Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9066 |
|---|---|
| ensemblid | ENSG00000011347.10 |
| hgncid | 11514 |
| symbol | SYT7 |
| name | synaptotagmin 7 |
| refseq_nuc | NM_001365809.2 |
| refseq_prot | NP_001352738.1 |
| ensembl_nuc | ENST00000539008.6 |
| ensembl_prot | ENSP00000439694.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 61513714 |
| end | 61581076 |
| strand | - |
| ver | v1.2 |
| region | chr11:61513714-61581076 |
| region5000 | chr11:61508714-61586076 |
| regionname0 | SYT7_chr11_61513714_61581076 |
| regionname5000 | SYT7_chr11_61508714_61586076 |
| 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 | 686 | 186 | 84 | 30 | 46 | 5 | 19 | 26 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0002 | 0/0 | 686 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0003 | 0/0 | 686 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0004 | 0/0 | 686 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2061 | 129 | 34 | 28 | 45 | 5 | 16 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0002 | 0/1 | 2061 | 51 | 45 | 2 | 0 | 0 | 3 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0003 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0004 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0005 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0006 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0007 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0008 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| c0009 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| 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 | 5170 | 50 | 11 | 16 | 13 | 1 | 9 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0002 | 0/0 | 5171 | 26 | 2 | 6 | 12 | 2 | 4 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0003 | 0/0 | 5172 | 7 | 0 | 0 | 7 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0004 | 1/0 | 5170 | 6 | 3 | 0 | 1 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0005 | 0/0 | 5170 | 6 | 6 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0006 | 0/0 | 5170 | 5 | 5 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0007 | 0/0 | 5169 | 5 | 5 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0008 | 0/0 | 5171 | 5 | 5 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0009 | 0/0 | 5169 | 4 | 3 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0010 | 0/0 | 5170 | 4 | 4 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0011 | 0/0 | 5168 | 4 | 4 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0012 | 0/0 | 5170 | 4 | 0 | 0 | 4 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0013 | 0/0 | 5170 | 3 | 3 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0014 | 0/0 | 5169 | 3 | 1 | 2 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0015 | 0/0 | 5171 | 3 | 3 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0016 | 0/0 | 5170 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0017 | 0/0 | 5171 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0018 | 0/0 | 5171 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0019 | 0/0 | 5171 | 2 | 0 | 1 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0020 | 0/0 | 5171 | 2 | 0 | 0 | 0 | 0 | 2 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0021 | 0/0 | 5168 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0022 | 0/0 | 5169 | 2 | 0 | 1 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0023 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0024 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0025 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0026 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0027 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0028 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0029 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0030 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0031 | 0/0 | 5171 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0032 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0033 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0034 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0035 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0036 | 0/0 | 5169 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0037 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0038 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0039 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0040 | 0/0 | 5170 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0041 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0042 | 0/0 | 5171 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0043 | 0/0 | 5171 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0044 | 0/0 | 5170 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0045 | 0/1 | 5170 | 1 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0046 | 0/0 | 5170 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0047 | 0/0 | 5170 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0048 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0049 | 0/0 | 5170 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0050 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0051 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0052 | 0/0 | 5170 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0053 | 0/0 | 5169 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0054 | 0/0 | 5170 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0055 | 0/0 | 5170 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0056 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0057 | 0/0 | 5168 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0058 | 0/0 | 5171 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0059 | 0/0 | 5170 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0060 | 0/0 | 5170 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0061 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0062 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| t0063 | 0/0 | 5172 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2061 | 129 | 34 | 28 | 45 | 5 | 16 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002 | 0/1 | 2061 | 51 | 45 | 2 | 0 | 0 | 3 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0003 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0005 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0008 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0009 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0002c0004 | 0/0 | 2061 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0003c0006 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0004c0007 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7230 | 42 | 6 | 16 | 13 | 1 | 6 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0002 | 0/0 | 7231 | 24 | 0 | 6 | 12 | 2 | 4 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0003 | 0/0 | 7232 | 7 | 0 | 0 | 7 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0004 | 1/0 | 7230 | 4 | 1 | 0 | 1 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0005 | 0/0 | 7230 | 6 | 6 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0006 | 0/0 | 7230 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0008 | 0/0 | 7231 | 5 | 5 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0010 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0012 | 0/0 | 7230 | 4 | 0 | 0 | 4 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0014 | 0/0 | 7229 | 3 | 1 | 2 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0015 | 0/0 | 7231 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0016 | 0/0 | 7230 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0019 | 0/0 | 7231 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0020 | 0/0 | 7231 | 2 | 0 | 0 | 0 | 0 | 2 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0021 | 0/0 | 7228 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0022 | 0/0 | 7229 | 2 | 0 | 1 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0024 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0025 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0029 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0031 | 0/0 | 7231 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0032 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0036 | 0/0 | 7229 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0040 | 0/0 | 7230 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0041 | 0/0 | 7231 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0042 | 0/0 | 7231 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0043 | 0/0 | 7231 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0044 | 0/0 | 7230 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0049 | 0/0 | 7230 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0052 | 0/0 | 7230 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0053 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0054 | 0/0 | 7230 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0055 | 0/0 | 7230 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0058 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0060 | 0/0 | 7230 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0061 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0001t0062 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0001 | 0/0 | 7230 | 7 | 5 | 0 | 0 | 0 | 2 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0002 | 0/0 | 7231 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0004 | 0/0 | 7230 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0006 | 0/0 | 7230 | 3 | 3 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0007 | 0/0 | 7229 | 5 | 5 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0009 | 0/0 | 7229 | 4 | 3 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0010 | 0/0 | 7230 | 3 | 3 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0011 | 0/0 | 7228 | 4 | 4 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0013 | 0/0 | 7230 | 3 | 3 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0018 | 0/0 | 7231 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0023 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0026 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0027 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0028 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0030 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0033 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0034 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0035 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0037 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0039 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0045 | 0/1 | 7230 | 1 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0046 | 0/0 | 7230 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0047 | 0/0 | 7230 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0048 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0050 | 0/0 | 7229 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0002t0057 | 0/0 | 7228 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0003t0017 | 0/0 | 7231 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0005t0051 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0005t0056 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0008t0063 | 0/0 | 7232 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0001c0009t0038 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0002c0004t0015 | 0/0 | 7231 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0002c0004t0059 | 0/0 | 7230 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0003c0006t0001 | 0/0 | 7230 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| a0004c0007t0019 | 0/0 | 7231 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | copy fasta | chr11 | 61508714 | 61586076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0004g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0008g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0012g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0014g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0014g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0016g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0016g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0019g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0020g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0021g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0021g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0022g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0022g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0024g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0025g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0029g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0031g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0032g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0036g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0040g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0041g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0042g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0043g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0044g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0049g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0052g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0053g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0054g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0055g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0058g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0060g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0061g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0001t0062g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0007g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0009g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0011g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0013g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0018g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0023g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0026g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0027g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0028g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0030g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0033g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0034g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0035g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0037g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0039g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0045g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0046g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0047g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0048g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0050g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0002t0057g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0003t0017g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0003t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0005t0051g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0005t0056g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0008t0063g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0001c0009t0038g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0002c0004t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0002c0004t0059g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0003c0006t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| a0004c0007t0019g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | GBR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00140 | hp2 | a0001 | c0001 | t0052 | g0073 | EUR | GBR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00323 | hp2 | a0004 | c0007 | t0019 | g0168 | EUR | FIN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00423 | hp1 | a0001 | c0001 | t0055 | g0142 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00741 | hp1 | a0001 | c0001 | t0014 | g0104 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01261 | hp2 | a0001 | c0002 | t0047 | g0156 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01346 | hp1 | a0001 | c0001 | t0036 | g0129 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01433 | hp2 | a0001 | c0001 | t0014 | g0130 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01496 | hp2 | a0001 | c0002 | t0009 | g0029 | AMR | CLM | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01515 | hp2 | a0001 | c0001 | t0060 | g0169 | EUR | IBS | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01884 | hp1 | a0001 | c0002 | t0013 | g0008 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01884 | hp2 | a0001 | c0001 | t0058 | g0076 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0081 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01943 | hp1 | a0001 | c0001 | t0022 | g0166 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG01978 | hp2 | a0001 | c0001 | t0044 | g0164 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02055 | hp1 | a0001 | c0002 | t0010 | g0022 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02083 | hp1 | a0001 | c0001 | t0042 | g0062 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02145 | hp1 | a0001 | c0002 | t0033 | g0145 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02145 | hp2 | a0001 | c0002 | t0035 | g0147 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02165 | hp1 | a0001 | c0001 | t0049 | g0084 | EAS | CDX | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02165 | hp2 | a0001 | c0001 | t0012 | g0044 | EAS | CDX | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0131 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02257 | hp2 | a0001 | c0002 | t0007 | g0024 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02258 | hp1 | a0001 | c0002 | t0010 | g0030 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02258 | hp2 | a0001 | c0002 | t0037 | g0095 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0058 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02451 | hp1 | a0001 | c0001 | t0029 | g0023 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02451 | hp2 | a0001 | c0002 | t0011 | g0018 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02572 | hp1 | a0002 | c0004 | t0015 | g0050 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02572 | hp2 | a0001 | c0001 | t0016 | g0127 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02602 | hp1 | a0001 | c0002 | t0046 | g0101 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02615 | hp1 | a0001 | c0001 | t0053 | g0046 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0047 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02622 | hp1 | a0001 | c0005 | t0051 | g0082 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02622 | hp2 | a0001 | c0002 | t0007 | g0002 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02630 | hp1 | a0001 | c0002 | t0039 | g0171 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02647 | hp2 | a0001 | c0002 | t0006 | g0015 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02698 | hp1 | a0001 | c0001 | t0031 | g0036 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02717 | hp1 | a0001 | c0001 | t0021 | g0063 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02886 | hp1 | a0001 | c0002 | t0011 | g0020 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0064 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0051 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02896 | hp1 | a0001 | c0003 | t0017 | g0066 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02896 | hp2 | a0001 | c0002 | t0018 | g0038 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0001 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02897 | hp2 | a0001 | c0003 | t0017 | g0065 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02965 | hp1 | a0002 | c0004 | t0059 | g0054 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02965 | hp2 | a0001 | c0002 | t0048 | g0155 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0069 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02976 | hp2 | a0001 | c0002 | t0009 | g0028 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03041 | hp1 | a0001 | c0002 | t0007 | g0002 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03041 | hp2 | a0001 | c0001 | t0025 | g0014 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0094 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03139 | hp1 | a0001 | c0002 | t0009 | g0032 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03139 | hp2 | a0001 | c0002 | t0011 | g0019 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03209 | hp1 | a0001 | c0002 | t0026 | g0013 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03209 | hp2 | a0001 | c0001 | t0015 | g0053 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03225 | hp1 | a0001 | c0009 | t0038 | g0161 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03225 | hp2 | a0001 | c0002 | t0030 | g0034 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03453 | hp1 | a0001 | c0005 | t0056 | g0052 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03486 | hp1 | a0001 | c0002 | t0010 | g0035 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03486 | hp2 | a0001 | c0001 | t0024 | g0010 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03491 | hp1 | a0001 | c0001 | t0054 | g0083 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03491 | hp2 | a0001 | c0001 | t0020 | g0004 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03492 | hp2 | a0001 | c0001 | t0020 | g0004 | SAS | PJL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03516 | hp1 | a0001 | c0002 | t0011 | g0021 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03540 | hp1 | a0001 | c0002 | t0027 | g0012 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03540 | hp2 | a0001 | c0002 | t0050 | g0149 | AFR | GWD | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03579 | hp1 | a0001 | c0002 | t0018 | g0039 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03831 | hp2 | a0001 | c0001 | t0043 | g0070 | SAS | BEB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0049 | SAS | BEB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0075 | SAS | STU | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG04228 | hp2 | a0003 | c0006 | t0001 | g0105 | SAS | STU | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0148 | AFR | YRI | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | YRI | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18947 | hp2 | a0001 | c0001 | t0062 | g0176 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18966 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18966 | hp2 | a0001 | c0001 | t0022 | g0048 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA18975 | hp2 | a0001 | c0008 | t0063 | g0179 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19000 | hp2 | a0001 | c0001 | t0061 | g0178 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19010 | hp2 | a0001 | c0001 | t0040 | g0137 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | LWK | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19030 | hp2 | a0001 | c0002 | t0023 | g0016 | AFR | LWK | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0026 | AFR | LWK | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | LWK | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19060 | hp1 | a0001 | c0001 | t0012 | g0068 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19074 | hp1 | a0001 | c0001 | t0041 | g0136 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA20129 | hp2 | a0001 | c0002 | t0034 | g0154 | AFR | ASW | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02486 | hp1 | a0001 | c0002 | t0013 | g0008 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG02559 | hp2 | a0001 | c0002 | t0057 | g0144 | AFR | ACB | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03471 | hp1 | a0001 | c0002 | t0007 | g0027 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| HG03471 | hp2 | a0001 | c0002 | t0013 | g0139 | AFR | MSL | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | USA | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0025 | AFR | USA | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA21309 | hp1 | a0001 | c0001 | t0032 | g0150 | AFR | LWK | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| NA21309 | hp2 | a0001 | c0002 | t0028 | g0011 | AFR | LWK | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0045 | g0170 | REF | REF | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0096 | REF | REF | SYT7_chr11_61508714_61586076 | SYT7 | chr11 | 61508714 | 61586076 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61533053
|
C | T | 1 | a0003 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1136G>A | p.Arg379His | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/13 | 1392/7230 | 1136/2061 | 379/686 | chr11 | 61533053 | ||
| chr11:61546053
|
C | T | 1 | a0004 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.550G>A | p.Ala184Thr | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/13 | 806/7230 | 550/2061 | 184/686 | chr11 | 61546053 | ||
| chr11:61546104
|
C | G | 1 | a0002 | 2 | HG02572.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.499G>C | p.Gly167Arg | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/13 | 755/7230 | 499/2061 | 167/686 | chr11 | 61546104 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61524450
|
A | G | 3 | a0001c0002a0001c0009a0004c0007 | 53 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(50): Show |
synonymous_variant | LOW | c.1554T>C | p.Ile518Ile | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 10/13 | 1810/7230 | 1554/2061 | 518/686 | chr11 | 61524450 | ||
| chr11:61524477
|
A | G | 1 | a0001c0005 | 2 | HG02622.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.1527T>C | p.Tyr509Tyr | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 10/13 | 1783/7230 | 1527/2061 | 509/686 | chr11 | 61524477 | ||
| chr11:61528057
|
C | T | 1 | a0001c0008 | 1 | NA18975.hp2 | synonymous_variant | LOW | c.1329G>A | p.Gln443Gln | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/13 | 1585/7230 | 1329/2061 | 443/686 | chr11 | 61528057 | ||
| chr11:61546156
|
G | A | 1 | a0001c0009 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.447C>T | p.Pro149Pro | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/13 | 703/7230 | 447/2061 | 149/686 | chr11 | 61546156 | ||
| chr11:61546162
|
C | T | 1 | a0003c0006 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.441G>A | p.Pro147Pro | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/13 | 697/7230 | 441/2061 | 147/686 | chr11 | 61546162 | ||
| chr11:61546207
|
C | T | 1 | a0001c0003 | 2 | HG02896.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.396G>A | p.Ala132Ala | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/13 | 652/7230 | 396/2061 | 132/686 | chr11 | 61546207 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61513815
|
G | C | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(23): Show | 67 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4812C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4812 | chr11 | 61513815 | |||||
| chr11:61513894
|
G | A | 1 | a0001c0002t0027 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4733C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4733 | chr11 | 61513894 | |||||
| chr11:61513901
|
C | T | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(16): Show | 53 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*4726G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4726 | chr11 | 61513901 | |||||
| chr11:61513958
|
G | A | 25 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(22): Show | 88 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*4669C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4669 | chr11 | 61513958 | |||||
| chr11:61514009
|
G | T | 1 | a0001c0002t0030 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4618C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4618 | chr11 | 61514009 | |||||
| chr11:61514012
|
TCA | T | 1 | a0001c0001t0021 | 2 | HG02717.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4613_*4614delTG | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4613 | chr11 | 61514012 | |||||
| chr11:61514047
|
C | T | 2 | a0001c0001t0019a0004c0007t0019 | 2 | HG00323.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4580G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4580 | chr11 | 61514047 | |||||
| chr11:61514061
|
G | A | 2 | a0001c0002t0034a0001c0002t0045 | 2 | NA20129.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4566C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4566 | chr11 | 61514061 | |||||
| chr11:61514079
|
G | A | 3 | a0001c0002t0007a0001c0002t0009a0001c0002t0037 | 10 | HG01496.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4548C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4548 | chr11 | 61514079 | |||||
| chr11:61514291
|
C | G | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(23): Show | 67 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*4336G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4336 | chr11 | 61514291 | |||||
| chr11:61514435
|
C | T | 6 | a0001c0002t0026a0001c0002t0035a0001c0002t0039others(3): Show | 6 | HG01261.hp2 HG02145.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4192G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4192 | chr11 | 61514435 | |||||
| chr11:61514541
|
T | C | 1 | a0001c0001t0042 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4086A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 4086 | chr11 | 61514541 | |||||
| chr11:61514809
|
C | T | 1 | a0001c0001t0053 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3818G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3818 | chr11 | 61514809 | |||||
| chr11:61514878
|
C | T | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(9): Show | 44 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3749G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3749 | chr11 | 61514878 | |||||
| chr11:61514945
|
G | A | 1 | a0001c0002t0050 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3682C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3682 | chr11 | 61514945 | |||||
| chr11:61515032
|
G | A | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(13): Show | 49 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3595C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3595 | chr11 | 61515032 | |||||
| chr11:61515160
|
C | T | 1 | a0001c0002t0023 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3467G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3467 | chr11 | 61515160 | |||||
| chr11:61515227
|
G | A | 1 | a0001c0002t0050 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3400C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3400 | chr11 | 61515227 | |||||
| chr11:61515301
|
C | T | 1 | a0001c0002t0046 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3326G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3326 | chr11 | 61515301 | |||||
| chr11:61515348
|
C | G | 2 | a0001c0002t0034a0001c0002t0045 | 2 | NA20129.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3279G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3279 | chr11 | 61515348 | |||||
| chr11:61515462
|
GT | G | 10 | a0001c0001t0014a0001c0001t0022a0001c0001t0029others(7): Show | 20 | HG00741.hp1 HG01346.hp1 HG01433.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3164delA | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3164 | chr11 | 61515462 | |||||
| chr11:61515508
|
A | AT | 21 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(18): Show | 54 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3118dupA | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3118 | chr11 | 61515508 | |||||
| chr11:61515530
|
G | A | 3 | a0001c0002t0011a0001c0002t0028a0001c0002t0057 | 6 | HG02451.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3097C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3097 | chr11 | 61515530 | |||||
| chr11:61515609
|
C | A | 3 | a0001c0002t0007a0001c0002t0009a0001c0002t0037 | 10 | HG01496.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3018G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 3018 | chr11 | 61515609 | |||||
| chr11:61516164
|
G | GC | 4 | a0001c0001t0008a0001c0003t0017a0001c0005t0051others(1): Show | 9 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2462dupG | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 2462 | chr11 | 61516164 | |||||
| chr11:61516226
|
C | T | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 2401 | chr11 | 61516226 | |||||
| chr11:61516230
|
T | A | 1 | a0001c0001t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2397A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 2397 | chr11 | 61516230 | |||||
| chr11:61516466
|
C | T | 2 | a0001c0001t0012a0001c0001t0040 | 5 | HG02165.hp2 NA18966.hp1 NA18969.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 2161 | chr11 | 61516466 | |||||
| chr11:61516771
|
T | C | 2 | a0001c0001t0029a0001c0001t0053 | 2 | HG02451.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1856A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1856 | chr11 | 61516771 | |||||
| chr11:61516850
|
G | T | 1 | a0001c0002t0039 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1777 | chr11 | 61516850 | |||||
| chr11:61517064
|
G | T | 2 | a0001c0002t0018a0001c0002t0023 | 3 | HG02896.hp2 HG03579.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1563C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1563 | chr11 | 61517064 | |||||
| chr11:61517169
|
C | T | 1 | a0001c0002t0023 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1458G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1458 | chr11 | 61517169 | |||||
| chr11:61517269
|
T | G | 1 | a0001c0001t0054 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1358A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1358 | chr11 | 61517269 | |||||
| chr11:61517477
|
G | A | 3 | a0001c0001t0022a0001c0001t0055a0001c0008t0063 | 4 | HG00423.hp1 HG01943.hp1 NA18966.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1150C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1150 | chr11 | 61517477 | |||||
| chr11:61517490
|
G | T | 1 | a0001c0002t0013 | 3 | HG01884.hp1 HG02486.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1137C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 1137 | chr11 | 61517490 | |||||
| chr11:61517826
|
G | C | 2 | a0001c0001t0005a0001c0005t0056 | 7 | HG02055.hp2 HG02647.hp1 HG02970.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*801C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 801 | chr11 | 61517826 | |||||
| chr11:61517853
|
C | T | 13 | a0001c0001t0016a0001c0001t0024a0001c0001t0025others(10): Show | 18 | HG01346.hp1 HG01496.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*774G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 774 | chr11 | 61517853 | |||||
| chr11:61518051
|
