52654450
|
A | G | 6 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+1347A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654450 | ||||||
| chr13:52654819
|
G | A | 1 | a0001c0001t0003g0035 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.96+1716G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654819 | ||||||
| chr13:52654882
|
A | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.96+1779A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654882 | ||||||
| chr13:52654927
|
T | C | 10 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0062others(7): Show | 11 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.96+1824T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52654927 | ||||||
| chr13:52655111
|
C | T | 1 | a0001c0001t0106g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.96+2008C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52655111 | ||||||
| chr13:52655117
|
A | G | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.96+2014A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52655117 | ||||||
| chr13:52655599
|
C | T | 1 | a0001c0001t0055g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.97-1933C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52655599 | ||||||
| chr13:52655683
|
A | AGATAGCA others(8): Show |
1 | a0001c0002t0039g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.97-1836_97-1822dup others(15): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 52655683 | |||||
| chr13:52655689
|
C | G | 1 | a0001c0001t0101g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-1843C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52655689 | ||||||
| chr13:52655746
|
A | T | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97-1786A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52655746 | ||||||
| chr13:52656179
|
G | C | 1 | a0001c0001t0004g0066 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.97-1353G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52656179 | ||||||
| chr13:52656253
|
G | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG00423.hp2 HG01175.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-1279G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52656253 | ||||||
| chr13:52656403
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | HG01346.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.97-1129T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52656403 | ||||||
| chr13:52656548
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.97-984G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52656548 | ||||||
| chr13:52656691
|
A | G | 1 | a0001c0001t0005g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97-841A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52656691 | ||||||
| chr13:52656848
|
T | C | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(240): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.97-684T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52656848 | ||||||
| chr13:52657030
|
C | T | 121 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(118): Show | 152 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.97-502C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657030 | ||||||
| chr13:52657120
|
G | A | 126 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(123): Show | 158 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.97-412G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657120 | ||||||
| chr13:52657308
|
G | A | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-224G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657308 | ||||||
| chr13:52657319
|
G | A | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.97-213G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657319 | ||||||
| chr13:52657329
|
A | G | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97-203A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657329 | ||||||
| chr13:52657388
|
G | A | 126 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(123): Show | 158 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.97-144G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657388 | ||||||
| chr13:52657442
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.97-90A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 2/12 | chr13 | 52657442 | ||||||
| chr13:52657655
|
T | G | 1 | a0001c0001t0002g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.187+33T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 3/12 | chr13 | 52657655 | ||||||
| chr13:52657911
|
G | A | 1 | a0001c0001t0063g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.187+289G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 3/12 | chr13 | 52657911 | ||||||
| chr13:52658354
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.188-45A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 3/12 | chr13 | 52658354 | ||||||
| chr13:52658371
|
G | A | 1 | a0001c0001t0053g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.188-28G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 3/12 | chr13 | 52658371 | ||||||
| chr13:52658379
|
A | T | 2 | a0001c0001t0055g0135a0001c0001t0056g0079 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.188-20A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 3/12 | chr13 | 52658379 | ||||||
| chr13:52658386
|
T | C | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-13T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 3/12 | chr13 | 52658386 | ||||||
| chr13:52658620
|
T | C | 1 | a0001c0001t0003g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.257+152T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | chr13 | 52658620 | ||||||
| chr13:52658738
|
CT | C | 11 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0016g0011others(8): Show | 12 | HG00544.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+288delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 52658738 | |||||
| chr13:52658738
|
CTT | C | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(240): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.257+287_257+288del others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 52658738 | |||||
| chr13:52658738
|
CTTT | C | 6 | a0001c0001t0001g0188a0001c0001t0002g0083a0001c0001t0017g0143others(3): Show | 6 | HG01169.hp1 HG02602.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+286_257+288del others(3): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr13 | 52658738 | |||||
| chr13:52658756
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(90): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.257+288T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | chr13 | 52658756 | ||||||
| chr13:52658853
|
G | A | 1 | a0001c0001t0024g0037 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.258-326G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | chr13 | 52658853 | ||||||
| chr13:52658992
|
A | G | 2 | a0001c0001t0098g0033a0002c0004t0099g0033 | 2 | HG01516.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.258-187A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | chr13 | 52658992 | ||||||
| chr13:52659059
|
A | T | 101 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(98): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.258-120A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | chr13 | 52659059 | ||||||
| chr13:52659167
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.258-12A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 4/12 | chr13 | 52659167 | ||||||
| chr13:52659457
|
C | T | 262 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(259): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.328+208C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659457 | ||||||
| chr13:52659765
|
CAT | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+520_328+521del others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659765 | |||||
| chr13:52659789
|
A | AAT | 3 | a0001c0001t0020g0158a0001c0001t0020g0160a0001c0001t0054g0034 | 3 | HG02896.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.328+565_328+566dup others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659789 | |||||
| chr13:52659806
|
ATATATAT others(12): Show |
A | 6 | a0001c0001t0015g0023a0001c0001t0015g0149a0001c0001t0045g0148others(3): Show | 6 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.328+559_328+577del others(19): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659806 | |||||
| chr13:52659806
|
ATATATAT others(13): Show |
A | 1 | a0001c0001t0015g0146 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.328+559_328+578del others(20): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659806 | |||||
| chr13:52659810
|
ATATATTT others(3): Show |
A | 1 | a0001c0001t0018g0174 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.328+563_328+572del others(10): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659810 | |||||
| chr13:52659812
|
ATATTT | A | 16 | a0001c0001t0001g0008a0001c0001t0001g0187a0001c0001t0001g0225others(13): Show | 20 | HG00099.hp1 HG00438.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.328+565_328+569del others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659812 | |||||
| chr13:52659812
|
ATATTTT | A | 32 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0032others(29): Show | 36 | HG00140.hp1 HG00423.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.328+565_328+570del others(6): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659812 | |||||
| chr13:52659812
|
ATATTTTT | A | 7 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(4): Show | 7 | HG01070.hp1 HG01257.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+565_328+571del others(7): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659812 | |||||
| chr13:52659812
|
ATATTTTT others(1): Show |
A | 9 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0005g0169others(6): Show | 9 | HG00408.hp1 HG02135.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+565_328+572del others(8): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659812 | |||||
| chr13:52659814
