Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 341359 |
|---|---|
| ensemblid | ENSG00000110975.8 |
| hgncid | 19266 |
| symbol | SYT10 |
| name | synaptotagmin 10 |
| refseq_nuc | NM_198992.4 |
| refseq_prot | NP_945343.1 |
| ensembl_nuc | ENST00000228567.7 |
| ensembl_prot | ENSP00000228567.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 33374238 |
| end | 33439819 |
| strand | - |
| ver | v1.2 |
| region | chr12:33374238-33439819 |
| region5000 | chr12:33369238-33444819 |
| regionname0 | SYT10_chr12_33374238_33439819 |
| regionname5000 | SYT10_chr12_33369238_33444819 |
| 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 | 523 | 312 | 85 | 67 | 125 | 6 | 27 | 99 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0002 | 0/0 | 523 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0003 | 0/0 | 523 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0004 | 0/0 | 523 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0005 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0006 | 0/0 | 523 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1572 | 238 | 61 | 42 | 112 | 3 | 18 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0002 | 0/0 | 1572 | 38 | 7 | 19 | 10 | 1 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0003 | 0/0 | 1572 | 13 | 0 | 6 | 1 | 2 | 4 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0004 | 0/0 | 1572 | 10 | 8 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0005 | 0/0 | 1572 | 8 | 7 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0006 | 0/0 | 1572 | 4 | 1 | 0 | 0 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0007 | 0/0 | 1572 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0008 | 0/0 | 1572 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0009 | 0/0 | 1572 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0010 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0011 | 0/0 | 1572 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| c0012 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| 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 | 2890 | 80 | 17 | 14 | 45 | 0 | 4 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0002 | 0/1 | 2890 | 75 | 7 | 7 | 50 | 1 | 9 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0003 | 1/0 | 2890 | 40 | 5 | 15 | 14 | 2 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0004 | 0/0 | 2890 | 38 | 7 | 18 | 11 | 1 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0005 | 0/0 | 2890 | 29 | 18 | 6 | 0 | 2 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0006 | 0/0 | 2890 | 10 | 9 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0007 | 0/0 | 2890 | 5 | 4 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0008 | 0/0 | 2890 | 4 | 1 | 0 | 0 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0009 | 0/0 | 2890 | 4 | 4 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0010 | 0/0 | 2890 | 4 | 4 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0011 | 0/0 | 2890 | 4 | 1 | 1 | 0 | 0 | 2 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0012 | 0/0 | 2890 | 3 | 3 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0013 | 0/0 | 2890 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0014 | 0/0 | 2890 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0015 | 0/0 | 2890 | 2 | 1 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0016 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0017 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0018 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0019 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0020 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0021 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0022 | 0/0 | 2890 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0023 | 0/0 | 2890 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0024 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0025 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0026 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0027 | 0/0 | 2890 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0028 | 0/0 | 2890 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0029 | 0/0 | 2890 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0030 | 0/0 | 2890 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0031 | 0/0 | 2890 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0032 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| t0033 | 0/0 | 2890 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1572 | 238 | 61 | 42 | 112 | 3 | 18 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0002 | 0/0 | 1572 | 38 | 7 | 19 | 10 | 1 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0003 | 0/0 | 1572 | 13 | 0 | 6 | 1 | 2 | 4 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0004 | 0/0 | 1572 | 10 | 8 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0005 | 0/0 | 1572 | 8 | 7 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0006 | 0/0 | 1572 | 4 | 1 | 0 | 0 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0012 | 0/0 | 1572 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0002c0009 | 0/0 | 1572 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0003c0007 | 0/0 | 1572 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0004c0008 | 0/0 | 1572 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0005c0010 | 0/0 | 1572 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0006c0011 | 0/0 | 1572 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4461 | 77 | 17 | 14 | 43 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0002 | 0/1 | 4461 | 73 | 7 | 7 | 48 | 1 | 9 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0003 | 1/0 | 4461 | 40 | 5 | 15 | 14 | 2 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0005 | 0/0 | 4461 | 9 | 9 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0006 | 0/0 | 4461 | 10 | 9 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0007 | 0/0 | 4461 | 5 | 4 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0009 | 0/0 | 4461 | 4 | 4 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0011 | 0/0 | 4461 | 4 | 1 | 1 | 0 | 0 | 2 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0014 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0016 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0017 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0018 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0020 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0021 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0022 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0023 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0024 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0025 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0026 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0027 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0028 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0030 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0001t0033 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0002t0004 | 0/0 | 4461 | 37 | 7 | 18 | 10 | 1 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0002t0031 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0003t0005 | 0/0 | 4461 | 11 | 0 | 6 | 0 | 2 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0003t0019 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0003t0029 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0004t0001 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0004t0005 | 0/0 | 4461 | 8 | 8 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0005t0010 | 0/0 | 4461 | 3 | 3 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0005t0012 | 0/0 | 4461 | 3 | 3 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0005t0015 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0005t0032 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0006t0008 | 0/0 | 4461 | 4 | 1 | 0 | 0 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0001c0012t0005 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0002c0009t0002 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0003c0007t0010 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0003c0007t0015 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0004c0008t0013 | 0/0 | 4461 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0005c0010t0004 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| a0006c0011t0001 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | copy fasta | chr12 | 33369238 | 33444819 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0178 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0246 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0007g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0011g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0011g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0014g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0014g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0018g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0021g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0023g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0024g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0025g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0026g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0027g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0028g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0030g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0033g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0002t0031g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0019g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0003t0029g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0004t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0010g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0012g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0015g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0005t0032g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0006t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0006t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0006t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0006t0008g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0012t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0002c0009t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0002c0009t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0003c0007t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0003c0007t0015g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0004c0008t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0004c0008t0013g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0005c0010t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0006c0011t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00597 | hp2 | a0001 | c0001 | t0025 | g0152 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0289 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00639 | hp2 | a0001 | c0003 | t0005 | g0138 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00733 | hp1 | a0001 | c0003 | t0005 | g0131 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0285 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0293 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0292 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0290 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01081 | hp1 | a0001 | c0003 | t0005 | g0158 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0248 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01099 | hp1 | a0001 | c0003 | t0005 | g0160 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0031 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01192 | hp1 | a0001 | c0001 | t0030 | g0226 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0267 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01243 | hp2 | a0001 | c0003 | t0005 | g0137 | AMR | PUR | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01256 | hp1 | a0004 | c0008 | t0013 | g0115 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0018 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0253 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0019 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01261 | hp1 | a0001 | c0001 | t0027 | g0189 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01346 | hp1 | a0001 | c0002 | t0004 | g0261 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01346 | hp2 | a0001 | c0002 | t0004 | g0295 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0251 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01358 | hp2 | a0001 | c0002 | t0004 | g0294 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0276 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01516 | hp2 | a0001 | c0003 | t0005 | g0145 | EUR | IBS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0199 | EUR | IBS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | IBS | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0283 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0018 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01934 | hp2 | a0001 | c0003 | t0005 | g0140 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01943 | hp2 | a0001 | c0002 | t0031 | g0268 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01975 | hp1 | a0001 | c0001 | t0023 | g0061 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0275 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01978 | hp2 | a0001 | c0002 | t0004 | g0269 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0291 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02055 | hp1 | a0001 | c0004 | t0005 | g0211 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0032 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02129 | hp2 | a0001 | c0003 | t0019 | g0142 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02145 | hp2 | a0001 | c0001 | t0016 | g0025 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02148 | hp1 | a0001 | c0002 | t0004 | g0019 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CDX | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0263 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02258 | hp1 | a0001 | c0001 | t0024 | g0169 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02258 | hp2 | a0001 | c0005 | t0032 | g0260 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02273 | hp1 | a0001 | c0002 | t0004 | g0270 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02280 | hp1 | a0001 | c0001 | t0011 | g0230 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0040 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0116 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0266 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02683 | hp1 | a0006 | c0011 | t0001 | g0056 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02683 | hp2 | a0001 | c0006 | t0008 | g0024 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02698 | hp1 | a0001 | c0001 | t0011 | g0252 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02723 | hp1 | a0001 | c0004 | t0005 | g0213 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02895 | hp2 | a0001 | c0004 | t0005 | g0216 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02897 | hp1 | a0001 | c0004 | t0005 | g0210 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02922 | hp1 | a0001 | c0012 | t0005 | g0209 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0020 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02965 | hp2 | a0001 | c0004 | t0005 | g0208 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02970 | hp2 | a0001 | c0005 | t0012 | g0014 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02976 | hp2 | a0001 | c0001 | t0017 | g0026 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03098 | hp2 | a0003 | c0007 | t0015 | g0277 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03130 | hp1 | a0001 | c0004 | t0005 | g0214 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03195 | hp1 | a0001 | c0005 | t0012 | g0014 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0006 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0284 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03239 | hp1 | a0001 | c0003 | t0005 | g0143 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03453 | hp1 | a0001 | c0005 | t0010 | g0221 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03516 | hp1 | a0001 | c0001 | t0020 | g0134 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03540 | hp1 | a0001 | c0005 | t0010 | g0223 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0265 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03669 | hp2 | a0001 | c0001 | t0022 | g0089 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03688 | hp1 | a0001 | c0003 | t0005 | g0083 | SAS | STU | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03688 | hp2 | a0001 | c0005 | t0015 | g0262 | SAS | STU | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03710 | hp2 | a0001 | c0003 | t0029 | g0141 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0250 | SAS | BEB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | BEB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03942 | hp2 | a0001 | c0003 | t0005 | g0139 | SAS | BEB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | STU | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG04228 | hp2 | a0001 | c0006 | t0008 | g0023 | SAS | STU | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18522 | hp1 | a0001 | c0004 | t0005 | g0215 | AFR | YRI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18522 | hp2 | a0001 | c0005 | t0012 | g0222 | AFR | YRI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18612 | hp1 | a0001 | c0001 | t0014 | g0084 | EAS | CHB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | YRI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0264 | AFR | YRI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18941 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18967 | hp2 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18968 | hp1 | a0001 | c0001 | t0018 | g0027 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18968 | hp2 | a0001 | c0001 | t0028 | g0148 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0273 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18986 | hp2 | a0001 | c0002 | t0004 | g0278 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18989 | hp1 | a0001 | c0002 | t0004 | g0274 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18995 | hp2 | a0001 | c0001 | t0026 | g0112 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19000 | hp2 | a0001 | c0001 | t0021 | g0073 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | LWK | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19043 | hp1 | a0003 | c0007 | t0010 | g0220 | AFR | LWK | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19043 | hp2 | a0001 | c0001 | t0033 | g0296 | AFR | LWK | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19065 | hp2 | a0002 | c0009 | t0002 | g0202 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19070 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19072 | hp1 | a0001 | c0004 | t0001 | g0094 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19078 | hp1 | a0001 | c0002 | t0004 | g0271 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19082 | hp1 | a0001 | c0002 | t0004 | g0279 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19085 | hp2 | a0005 | c0010 | t0004 | g0286 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19086 | hp2 | a0002 | c0009 | t0002 | g0201 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19089 | hp2 | a0001 | c0001 | t0014 | g0183 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0020 | AFR | YRI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | YRI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA20752 | hp1 | a0001 | c0003 | t0005 | g0205 | EUR | TSI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0282 | EUR | TSI | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | GIH | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA20905 | hp2 | a0001 | c0006 | t0008 | g0021 | SAS | GIH | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02486 | hp2 | a0001 | c0006 | t0008 | g0022 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02559 | hp2 | a0001 | c0004 | t0005 | g0212 | AFR | ACB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18955 | hp2 | a0001 | c0004 | t0001 | g0098 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | USA | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA20300 | hp2 | a0004 | c0008 | t0013 | g0114 | AFR | USA | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA21309 | hp1 | a0001 | c0005 | t0010 | g0219 | AFR | LWK | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | LWK | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0178 | REF | REF | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0246 | REF | REF | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:33376888