ACG | A | 2 | a0001c0002t0011a0001c0002t0057 | 5 | HG02451.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*574_*575delCG | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 574 | chr11 | 61518051 | |||||
| chr11:61518056
|
C | A | 2 | a0001c0002t0011a0001c0002t0057 | 5 | HG02451.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*571G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 571 | chr11 | 61518056 | |||||
| chr11:61518086
|
G | C | 5 | a0001c0001t0015a0001c0001t0058a0001c0002t0030others(2): Show | 6 | HG01884.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*541C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 541 | chr11 | 61518086 | |||||
| chr11:61518230
|
T | C | 1 | a0001c0001t0060 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 397 | chr11 | 61518230 | |||||
| chr11:61518257
|
C | T | 1 | a0001c0001t0032 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 13/13 | 370 | chr11 | 61518257 | |||||
| chr11:61580892
|
G | A | 1 | a0001c0001t0031 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/13 | 72 | chr11 | 61580892 | |||||
| chr11:61580895
|
G | T | 16 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(13): Show | 31 | HG01496.hp2 HG02055.hp1 HG02257.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/13 | 75 | chr11 | 61580895 | |||||
| chr11:61580934
|
G | GC | 4 | a0001c0001t0003a0001c0001t0061a0001c0001t0062others(1): Show | 10 | NA18947.hp1 NA18947.hp2 NA18959.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-115dupG | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/13 | 115 | chr11 | 61580934 | |||||
| chr11:61581047
|
G | T | 16 | a0001c0001t0006a0001c0001t0010a0001c0001t0024others(13): Show | 31 | HG01496.hp2 HG02055.hp1 HG02257.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-227C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/13 | 227 | chr11 | 61581047 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:61518856
|
T | TACCCCAC others(2): Show |
7 | a0001c0001t0001g0158a0001c0001t0024g0010a0001c0002t0001g0075others(4): Show | 7 | HG02602.hp1 HG03486.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-126_1957-125i others(11): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61518856 | ||||||
| chr11:61518952
|
C | T | 7 | a0001c0001t0001g0158a0001c0001t0024g0010a0001c0002t0001g0075others(4): Show | 7 | HG02602.hp1 HG03486.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-221G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61518952 | ||||||
| chr11:61519072
|
C | G | 1 | a0001c0001t0053g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1957-341G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519072 | ||||||
| chr11:61519220
|
G | A | 45 | a0001c0001t0001g0158a0001c0001t0005g0097a0001c0001t0005g0098others(42): Show | 48 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(45): Show |
intron_variant | MODIFIER | c.1957-489C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519220 | ||||||
| chr11:61519525
|
A | T | 50 | a0001c0001t0001g0158a0001c0001t0005g0097a0001c0001t0005g0098others(47): Show | 54 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(51): Show |
intron_variant | MODIFIER | c.1957-794T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519525 | ||||||
| chr11:61519544
|
G | A | 11 | a0001c0002t0001g0146a0001c0002t0007g0002a0001c0002t0007g0024others(8): Show | 12 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1957-813C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519544 | ||||||
| chr11:61519619
|
T | C | 12 | a0001c0002t0001g0037a0001c0002t0001g0157a0001c0002t0001g0162others(9): Show | 13 | HG02486.hp2 HG02630.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1957-888A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519619 | ||||||
| chr11:61519907
|
G | A | 3 | a0001c0002t0018g0038a0001c0002t0018g0039a0001c0009t0038g0161 | 3 | HG02896.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1957-1176C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519907 | ||||||
| chr11:61519914
|
A | G | 50 | a0001c0001t0005g0097a0001c0001t0005g0098a0001c0001t0006g0031others(47): Show | 54 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(51): Show |
intron_variant | MODIFIER | c.1957-1183T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61519914 | ||||||
| chr11:61520011
|
G | C | 3 | a0001c0002t0018g0038a0001c0002t0018g0039a0001c0009t0038g0161 | 3 | HG02896.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1957-1280C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520011 | ||||||
| chr11:61520023
|
T | TTGGGCAA others(29): Show |
1 | a0001c0001t0001g0103 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1957-1328_1957-129 others(40): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520023 | ||||||
| chr11:61520023
|
T | TTGGGCAA others(65): Show |
6 | a0001c0001t0001g0128a0001c0001t0014g0104a0001c0001t0014g0130others(3): Show | 6 | HG00741.hp1 HG01256.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-1364_1957-129 others(76): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520023 | ||||||
| chr11:61520023
|
TTGGGCAA others(29): Show |
T | 41 | a0001c0001t0001g0118a0001c0001t0024g0010a0001c0001t0053g0046others(38): Show | 44 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.1957-1328_1957-129 others(40): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520023 | ||||||
| chr11:61520023
|
TTGGGCAA others(65): Show |
T | 17 | a0001c0001t0005g0097a0001c0001t0005g0098a0001c0001t0006g0031others(14): Show | 18 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1957-1364_1957-129 others(76): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520023 | ||||||
| chr11:61520126
|
G | A | 3 | a0001c0002t0035g0147a0001c0002t0047g0156a0001c0002t0048g0155 | 3 | HG01261.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1957-1395C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520126 | ||||||
| chr11:61520181
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1957-1450G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520181 | ||||||
| chr11:61520217
|
T | A | 18 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0109others(15): Show | 19 | HG00408.hp1 HG00423.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.1957-1486A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520217 | ||||||
| chr11:61520555
|
T | G | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1957-1824A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520555 | ||||||
| chr11:61520574
|
C | T | 2 | a0001c0001t0004g0049a0001c0001t0020g0004 | 3 | HG03491.hp2 HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1957-1843G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520574 | ||||||
| chr11:61520706
|
C | T | 1 | a0001c0001t0060g0169 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1957-1975G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520706 | ||||||
| chr11:61520729
|
A | T | 2 | a0001c0002t0006g0001a0001c0002t0027g0012 | 3 | HG02895.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1957-1998T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520729 | ||||||
| chr11:61520797
|
C | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1957-2066G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520797 | ||||||
| chr11:61520885
|
C | T | 39 | a0001c0001t0024g0010a0001c0001t0053g0046a0001c0002t0001g0037others(36): Show | 42 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.1957-2154G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520885 | ||||||
| chr11:61520928
|
G | A | 7 | a0001c0002t0001g0160a0001c0002t0004g0138a0001c0002t0013g0008others(4): Show | 8 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1956+2147C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61520928 | ||||||
| chr11:61521198
|
G | A | 22 | a0001c0001t0005g0097a0001c0001t0005g0098a0001c0001t0006g0031others(19): Show | 23 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1956+1877C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521198 | ||||||
| chr11:61521350
|
T | C | 54 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(51): Show | 58 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.1956+1725A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521350 | ||||||
| chr11:61521360
|
C | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1956+1715G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521360 | ||||||
| chr11:61521368
|
G | A | 8 | a0001c0002t0001g0160a0001c0002t0004g0138a0001c0002t0013g0008others(5): Show | 9 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1956+1707C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521368 | ||||||
| chr11:61521444
|
A | G | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1956+1631T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521444 | ||||||
| chr11:61521660
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1956+1415G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521660 | ||||||
| chr11:61521711
|
A | G | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1956+1364T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521711 | ||||||
| chr11:61521747
|
C | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1956+1328G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521747 | ||||||
| chr11:61521921
|
A | C | 7 | a0001c0002t0010g0022a0001c0002t0010g0035a0001c0002t0011g0018others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+1154T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521921 | ||||||
| chr11:61521954
|
A | G | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1956+1121T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61521954 | ||||||
| chr11:61522187
|
C | CT | 24 | a0001c0001t0002g0072a0001c0002t0001g0037a0001c0002t0001g0146others(21): Show | 25 | HG02027.hp2 HG02055.hp1 HG02451.hp2 others(22): Show |
intron_variant | MODIFIER | c.1956+887dupA | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522187 | ||||||
| chr11:61522187
|
CT | C | 18 | a0001c0001t0001g0040a0001c0001t0001g0167a0001c0001t0002g0041others(15): Show | 19 | HG00423.hp1 HG01891.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1956+887delA | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522187 | ||||||
| chr11:61522187
|
CTT | C | 9 | a0001c0001t0005g0134a0001c0002t0001g0162a0001c0002t0004g0138others(6): Show | 10 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+886_1956+887d others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522187 | ||||||
| chr11:61522421
|
C | T | 4 | a0001c0001t0001g0124a0001c0002t0018g0038a0001c0002t0018g0039others(1): Show | 4 | HG02896.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+654G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522421 | ||||||
| chr11:61522465
|
C | T | 8 | a0001c0002t0001g0162a0001c0002t0004g0138a0001c0002t0013g0008others(5): Show | 9 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1956+610G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522465 | ||||||
| chr11:61522509
|
A | G | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1956+566T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522509 | ||||||
| chr11:61522730
|
A | G | 6 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(3): Show | 6 | HG02602.hp1 HG02809.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1956+345T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522730 | ||||||
| chr11:61522757
|
C | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1956+318G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522757 | ||||||
| chr11:61522965
|
A | G | 15 | a0001c0002t0001g0037a0001c0002t0002g0148a0001c0002t0004g0094others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1956+110T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 12/12 | chr11 | 61522965 | ||||||
| chr11:61523297
|
G | A | 1 | a0001c0001t0049g0084 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1757-23C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 11/12 | chr11 | 61523297 | ||||||
| chr11:61523309
|
G | A | 6 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(3): Show | 6 | HG02602.hp1 HG02809.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1757-35C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 11/12 | chr11 | 61523309 | ||||||
| chr11:61523605
|
A | G | 40 | a0001c0002t0001g0037a0001c0002t0001g0075a0001c0002t0001g0146others(37): Show | 43 | HG00323.hp2 HG01261.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.1756+222T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 11/12 | chr11 | 61523605 | ||||||
| chr11:61523735
|
C | T | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1756+92G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 11/12 | chr11 | 61523735 | ||||||
| chr11:61523960
|
G | A | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1642-19C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 10/12 | chr11 | 61523960 | ||||||
| chr11:61524313
|
C | T | 11 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0109others(8): Show | 11 | HG00408.hp1 HG00423.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1641+50G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 10/12 | chr11 | 61524313 | ||||||
| chr11:61524566
|
G | C | 1 | a0001c0001t0002g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1472-34C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61524566 | ||||||
| chr11:61524619
|
G | A | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1472-87C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61524619 | ||||||
| chr11:61524754
|
C | T | 1 | a0001c0002t0050g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1472-222G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61524754 | ||||||
| chr11:61524825
|
T | C | 9 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0015g0051others(6): Show | 9 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1472-293A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61524825 | ||||||
| chr11:61525119
|
C | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1472-587G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525119 | ||||||
| chr11:61525226
|
A | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1472-694T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525226 | ||||||
| chr11:61525385
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1472-853G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525385 | ||||||
| chr11:61525387
|
T | G | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1472-855A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525387 | ||||||
| chr11:61525573
|
G | A | 1 | a0001c0002t0023g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1472-1041C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525573 | ||||||
| chr11:61525583
|
C | CT | 14 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0015g0051others(11): Show | 15 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1472-1052dupA | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525583 | ||||||
| chr11:61525894
|
G | A | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1472-1362C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525894 | ||||||
| chr11:61525910
|
G | A | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1472-1378C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61525910 | ||||||
| chr11:61526174
|
T | C | 1 | a0001c0001t0006g0031 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1472-1642A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61526174 | ||||||
| chr11:61526175
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1472-1643C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61526175 | ||||||
| chr11:61526342
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 5 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1471+1573C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61526342 | ||||||
| chr11:61526661
|
C | T | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1471+1254G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61526661 | ||||||
| chr11:61526748
|
A | G | 8 | a0001c0002t0001g0160a0001c0002t0002g0152a0001c0002t0018g0038others(5): Show | 8 | HG02630.hp1 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1471+1167T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61526748 | ||||||
| chr11:61526786
|
C | T | 2 | a0001c0002t0050g0149a0004c0007t0019g0168 | 2 | HG00323.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1471+1129G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61526786 | ||||||
| chr11:61527561
|
G | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1471+354C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61527561 | ||||||
| chr11:61527711
|
G | A | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1471+204C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61527711 | ||||||
| chr11:61527844
|
A | T | 65 | a0001c0001t0005g0097a0001c0001t0005g0098a0001c0001t0006g0031others(62): Show | 69 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(66): Show |
intron_variant | MODIFIER | c.1471+71T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 9/12 | chr11 | 61527844 | ||||||
| chr11:61528337
|
T | C | 14 | a0001c0002t0001g0037a0001c0002t0004g0094a0001c0002t0006g0001others(11): Show | 15 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1201-152A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528337 | ||||||
| chr11:61528369
|
G | T | 4 | a0001c0001t0001g0151a0001c0001t0002g0071a0001c0001t0031g0036others(1): Show | 4 | HG02602.hp2 HG02698.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-184C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528369 | ||||||
| chr11:61528372
|