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0030g0180 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.328+566_328+567ins others(11): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0008g0179 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.328+566_328+567ins others(15): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0010g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(17): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0010g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(19): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0056g0079 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328+566_328+567ins others(24): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0010g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.328+566_328+567ins others(22): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0010g0076 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(18): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0055g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(21): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0008g0181 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(13): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0008g0182 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(14): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTT | A | 9 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 10 | HG01943.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+594_328+597del others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTT | A | 9 | a0001c0001t0001g0190a0001c0001t0002g0085a0001c0001t0002g0088others(6): Show | 10 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.328+593_328+597del others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT | A | 12 | a0001c0001t0002g0096a0001c0001t0011g0039a0001c0001t0013g0004others(9): Show | 15 | HG00323.hp2 HG01074.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.328+591_328+597del others(7): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(1): Show |
A | 6 | a0001c0001t0002g0109a0001c0001t0005g0024a0001c0001t0005g0163others(3): Show | 7 | HG00323.hp1 HG01081.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+590_328+597del others(8): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(2): Show |
A | 23 | a0001c0001t0002g0002a0001c0001t0002g0067a0001c0001t0002g0068others(20): Show | 28 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.328+589_328+597del others(9): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0101 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.328+588_328+597del others(10): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(4): Show |
A | 11 | a0001c0001t0003g0015a0001c0001t0003g0035a0001c0001t0003g0036others(8): Show | 13 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.328+587_328+597del others(11): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0003g0053a0001c0001t0022g0048a0001c0001t0043g0050others(1): Show | 4 | HG00597.hp2 NA18960.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+586_328+597del others(12): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(6): Show |
A | 31 | a0001c0001t0002g0003a0001c0001t0002g0041a0001c0001t0002g0099others(28): Show | 41 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.328+585_328+597del others(13): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0003g0054a0001c0001t0004g0128a0001c0001t0100g0134 | 3 | HG02970.hp1 HG04199.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.328+584_328+597del others(14): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(8): Show |
A | 31 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0112others(28): Show | 39 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.328+583_328+597del others(15): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0002g0145a0001c0001t0014g0121 | 2 | HG01168.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.328+582_328+597del others(16): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659814
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0001t0004g0009a0001c0001t0004g0131 | 5 | HG02055.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+581_328+597del others(17): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52659814 | |||||
| chr13:52659815
|
T | TA | 4 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(1): Show | 5 | HG00544.hp1 HG01099.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+566_328+567ins others(1): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659815 | ||||||
| chr13:52659815
|
T | TATATATA others(6): Show |
1 | a0001c0001t0008g0178 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.328+566_328+567ins others(13): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659815 | ||||||
| chr13:52659815
|
T | TATATATA others(8): Show |
2 | a0001c0001t0008g0176a0001c0001t0008g0177 | 2 | HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.328+566_328+567ins others(15): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659815 | ||||||
| chr13:52659815
|
T | TATATATA others(16): Show |
1 | a0001c0001t0030g0175 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.328+566_328+567ins others(23): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659815 | ||||||
| chr13:52659817
|
T | A | 1 | a0001c0001t0023g0153 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.328+568T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659817 | ||||||
| chr13:52659818
|
T | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.328+569T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659818 | ||||||
| chr13:52659820
|
T | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.328+571T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659820 | ||||||
| chr13:52659821
|
T | A | 7 | a0001c0001t0002g0085a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 8 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+572T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659821 | ||||||
| chr13:52659822
|
T | A | 2 | a0001c0001t0002g0129a0001c0001t0002g0130 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.328+573T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659822 | ||||||
| chr13:52659823
|
T | A | 17 | a0001c0001t0002g0085a0001c0001t0002g0088a0001c0001t0002g0089others(14): Show | 21 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.328+574T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659823 | ||||||
| chr13:52659824
|
T | A | 4 | a0001c0001t0002g0109a0001c0001t0002g0129a0001c0001t0002g0130others(1): Show | 4 | HG01516.hp2 HG01517.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+575T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659824 | ||||||
| chr13:52659825
|
T | A | 40 | a0001c0001t0002g0002a0001c0001t0002g0067a0001c0001t0002g0068others(37): Show | 49 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.328+576T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659825 | ||||||
| chr13:52659826
|
T | A | 4 | a0001c0001t0002g0101a0001c0001t0002g0109a0001c0001t0002g0129others(1): Show | 4 | HG01516.hp2 HG01517.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+577T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659826 | ||||||
| chr13:52659827
|
T | A | 50 | a0001c0001t0002g0002a0001c0001t0002g0067a0001c0001t0002g0068others(47): Show | 61 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.328+578T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659827 | ||||||
| chr13:52659828
|
T | A | 8 | a0001c0001t0002g0101a0001c0001t0002g0109a0001c0001t0002g0129others(5): Show | 8 | HG00597.hp2 HG01516.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.328+579T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659828 | ||||||
| chr13:52659829
|
T | A | 76 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0041others(73): Show | 97 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.328+580T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659829 | ||||||
| chr13:52659830
|
T | A | 9 | a0001c0001t0002g0101a0001c0001t0002g0129a0001c0001t0002g0130others(6): Show | 9 | HG00597.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.328+581T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659830 | ||||||
| chr13:52659831
|
T | A | 84 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0022others(81): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.328+582T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659831 | ||||||
| chr13:52659832
|
T | A | 5 | a0001c0001t0002g0145a0001c0001t0014g0121a0001c0001t0022g0048others(2): Show | 5 | HG01168.hp1 HG06807.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+583T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659832 | ||||||
| chr13:52659833
|
T | A | 44 | a0001c0001t0002g0005a0001c0001t0002g0022a0001c0001t0002g0041others(41): Show | 59 | HG00140.hp2 HG00621.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.328+584T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659833 | ||||||
| chr13:52659835
|
T | A | 8 | a0001c0001t0002g0041a0001c0001t0003g0013a0001c0001t0003g0040others(5): Show | 9 | HG00738.hp1 HG01168.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.328+586T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659835 | ||||||
| chr13:52659851
|
C | T | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+602C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659851 | ||||||
| chr13:52659953
|
C | T | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.328+704C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659953 | ||||||
| chr13:52659985
|
C | T | 2 | a0001c0001t0005g0025a0001c0001t0084g0025 | 2 | HG00621.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.328+736C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659985 | ||||||
| chr13:52659989
|
C | T | 2 | a0001c0001t0002g0108a0001c0001t0043g0050 | 2 | NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.328+740C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52659989 | ||||||
| chr13:52660005
|
A | G | 3 | a0001c0001t0012g0019a0001c0001t0012g0070a0001c0001t0012g0071 | 4 | HG01243.hp2 HG02965.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.328+756A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660005 | ||||||
| chr13:52660073
|
C | T | 1 | a0001c0001t0063g0081 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.328+824C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660073 | ||||||
| chr13:52660122
|
C | G | 1 | a0001c0001t0001g0224 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.328+873C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660122 | ||||||
| chr13:52660190
|