|
G | A | 1 | a0003 | 2 | HG03098.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1514C>T | p.Ala505Val | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1811/4461 | 1514/1572 | 505/523 | chr12 | 33376888 | ||
| chr12:33379869
|
T | G | 1 | a0004 | 2 | HG01256.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1463A>C | p.His488Pro | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/7 | 1760/4461 | 1463/1572 | 488/523 | chr12 | 33379869 | ||
| chr12:33406979
|
A | G | 1 | a0005 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.887T>C | p.Phe296Ser | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/7 | 1184/4461 | 887/1572 | 296/523 | chr12 | 33406979 | ||
| chr12:33407093
|
A | C | 1 | a0006 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.773T>G | p.Leu258Arg | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/7 | 1070/4461 | 773/1572 | 258/523 | chr12 | 33407093 | ||
| chr12:33426283
|
G | C | 1 | a0002 | 2 | NA19065.hp2 NA19086.hp2 |
missense_variant | MODERATE | c.364C>G | p.Pro122Ala | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/7 | 661/4461 | 364/1572 | 122/523 | chr12 | 33426283 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:33382354
|
G | A | 4 | a0001c0002a0001c0003a0001c0012others(1): Show | 53 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
synonymous_variant | LOW | c.1365C>T | p.Tyr455Tyr | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/7 | 1662/4461 | 1365/1572 | 455/523 | chr12 | 33382354 | ||
| chr12:33385244
|
C | T | 1 | a0001c0006 | 4 | HG02486.hp2 HG02683.hp2 HG04228.hp2 others(1): Show |
synonymous_variant | LOW | c.1125G>A | p.Pro375Pro | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/7 | 1422/4461 | 1125/1572 | 375/523 | chr12 | 33385244 | ||
| chr12:33407124
|
G | A | 1 | a0004c0008 | 2 | HG01256.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.742C>T | p.Leu248Leu | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/7 | 1039/4461 | 742/1572 | 248/523 | chr12 | 33407124 | ||
| chr12:33426278
|
G | A | 2 | a0001c0004a0001c0012 | 11 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(8): Show |
synonymous_variant | LOW | c.369C>T | p.Ala123Ala | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/7 | 666/4461 | 369/1572 | 123/523 | chr12 | 33426278 | ||
| chr12:33426362
|
C | G | 4 | a0001c0002a0001c0005a0003c0007others(1): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
synonymous_variant | LOW | c.285G>C | p.Thr95Thr | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/7 | 582/4461 | 285/1572 | 95/523 | chr12 | 33426362 | ||
| chr12:33426473
|
A | T | 4 | a0001c0002a0001c0005a0003c0007others(1): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
synonymous_variant | LOW | c.174T>A | p.Ala58Ala | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/7 | 471/4461 | 174/1572 | 58/523 | chr12 | 33426473 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:33374511
|
T | G | 16 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(13): Show | 90 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2319A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 2319 | chr12 | 33374511 | |||||
| chr12:33374545
|
A | G | 1 | a0001c0001t0023 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2285T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 2285 | chr12 | 33374545 | |||||
| chr12:33374733
|
A | C | 1 | a0001c0003t0019 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2097T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 2097 | chr12 | 33374733 | |||||
| chr12:33374790
|
T | C | 1 | a0001c0001t0009 | 4 | HG01891.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2040A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 2040 | chr12 | 33374790 | |||||
| chr12:33374885
|
C | T | 1 | a0004c0008t0013 | 2 | HG01256.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1945G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1945 | chr12 | 33374885 | |||||
| chr12:33374964
|
T | C | 1 | a0001c0001t0024 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1866A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1866 | chr12 | 33374964 | |||||
| chr12:33375208
|
A | T | 2 | a0001c0001t0024a0001c0001t0033 | 2 | HG02258.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1622T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1622 | chr12 | 33375208 | |||||
| chr12:33375361
|
C | T | 1 | a0001c0001t0027 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1469 | chr12 | 33375361 | |||||
| chr12:33375403
|
T | G | 1 | a0001c0001t0020 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1427A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1427 | chr12 | 33375403 | |||||
| chr12:33375520
|
C | T | 1 | a0001c0001t0026 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 1310 | chr12 | 33375520 | |||||
| chr12:33375954
|
C | T | 1 | a0001c0001t0025 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*876G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 876 | chr12 | 33375954 | |||||
| chr12:33376064
|
A | T | 1 | a0001c0001t0006 | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*766T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 766 | chr12 | 33376064 | |||||
| chr12:33376127
|
G | A | 16 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(13): Show | 90 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*703C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 703 | chr12 | 33376127 | |||||
| chr12:33376133
|
T | G | 1 | a0001c0002t0031 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 697 | chr12 | 33376133 | |||||
| chr12:33376229
|
A | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(36): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 601 | chr12 | 33376229 | |||||
| chr12:33376278
|
C | G | 9 | a0001c0001t0001a0001c0001t0011a0001c0001t0016others(6): Show | 89 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*552G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 552 | chr12 | 33376278 | |||||
| chr12:33376328
|
C | A | 1 | a0001c0001t0028 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*502G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 502 | chr12 | 33376328 | |||||
| chr12:33376353
|
T | C | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(36): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*477A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 477 | chr12 | 33376353 | |||||
| chr12:33376416
|
C | G | 26 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(23): Show | 181 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 414 | chr12 | 33376416 | |||||
| chr12:33376552
|
C | G | 15 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(12): Show | 89 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*278G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 278 | chr12 | 33376552 | |||||
| chr12:33376603
|
C | T | 2 | a0001c0001t0021a0001c0005t0012 | 4 | HG02970.hp2 HG03195.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 227 | chr12 | 33376603 | |||||
| chr12:33376712
|
A | T | 14 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(11): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*118T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 118 | chr12 | 33376712 | |||||
| chr12:33376784
|
G | C | 1 | a0001c0003t0029 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 7/7 | 46 | chr12 | 33376784 | |||||
| chr12:33439562
|
A | G | 1 | a0001c0001t0007 | 5 | HG00741.hp1 HG02109.hp1 HG03139.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-40T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 40 | chr12 | 33439562 | |||||
| chr12:33439580
|
C | T | 1 | a0001c0001t0018 | 1 | NA18968.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 58 | chr12 | 33439580 | |||||
| chr12:33439610
|
C | T | 3 | a0001c0005t0010a0001c0005t0012a0003c0007t0010 | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-88G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 88 | chr12 | 33439610 | |||||
| chr12:33439655
|
G | C | 6 | a0001c0002t0004a0001c0002t0031a0001c0005t0015others(3): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | chr12 | 33439655 | ||||||
| chr12:33439746
|
C | G | 29 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(26): Show | 222 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(219): Show |
5_prime_UTR_variant | MODIFIER | c.-224G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 224 | chr12 | 33439746 | |||||
| chr12:33439768
|
C | T | 1 | a0001c0001t0017 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-246G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 246 | chr12 | 33439768 | |||||
| chr12:33439785
|
C | T | 1 | a0001c0001t0016 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-263G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 263 | chr12 | 33439785 | |||||
| chr12:33439811
|
G | T | 1 | a0001c0006t0008 | 4 | HG02486.hp2 HG02683.hp2 HG04228.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-289C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | 289 | chr12 | 33439811 | |||||
| chr12:33439814
|
T | A | 1 | a0001c0001t0033 | 1 | NA19043.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-292A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/7 | chr12 | 33439814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:33377157
|