G | T | 1 | a0001c0001t0029g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1201-187C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528372 | ||||||
| chr11:61528448
|
G | A | 17 | a0001c0001t0001g0040a0001c0001t0001g0167a0001c0001t0002g0041others(14): Show | 18 | HG00423.hp1 HG00558.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-263C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528448 | ||||||
| chr11:61528596
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1201-411C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528596 | ||||||
| chr11:61528963
|
A | G | 1 | a0001c0001t0042g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1201-778T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528963 | ||||||
| chr11:61528986
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1201-801T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61528986 | ||||||
| chr11:61529150
|
C | A | 1 | a0001c0001t0055g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1201-965G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61529150 | ||||||
| chr11:61529412
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1201-1227C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61529412 | ||||||
| chr11:61530071
|
C | G | 14 | a0001c0002t0001g0037a0001c0002t0002g0152a0001c0002t0004g0094others(11): Show | 15 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1201-1886G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61530071 | ||||||
| chr11:61530271
|
A | G | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1201-2086T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61530271 | ||||||
| chr11:61530288
|
T | TG | 4 | a0001c0001t0005g0097a0001c0001t0005g0098a0001c0001t0029g0023others(1): Show | 4 | HG02055.hp2 HG02451.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201-2104dupC | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61530288 | ||||||
| chr11:61530569
|
G | A | 1 | a0001c0002t0046g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1201-2384C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61530569 | ||||||
| chr11:61530917
|
G | A | 5 | a0001c0002t0011g0018a0001c0002t0011g0019a0001c0002t0011g0020others(2): Show | 5 | HG02451.hp2 HG02559.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+2072C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61530917 | ||||||
| chr11:61531053
|
T | G | 5 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(2): Show | 6 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+1936A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531053 | ||||||
| chr11:61531060
|
T | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1200+1929A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531060 | ||||||
| chr11:61531180
|
T | C | 1 | a0001c0001t0032g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1200+1809A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531180 | ||||||
| chr11:61531421
|
C | T | 1 | a0001c0002t0026g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1200+1568G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531421 | ||||||
| chr11:61531425
|
C | G | 1 | a0001c0002t0010g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1200+1564G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531425 | ||||||
| chr11:61531459
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 5 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+1530C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531459 | ||||||
| chr11:61531461
|
G | C | 8 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(5): Show | 8 | HG02602.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+1528C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531461 | ||||||
| chr11:61531537
|
G | C | 2 | a0001c0003t0017g0065a0001c0003t0017g0066 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1200+1452C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531537 | ||||||
| chr11:61531818
|
C | T | 1 | a0001c0001t0036g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1200+1171G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531818 | ||||||
| chr11:61531891
|
C | CA | 41 | a0001c0001t0001g0061a0001c0001t0001g0158a0001c0001t0002g0072others(38): Show | 44 | HG00741.hp2 HG01175.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.1200+1097dupT | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531891 | ||||||
| chr11:61531891
|
C | CAA | 6 | a0001c0002t0001g0146a0001c0002t0001g0157a0001c0002t0007g0025others(3): Show | 6 | HG02572.hp1 HG02809.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+1096_1200+109 others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531891 | ||||||
| chr11:61531891
|
CAAAAAAA others(3): Show |
C | 14 | a0001c0002t0001g0037a0001c0002t0002g0152a0001c0002t0004g0094others(11): Show | 15 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1200+1088_1200+109 others(14): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531891 | ||||||
| chr11:61531891
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0002g0077a0001c0001t0002g0088 | 2 | NA18970.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1200+1087_1200+109 others(15): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61531891 | ||||||
| chr11:61532108
|
G | C | 8 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(5): Show | 8 | HG02602.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+881C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61532108 | ||||||
| chr11:61532263
|
T | G | 1 | a0001c0001t0062g0176 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1200+726A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61532263 | ||||||
| chr11:61532313
|
C | T | 8 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(5): Show | 8 | HG02602.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+676G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61532313 | ||||||
| chr11:61532379
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1200+610T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61532379 | ||||||
| chr11:61532773
|
G | A | 1 | a0001c0002t0050g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1200+216C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61532773 | ||||||
| chr11:61532824
|
G | A | 16 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0015g0051others(13): Show | 17 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1200+165C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 8/12 | chr11 | 61532824 | ||||||
| chr11:61533232
|
G | C | 180 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0045others(177): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1065-108C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61533232 | ||||||
| chr11:61533325
|
C | G | 5 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(2): Show | 6 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-201G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61533325 | ||||||
| chr11:61533438
|
G | A | 2 | a0001c0001t0014g0130a0001c0001t0014g0131 | 2 | HG01433.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1065-314C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61533438 | ||||||
| chr11:61533448
|
G | C | 26 | a0001c0002t0001g0037a0001c0002t0002g0152a0001c0002t0004g0094others(23): Show | 28 | HG01496.hp2 HG02055.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.1065-324C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61533448 | ||||||
| chr11:61533549
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1065-425G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61533549 | ||||||
| chr11:61534214
|
G | A | 2 | a0001c0002t0001g0075a0001c0002t0001g0153 | 2 | HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1065-1090C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534214 | ||||||
| chr11:61534227
|
T | A | 15 | a0001c0002t0001g0037a0001c0002t0002g0152a0001c0002t0004g0094others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1065-1103A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534227 | ||||||
| chr11:61534282
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1065-1158A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534282 | ||||||
| chr11:61534368
|
C | T | 1 | a0001c0002t0037g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1065-1244G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534368 | ||||||
| chr11:61534371
|
A | G | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1065-1247T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534371 | ||||||
| chr11:61534409
|
G | A | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1065-1285C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534409 | ||||||
| chr11:61534413
|
G | GCACACAC others(15): Show |
9 | a0001c0002t0007g0002a0001c0002t0007g0025a0001c0002t0007g0027others(6): Show | 10 | HG01496.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1065-1290_1065-128 others(26): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534413 | ||||||
| chr11:61534420
|
T | C | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1296A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534420 | ||||||
| chr11:61534421
|
G | A | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1297C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534421 | ||||||
| chr11:61534429
|
A | G | 9 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0015g0051others(6): Show | 9 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1065-1305T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534429 | ||||||
| chr11:61534441
|
G | A | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1317C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534441 | ||||||
| chr11:61534445
|
G | GCA | 2 | a0001c0001t0014g0130a0001c0001t0014g0131 | 2 | HG01433.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1065-1323_1065-132 others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534445 | ||||||
| chr11:61534445
|
G | GCACA | 176 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0045others(173): Show | 185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1065-1325_1065-132 others(8): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534445 | ||||||
| chr11:61534448
|
C | T | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1324G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534448 | ||||||
| chr11:61534453
|
G | A | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1329C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534453 | ||||||
| chr11:61534458
|
T | C | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1334A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534458 | ||||||
| chr11:61534459
|
G | A | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1335C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534459 | ||||||
| chr11:61534461
|
G | A | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1337C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534461 | ||||||
| chr11:61534462
|
T | C | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1338A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534462 | ||||||
| chr11:61534470
|
T | C | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1065-1346A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534470 | ||||||
| chr11:61534474
|
C | T | 8 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(5): Show | 8 | HG02602.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-1350G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534474 | ||||||
| chr11:61534610
|
C | T | 12 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(9): Show | 14 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1065-1486G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534610 | ||||||
| chr11:61534662
|
C | T | 1 | a0001c0002t0001g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1065-1538G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534662 | ||||||
| chr11:61534751
|
A | G | 8 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0157others(5): Show | 8 | HG02602.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-1627T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534751 | ||||||
| chr11:61534772
|
C | T | 8 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0099others(5): Show | 8 | HG00735.hp2 HG00738.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1065-1648G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534772 | ||||||
| chr11:61534843
|
TAC | T | 46 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(43): Show | 50 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.1065-1721_1065-172 others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534843 | ||||||
| chr11:61534861
|
C | T | 5 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(2): Show | 6 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1065-1737G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534861 | ||||||
| chr11:61534995
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1065-1871C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61534995 | ||||||
| chr11:61535026
|
G | C | 2 | a0001c0001t0053g0046a0001c0002t0002g0148 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1065-1902C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61535026 | ||||||
| chr11:61535232
|
G | T | 46 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(43): Show | 50 | HG01261.hp2 HG01496.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.1065-2108C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61535232 | ||||||
| chr11:61535234
|
C | T | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1065-2110G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61535234 | ||||||
| chr11:61535726
|
C | T | 15 | a0001c0002t0001g0037a0001c0002t0002g0152a0001c0002t0006g0001others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1064+2418G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61535726 | ||||||
| chr11:61536138
|
T | C | 85 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0167others(82): Show | 91 | HG00423.hp1 HG00558.hp2 HG01261.hp2 others(88): Show |
intron_variant | MODIFIER | c.1064+2006A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536138 | ||||||
| chr11:61536331
|
C | T | 68 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0055others(65): Show | 72 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.1064+1813G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536331 | ||||||
| chr11:61536390
|
C | T | 1 | a0001c0002t0045g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1064+1754G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536390 | ||||||
| chr11:61536518
|
C | G | 1 | a0001c0001t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1064+1626G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536518 | ||||||
| chr11:61536590
|
G | A | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1064+1554C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536590 | ||||||
| chr11:61536592
|
T | C | 7 | a0001c0001t0005g0097a0001c0002t0001g0162a0001c0002t0004g0138others(4): Show | 8 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1064+1552A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536592 | ||||||
| chr11:61536630
|
G | C | 16 | a0001c0001t0006g0031a0001c0001t0008g0003a0001c0001t0008g0042others(13): Show | 18 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1064+1514C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61536630 | ||||||
| chr11:61537001
|
T | C | 14 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0109others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1064+1143A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537001 | ||||||
| chr11:61537256
|
CAG | C | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1064+886_1064+887d others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537256 | ||||||
| chr11:61537395
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1064+749T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537395 | ||||||
| chr11:61537511
|
G | A | 1 | a0001c0002t0010g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1064+633C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537511 | ||||||
| chr11:61537634
|
GC | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0055a0001c0001t0001g0091others(1): Show | 5 | HG01261.hp1 HG01346.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+509delG | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537634 | ||||||
| chr11:61537680
|
C | T | 2 | a0001c0003t0017g0065a0001c0003t0017g0066 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1064+464G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537680 | ||||||
| chr11:61537745
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1064+399G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61537745 | ||||||
| chr11:61538085
|
G | A | 1 | a0001c0002t0045g0170 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1064+59C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 7/12 | chr11 | 61538085 | ||||||
| chr11:61538346
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.942-80C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GAGAGA | 2 | a0001c0001t0002g0059a0001c0001t0002g0074 | 2 | HG01515.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.942-81_942-80insTC others(3): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GAGAGAGA others(4): Show |