G | A | 2 | a0001c0001t0055g0135a0001c0001t0056g0079 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.328+941G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660190 | ||||||
| chr13:52660350
|
A | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+1101A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660350 | ||||||
| chr13:52660413
|
T | C | 2 | a0001c0001t0007g0110a0001c0001t0079g0111 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.328+1164T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660413 | ||||||
| chr13:52660448
|
G | A | 236 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0032others(233): Show | 276 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.328+1199G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660448 | ||||||
| chr13:52660508
|
T | G | 1 | a0001c0001t0003g0118 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.328+1259T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660508 | ||||||
| chr13:52660523
|
GT | G | 5 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.328+1278delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 52660523 | |||||
| chr13:52660557
|
T | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+1308T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660557 | ||||||
| chr13:52660623
|
G | A | 126 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(123): Show | 158 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.328+1374G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660623 | ||||||
| chr13:52660690
|
C | T | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+1441C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660690 | ||||||
| chr13:52660832
|
G | A | 1 | a0001c0001t0055g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.328+1583G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660832 | ||||||
| chr13:52660845
|
C | T | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+1596C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660845 | ||||||
| chr13:52660931
|
T | A | 4 | a0001c0001t0001g0196a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG00438.hp2 HG00609.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+1682T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660931 | ||||||
| chr13:52660962
|
A | T | 1 | a0001c0001t0002g0116 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.329-1687A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52660962 | ||||||
| chr13:52661005
|
A | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.329-1644A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661005 | ||||||
| chr13:52661063
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.329-1586C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661063 | ||||||
| chr13:52661122
|
T | C | 3 | a0001c0001t0002g0080a0001c0001t0002g0083a0001c0001t0002g0101 | 3 | NA18997.hp1 NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.329-1527T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661122 | ||||||
| chr13:52661290
|
G | T | 2 | a0001c0001t0034g0157a0001c0001t0034g0161 | 2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.329-1359G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661290 | ||||||
| chr13:52661291
|
T | G | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(240): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.329-1358T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661291 | ||||||
| chr13:52661322
|
G | C | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.329-1327G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661322 | ||||||
| chr13:52661482
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.329-1167G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661482 | ||||||
| chr13:52661765
|
G | T | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(244): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.329-884G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52661765 | ||||||
| chr13:52662078
|
A | G | 11 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0062others(8): Show | 12 | HG00609.hp1 HG00673.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.329-571A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52662078 | ||||||
| chr13:52662186
|
A | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.329-463A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52662186 | ||||||
| chr13:52662238
|
G | A | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-411G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52662238 | ||||||
| chr13:52662246
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.329-403A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 5/12 | chr13 | 52662246 | ||||||
| chr13:52662723
|
ATTTG | A | 6 | a0001c0001t0010g0073a0001c0001t0010g0074a0001c0001t0010g0075others(3): Show | 6 | HG01192.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.382+25_382+28delGT others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 52662723 | |||||
| chr13:52662737
|
A | G | 2 | a0001c0001t0007g0064a0001c0001t0068g0065 | 2 | HG02040.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.382+35A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 6/12 | chr13 | 52662737 | ||||||
| chr13:52663007
|
C | T | 1 | a0001c0001t0035g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.383-89C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 6/12 | chr13 | 52663007 | ||||||
| chr13:52663500
|
G | C | 1 | a0001c0001t0009g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.399+388G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 7/12 | chr13 | 52663500 | ||||||
| chr13:52663585
|
C | T | 1 | a0001c0001t0079g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.400-450C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 7/12 | chr13 | 52663585 | ||||||
| chr13:52663612
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.400-423A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 7/12 | chr13 | 52663612 | ||||||
| chr13:52663634
|
A | G | 1 | a0001c0001t0003g0035 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.400-401A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 7/12 | chr13 | 52663634 | ||||||
| chr13:52663874
|
A | G | 2 | a0001c0001t0030g0175a0001c0001t0030g0180 | 2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.400-161A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 7/12 | chr13 | 52663874 | ||||||
| chr13:52664013
|
C | T | 6 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(3): Show | 6 | HG01255.hp2 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-22C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 7/12 | chr13 | 52664013 | ||||||
| chr13:52664630
|
A | C | 5 | a0001c0001t0001g0209a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG00735.hp1 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.422+573A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52664630 | ||||||
| chr13:52664699
|
C | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.422+642C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52664699 | ||||||
| chr13:52664708
|
A | G | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.422+651A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52664708 | ||||||
| chr13:52664772
|
G | A | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+715G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52664772 | ||||||
| chr13:52664848
|
C | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.423-789C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52664848 | ||||||
| chr13:52664874
|
G | A | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-763G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52664874 | ||||||
| chr13:52665017
|
C | G | 1 | a0001c0001t0012g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.423-620C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665017 | ||||||
| chr13:52665125
|
C | T | 128 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(125): Show | 160 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.423-512C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665125 | ||||||
| chr13:52665230
|
A | G | 1 | a0001c0001t0060g0047 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.423-407A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665230 | ||||||
| chr13:52665242
|
G | C | 1 | a0001c0001t0006g0210 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.423-395G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665242 | ||||||
| chr13:52665281
|
G | T | 1 | a0001c0001t0012g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.423-356G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665281 | ||||||
| chr13:52665294
|
C | G | 1 | a0001c0002t0042g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.423-343C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665294 | ||||||
| chr13:52665323
|
TTAAAA | T | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-309_423-305del others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 52665323 | |||||
| chr13:52665406
|
A | G | 5 | a0001c0001t0005g0163a0001c0001t0005g0165a0001c0001t0005g0170others(2): Show | 5 | HG02135.hp2 NA18970.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.423-231A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | chr13 | 52665406 | ||||||
| chr13:52665512
|
G | GTAGT | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.423-123_423-120dup others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 52665512 | |||||
| chr13:52665794
|
C | T | 1 | a0001c0001t0061g0042 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.519+61C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52665794 | ||||||
| chr13:52665896
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.519+163T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52665896 | ||||||
| chr13:52665897
|
G | A | 1 | a0001c0001t0004g0122 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.519+164G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52665897 | ||||||
| chr13:52665986
|
C | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.519+253C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52665986 | ||||||
| chr13:52666048
|
T | C | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(96): Show | 112 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.519+315T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666048 | ||||||