A | T | 84 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(81): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1501-256T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377157 | ||||||
| chr12:33377329
|
C | A | 84 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(81): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1501-428G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377329 | ||||||
| chr12:33377547
|
G | A | 84 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(81): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1501-646C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377547 | ||||||
| chr12:33377578
|
C | G | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1501-677G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377578 | ||||||
| chr12:33377624
|
T | TTTTC | 77 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(74): Show | 80 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1501-724_1501-723i others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377624 | ||||||
| chr12:33377628
|
T | C | 9 | a0001c0001t0005g0043a0001c0001t0005g0117a0001c0001t0005g0118others(6): Show | 10 | HG00741.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1501-727A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377628 | ||||||
| chr12:33377629
|
C | CT | 45 | a0001c0001t0001g0051a0001c0001t0001g0080a0001c0001t0001g0218others(42): Show | 49 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1501-729dupA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377629 | ||||||
| chr12:33377629
|
C | CTT | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(119): Show | 133 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1501-730_1501-729d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377629 | ||||||
| chr12:33377629
|
C | T | 9 | a0001c0001t0005g0043a0001c0001t0005g0117a0001c0001t0005g0118others(6): Show | 10 | HG00741.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1501-728G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377629 | ||||||
| chr12:33377633
|
T | C | 9 | a0001c0001t0005g0043a0001c0001t0005g0117a0001c0001t0005g0118others(6): Show | 10 | HG00741.hp1 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1501-732A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377633 | ||||||
| chr12:33377633
|
T | TC | 75 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(72): Show | 78 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1501-733_1501-732i others(3): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377633 | ||||||
| chr12:33377710
|
C | A | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1501-809G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377710 | ||||||
| chr12:33377790
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(59): Show | 69 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1501-889C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377790 | ||||||
| chr12:33377872
|
C | A | 2 | a0001c0002t0004g0263a0001c0002t0004g0264 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1501-971G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377872 | ||||||
| chr12:33377906
|
T | G | 86 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(83): Show | 90 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1501-1005A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33377906 | ||||||
| chr12:33378257
|
A | G | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1501-1356T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378257 | ||||||
| chr12:33378322
|
A | T | 86 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(83): Show | 90 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1501-1421T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378322 | ||||||
| chr12:33378344
|
TAATA | T | 3 | a0001c0001t0002g0111a0001c0001t0002g0113a0001c0001t0026g0112 | 3 | NA18995.hp2 NA19007.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1501-1447_1501-144 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378344 | ||||||
| chr12:33378360
|
T | C | 50 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(47): Show | 53 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1501-1459A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378360 | ||||||
| chr12:33378376
|
G | A | 1 | a0001c0001t0007g0028 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1500+1456C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378376 | ||||||
| chr12:33378503
|
G | A | 84 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(81): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1500+1329C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378503 | ||||||
| chr12:33378814
|
C | CTG | 29 | a0001c0001t0001g0048a0001c0001t0001g0144a0001c0001t0001g0217others(26): Show | 31 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1500+1016_1500+101 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378814 | ||||||
| chr12:33378814
|
C | CTGTG | 3 | a0001c0001t0001g0103a0001c0001t0002g0176a0001c0001t0002g0179 | 3 | HG02132.hp2 HG03704.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1500+1014_1500+101 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378814 | ||||||
| chr12:33378814
|
CTG | C | 24 | a0001c0001t0001g0091a0001c0001t0003g0224a0001c0001t0003g0242others(21): Show | 25 | HG00741.hp1 HG01169.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.1500+1016_1500+101 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378814 | ||||||
| chr12:33378814
|
CTGTG | C | 33 | a0001c0001t0001g0068a0001c0001t0001g0132a0001c0001t0005g0117others(30): Show | 36 | HG00639.hp2 HG00733.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1500+1014_1500+101 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378814 | ||||||
| chr12:33378814
|
CTGTGTG | C | 40 | a0001c0001t0006g0040a0001c0001t0007g0030a0001c0001t0030g0226others(37): Show | 41 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1500+1012_1500+101 others(10): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378814 | ||||||
| chr12:33378832
|
GTGTGTGT others(23): Show |
G | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1500+970_1500+999d others(32): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378832 | ||||||
| chr12:33378948
|
T | C | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1500+884A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33378948 | ||||||
| chr12:33379195
|
G | GTTTACCA others(136): Show |
1 | a0001c0001t0014g0183 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1500+494_1500+636d others(145): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379195 | ||||||
| chr12:33379297
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1500+535C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379297 | ||||||
| chr12:33379313
|
C | G | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1500+519G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379313 | ||||||
| chr12:33379383
|
C | T | 84 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(81): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1500+449G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379383 | ||||||
| chr12:33379549
|
C | CA | 36 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0048others(33): Show | 37 | HG00544.hp2 HG00621.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1500+282dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379549 | ||||||
| chr12:33379549
|
C | CAA | 11 | a0001c0001t0001g0049a0001c0001t0001g0067a0001c0001t0001g0071others(8): Show | 11 | HG01346.hp1 HG01981.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.1500+281_1500+282d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379549 | ||||||
| chr12:33379549
|
CA | C | 88 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0108others(85): Show | 96 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1500+282delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379549 | ||||||
| chr12:33379549
|
CAA | C | 7 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0003g0004others(4): Show | 10 | HG01069.hp2 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+281_1500+282d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379549 | ||||||
| chr12:33379549
|
CAAAAAAA others(5): Show |
C | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1500+271_1500+282d others(14): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379549 | ||||||
| chr12:33379565
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0006g0040 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1500+251_1500+266d others(18): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379565 | ||||||
| chr12:33379578
|
AAAG | A | 11 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(8): Show | 11 | HG01192.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1500+251_1500+253d others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379578 | ||||||
| chr12:33379579
|
AAG | A | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+251_1500+252d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379579 | ||||||
| chr12:33379580
|
AG | A | 9 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(6): Show | 10 | HG00741.hp1 HG02109.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1500+251delC | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379580 | ||||||
| chr12:33379581
|
G | A | 53 | a0001c0001t0005g0043a0001c0001t0005g0120a0001c0001t0005g0121others(50): Show | 56 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1500+251C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379581 | ||||||
| chr12:33379629
|
T | G | 84 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(81): Show | 88 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.1500+203A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379629 | ||||||
| chr12:33379657
|
A | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1500+175T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379657 | ||||||
| chr12:33379730
|
C | T | 20 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0085others(17): Show | 22 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1500+102G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379730 | ||||||
| chr12:33379785