1 | a0001c0001t0001g0128 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.942-81_942-80insTC others(9): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGA | 20 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0067others(17): Show | 22 | HG00738.hp1 HG01346.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.942-82_942-81dupTC | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGA | 45 | a0001c0001t0001g0006a0001c0001t0001g0078a0001c0001t0001g0090others(42): Show | 47 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.942-84_942-81dupTC others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGA | 31 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0103others(28): Show | 33 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.942-86_942-81dupTC others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGAG others(1): Show |
11 | a0001c0001t0001g0087a0001c0001t0001g0114a0001c0001t0002g0072others(8): Show | 11 | HG02027.hp2 HG02698.hp1 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.942-88_942-81dupTC others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGAG others(3): Show |
5 | a0001c0001t0001g0123a0001c0001t0002g0115a0001c0001t0036g0129others(2): Show | 5 | HG00438.hp2 HG01261.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.942-90_942-81dupTC others(8): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGAG others(5): Show |
4 | a0001c0001t0014g0130a0001c0001t0014g0131a0001c0002t0001g0037others(1): Show | 4 | HG01433.hp2 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.942-92_942-81dupTC others(10): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGAG others(7): Show |
1 | a0001c0002t0048g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.942-94_942-81dupTC others(12): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGAG others(3): Show |
1 | a0001c0001t0008g0003 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.942-81_942-80insTC others(8): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
G | GGAGAGAG others(5): Show |
1 | a0001c0001t0008g0043 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.942-81_942-80insTC others(10): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
GGA | G | 22 | a0001c0001t0001g0040a0001c0001t0001g0126a0001c0001t0002g0041others(19): Show | 23 | HG01884.hp2 HG01891.hp2 HG02165.hp1 others(20): Show |
intron_variant | MODIFIER | c.942-82_942-81delTC | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538346
|
GGAGA | G | 5 | a0001c0001t0003g0173a0001c0001t0020g0004a0001c0002t0002g0152others(2): Show | 6 | HG02257.hp2 HG02723.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.942-84_942-81delTC others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538346 | ||||||
| chr11:61538348
|
A | AGAGAGG | 2 | a0001c0001t0008g0042a0001c0001t0053g0046 | 2 | HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.942-83_942-82insCC others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538348 | ||||||
| chr11:61538354
|
A | G | 12 | a0001c0001t0001g0040a0001c0001t0002g0041a0001c0001t0003g0177others(9): Show | 13 | HG01891.hp2 HG02165.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.942-88T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538354 | ||||||
| chr11:61538388
|
A | AGAGAGAG others(2): Show |
2 | a0001c0001t0001g0086a0001c0001t0002g0057 | 2 | HG00323.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.942-123_942-122ins others(9): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538388 | ||||||
| chr11:61538388
|
A | AGAGAGAG others(6): Show |
1 | a0001c0001t0002g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.942-123_942-122ins others(13): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538388 | ||||||
| chr11:61538389
|
A | G | 2 | a0001c0001t0024g0010a0001c0001t0043g0070 | 2 | HG03486.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.942-123T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538389 | ||||||
| chr11:61538399
|
G | GAGAGAGA others(7): Show |
1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.942-134_942-133ins others(14): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538399 | ||||||
| chr11:61538512
|
C | G | 1 | a0001c0002t0001g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.942-246G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538512 | ||||||
| chr11:61538650
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.942-384G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538650 | ||||||
| chr11:61538732
|
G | C | 5 | a0001c0001t0006g0031a0001c0001t0008g0003a0001c0001t0008g0042others(2): Show | 6 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.942-466C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538732 | ||||||
| chr11:61538774
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.942-508C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61538774 | ||||||
| chr11:61539165
|
T | C | 11 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0001t0006g0033others(8): Show | 11 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.942-899A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539165 | ||||||
| chr11:61539247
|
G | A | 1 | a0001c0002t0023g0016 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.942-981C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539247 | ||||||
| chr11:61539275
|
G | A | 5 | a0001c0001t0001g0165a0001c0001t0002g0009a0001c0001t0002g0163others(2): Show | 6 | HG00735.hp1 HG01175.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.942-1009C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539275 | ||||||
| chr11:61539398
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0004g0159 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.942-1132A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539398 | ||||||
| chr11:61539457
|
G | C | 101 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0055others(98): Show | 105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.942-1191C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539457 | ||||||
| chr11:61539632
|
G | A | 2 | a0001c0002t0001g0160a0001c0002t0039g0171 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.942-1366C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539632 | ||||||
| chr11:61539766
|
T | C | 26 | a0001c0001t0001g0040a0001c0001t0001g0158a0001c0001t0002g0041others(23): Show | 27 | HG01891.hp2 HG02165.hp1 HG02572.hp1 others(24): Show |
intron_variant | MODIFIER | c.942-1500A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539766 | ||||||
| chr11:61539995
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.942-1729A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61539995 | ||||||
| chr11:61540115
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.942-1849G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61540115 | ||||||
| chr11:61540798
|
C | T | 1 | a0001c0001t0016g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.941+1413G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61540798 | ||||||
| chr11:61541075
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.941+1136G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61541075 | ||||||
| chr11:61541085
|
G | C | 1 | a0001c0001t0055g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.941+1126C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61541085 | ||||||
| chr11:61541503
|
T | C | 25 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0158others(22): Show | 26 | HG02055.hp1 HG02451.hp2 HG02559.hp2 others(23): Show |
intron_variant | MODIFIER | c.941+708A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61541503 | ||||||
| chr11:61541772
|
G | A | 1 | a0001c0001t0005g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.941+439C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61541772 | ||||||
| chr11:61542186
|
C | T | 2 | a0001c0002t0047g0156a0001c0002t0048g0155 | 2 | HG01261.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.941+25G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 6/12 | chr11 | 61542186 | ||||||
| chr11:61542650
|
C | T | 2 | a0001c0001t0019g0058a0001c0001t0052g0073 | 2 | HG00140.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.573-71G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61542650 | ||||||
| chr11:61542750
|
G | A | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.573-171C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61542750 | ||||||
| chr11:61542866
|
C | T | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.573-287G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61542866 | ||||||
| chr11:61543154
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.573-575C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61543154 | ||||||
| chr11:61543858
|
T | A | 11 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0001t0006g0033others(8): Show | 11 | HG02145.hp2 HG02630.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.573-1279A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61543858 | ||||||
| chr11:61544371
|
G | A | 2 | a0001c0001t0058g0076a0001c0009t0038g0161 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.572+1660C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544371 | ||||||
| chr11:61544524
|
C | G | 1 | a0001c0001t0003g0172 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.572+1507G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544524 | ||||||
| chr11:61544600
|
C | A | 1 | a0001c0001t0004g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.572+1431G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544600 | ||||||
| chr11:61544647
|
T | C | 2 | a0001c0002t0001g0160a0001c0002t0039g0171 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.572+1384A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544647 | ||||||
| chr11:61544745
|
C | T | 1 | a0001c0001t0029g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.572+1286G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544745 | ||||||
| chr11:61544886
|
C | A | 10 | a0001c0002t0007g0002a0001c0002t0007g0024a0001c0002t0007g0025others(7): Show | 11 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.572+1145G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544886 | ||||||
| chr11:61544898
|
G | T | 1 | a0001c0002t0011g0018 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.572+1133C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544898 | ||||||
| chr11:61544946
|
A | G | 173 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0045others(170): Show | 182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.572+1085T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61544946 | ||||||
| chr11:61545731
|
G | C | 3 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0002t0030g0034 | 3 | HG02717.hp2 HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.572+300C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 5/12 | chr11 | 61545731 | ||||||
| chr11:61546295
|
G | A | 1 | a0001c0002t0033g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.348-40C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61546295 | ||||||
| chr11:61546330
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.348-75C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61546330 | ||||||
| chr11:61546761
|
C | A | 2 | a0001c0003t0017g0065a0001c0003t0017g0066 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.347+416G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61546761 | ||||||
| chr11:61546969
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.347+208C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61546969 | ||||||
| chr11:61547037
|
G | T | 1 | a0001c0001t0058g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+140C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61547037 | ||||||
| chr11:61547058
|
G | T | 8 | a0001c0001t0006g0033a0001c0001t0021g0063a0001c0001t0021g0064others(5): Show | 8 | HG02145.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.347+119C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61547058 | ||||||
| chr11:61547080
|
G | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0055a0001c0001t0001g0091others(1): Show | 5 | HG01261.hp1 HG01346.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+97C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 4/12 | chr11 | 61547080 | ||||||
| chr11:61547499
|
T | TACACGC | 10 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0001t0021g0063others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.216-197_216-192dup others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61547499 | ||||||
| chr11:61548043
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.216-735A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548043 | ||||||
| chr11:61548345
|
C | A | 1 | a0001c0001t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.216-1037G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548345 | ||||||
| chr11:61548401
|
G | A | 3 | a0001c0002t0004g0138a0001c0002t0013g0008a0001c0002t0013g0139 | 4 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-1093C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548401 | ||||||
| chr11:61548418
|
G | A | 4 | a0001c0001t0015g0051a0001c0005t0056g0052a0002c0004t0015g0050others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-1110C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548418 | ||||||
| chr11:61548572
|
C | T | 5 | a0001c0001t0021g0063a0001c0001t0021g0064a0001c0002t0033g0145others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.216-1264G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548572 | ||||||
| chr11:61548584
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.216-1276C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548584 | ||||||
| chr11:61548618
|
C | T | 2 | a0001c0001t0006g0031a0001c0001t0053g0046 | 2 | HG02615.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.216-1310G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548618 | ||||||
| chr11:61548662
|
C | T | 98 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0055others(95): Show | 102 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.216-1354G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548662 | ||||||
| chr11:61548835
|
T | C | 99 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0055others(96): Show | 103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.216-1527A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548835 | ||||||
| chr11:61548929
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0002g0041a0001c0001t0003g0177others(1): Show | 4 | NA18959.hp1 NA18962.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-1621C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61548929 | ||||||
| chr11:61549057
|
C | T | 1 | a0001c0001t0058g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.216-1749G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549057 | ||||||
| chr11:61549474
|
C | T | 1 | a0001c0001t0053g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.215+1910G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549474 | ||||||
| chr11:61549532
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.215+1852G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549532 | ||||||
| chr11:61549738
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0054g0083 | 2 | HG02698.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.215+1646G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549738 | ||||||
| chr11:61549850
|
T | C | 6 | a0001c0001t0008g0042a0001c0002t0001g0157a0001c0002t0002g0152others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.215+1534A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549850 | ||||||
| chr11:61549915
|
G | A | 61 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0055others(58): Show | 64 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.215+1469C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549915 | ||||||
| chr11:61549995
|
T | C | 23 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0001t0006g0031others(20): Show | 24 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.215+1389A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61549995 | ||||||
| chr11:61550601
|
A | G | 172 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0045others(169): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.215+783T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61550601 | ||||||
| chr11:61550732
|
G | T | 2 | a0001c0002t0010g0022a0001c0002t0010g0035 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.215+652C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61550732 | ||||||
| chr11:61551099
|
G | T | 6 | a0001c0001t0005g0005a0001c0001t0005g0069a0001c0001t0005g0134others(3): Show | 7 | HG01891.hp2 HG02622.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+285C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61551099 | ||||||
| chr11:61551177
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.215+207G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61551177 | ||||||
| chr11:61551187
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.215+197G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61551187 | ||||||
| chr11:61551278
|
G | T | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.215+106C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61551278 | ||||||
| chr11:61551296
|
C | T | 1 | a0001c0002t0001g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.215+88G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61551296 | ||||||
| chr11:61551337
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.215+47A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 3/12 | chr11 | 61551337 | ||||||
| chr11:61551567
|
C | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.136-104G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61551567 | ||||||
| chr11:61551719