| chr13:52666049
|
G | A | 5 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0050g0162others(2): Show | 5 | HG01175.hp2 HG01943.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+316G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666049 | ||||||
| chr13:52666126
|
C | T | 1 | a0001c0001t0049g0152 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.519+393C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666126 | ||||||
| chr13:52666127
|
G | A | 1 | a0001c0001t0028g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.519+394G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666127 | ||||||
| chr13:52666141
|
A | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+408A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666141 | ||||||
| chr13:52666218
|
TGGGACTA others(8): Show |
T | 4 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+486_519+500del others(15): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666218 | ||||||
| chr13:52666232
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.519+499C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666232 | ||||||
| chr13:52666234
|
T | A | 4 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+501T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666234 | ||||||
| chr13:52666287
|
G | A | 1 | a0001c0002t0039g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.520-525G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666287 | ||||||
| chr13:52666386
|
T | C | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-426T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666386 | ||||||
| chr13:52666411
|
C | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.520-401C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666411 | ||||||
| chr13:52666621
|
C | G | 1 | a0001c0001t0043g0050 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.520-191C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666621 | ||||||
| chr13:52666664
|
AC | A | 3 | a0001c0001t0012g0019a0001c0001t0012g0070a0001c0001t0012g0071 | 4 | HG01243.hp2 HG02965.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-146delC | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 52666664 | |||||
| chr13:52666700
|
A | G | 1 | a0001c0001t0003g0046 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.520-112A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666700 | ||||||
| chr13:52666749
|
G | C | 260 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(257): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.520-63G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 9/12 | chr13 | 52666749 | ||||||
| chr13:52666956
|
T | G | 1 | a0001c0001t0002g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.627+37T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52666956 | ||||||
| chr13:52667156
|
T | C | 104 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(101): Show | 129 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.627+237T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667156 | ||||||
| chr13:52667368
|
G | A | 250 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(247): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.627+449G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667368 | ||||||
| chr13:52667405
|
C | T | 1 | a0001c0001t0104g0084 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.627+486C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667405 | ||||||
| chr13:52667411
|
C | G | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+492C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667411 | ||||||
| chr13:52667510
|
T | A | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.627+591T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667510 | ||||||
| chr13:52667576
|
CT | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(250): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.627+667delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52667576 | |||||
| chr13:52667586
|
T | A | 19 | a0001c0001t0005g0012a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 21 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.627+667T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667586 | ||||||
| chr13:52667629
|
A | G | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+710A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667629 | ||||||
| chr13:52667665
|
G | T | 2 | a0001c0001t0003g0053a0001c0001t0003g0055 | 2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.627+746G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667665 | ||||||
| chr13:52667789
|
T | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+870T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667789 | ||||||
| chr13:52667791
|
G | A | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.627+872G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667791 | ||||||
| chr13:52667865
|
G | A | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+946G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667865 | ||||||
| chr13:52667972
|
C | CT | 15 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(12): Show | 15 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.627+1066dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52667972 | |||||
| chr13:52667985
|
T | C | 1 | a0001c0001t0075g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.627+1066T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52667985 | ||||||
| chr13:52668395
|
T | C | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+1476T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52668395 | ||||||
| chr13:52668625
|
A | G | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+1706A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52668625 | ||||||
| chr13:52668789
|
A | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.627+1870A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52668789 | ||||||
| chr13:52668830
|
C | CA | 42 | a0001c0001t0001g0030a0001c0001t0001g0211a0001c0001t0001g0227others(39): Show | 46 | HG00408.hp1 HG00621.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.627+1928dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52668830 | |||||
| chr13:52669025
|
T | G | 1 | a0001c0002t0040g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.627+2106T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669025 | ||||||
| chr13:52669047
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.627+2128T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669047 | ||||||
| chr13:52669157
|
T | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+2238T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669157 | ||||||
| chr13:52669299
|
A | G | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.627+2380A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669299 | ||||||
| chr13:52669484
|
A | G | 1 | a0001c0001t0020g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.627+2565A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669484 | ||||||
| chr13:52669828
|
A | G | 4 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0047g0150others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+2909A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669828 | ||||||
| chr13:52669836
|
A | C | 4 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(1): Show | 4 | HG01255.hp2 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+2917A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52669836 | ||||||
| chr13:52670140
|
C | T | 3 | a0001c0001t0002g0080a0001c0001t0002g0083a0001c0001t0002g0101 | 3 | NA18997.hp1 NA19059.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.627+3221C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670140 | ||||||
| chr13:52670252
|
A | G | 9 | a0001c0001t0006g0027a0001c0001t0006g0028a0001c0001t0006g0031others(6): Show | 11 | HG01106.hp1 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.627+3333A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670252 | ||||||
| chr13:52670632
|
A | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.627+3713A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670632 | ||||||
| chr13:52670675
|
A | G | 262 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(259): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.627+3756A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670675 | ||||||
| chr13:52670680
|
T | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | NA18965.hp2 NA18981.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.627+3761T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670680 | ||||||
| chr13:52670826
|
A | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+3907A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670826 | ||||||
| chr13:52670927
|
A | G | 1 | a0001c0001t0005g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.627+4008A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52670927 | ||||||
| chr13:52671043
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.627+4124A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671043 | ||||||
| chr13:52671062
|
T | C | 2 | a0001c0001t0030g0175a0001c0001t0030g0180 | 2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.627+4143T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671062 | ||||||
| chr13:52671144
|
A | T | 1 | a0001c0001t0015g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.627+4225A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671144 | ||||||
| chr13:52671148
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.627+4229A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671148 | ||||||
| chr13:52671256
|
T | C | 1 | a0001c0001t0096g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.627+4337T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671256 | ||||||
| chr13:52671321
|
A | AAAG | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.627+4405_627+4407d others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52671321 | |||||
| chr13:52671389
|
A | G | 5 | a0001c0001t0002g0114a0001c0001t0002g0132a0001c0001t0009g0006others(2): Show | 8 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.627+4470A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671389 | ||||||
| chr13:52671396
|