|
C | T | 5 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG02818.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1500+47G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 6/6 | chr12 | 33379785 | ||||||
| chr12:33380088
|
C | T | 24 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(21): Show | 25 | HG00741.hp1 HG01192.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1371-127G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380088 | ||||||
| chr12:33380106
|
C | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1371-145G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380106 | ||||||
| chr12:33380133
|
C | G | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1371-172G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380133 | ||||||
| chr12:33380191
|
C | T | 1 | a0001c0002t0004g0261 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1371-230G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380191 | ||||||
| chr12:33380195
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1371-234C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380195 | ||||||
| chr12:33380218
|
A | C | 3 | a0001c0001t0002g0010a0001c0001t0002g0129a0001c0001t0002g0130 | 4 | HG01106.hp2 HG03491.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371-257T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380218 | ||||||
| chr12:33380363
|
A | G | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1371-402T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380363 | ||||||
| chr12:33380439
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.1371-478G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380439 | ||||||
| chr12:33380533
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(78): Show | 89 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1371-572G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380533 | ||||||
| chr12:33380564
|
C | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(78): Show | 89 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1371-603G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380564 | ||||||
| chr12:33380577
|
A | G | 23 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(20): Show | 25 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1371-616T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380577 | ||||||
| chr12:33380757
|
G | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1371-796C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380757 | ||||||
| chr12:33380900
|
A | G | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1371-939T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380900 | ||||||
| chr12:33380980
|
A | G | 1 | a0001c0001t0002g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1371-1019T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380980 | ||||||
| chr12:33380984
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1371-1023A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33380984 | ||||||
| chr12:33381006
|
G | C | 26 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0265others(23): Show | 28 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1371-1045C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381006 | ||||||
| chr12:33381192
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1370+1157G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381192 | ||||||
| chr12:33381202
|
T | C | 4 | a0001c0001t0003g0242a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG01109.hp2 HG01261.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370+1147A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381202 | ||||||
| chr12:33381320
|
C | A | 1 | a0001c0001t0016g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1370+1029G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381320 | ||||||
| chr12:33381361
|
T | C | 75 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(72): Show | 78 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1370+988A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381361 | ||||||
| chr12:33381419
|
G | T | 1 | a0001c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+930C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381419 | ||||||
| chr12:33381433
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.1370+916A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381433 | ||||||
| chr12:33381516
|
T | C | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1370+833A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381516 | ||||||
| chr12:33381710
|
G | T | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1370+639C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381710 | ||||||
| chr12:33381770
|
A | G | 86 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0012others(83): Show | 93 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1370+579T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381770 | ||||||
| chr12:33381860
|
A | G | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1370+489T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381860 | ||||||
| chr12:33381873
|
C | A | 47 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(44): Show | 50 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1370+476G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381873 | ||||||
| chr12:33381884
|
C | A | 10 | a0001c0001t0005g0043a0001c0001t0005g0117a0001c0001t0005g0118others(7): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1370+465G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381884 | ||||||
| chr12:33381903
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1370+446C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381903 | ||||||
| chr12:33381924
|
A | T | 75 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(72): Show | 78 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1370+425T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381924 | ||||||
| chr12:33381936
|
G | C | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1370+413C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381936 | ||||||
| chr12:33381953
|
T | C | 10 | a0001c0001t0007g0030a0001c0001t0030g0226a0001c0004t0005g0208others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370+396A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33381953 | ||||||
| chr12:33382045
|
G | A | 1 | a0001c0012t0005g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1370+304C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33382045 | ||||||
| chr12:33382052
|
G | A | 75 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(72): Show | 78 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.1370+297C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33382052 | ||||||
| chr12:33382122
|
G | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1370+227C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33382122 | ||||||
| chr12:33382274
|
T | C | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1370+75A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33382274 | ||||||
| chr12:33382313
|
A | G | 10 | a0001c0001t0005g0043a0001c0001t0005g0117a0001c0001t0005g0118others(7): Show | 11 | HG00741.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1370+36T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 5/6 | chr12 | 33382313 | ||||||
| chr12:33382575
|
T | G | 91 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0012others(88): Show | 98 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1199-55A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33382575 | ||||||
| chr12:33382885
|
A | G | 10 | a0001c0001t0007g0030a0001c0001t0030g0226a0001c0004t0005g0208others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1199-365T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33382885 | ||||||
| chr12:33382921
|
C | A | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1199-401G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33382921 | ||||||
| chr12:33383104
|
A | C | 3 | a0001c0001t0007g0005a0001c0001t0007g0028a0001c0001t0007g0029 | 4 | HG00741.hp1 HG02109.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1199-584T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383104 | ||||||
| chr12:33383158
|
T | G | 47 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(44): Show | 50 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1199-638A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383158 | ||||||
| chr12:33383293
|
AT | A | 50 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(47): Show | 53 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1199-774delA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383293 | ||||||
| chr12:33383493
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1199-973G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383493 | ||||||
| chr12:33383513
|
G | A | 50 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(47): Show | 53 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1199-993C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383513 | ||||||
| chr12:33383637
|
C | A | 48 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0013others(45): Show | 51 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1199-1117G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383637 | ||||||
| chr12:33383716
|
C | T | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1199-1196G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383716 | ||||||
| chr12:33383720
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1199-1200T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383720 | ||||||
| chr12:33383821
|
C | T | 1 | a0002c0009t0002g0201 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1199-1301G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33383821 | ||||||
| chr12:33384054
|
G | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1198+1117C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384054 | ||||||
| chr12:33384398
|
T | C | 4 | a0001c0002t0004g0282a0001c0002t0004g0289a0001c0002t0004g0290others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198+773A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384398 | ||||||