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.136-256T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61551719 | ||||||
| chr11:61551846
|
C | T | 1 | a0001c0002t0057g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.136-383G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61551846 | ||||||
| chr11:61552370
|
G | A | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.136-907C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552370 | ||||||
| chr11:61552387
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.136-924G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552387 | ||||||
| chr11:61552396
|
G | C | 1 | a0001c0002t0002g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.136-933C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552396 | ||||||
| chr11:61552452
|
GCA | G | 26 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(23): Show | 27 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.136-991_136-990del others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552452 | ||||||
| chr11:61552454
|
ACACACAC others(11): Show |
A | 20 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(17): Show | 21 | HG01261.hp2 HG02055.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.136-1009_136-992de others(19): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552454 | ||||||
| chr11:61552476
|
ACACACAC others(5): Show |
A | 1 | a0001c0002t0039g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.136-1025_136-1014d others(14): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552476 | ||||||
| chr11:61552503
|
C | T | 1 | a0001c0001t0001g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.136-1040G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552503 | ||||||
| chr11:61552641
|
C | A | 11 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0002t0007g0002others(8): Show | 12 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-1178G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552641 | ||||||
| chr11:61552781
|
C | T | 3 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0009t0038g0161 | 3 | HG02970.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.136-1318G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552781 | ||||||
| chr11:61552956
|
G | A | 6 | a0001c0001t0015g0051a0001c0001t0015g0053a0001c0002t0057g0144others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-1493C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61552956 | ||||||
| chr11:61553047
|
C | T | 6 | a0001c0001t0001g0151a0001c0001t0032g0150a0001c0002t0001g0153others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-1584G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61553047 | ||||||
| chr11:61553256
|
C | T | 1 | a0001c0001t0002g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.136-1793G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61553256 | ||||||
| chr11:61553406
|
G | A | 1 | a0001c0002t0009g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136-1943C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61553406 | ||||||
| chr11:61553544
|
C | T | 4 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0001t0029g0023others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-2081G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61553544 | ||||||
| chr11:61553651
|
C | G | 1 | a0001c0002t0002g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.136-2188G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61553651 | ||||||
| chr11:61553950
|
C | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.135+2154G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61553950 | ||||||
| chr11:61554007
|
A | C | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.135+2097T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554007 | ||||||
| chr11:61554098
|
G | A | 1 | a0001c0001t0029g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135+2006C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554098 | ||||||
| chr11:61554286
|
C | CCGCACA | 5 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0002t0002g0148others(2): Show | 5 | HG02970.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+1817_135+1818i others(8): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554286 | ||||||
| chr11:61554288
|
A | G | 168 | a0001c0001t0001g0006a0001c0001t0001g0040a0001c0001t0001g0045others(165): Show | 176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.135+1816T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554288 | ||||||
| chr11:61554290
|
A | C | 5 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0002t0002g0148others(2): Show | 5 | HG02970.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+1814T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554290 | ||||||
| chr11:61554433
|
CACAG | C | 5 | a0001c0001t0015g0051a0001c0001t0015g0053a0001c0005t0056g0052others(2): Show | 5 | HG02572.hp1 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.135+1667_135+1670d others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554433 | ||||||
| chr11:61554449
|
G | C | 5 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0002t0002g0148others(2): Show | 5 | HG02970.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+1655C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554449 | ||||||
| chr11:61554535
|
A | T | 1 | a0001c0001t0006g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.135+1569T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554535 | ||||||
| chr11:61554617
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.135+1487G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61554617 | ||||||
| chr11:61555007
|
G | A | 4 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043others(1): Show | 5 | HG02280.hp2 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+1097C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555007 | ||||||
| chr11:61555119
|
C | T | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135+985G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555119 | ||||||
| chr11:61555175
|
C | T | 1 | a0004c0007t0019g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.135+929G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555175 | ||||||
| chr11:61555290
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.135+814G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555290 | ||||||
| chr11:61555293
|
G | T | 2 | a0001c0001t0058g0076a0001c0002t0001g0037 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.135+811C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555293 | ||||||
| chr11:61555360
|
G | C | 9 | a0001c0001t0001g0060a0001c0001t0001g0099a0001c0001t0001g0100others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+744C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555360 | ||||||
| chr11:61555406
|
G | C | 2 | a0001c0001t0058g0076a0001c0002t0001g0037 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.135+698C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555406 | ||||||
| chr11:61555436
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.135+668G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555436 | ||||||
| chr11:61555681
|
G | C | 15 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(12): Show | 15 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.135+423C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555681 | ||||||
| chr11:61555772
|
C | CGT | 22 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(19): Show | 22 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(19): Show |
intron_variant | MODIFIER | c.135+330_135+331dup others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555772 | ||||||
| chr11:61555772
|
C | CGTGT | 14 | a0001c0001t0010g0017a0001c0001t0025g0014a0001c0002t0006g0001others(11): Show | 15 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+328_135+331dup others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555772 | ||||||
| chr11:61555873
|
T | C | 4 | a0001c0001t0001g0128a0001c0001t0014g0130a0001c0001t0014g0131others(1): Show | 4 | HG01256.hp1 HG01346.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+231A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61555873 | ||||||
| chr11:61556041
|
T | G | 1 | a0001c0002t0009g0026 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+63A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61556041 | ||||||
| chr11:61556049
|
G | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.135+55C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61556049 | ||||||
| chr11:61556066
|
C | A | 1 | a0001c0002t0057g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.135+38G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 2/12 | chr11 | 61556066 | ||||||
| chr11:61556343
|
C | T | 3 | a0001c0002t0004g0138a0001c0002t0013g0008a0001c0002t0013g0139 | 4 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-136G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556343 | ||||||
| chr11:61556430
|
T | C | 1 | a0001c0009t0038g0161 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.32-223A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556430 | ||||||
| chr11:61556432
|
G | A | 2 | a0001c0001t0032g0150a0001c0002t0001g0153 | 2 | HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.32-225C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556432 | ||||||
| chr11:61556451
|
C | T | 3 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0174 | 3 | NA18959.hp2 NA18975.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.32-244G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556451 | ||||||
| chr11:61556516
|
G | T | 11 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0002t0007g0002others(8): Show | 12 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.32-309C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556516 | ||||||
| chr11:61556570
|
C | T | 35 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(32): Show | 36 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.32-363G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556570 | ||||||
| chr11:61556643
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.32-436T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556643 | ||||||
| chr11:61556993
|
A | ATGAGACC | 35 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(32): Show | 36 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.32-787_32-786insGG others(5): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61556993 | ||||||
| chr11:61557165
|
T | G | 35 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(32): Show | 36 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.32-958A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61557165 | ||||||
| chr11:61557352
|
A | G | 47 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(44): Show | 49 | HG01261.hp2 HG01496.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.32-1145T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61557352 | ||||||
| chr11:61557365
|
T | G | 2 | a0001c0002t0018g0038a0001c0002t0018g0039 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.32-1158A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61557365 | ||||||
| chr11:61557941
|
G | A | 13 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(10): Show | 13 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.32-1734C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61557941 | ||||||
| chr11:61557980
|
C | T | 2 | a0001c0002t0047g0156a0001c0002t0048g0155 | 2 | HG01261.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.32-1773G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61557980 | ||||||
| chr11:61558229
|
G | C | 3 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0001t0029g0023 | 3 | HG02451.hp1 HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.32-2022C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558229 | ||||||
| chr11:61558239
|
T | C | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-2032A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558239 | ||||||
| chr11:61558477
|
T | A | 2 | a0001c0003t0017g0065a0001c0003t0017g0066 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.32-2270A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558477 | ||||||
| chr11:61558483
|
T | C | 2 | a0001c0001t0001g0045a0001c0002t0002g0152 | 2 | HG02723.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.32-2276A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558483 | ||||||
| chr11:61558483
|
T | TAC | 2 | a0001c0002t0001g0157a0001c0002t0034g0154 | 2 | HG02809.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.32-2277_32-2276ins others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558483 | ||||||
| chr11:61558483
|
T | TATATACA others(13): Show |
1 | a0001c0002t0010g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.32-2277_32-2276ins others(20): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558483 | ||||||
| chr11:61558483
|
TATACACA others(3): Show |
T | 1 | a0001c0002t0039g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.32-2286_32-2277del others(10): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558483 | ||||||
| chr11:61558485
|
T | C | 16 | a0001c0001t0001g0045a0001c0001t0001g0158a0001c0001t0004g0159others(13): Show | 16 | HG01261.hp2 HG02451.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-2278A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558485 | ||||||
| chr11:61558485
|
T | TAC | 14 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0109others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(11): Show |
intron_variant | MODIFIER | c.32-2280_32-2279dup others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558485 | ||||||
| chr11:61558487
|
C | T | 18 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(15): Show | 19 | HG01884.hp2 HG02055.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-2280G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558487 | ||||||
| chr11:61558503
|
C | CACAT | 3 | a0001c0001t0032g0150a0001c0002t0001g0153a0001c0002t0002g0152 | 3 | HG02723.hp1 HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.32-2297_32-2296ins others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558503 | ||||||
| chr11:61558505
|
T | C | 6 | a0001c0001t0031g0036a0001c0001t0032g0150a0001c0002t0001g0153others(3): Show | 6 | HG02630.hp1 HG02698.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-2298A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TAC | 5 | a0001c0001t0002g0071a0001c0001t0008g0003a0001c0001t0008g0042others(2): Show | 6 | HG02280.hp2 HG02559.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.32-2300_32-2299dup others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TACAC | 17 | a0001c0001t0001g0116a0001c0001t0002g0041a0001c0001t0006g0031others(14): Show | 18 | HG00558.hp1 HG01496.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.32-2302_32-2299dup others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TACACAC | 4 | a0001c0001t0006g0033a0001c0002t0006g0001a0001c0002t0026g0013others(1): Show | 5 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-2304_32-2299dup others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TACACACA others(3): Show |
1 | a0001c0001t0025g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.32-2308_32-2299dup others(10): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TACACACA others(5): Show |
4 | a0001c0002t0011g0018a0001c0002t0011g0019a0001c0002t0011g0020others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-2310_32-2299dup others(12): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TACACACA others(7): Show |
4 | a0001c0001t0010g0017a0001c0002t0006g0015a0001c0002t0023g0016others(1): Show | 4 | HG02647.hp2 HG03225.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-2312_32-2299dup others(14): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
T | TACACACA others(9): Show |
1 | a0001c0002t0010g0022 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.32-2314_32-2299dup others(16): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
TAC | T | 13 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0128others(10): Show | 14 | HG00140.hp2 HG01256.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.32-2300_32-2299del others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558505
|
TACAC | T | 3 | a0001c0001t0036g0129a0001c0002t0001g0162a0001c0009t0038g0161 | 3 | HG01346.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.32-2302_32-2299del others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558505 | ||||||
| chr11:61558511
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.32-2304G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558511 | ||||||
| chr11:61558527
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0158a0001c0001t0004g0159 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.32-2330_32-2321del others(10): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558527 | ||||||
| chr11:61558533
|
CACAT | C | 2 | a0001c0002t0018g0038a0001c0002t0018g0039 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.32-2330_32-2327del others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558533 | ||||||
| chr11:61558535
|
C | A | 4 | a0001c0001t0021g0063a0001c0001t0021g0064a0001c0003t0017g0065others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-2328G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558535 | ||||||
| chr11:61558535
|
C | CAT | 3 | a0001c0001t0001g0117a0001c0001t0002g0106a0003c0006t0001g0105 | 3 | HG03017.hp1 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.32-2330_32-2329dup others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558535 | ||||||