A | G | 1 | a0001c0001t0104g0084 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.627+4477A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671396 | ||||||
| chr13:52671637
|
G | T | 1 | a0001c0001t0032g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.628-4593G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671637 | ||||||
| chr13:52671841
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.628-4389A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671841 | ||||||
| chr13:52671919
|
G | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.628-4311G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52671919 | ||||||
| chr13:52672100
|
C | T | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-4130C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672100 | ||||||
| chr13:52672158
|
A | G | 2 | a0001c0001t0036g0018a0001c0001t0037g0018 | 2 | HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.628-4072A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672158 | ||||||
| chr13:52672175
|
G | A | 1 | a0001c0001t0017g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.628-4055G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672175 | ||||||
| chr13:52672180
|
C | T | 2 | a0001c0001t0030g0175a0001c0001t0030g0180 | 2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.628-4050C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672180 | ||||||
| chr13:52672194
|
A | G | 2 | a0001c0001t0003g0036a0001c0001t0044g0093 | 2 | NA18961.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.628-4036A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672194 | ||||||
| chr13:52672694
|
T | A | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-3536T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672694 | ||||||
| chr13:52672957
|
T | C | 1 | a0001c0001t0097g0168 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.628-3273T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672957 | ||||||
| chr13:52672990
|
C | T | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-3240C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52672990 | ||||||
| chr13:52673243
|
T | C | 1 | a0001c0001t0008g0176 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.628-2987T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673243 | ||||||
| chr13:52673254
|
T | TG | 3 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011 | 4 | HG00544.hp1 NA18994.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-2976_628-2975i others(3): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673254 | ||||||
| chr13:52673255
|
TG | T | 252 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(249): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.628-2974delG | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673255 | ||||||
| chr13:52673256
|
G | T | 2 | a0001c0001t0021g0077a0001c0001t0021g0078 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.628-2974G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673256 | ||||||
| chr13:52673289
|
C | T | 1 | a0001c0001t0004g0021 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.628-2941C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673289 | ||||||
| chr13:52673318
|
C | T | 2 | a0001c0001t0002g0114a0001c0001t0002g0132 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.628-2912C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673318 | ||||||
| chr13:52673390
|
G | A | 1 | a0001c0001t0003g0051 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.628-2840G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673390 | ||||||
| chr13:52673490
|
C | G | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-2740C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673490 | ||||||
| chr13:52673565
|
T | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-2665T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52673565 | ||||||
| chr13:52674013
|
T | C | 1 | a0001c0001t0002g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.628-2217T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674013 | ||||||
| chr13:52674053
|
C | CT | 82 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(79): Show | 95 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.628-2156dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52674053 | |||||
| chr13:52674053
|
C | CTT | 43 | a0001c0001t0001g0196a0001c0001t0001g0211a0001c0001t0001g0215others(40): Show | 44 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.628-2157_628-2156d others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52674053 | |||||
| chr13:52674053
|
C | CTTT | 114 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(111): Show | 145 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.628-2158_628-2156d others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52674053 | |||||
| chr13:52674053
|
C | CTTTT | 9 | a0001c0001t0003g0044a0001c0001t0004g0127a0001c0001t0004g0128others(6): Show | 10 | HG01109.hp2 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.628-2159_628-2156d others(6): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52674053 | |||||
| chr13:52674060
|
T | TTC | 6 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-2169_628-2168i others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 52674060 | |||||
| chr13:52674082
|
T | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-2148T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674082 | ||||||
| chr13:52674109
|
C | T | 1 | a0001c0001t0055g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.628-2121C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674109 | ||||||
| chr13:52674214
|
G | A | 1 | a0001c0002t0039g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.628-2016G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674214 | ||||||
| chr13:52674226
|
A | G | 1 | a0001c0001t0002g0107 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.628-2004A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674226 | ||||||
| chr13:52674244
|
G | A | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-1986G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674244 | ||||||
| chr13:52674263
|
G | A | 1 | a0001c0001t0008g0177 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.628-1967G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674263 | ||||||
| chr13:52674447
|
C | T | 3 | a0001c0001t0012g0019a0001c0001t0012g0070a0001c0001t0012g0071 | 4 | HG01243.hp2 HG02965.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-1783C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674447 | ||||||
| chr13:52674547
|
G | C | 6 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(3): Show | 6 | HG01255.hp2 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-1683G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674547 | ||||||
| chr13:52674752
|
T | C | 1 | a0001c0001t0007g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.628-1478T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674752 | ||||||
| chr13:52674780
|
T | C | 250 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(247): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.628-1450T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674780 | ||||||
| chr13:52674990
|
A | G | 4 | a0001c0001t0010g0073a0001c0001t0010g0074a0001c0001t0010g0075others(1): Show | 4 | HG01192.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-1240A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52674990 | ||||||
| chr13:52675038
|
C | T | 2 | a0001c0001t0030g0175a0001c0001t0030g0180 | 2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.628-1192C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675038 | ||||||
| chr13:52675081
|
C | T | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1149C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675081 | ||||||
| chr13:52675084
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.628-1146A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675084 | ||||||
| chr13:52675125
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.628-1105A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675125 | ||||||
| chr13:52675187
|
C | T | 136 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(133): Show | 168 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.628-1043C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675187 | ||||||
| chr13:52675221
|
C | T | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.628-1009C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675221 | ||||||
| chr13:52675279
|
A | G | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(97): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.628-951A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675279 | ||||||
| chr13:52675328
|
C | T | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.628-902C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675328 | ||||||
| chr13:52675410
|
C | T | 1 | a0001c0002t0040g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.628-820C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675410 | ||||||
| chr13:52675530
|
T | C | 1 | a0001c0001t0100g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.628-700T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675530 | ||||||
| chr13:52675859
|
A | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-371A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675859 | ||||||
| chr13:52675862
|
T | C | 25 | a0001c0001t0005g0012a0001c0001t0005g0024a0001c0001t0005g0025others(22): Show | 27 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.628-368T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675862 | ||||||
| chr13:52675863
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.628-367C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675863 | ||||||
| chr13:52675965
|
C | T | 3 | a0001c0001t0009g0006a0001c0001t0009g0098a0001c0001t0073g0006 | 6 | HG02258.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-265C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675965 | ||||||
| chr13:52675995
|
A | G | 4 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0047g0150others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-235A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52675995 | ||||||
| chr13:52676052
|
A | G | 1 | a0001c0001t0045g0148 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.628-178A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 10/12 | chr13 | 52676052 | ||||||