| chr12:33384405
|
T | C | 1 | a0001c0001t0020g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1198+766A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384405 | ||||||
| chr12:33384422
|
T | C | 3 | a0001c0001t0002g0111a0001c0001t0002g0113a0001c0001t0026g0112 | 3 | NA18995.hp2 NA19007.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1198+749A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384422 | ||||||
| chr12:33384452
|
T | C | 108 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0013others(105): Show | 116 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.1198+719A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384452 | ||||||
| chr12:33384907
|
T | C | 1 | a0001c0002t0004g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1198+264A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384907 | ||||||
| chr12:33384958
|
A | G | 43 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(40): Show | 45 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198+213T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 4/6 | chr12 | 33384958 | ||||||
| chr12:33385679
|
C | G | 1 | a0001c0001t0002g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1078-388G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33385679 | ||||||
| chr12:33385795
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1078-504A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33385795 | ||||||
| chr12:33385859
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0204 | 2 | HG02132.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1078-568T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33385859 | ||||||
| chr12:33386025
|
G | A | 1 | a0001c0003t0005g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1078-734C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386025 | ||||||
| chr12:33386051
|
T | G | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-760A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386051 | ||||||
| chr12:33386055
|
G | A | 10 | a0001c0001t0007g0030a0001c0001t0030g0226a0001c0004t0005g0208others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-764C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386055 | ||||||
| chr12:33386163
|
G | A | 8 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(5): Show | 8 | HG00738.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-872C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386163 | ||||||
| chr12:33386280
|
A | G | 1 | a0001c0012t0005g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1078-989T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386280 | ||||||
| chr12:33386325
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1078-1034G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386325 | ||||||
| chr12:33386331
|
G | C | 1 | a0001c0001t0003g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1078-1040C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386331 | ||||||
| chr12:33386343
|
T | C | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-1052A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386343 | ||||||
| chr12:33386410
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1078-1119A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386410 | ||||||
| chr12:33386549
|
A | G | 3 | a0001c0001t0002g0171a0001c0001t0002g0196a0001c0001t0002g0198 | 3 | HG02148.hp2 HG02293.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1078-1258T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386549 | ||||||
| chr12:33386558
|
A | AACTC | 2 | a0001c0001t0002g0013a0001c0001t0002g0190 | 3 | NA18967.hp1 NA18969.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1078-1271_1078-126 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386558 | ||||||
| chr12:33386908
|
C | T | 1 | a0001c0005t0010g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1078-1617G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386908 | ||||||
| chr12:33386997
|
A | C | 23 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(20): Show | 25 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1078-1706T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33386997 | ||||||
| chr12:33387747
|
G | GTTT | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(137): Show | 151 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.1078-2459_1078-245 others(7): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33387747 | ||||||
| chr12:33387747
|
G | GTTTT | 39 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0066others(36): Show | 42 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1078-2460_1078-245 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33387747 | ||||||
| chr12:33387747
|
G | GTTTTT | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0048others(8): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-2461_1078-245 others(9): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33387747 | ||||||
| chr12:33387753
|
T | TG | 48 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(45): Show | 51 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-2463_1078-246 others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33387753 | ||||||
| chr12:33388066
|
G | A | 23 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(20): Show | 25 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1078-2775C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388066 | ||||||
| chr12:33388112
|
C | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-2821G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388112 | ||||||
| chr12:33388121
|
TA | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(190): Show | 209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1078-2831delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388121 | ||||||
| chr12:33388167
|
T | A | 49 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(46): Show | 52 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1078-2876A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388167 | ||||||
| chr12:33388328
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(169): Show | 185 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.1078-3037C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388328 | ||||||
| chr12:33388335
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(169): Show | 185 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.1078-3044G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388335 | ||||||
| chr12:33388410
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1078-3119C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388410 | ||||||
| chr12:33388447
|
T | C | 7 | a0001c0001t0002g0010a0001c0001t0002g0129a0001c0001t0002g0130others(4): Show | 8 | HG01106.hp2 HG02300.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-3156A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388447 | ||||||
| chr12:33388531
|
T | G | 1 | a0001c0002t0004g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1078-3240A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388531 | ||||||
| chr12:33388539
|
A | G | 1 | a0001c0001t0002g0200 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1078-3248T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388539 | ||||||
| chr12:33388631
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1078-3340G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388631 | ||||||
| chr12:33388757
|
T | C | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1078-3466A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388757 | ||||||
| chr12:33388903
|
C | G | 1 | a0001c0001t0001g0064 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1078-3612G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388903 | ||||||
| chr12:33388953
|
A | T | 23 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(20): Show | 25 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.1078-3662T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388953 | ||||||
| chr12:33389006
|
G | A | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-3715C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33389006 | ||||||
| chr12:33389136
|
C | T | 21 | a0001c0001t0005g0043a0001c0001t0005g0117a0001c0001t0005g0118others(18): Show | 24 | HG00741.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1078-3845G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33389136 | ||||||
| chr12:33389549
|
C | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-4258G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33389549 | ||||||
| chr12:33390083
|
A | T | 8 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(5): Show | 8 | HG00738.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-4792T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390083 | ||||||
| chr12:33390085
|
A | G | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-4794T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390085 | ||||||
| chr12:33390089
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.1078-4798A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390089 | ||||||
| chr12:33390157
|
C | T | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078-4866G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390157 | ||||||
| chr12:33390187
|
C | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0106others(13): Show | 17 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-4896G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390187 | ||||||
| chr12:33390273
|
A | C | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1078-4982T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390273 | ||||||
| chr12:33390285
|
C | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-4994G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390285 | ||||||
| chr12:33390304
|
G | C | 1 | a0001c0001t0020g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-5013C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390304 | ||||||
| chr12:33390432
|
C | T | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078-5141G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390432 | ||||||