| chr11:61558535
|
CAT | C | 4 | a0001c0001t0001g0045a0001c0001t0029g0023a0001c0002t0047g0156others(1): Show | 4 | HG01261.hp2 HG02451.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-2330_32-2329del others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558535 | ||||||
| chr11:61558537
|
T | C | 34 | a0001c0001t0001g0151a0001c0001t0006g0031a0001c0001t0006g0033others(31): Show | 36 | HG01496.hp2 HG02055.hp1 HG02257.hp2 others(33): Show |
intron_variant | MODIFIER | c.32-2330A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558537 | ||||||
| chr11:61558539
|
T | C | 1 | a0001c0002t0002g0152 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32-2332A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558539 | ||||||
| chr11:61558742
|
C | T | 29 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0109others(26): Show | 30 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.32-2535G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558742 | ||||||
| chr11:61558899
|
C | T | 1 | a0001c0001t0022g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.32-2692G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61558899 | ||||||
| chr11:61559300
|
G | A | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-3093C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61559300 | ||||||
| chr11:61559453
|
C | G | 6 | a0001c0001t0001g0151a0001c0001t0032g0150a0001c0002t0001g0153others(3): Show | 6 | HG02723.hp1 HG02809.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-3246G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61559453 | ||||||
| chr11:61559635
|
C | T | 3 | a0001c0002t0004g0138a0001c0002t0013g0008a0001c0002t0013g0139 | 4 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-3428G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61559635 | ||||||
| chr11:61559920
|
C | T | 2 | a0001c0002t0018g0038a0001c0002t0018g0039 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.32-3713G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61559920 | ||||||
| chr11:61560240
|
T | C | 2 | a0001c0001t0032g0150a0001c0002t0001g0153 | 2 | HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.32-4033A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560240 | ||||||
| chr11:61560366
|
T | C | 53 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(50): Show | 55 | HG01261.hp2 HG01496.hp2 HG02055.hp1 others(52): Show |
intron_variant | MODIFIER | c.32-4159A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560366 | ||||||
| chr11:61560545
|
G | A | 1 | a0001c0001t0029g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32-4338C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560545 | ||||||
| chr11:61560638
|
T | A | 15 | a0001c0001t0001g0056a0001c0001t0001g0107a0001c0001t0001g0109others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.32-4431A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560638 | ||||||
| chr11:61560699
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.32-4492G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560699 | ||||||
| chr11:61560700
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.32-4493C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560700 | ||||||
| chr11:61560732
|
A | G | 1 | a0001c0001t0053g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.32-4525T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560732 | ||||||
| chr11:61560773
|
C | A | 1 | a0001c0001t0004g0049 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.32-4566G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61560773 | ||||||
| chr11:61561129
|
A | G | 1 | a0001c0001t0029g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.32-4922T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561129 | ||||||
| chr11:61561165
|
C | T | 1 | a0001c0002t0039g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.32-4958G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561165 | ||||||
| chr11:61561199
|
C | A | 1 | a0001c0002t0050g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32-4992G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561199 | ||||||
| chr11:61561260
|
C | G | 8 | a0001c0001t0001g0151a0001c0001t0032g0150a0001c0002t0001g0153others(5): Show | 8 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-5053G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561260 | ||||||
| chr11:61561403
|
A | G | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-5196T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561403 | ||||||
| chr11:61561498
|
C | G | 1 | a0001c0002t0057g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.32-5291G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561498 | ||||||
| chr11:61561901
|
A | G | 2 | a0001c0001t0002g0071a0001c0001t0043g0070 | 2 | HG02602.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.32-5694T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61561901 | ||||||
| chr11:61562013
|
C | T | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-5806G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562013 | ||||||
| chr11:61562031
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.32-5824A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562031 | ||||||
| chr11:61562048
|
G | GCA | 2 | a0001c0001t0001g0116a0001c0001t0002g0143 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.32-5843_32-5842dup others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562048 | ||||||
| chr11:61562048
|
GCA | G | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-5843_32-5842del others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562048 | ||||||
| chr11:61562048
|
GCACA | G | 19 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(16): Show | 19 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.32-5845_32-5842del others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562048 | ||||||
| chr11:61562075
|
C | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-5868G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562075 | ||||||
| chr11:61562138
|
C | T | 15 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(12): Show | 15 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.32-5931G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562138 | ||||||
| chr11:61562309
|
T | C | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-6102A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562309 | ||||||
| chr11:61562586
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.32-6379C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562586 | ||||||
| chr11:61562732
|
G | A | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-6525C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562732 | ||||||
| chr11:61562838
|
G | A | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.32-6631C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562838 | ||||||
| chr11:61562869
|
G | GCC | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-6663_32-6662ins others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562869 | ||||||
| chr11:61562887
|
A | C | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-6680T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562887 | ||||||
| chr11:61562977
|
G | A | 1 | a0001c0001t0020g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.32-6770C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562977 | ||||||
| chr11:61562985
|
C | T | 1 | a0001c0001t0005g0069 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.32-6778G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61562985 | ||||||
| chr11:61563043
|
CA | C | 9 | a0001c0001t0002g0135a0001c0001t0003g0172a0001c0001t0003g0180others(6): Show | 10 | NA18947.hp1 NA18966.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-6837delT | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563043 | ||||||
| chr11:61563119
|
C | T | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-6912G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563119 | ||||||
| chr11:61563140
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.32-6933T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563140 | ||||||
| chr11:61563285
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.32-7078A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563285 | ||||||
| chr11:61563475
|
C | G | 5 | a0001c0001t0001g0165a0001c0001t0002g0009a0001c0001t0002g0163others(2): Show | 6 | HG00735.hp1 HG01175.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.32-7268G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563475 | ||||||
| chr11:61563505
|
A | G | 47 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(44): Show | 49 | HG01261.hp2 HG01496.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.32-7298T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563505 | ||||||
| chr11:61563812
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.32-7605C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563812 | ||||||
| chr11:61563871
|
C | A | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-7664G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61563871 | ||||||
| chr11:61564750
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.32-8543C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61564750 | ||||||
| chr11:61565076
|
C | T | 5 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0002t0002g0148others(2): Show | 5 | HG02970.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-8869G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565076 | ||||||
| chr11:61565121
|
A | G | 8 | a0001c0001t0001g0151a0001c0001t0032g0150a0001c0002t0001g0153others(5): Show | 8 | HG01261.hp2 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.32-8914T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565121 | ||||||
| chr11:61565175
|
T | C | 3 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043 | 4 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-8968A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565175 | ||||||
| chr11:61565444
|
C | T | 4 | a0001c0001t0021g0063a0001c0001t0021g0064a0001c0003t0017g0065others(1): Show | 4 | HG02717.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-9237G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565444 | ||||||
| chr11:61565578
|
A | C | 1 | a0001c0001t0042g0062 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.32-9371T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565578 | ||||||
| chr11:61565672
|
C | T | 2 | a0001c0002t0047g0156a0001c0002t0048g0155 | 2 | HG01261.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.32-9465G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565672 | ||||||
| chr11:61565691
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.32-9484A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565691 | ||||||
| chr11:61565899
|
C | T | 1 | a0001c0002t0018g0038 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.32-9692G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61565899 | ||||||
| chr11:61566327
|
G | T | 1 | a0001c0002t0028g0011 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32-10120C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566327 | ||||||
| chr11:61566330
|
C | T | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-10123G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566330 | ||||||
| chr11:61566526
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.32-10319C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566526 | ||||||
| chr11:61566598
|
C | T | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-10391G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566598 | ||||||
| chr11:61566794
|
C | T | 1 | a0001c0001t0008g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.32-10587G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566794 | ||||||
| chr11:61566956
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0002g0119 | 3 | HG01978.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.32-10749C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566956 | ||||||
| chr11:61566957
|
T | C | 1 | a0001c0002t0035g0147 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.32-10750A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61566957 | ||||||
| chr11:61567331
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0002g0041a0001c0001t0003g0177 | 3 | NA18959.hp1 NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.32-11124T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567331 | ||||||
| chr11:61567343
|
G | GC | 11 | a0001c0001t0004g0049a0001c0001t0008g0003a0001c0001t0008g0042others(8): Show | 13 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.32-11137dupG | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567343 | ||||||
| chr11:61567343
|
G | GCC | 14 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0015g0053others(11): Show | 15 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.32-11138_32-11137d others(4): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567343 | ||||||
| chr11:61567343
|
G | GCCC | 11 | a0001c0001t0001g0151a0001c0001t0010g0017a0001c0001t0025g0014others(8): Show | 11 | HG02630.hp1 HG02647.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.32-11139_32-11137d others(5): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567343 | ||||||
| chr11:61567343
|
G | GCCCC | 12 | a0001c0001t0001g0045a0001c0002t0001g0153a0001c0002t0001g0157others(9): Show | 12 | HG01261.hp2 HG02451.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.32-11140_32-11137d others(6): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567343 | ||||||
| chr11:61567712
|
G | A | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.32-11505C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567712 | ||||||
| chr11:61567738
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.32-11531C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61567738 | ||||||
| chr11:61568020
|
A | G | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.32-11813T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568020 | ||||||
| chr11:61568124
|
T | C | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.32-11917A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568124 | ||||||
| chr11:61568202
|
T | TG | 53 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(50): Show | 55 | HG01261.hp2 HG01496.hp2 HG02055.hp1 others(52): Show |
intron_variant | MODIFIER | c.32-11996dupC | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568202 | ||||||
| chr11:61568328
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32-12121G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568328 | ||||||
| chr11:61568413
|
A | G | 1 | a0001c0001t0004g0049 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.32-12206T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568413 | ||||||
| chr11:61568588
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.31+12202C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568588 | ||||||
| chr11:61568723
|
C | A | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.31+12067G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568723 | ||||||
| chr11:61568747
|
A | C | 2 | a0001c0002t0010g0022a0001c0002t0010g0035 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.31+12043T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568747 | ||||||
| chr11:61568782
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.31+12008A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61568782 | ||||||
| chr11:61569469
|
C | T | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.31+11321G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569469 | ||||||
| chr11:61569525
|
G | T | 2 | a0001c0002t0001g0162a0001c0009t0038g0161 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.31+11265C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569525 | ||||||
| chr11:61569577
|
C | T | 1 | a0001c0002t0057g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31+11213G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569577 | ||||||
| chr11:61569647
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.31+11143G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569647 | ||||||
| chr11:61569657
|
T | TACAGAAG others(1): Show |
2 | a0001c0001t0001g0158a0001c0001t0004g0159 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.31+11125_31+11132d others(10): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569657 | ||||||
| chr11:61569682
|
C | A | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.31+11108G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569682 | ||||||
| chr11:61569686
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.31+11104A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569686 | ||||||
| chr11:61569780
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.31+11010G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569780 | ||||||
| chr11:61569971
|
C | T | 3 | a0001c0001t0060g0169a0001c0002t0045g0170a0004c0007t0019g0168 | 3 | HG00323.hp2 HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.31+10819G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61569971 | ||||||
| chr11:61570307
|
G | A | 1 | a0001c0002t0034g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.31+10483C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61570307 | ||||||
| chr11:61570359
|
G | A | 2 | a0001c0002t0010g0022a0001c0002t0010g0035 | 2 | HG02055.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.31+10431C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61570359 | ||||||
| chr11:61570659