| chr13:52676612
|
G | A | 1 | a0001c0001t0024g0037 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.718+292G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52676612 | ||||||
| chr13:52676704
|
G | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.718+384G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52676704 | ||||||
| chr13:52676823
|
A | G | 2 | a0001c0001t0028g0219a0001c0001t0028g0233 | 2 | HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.718+503A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52676823 | ||||||
| chr13:52676876
|
C | A | 1 | a0001c0001t0100g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.718+556C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52676876 | ||||||
| chr13:52676905
|
C | G | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(97): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.718+585C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52676905 | ||||||
| chr13:52676952
|
A | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.718+632A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52676952 | ||||||
| chr13:52677078
|
CAT | C | 6 | a0001c0001t0004g0009a0001c0001t0032g0139a0001c0001t0032g0141others(3): Show | 9 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.718+759_718+760del others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677078 | ||||||
| chr13:52677327
|
T | A | 1 | a0001c0001t0083g0198 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.718+1007T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677327 | ||||||
| chr13:52677487
|
A | AT | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+1171dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52677487 | |||||
| chr13:52677598
|
T | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.718+1278T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677598 | ||||||
| chr13:52677627
|
G | T | 2 | a0001c0001t0013g0004a0001c0001t0078g0004 | 5 | HG01074.hp2 HG01496.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+1307G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677627 | ||||||
| chr13:52677631
|
A | G | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(240): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.718+1311A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677631 | ||||||
| chr13:52677632
|
G | T | 1 | a0001c0001t0043g0050 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.718+1312G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677632 | ||||||
| chr13:52677703
|
CTGTTAAC others(4): Show |
C | 250 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(247): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.718+1387_718+1397d others(13): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52677703 | |||||
| chr13:52677726
|
T | C | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.718+1406T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677726 | ||||||
| chr13:52677788
|
A | AT | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.718+1468_718+1469i others(3): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677788 | ||||||
| chr13:52677848
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.718+1528T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52677848 | ||||||
| chr13:52678116
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.718+1796C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678116 | ||||||
| chr13:52678148
|
A | G | 1 | a0001c0001t0047g0150 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.719-1826A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678148 | ||||||
| chr13:52678171
|
C | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.719-1803C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678171 | ||||||
| chr13:52678311
|
GTGT | G | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-1658_719-1656d others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52678311 | |||||
| chr13:52678523
|
C | T | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-1451C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678523 | ||||||
| chr13:52678591
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.719-1383A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678591 | ||||||
| chr13:52678651
|
GAA | G | 6 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.719-1322_719-1321d others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678651 | ||||||
| chr13:52678681
|
G | GT | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.719-1278dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52678681 | |||||
| chr13:52678681
|
GT | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.719-1278delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52678681 | |||||
| chr13:52678787
|
T | TC | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.719-1186dupC | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52678787 | |||||
| chr13:52678853
|
A | AT | 8 | a0001c0001t0004g0126a0001c0001t0015g0023a0001c0001t0015g0146others(5): Show | 8 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.719-1112dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52678853 | |||||
| chr13:52678856
|
T | A | 1 | a0001c0001t0001g0215 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.719-1118T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52678856 | ||||||
| chr13:52679104
|
A | G | 1 | a0001c0001t0047g0150 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.719-870A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679104 | ||||||
| chr13:52679151
|
C | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.719-823C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679151 | ||||||
| chr13:52679257
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.719-717G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679257 | ||||||
| chr13:52679429
|
TCTTA | T | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.719-541_719-538del others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52679429 | |||||
| chr13:52679566
|
A | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0223 | 2 | HG01261.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.719-408A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679566 | ||||||
| chr13:52679583
|
T | TA | 236 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(233): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.719-385dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 52679583 | |||||
| chr13:52679602
|
A | G | 1 | a0001c0001t0075g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.719-372A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679602 | ||||||
| chr13:52679721
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.719-253A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679721 | ||||||
| chr13:52679785
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.719-189T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679785 | ||||||
| chr13:52679803
|
T | C | 236 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(233): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.719-171T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679803 | ||||||
| chr13:52679844
|
T | C | 1 | a0001c0001t0079g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.719-130T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679844 | ||||||
| chr13:52679897
|
A | G | 2 | a0001c0001t0083g0198a0001c0001t0091g0200 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.719-77A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679897 | ||||||
| chr13:52679936
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.719-38A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679936 | ||||||
| chr13:52679947
|
T | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.719-27T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 11/12 | chr13 | 52679947 | ||||||
| chr13:52680161
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
splice_region_variant&intron_variant | LOW | c.900+6A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680161 | ||||||
| chr13:52680181
|
T | C | 1 | a0001c0002t0041g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.900+26T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680181 | ||||||
| chr13:52680330
|
TTATGGAA others(32): Show |
T | 1 | a0001c0001t0002g0083 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.900+176_900+214del others(39): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680330 | ||||||
| chr13:52680362
|
T | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(250): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.900+207T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680362 | ||||||
| chr13:52680370
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.900+215G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680370 | ||||||
| chr13:52680504
|
G | A | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+349G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680504 | ||||||
| chr13:52680512
|
TC | T | 4 | a0001c0001t0010g0073a0001c0001t0010g0074a0001c0001t0010g0075others(1): Show | 4 | HG01192.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+358delC | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680512 | ||||||
| chr13:52680598
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.900+443G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680598 | ||||||
| chr13:52680645
|
G | A | 2 | a0001c0001t0029g0056a0003c0003t0029g0167 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.900+490G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680645 | ||||||
| chr13:52680691
|
A | G | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.900+536A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680691 | ||||||
| chr13:52680713
|
G | A | 6 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+558G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680713 | ||||||
| chr13:52680877
|
T | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(92): Show | 107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.900+722T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680877 | ||||||
| chr13:52680878
|
G | C | 134 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(131): Show | 167 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.900+723G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680878 | ||||||