| chr12:33390521
|
T | C | 1 | a0001c0001t0003g0243 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1078-5230A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390521 | ||||||
| chr12:33390565
|
C | CCT | 22 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(19): Show | 24 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1078-5276_1078-527 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390565 | ||||||
| chr12:33390568
|
C | CTA | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(168): Show | 185 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.1078-5279_1078-527 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390568 | ||||||
| chr12:33390625
|
G | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-5334C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390625 | ||||||
| chr12:33390665
|
T | TAC | 8 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(5): Show | 9 | HG00741.hp1 HG02109.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-5376_1078-537 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390665 | ||||||
| chr12:33390918
|
T | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1078-5627A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390918 | ||||||
| chr12:33390929
|
T | G | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1078-5638A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390929 | ||||||
| chr12:33390929
|
T | TTTG | 21 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0085others(18): Show | 23 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1078-5641_1078-563 others(7): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390929 | ||||||
| chr12:33390932
|
G | T | 30 | a0001c0001t0005g0043a0001c0001t0006g0031a0001c0001t0006g0032others(27): Show | 31 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1078-5641C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390932 | ||||||
| chr12:33390935
|
G | T | 3 | a0001c0001t0009g0006a0001c0001t0009g0044a0001c0001t0009g0116 | 4 | HG01891.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-5644C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390935 | ||||||
| chr12:33390993
|
C | T | 1 | a0001c0006t0008g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1078-5702G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33390993 | ||||||
| chr12:33391071
|
G | T | 1 | a0001c0001t0002g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1078-5780C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391071 | ||||||
| chr12:33391093
|
A | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-5802T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391093 | ||||||
| chr12:33391217
|
G | A | 2 | a0001c0001t0005g0120a0001c0001t0005g0121 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-5926C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391217 | ||||||
| chr12:33391236
|
C | CT | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-5946dupA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391236 | ||||||
| chr12:33391242
|
A | T | 60 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(57): Show | 63 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1078-5951T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391242 | ||||||
| chr12:33391251
|
TA | T | 9 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0269others(6): Show | 11 | HG01256.hp2 HG01258.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078-5961delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391251 | ||||||
| chr12:33391381
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1078-6090A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391381 | ||||||
| chr12:33391736
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(136): Show | 150 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.1078-6445G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391736 | ||||||
| chr12:33391855
|
G | C | 10 | a0001c0001t0030g0226a0001c0004t0005g0208a0001c0004t0005g0210others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-6564C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391855 | ||||||
| chr12:33391891
|
A | G | 1 | a0001c0001t0006g0031 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1078-6600T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391891 | ||||||
| chr12:33392200
|
A | C | 1 | a0001c0002t0004g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1078-6909T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392200 | ||||||
| chr12:33392402
|
C | T | 1 | a0001c0001t0006g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1078-7111G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392402 | ||||||
| chr12:33392420
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(191): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-7129C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392420 | ||||||
| chr12:33392581
|
T | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(192): Show | 211 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.1078-7290A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392581 | ||||||
| chr12:33392673
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(193): Show | 212 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.1078-7382A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392673 | ||||||
| chr12:33392913
|
T | A | 1 | a0001c0001t0011g0251 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1078-7622A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392913 | ||||||
| chr12:33392969
|
T | C | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1078-7678A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392969 | ||||||
| chr12:33392979
|
T | C | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1078-7688A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392979 | ||||||
| chr12:33392985
|
T | TA | 15 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0105others(12): Show | 17 | HG00735.hp1 HG01516.hp1 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-7695dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAA | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0051others(32): Show | 39 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1078-7696_1078-769 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAA | 35 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(32): Show | 38 | HG00544.hp2 HG00621.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1078-7697_1078-769 others(7): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAA | 30 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0048others(27): Show | 32 | HG01106.hp2 HG01109.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1078-7698_1078-769 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAA | 24 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0144others(21): Show | 25 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.1078-7699_1078-769 others(9): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAA | 16 | a0001c0001t0001g0011a0001c0001t0001g0165a0001c0001t0001g0166others(13): Show | 17 | HG01175.hp2 HG01256.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-7700_1078-769 others(10): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA | 12 | a0001c0001t0001g0167a0001c0001t0002g0102a0001c0001t0002g0113others(9): Show | 12 | HG00544.hp1 HG00642.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.1078-7701_1078-769 others(11): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(2): Show |
7 | a0001c0001t0005g0033a0001c0001t0005g0118a0001c0001t0005g0120others(4): Show | 7 | HG01884.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-7703_1078-769 others(13): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(3): Show |
5 | a0001c0001t0005g0034a0001c0001t0005g0117a0001c0001t0005g0119others(2): Show | 6 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-7704_1078-769 others(14): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(4): Show |
10 | a0001c0001t0002g0054a0001c0001t0002g0147a0001c0001t0007g0005others(7): Show | 11 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1078-7705_1078-769 others(15): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(5): Show |
6 | a0001c0001t0002g0157a0001c0001t0007g0028a0001c0001t0028g0148others(3): Show | 6 | HG00438.hp1 HG01358.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-7706_1078-769 others(16): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(6): Show |
9 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0002t0004g0264others(6): Show | 9 | HG00639.hp1 HG01346.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-7707_1078-769 others(17): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(7): Show |
11 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0088others(8): Show | 13 | HG01074.hp2 NA18612.hp1 NA18945.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-7708_1078-769 others(18): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(8): Show |
6 | a0001c0001t0002g0086a0001c0001t0002g0153a0001c0001t0002g0154others(3): Show | 6 | HG00597.hp2 HG02155.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-7709_1078-769 others(19): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(9): Show |
3 | a0001c0001t0002g0085a0001c0001t0002g0128a0001c0001t0002g0155 | 3 | HG00621.hp1 HG02523.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1078-7710_1078-769 others(20): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(11): Show |
1 | a0001c0001t0002g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1078-7712_1078-769 others(22): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
T | TAAAAAAA others(13): Show |
1 | a0001c0001t0002g0146 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1078-7714_1078-769 others(24): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
TA | T | 7 | a0001c0001t0003g0004a0001c0001t0003g0224a0001c0001t0003g0235others(4): Show | 9 | HG01069.hp2 HG01496.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078-7695delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