|
G | A | 1 | a0001c0001t0016g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+10131C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61570659 | ||||||
| chr11:61570681
|
T | C | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+10109A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61570681 | ||||||
| chr11:61570773
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0014g0130a0001c0001t0014g0131others(1): Show | 4 | HG01256.hp1 HG01346.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+10017C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61570773 | ||||||
| chr11:61570921
|
A | ACT | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.31+9867_31+9868dup others(2): Show |
SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61570921 | ||||||
| chr11:61571185
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0002g0041a0001c0001t0003g0177others(1): Show | 4 | NA18959.hp1 NA18962.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+9605C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61571185 | ||||||
| chr11:61571220
|
A | T | 1 | a0001c0001t0019g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.31+9570T>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61571220 | ||||||
| chr11:61571291
|
T | C | 11 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0002t0007g0002others(8): Show | 12 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+9499A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61571291 | ||||||
| chr11:61571395
|
T | C | 36 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(33): Show | 37 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(34): Show |
intron_variant | MODIFIER | c.31+9395A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61571395 | ||||||
| chr11:61571717
|
A | C | 20 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(17): Show | 20 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.31+9073T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61571717 | ||||||
| chr11:61571976
|
A | G | 1 | a0001c0001t0002g0163 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.31+8814T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61571976 | ||||||
| chr11:61572116
|
TG | T | 18 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(15): Show | 18 | HG00323.hp1 HG00741.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.31+8673delC | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572116 | ||||||
| chr11:61572119
|
G | A | 2 | a0001c0002t0001g0162a0001c0009t0038g0161 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.31+8671C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572119 | ||||||
| chr11:61572119
|
G | C | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.31+8671C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572119 | ||||||
| chr11:61572121
|
G | C | 1 | a0001c0001t0005g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.31+8669C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572121 | ||||||
| chr11:61572122
|
G | C | 8 | a0001c0001t0002g0135a0001c0001t0003g0180a0001c0001t0003g0181others(5): Show | 9 | HG02165.hp2 NA18947.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+8668C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572122 | ||||||
| chr11:61572237
|
C | T | 14 | a0001c0001t0010g0017a0001c0001t0025g0014a0001c0002t0006g0001others(11): Show | 15 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.31+8553G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572237 | ||||||
| chr11:61572255
|
T | A | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+8535A>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572255 | ||||||
| chr11:61572281
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.31+8509G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572281 | ||||||
| chr11:61572298
|
A | G | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+8492T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572298 | ||||||
| chr11:61572303
|
G | A | 2 | a0001c0002t0047g0156a0001c0002t0048g0155 | 2 | HG01261.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.31+8487C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572303 | ||||||
| chr11:61572495
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.31+8295G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572495 | ||||||
| chr11:61572608
|
C | A | 2 | a0001c0002t0018g0038a0001c0002t0018g0039 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.31+8182G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61572608 | ||||||
| chr11:61573071
|
GA | G | 11 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0002t0007g0002others(8): Show | 12 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+7718delT | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573071 | ||||||
| chr11:61573072
|
A | AG | 15 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(12): Show | 16 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.31+7717dupC | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573072 | ||||||
| chr11:61573342
|
C | G | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31+7448G>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573342 | ||||||
| chr11:61573428
|
T | G | 3 | a0001c0002t0004g0138a0001c0002t0013g0008a0001c0002t0013g0139 | 4 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.31+7362A>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573428 | ||||||
| chr11:61573452
|
G | T | 11 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0002t0007g0002others(8): Show | 12 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+7338C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573452 | ||||||
| chr11:61573526
|
C | T | 1 | a0001c0002t0001g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.31+7264G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573526 | ||||||
| chr11:61573567
|
T | C | 1 | a0002c0004t0059g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.31+7223A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573567 | ||||||
| chr11:61573774
|
T | C | 13 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(10): Show | 13 | HG01261.hp2 HG02451.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.31+7016A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573774 | ||||||
| chr11:61573792
|
T | C | 57 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(54): Show | 60 | HG01261.hp2 HG01496.hp2 HG02055.hp1 others(57): Show |
intron_variant | MODIFIER | c.31+6998A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573792 | ||||||
| chr11:61573963
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0002g0141 | 2 | HG00408.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.31+6827C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61573963 | ||||||
| chr11:61574076
|
C | T | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31+6714G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574076 | ||||||
| chr11:61574314
|
G | T | 12 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(9): Show | 12 | HG01261.hp2 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+6476C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574314 | ||||||
| chr11:61574435
|
A | G | 3 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0009t0038g0161 | 3 | HG02970.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.31+6355T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574435 | ||||||
| chr11:61574573
|
G | A | 1 | a0001c0002t0039g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31+6217C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574573 | ||||||
| chr11:61574805
|
C | T | 1 | a0001c0002t0007g0024 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31+5985G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574805 | ||||||
| chr11:61574882
|
G | A | 1 | a0001c0001t0055g0142 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.31+5908C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574882 | ||||||
| chr11:61574886
|
G | A | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31+5904C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574886 | ||||||
| chr11:61574905
|
C | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+5885G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61574905 | ||||||
| chr11:61575185
|
C | T | 35 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(32): Show | 36 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.31+5605G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575185 | ||||||
| chr11:61575224
|
C | T | 53 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(50): Show | 55 | HG01261.hp2 HG01496.hp2 HG02055.hp1 others(52): Show |
intron_variant | MODIFIER | c.31+5566G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575224 | ||||||
| chr11:61575490
|
C | T | 16 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(13): Show | 17 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.31+5300G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575490 | ||||||
| chr11:61575516
|
A | C | 16 | a0001c0001t0010g0017a0001c0001t0024g0010a0001c0001t0025g0014others(13): Show | 17 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.31+5274T>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575516 | ||||||
| chr11:61575601
|
G | A | 12 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(9): Show | 12 | HG01261.hp2 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+5189C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575601 | ||||||
| chr11:61575750
|
C | T | 1 | a0001c0002t0039g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31+5040G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575750 | ||||||
| chr11:61575841
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.31+4949C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575841 | ||||||
| chr11:61575906
|
G | A | 1 | a0001c0002t0001g0157 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.31+4884C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61575906 | ||||||
| chr11:61576062
|
G | A | 2 | a0001c0002t0002g0148a0001c0002t0050g0149 | 2 | HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.31+4728C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576062 | ||||||
| chr11:61576224
|
A | G | 2 | a0001c0001t0004g0049a0001c0001t0020g0004 | 3 | HG03491.hp2 HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.31+4566T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576224 | ||||||
| chr11:61576334
|
C | T | 1 | a0001c0001t0022g0048 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.31+4456G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576334 | ||||||
| chr11:61576553
|
C | T | 19 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(16): Show | 19 | HG01261.hp2 HG02630.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+4237G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576553 | ||||||
| chr11:61576660
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.31+4130C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576660 | ||||||
| chr11:61576851
|
G | T | 2 | a0001c0001t0001g0158a0001c0001t0004g0159 | 2 | HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.31+3939C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576851 | ||||||
| chr11:61576994
|
C | T | 12 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(9): Show | 12 | HG01261.hp2 HG02630.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.31+3796G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61576994 | ||||||
| chr11:61577147
|
C | A | 34 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0004g0159others(31): Show | 35 | HG01261.hp2 HG02055.hp1 HG02451.hp1 others(32): Show |
intron_variant | MODIFIER | c.31+3643G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577147 | ||||||
| chr11:61577473
|
C | A | 2 | a0001c0002t0018g0038a0001c0002t0018g0039 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.31+3317G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577473 | ||||||
| chr11:61577585
|
A | G | 1 | a0001c0001t0008g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.31+3205T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577585 | ||||||
| chr11:61577624
|
G | A | 11 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0004g0159others(8): Show | 11 | HG01261.hp2 HG02630.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.31+3166C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577624 | ||||||
| chr11:61577636
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0004g0159a0001c0002t0039g0171 | 3 | HG02630.hp1 HG02717.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.31+3154C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577636 | ||||||
| chr11:61577709
|
G | A | 1 | a0001c0002t0057g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31+3081C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577709 | ||||||
| chr11:61577892
|
C | T | 1 | a0001c0001t0053g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.31+2898G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577892 | ||||||
| chr11:61577893
|
G | A | 3 | a0001c0002t0001g0160a0001c0002t0001g0162a0001c0009t0038g0161 | 3 | HG02970.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.31+2897C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61577893 | ||||||
| chr11:61578020
|
A | G | 38 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0158others(35): Show | 39 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.31+2770T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578020 | ||||||
| chr11:61578036
|
T | C | 37 | a0001c0001t0001g0151a0001c0001t0001g0158a0001c0001t0004g0159others(34): Show | 38 | HG01261.hp2 HG02055.hp1 HG02145.hp1 others(35): Show |
intron_variant | MODIFIER | c.31+2754A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578036 | ||||||
| chr11:61578042
|
G | A | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+2748C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578042 | ||||||
| chr11:61578149
|
C | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+2641G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578149 | ||||||
| chr11:61578206
|
G | C | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+2584C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578206 | ||||||
| chr11:61578484
|
A | G | 16 | a0001c0001t0010g0017a0001c0001t0025g0014a0001c0001t0029g0023others(13): Show | 17 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.31+2306T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578484 | ||||||
| chr11:61578565
|
G | A | 1 | a0001c0002t0030g0034 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31+2225C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578565 | ||||||
| chr11:61578749
|
C | A | 1 | a0001c0002t0010g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.31+2041G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61578749 | ||||||
| chr11:61579016
|
C | T | 1 | a0001c0001t0012g0044 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.31+1774G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579016 | ||||||
| chr11:61579152
|
C | A | 6 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0002g0009others(3): Show | 7 | HG00735.hp1 HG01175.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.31+1638G>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579152 | ||||||
| chr11:61579299
|
C | T | 3 | a0001c0001t0008g0003a0001c0001t0008g0042a0001c0001t0008g0043 | 4 | HG02280.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+1491G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579299 | ||||||
| chr11:61579300
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0002g0041 | 2 | NA18959.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.31+1490G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579300 | ||||||
| chr11:61579492
|
C | T | 2 | a0001c0002t0018g0038a0001c0002t0018g0039 | 2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.31+1298G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579492 | ||||||
| chr11:61579561
|
G | C | 3 | a0001c0001t0060g0169a0001c0002t0045g0170a0004c0007t0019g0168 | 3 | HG00323.hp2 HG01515.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.31+1229C>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579561 | ||||||
| chr11:61579959
|
G | A | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+831C>T | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61579959 | ||||||
| chr11:61580028
|
G | T | 1 | a0001c0001t0031g0036 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.31+762C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61580028 | ||||||
| chr11:61580197
|
C | T | 1 | a0001c0002t0001g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+593G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61580197 | ||||||
| chr11:61580198
|
T | C | 1 | a0001c0002t0039g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31+592A>G | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61580198 | ||||||
| chr11:61580265
|
A | G | 29 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0010g0017others(26): Show | 31 | HG01496.hp2 HG02055.hp1 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.31+525T>C | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61580265 | ||||||
| chr11:61580435
|
G | T | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.31+355C>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61580435 | ||||||
| chr11:61580436
|
C | T | 1 | a0001c0001t0024g0010 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.31+354G>A | SYT7 | ENSG00000011347.10 | transcript | ENST00000539008.6 | protein_coding | 1/12 | chr11 | 61580436 |