| chr13:52680949
|
T | C | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.900+794T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680949 | ||||||
| chr13:52680998
|
C | T | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+843C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52680998 | ||||||
| chr13:52681077
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.900+922A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681077 | ||||||
| chr13:52681135
|
G | C | 2 | a0001c0001t0030g0175a0001c0001t0030g0180 | 2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.900+980G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681135 | ||||||
| chr13:52681196
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.900+1041A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681196 | ||||||
| chr13:52681219
|
T | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.900+1064T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681219 | ||||||
| chr13:52681252
|
C | CA | 14 | a0001c0001t0001g0191a0001c0001t0001g0203a0001c0001t0002g0085others(11): Show | 14 | HG00544.hp2 HG01891.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.900+1113dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52681252 | |||||
| chr13:52681291
|
G | A | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+1136G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681291 | ||||||
| chr13:52681302
|
T | C | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.900+1147T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681302 | ||||||
| chr13:52681669
|
C | T | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(84): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.900+1514C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681669 | ||||||
| chr13:52681737
|
C | T | 2 | a0001c0001t0034g0157a0001c0001t0034g0161 | 2 | HG06807.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.900+1582C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681737 | ||||||
| chr13:52681738
|
G | A | 1 | a0001c0001t0062g0123 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.900+1583G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681738 | ||||||
| chr13:52681813
|
A | C | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+1658A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681813 | ||||||
| chr13:52681836
|
T | TA | 213 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(210): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.900+1695dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52681836 | |||||
| chr13:52681836
|
T | TAA | 10 | a0001c0001t0005g0172a0001c0001t0008g0182a0001c0001t0015g0023others(7): Show | 10 | HG01256.hp2 HG01891.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.900+1694_900+1695d others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52681836 | |||||
| chr13:52681849
|
A | AG | 5 | a0001c0001t0001g0188a0001c0001t0001g0207a0001c0001t0001g0215others(2): Show | 5 | HG00323.hp2 HG01257.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+1694_900+1695i others(3): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681849 | ||||||
| chr13:52681865
|
T | G | 1 | a0001c0001t0001g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.900+1710T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52681865 | ||||||
| chr13:52681917
|
T | TACTC | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.900+1765_900+1766i others(6): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52681917 | |||||
| chr13:52682022
|
T | A | 1 | a0001c0001t0065g0072 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.900+1867T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682022 | ||||||
| chr13:52682047
|
A | G | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.900+1892A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682047 | ||||||
| chr13:52682082
|
C | T | 4 | a0001c0001t0010g0073a0001c0001t0010g0074a0001c0001t0010g0075others(1): Show | 4 | HG01192.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+1927C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682082 | ||||||
| chr13:52682086
|
T | G | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.900+1931T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682086 | ||||||
| chr13:52682388
|
TG | T | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.900+2238delG | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52682388 | |||||
| chr13:52682421
|
G | C | 1 | a0001c0001t0038g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.900+2266G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682421 | ||||||
| chr13:52682500
|
C | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+2345C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682500 | ||||||
| chr13:52682663
|
G | A | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.900+2508G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682663 | ||||||
| chr13:52682690
|
C | T | 6 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+2535C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682690 | ||||||
| chr13:52682695
|
C | T | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.900+2540C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52682695 | ||||||
| chr13:52683317
|
C | T | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.900+3162C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683317 | ||||||
| chr13:52683363
|
T | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.900+3208T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683363 | ||||||
| chr13:52683445
|
C | A | 1 | a0001c0001t0053g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.900+3290C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683445 | ||||||
| chr13:52683558
|
T | A | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+3403T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683558 | ||||||
| chr13:52683595
|
T | G | 1 | a0001c0001t0089g0213 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.900+3440T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683595 | ||||||
| chr13:52683611
|
G | A | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+3456G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683611 | ||||||
| chr13:52683619
|
G | A | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.900+3464G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683619 | ||||||
| chr13:52683711
|
C | T | 2 | a0001c0001t0005g0025a0001c0001t0084g0025 | 2 | HG00621.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.900+3556C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683711 | ||||||
| chr13:52683744
|
A | G | 4 | a0001c0001t0010g0073a0001c0001t0010g0074a0001c0001t0010g0075others(1): Show | 4 | HG01192.hp2 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+3589A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683744 | ||||||
| chr13:52683905
|
C | T | 1 | a0001c0001t0057g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.900+3750C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683905 | ||||||
| chr13:52683907
|
G | C | 1 | a0001c0001t0074g0038 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.900+3752G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683907 | ||||||
| chr13:52683958
|
G | A | 2 | a0001c0001t0030g0175a0001c0001t0030g0180 | 2 | HG01074.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.901-3776G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683958 | ||||||
| chr13:52683990
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.901-3744C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52683990 | ||||||
| chr13:52684038
|
A | G | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.901-3696A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684038 | ||||||
| chr13:52684071
|
T | A | 4 | a0001c0001t0006g0205a0001c0001t0006g0210a0001c0001t0006g0212others(1): Show | 4 | HG01496.hp1 HG02809.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.901-3663T>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684071 | ||||||
| chr13:52684128
|
T | G | 2 | a0001c0001t0007g0110a0001c0001t0079g0111 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.901-3606T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684128 | ||||||
| chr13:52684154
|
G | A | 72 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(69): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.901-3580G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684154 | ||||||
| chr13:52684348
|
A | G | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-3386A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684348 | ||||||
| chr13:52684362
|
T | C | 1 | a0001c0001t0100g0134 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.901-3372T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684362 | ||||||
| chr13:52684420
|
TG | T | 233 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(230): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.901-3313delG | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684420 | ||||||
| chr13:52684421
|
G | T | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-3313G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684421 | ||||||
| chr13:52684462
|
T | C | 1 | a0001c0001t0004g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.901-3272T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684462 | ||||||
| chr13:52684602
|
G | A | 1 | a0001c0001t0065g0072 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.901-3132G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684602 | ||||||
| chr13:52684624
|
G | C | 1 | a0001c0002t0039g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901-3110G>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684624 | ||||||
| chr13:52684730
|
A | G | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-3004A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684730 | ||||||
| chr13:52684908
|
CT | C | 254 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(251): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.901-2813delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52684908 | |||||
| chr13:52684930
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.901-2804G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684930 | ||||||
| chr13:52684977
|
T | C | 1 | a0001c0001t0096g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.901-2757T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52684977 | ||||||
| chr13:52685069
|
CT | C | 233 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(230): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.901-2651delT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52685069 | |||||
| chr13:52685069
|
CTT | C | 8 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(5): Show | 8 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-2652_901-2651d others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52685069 | |||||
| chr13:52685200
|
T | G | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.901-2534T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685200 | ||||||
| chr13:52685256
|
C | CT | 5 | a0001c0001t0016g0011a0001c0001t0016g0151a0001c0001t0023g0011others(2): Show | 6 | HG00544.hp1 HG01099.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-2458dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52685256 | |||||
| chr13:52685256
|
CTT | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0199a0001c0001t0002g0108others(3): Show | 6 | HG00642.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-2459_901-2458d others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52685256 | |||||
| chr13:52685256
|
CTTT | C | 243 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(240): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.901-2460_901-2458d others(5): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52685256 | |||||
| chr13:52685261
|
T | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0199a0001c0001t0019g0032 | 3 | HG01175.hp1 HG01192.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.901-2473T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685261 | ||||||
| chr13:52685262
|
T | C | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(93): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.901-2472T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685262 | ||||||
| chr13:52685413
|
C | A | 2 | a0001c0001t0055g0135a0001c0001t0056g0079 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.901-2321C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685413 | ||||||
| chr13:52685484
|
T | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-2250T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685484 | ||||||
| chr13:52685576
|
G | A | 2 | a0001c0001t0055g0135a0001c0001t0056g0079 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.901-2158G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685576 | ||||||
| chr13:52685593
|
A | G | 1 | a0001c0001t0096g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.901-2141A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685593 | ||||||
| chr13:52685622
|
A | T | 128 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(125): Show | 160 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.901-2112A>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685622 | ||||||
| chr13:52685628
|
T | G | 2 | a0001c0001t0055g0135a0001c0001t0056g0079 | 2 | HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.901-2106T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685628 | ||||||
| chr13:52685681
|
A | G | 2 | a0001c0001t0005g0025a0001c0001t0084g0025 | 2 | HG00621.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.901-2053A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685681 | ||||||
| chr13:52685886
|
T | C | 5 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(2): Show | 5 | HG02559.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-1848T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52685886 | ||||||
| chr13:52686052
|
A | G | 4 | a0001c0002t0039g0060a0001c0002t0040g0057a0001c0002t0041g0058others(1): Show | 4 | HG01243.hp1 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-1682A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686052 | ||||||
| chr13:52686085
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.901-1649G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686085 | ||||||
| chr13:52686123
|
T | C | 1 | a0001c0001t0012g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.901-1611T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686123 | ||||||
| chr13:52686192
|
T | C | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-1542T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686192 | ||||||
| chr13:52686250
|
C | A | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-1484C>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686250 | ||||||
| chr13:52686286
|
C | T | 1 | a0001c0001t0035g0063 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.901-1448C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686286 | ||||||
| chr13:52686307
|
G | T | 1 | a0001c0001t0068g0065 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.901-1427G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686307 | ||||||
| chr13:52686442
|
T | G | 1 | a0001c0001t0002g0083 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.901-1292T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686442 | ||||||
| chr13:52686443
|
G | T | 1 | a0001c0001t0002g0083 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.901-1291G>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686443 | ||||||
| chr13:52686528
|
G | A | 2 | a0001c0001t0007g0016a0001c0001t0067g0061 | 3 | HG00609.hp1 HG02165.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.901-1206G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686528 | ||||||
| chr13:52686587
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.901-1147G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686587 | ||||||
| chr13:52686588
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.901-1146C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686588 | ||||||
| chr13:52686618
|
G | A | 1 | a0001c0001t0054g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.901-1116G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686618 | ||||||
| chr13:52686726
|
A | C | 1 | a0001c0001t0038g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.901-1008A>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686726 | ||||||
| chr13:52686792
|
T | C | 259 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(256): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.901-942T>C | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686792 | ||||||
| chr13:52686825
|
C | T | 3 | a0001c0001t0032g0139a0001c0001t0102g0137a0001c0001t0103g0138 | 3 | HG02486.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.901-909C>T | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686825 | ||||||
| chr13:52686840
|
G | A | 1 | a0001c0002t0040g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.901-894G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686840 | ||||||
| chr13:52686899
|
C | G | 19 | a0001c0001t0005g0012a0001c0001t0005g0024a0001c0001t0005g0025others(16): Show | 21 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.901-835C>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686899 | ||||||
| chr13:52686928
|
G | A | 7 | a0001c0001t0015g0023a0001c0001t0015g0146a0001c0001t0015g0149others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-806G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686928 | ||||||
| chr13:52686948
|
G | A | 6 | a0001c0001t0004g0020a0001c0001t0004g0128a0001c0001t0014g0117others(3): Show | 7 | HG00099.hp2 HG00140.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.901-786G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52686948 | ||||||
| chr13:52687036
|
A | G | 93 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(90): Show | 106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.901-698A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52687036 | ||||||
| chr13:52687068
|
C | CA | 17 | a0001c0001t0003g0043a0001c0001t0010g0073a0001c0001t0010g0074others(14): Show | 17 | HG01192.hp2 HG01243.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.901-642dupA | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687068 | |||||
| chr13:52687068
|
C | CAA | 118 | a0001c0001t0001g0190a0001c0001t0001g0208a0001c0001t0002g0003others(115): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.901-643_901-642dup others(2): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687068 | |||||
| chr13:52687068
|
C | CAAA | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(93): Show | 113 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.901-644_901-642dup others(3): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687068 | |||||
| chr13:52687068
|
C | CAAAA | 18 | a0001c0001t0001g0188a0001c0001t0001g0201a0001c0001t0001g0207others(15): Show | 19 | HG00544.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.901-645_901-642dup others(4): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687068 | |||||
| chr13:52687068
|
CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0032g0139a0001c0001t0032g0141a0001c0001t0051g0140others(4): Show | 7 | HG01891.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.901-650_901-642del others(9): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687068 | |||||
| chr13:52687068
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0039g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.901-653_901-642del others(12): Show |
SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687068 | |||||
| chr13:52687274
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.901-460A>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52687274 | ||||||
| chr13:52687378
|
A | AT | 137 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0005others(134): Show | 169 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.901-348dupT | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr13 | 52687378 | |||||
| chr13:52687396
|
T | G | 1 | a0001c0001t0004g0020 | 2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.901-338T>G | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52687396 | ||||||
| chr13:52687456
|
G | A | 6 | a0001c0001t0008g0176a0001c0001t0008g0177a0001c0001t0008g0178others(3): Show | 6 | HG01255.hp2 HG01256.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-278G>A | SUGT1 | ENSG00000165416.15 | transcript | ENST00000310528.9 | protein_coding | 12/12 | chr13 | 52687456 |