TAAAA | T | 7 | a0001c0001t0009g0044a0001c0001t0009g0116a0001c0003t0005g0137others(4): Show | 8 | HG01243.hp2 HG02129.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1078-7698_1078-769 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
TAAAAA | T | 10 | a0001c0002t0004g0269a0001c0002t0004g0272a0001c0003t0005g0131others(7): Show | 10 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1078-7699_1078-769 others(9): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33392985
|
TAAAAAA | T | 17 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0265others(14): Show | 19 | HG01256.hp2 HG01258.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.1078-7700_1078-769 others(10): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392985 | ||||||
| chr12:33393063
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | NA18953.hp1 NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1078-7772C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393063 | ||||||
| chr12:33393371
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(62): Show | 72 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1078-8080A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393371 | ||||||
| chr12:33393622
|
G | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-8331C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393622 | ||||||
| chr12:33393644
|
CA | C | 49 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(46): Show | 52 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1078-8354delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393644 | ||||||
| chr12:33393650
|
C | G | 49 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(46): Show | 52 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1078-8359G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393650 | ||||||
| chr12:33393703
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1078-8412G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393703 | ||||||
| chr12:33393721
|
C | T | 1 | a0001c0001t0022g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1078-8430G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393721 | ||||||
| chr12:33393845
|
G | A | 4 | a0001c0001t0003g0242a0001c0001t0003g0243a0001c0001t0003g0244others(1): Show | 4 | HG01109.hp2 HG01261.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-8554C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393845 | ||||||
| chr12:33393856
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1078-8565A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393856 | ||||||
| chr12:33393858
|
C | G | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-8567G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393858 | ||||||
| chr12:33393880
|
T | C | 3 | a0001c0001t0009g0006a0001c0001t0009g0044a0001c0001t0009g0116 | 4 | HG01891.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-8589A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393880 | ||||||
| chr12:33393890
|
C | T | 1 | a0001c0005t0032g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1078-8599G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393890 | ||||||
| chr12:33393940
|
G | C | 1 | a0001c0001t0002g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1078-8649C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393940 | ||||||
| chr12:33393991
|
T | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(196): Show | 215 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-8700A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393991 | ||||||
| chr12:33394032
|
C | T | 48 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0013others(45): Show | 51 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-8741G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394032 | ||||||
| chr12:33394035
|
C | T | 46 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(43): Show | 49 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1078-8744G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394035 | ||||||
| chr12:33394043
|
A | G | 1 | a0001c0001t0023g0061 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1078-8752T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394043 | ||||||
| chr12:33394139
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | NA18960.hp1 NA18977.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1078-8848C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394139 | ||||||
| chr12:33394301
|
T | C | 10 | a0001c0001t0030g0226a0001c0004t0005g0208a0001c0004t0005g0210others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-9010A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394301 | ||||||
| chr12:33394306
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(196): Show | 215 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-9015T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394306 | ||||||
| chr12:33394460
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 276 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1078-9169A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394460 | ||||||
| chr12:33394817
|
G | A | 48 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(45): Show | 51 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-9526C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394817 | ||||||
| chr12:33394948
|
C | T | 48 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(45): Show | 51 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-9657G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394948 | ||||||
| chr12:33394955
|
G | A | 48 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(45): Show | 51 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-9664C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394955 | ||||||
| chr12:33394981
|
G | A | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-9690C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394981 | ||||||
| chr12:33394984
|
A | T | 1 | a0001c0002t0031g0268 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1078-9693T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394984 | ||||||
| chr12:33394996
|
G | A | 48 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(45): Show | 51 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1078-9705C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394996 | ||||||
| chr12:33395002
|
G | A | 17 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(14): Show | 18 | HG00738.hp1 HG00741.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1078-9711C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395002 | ||||||
| chr12:33395062
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1078-9771A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395062 | ||||||
| chr12:33395066
|
C | T | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1078-9775G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395066 | ||||||
| chr12:33395069
|
C | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-9778G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395069 | ||||||
| chr12:33395082
|
C | T | 13 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-9791G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395082 | ||||||
| chr12:33395229
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1078-9938C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395229 | ||||||
| chr12:33395305
|
C | G | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1078-10014G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395305 | ||||||
| chr12:33395416
|
A | T | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1078-10125T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395416 | ||||||
| chr12:33395544
|
A | G | 15 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(12): Show | 16 | HG00738.hp1 HG00741.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-10253T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395544 | ||||||
| chr12:33395595
|
C | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(244): Show | 266 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.1078-10304G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395595 | ||||||
| chr12:33395688
|
A | G | 20 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(17): Show | 20 | HG01169.hp2 HG01192.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1078-10397T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395688 | ||||||
| chr12:33395753
|
A | G | 2 | a0001c0002t0004g0271a0001c0002t0004g0273 | 2 | NA18970.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1078-10462T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395753 | ||||||
| chr12:33395868
|
C | CATT | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(196): Show | 215 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-10580_1078-10 others(9): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395868 | ||||||
| chr12:33395899
|
A | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(196): Show | 215 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-10608T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33395899 | ||||||
| chr12:33396496
|
T | A | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+10293A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33396496 | ||||||
| chr12:33396715
|
C | T | 1 | a0001c0001t0006g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1077+10074G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33396715 | ||||||
| chr12:33396928
|
G | A | 48 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(45): Show | 51 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.1077+9861C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33396928 | ||||||
| chr12:33396939
|
A | G | 1 | a0001c0003t0005g0138 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1077+9850T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33396939 | ||||||
| chr12:33397061
|
G | C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(207): Show | 226 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1077+9728C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397061 | ||||||
| chr12:33397306
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(206): Show | 225 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1077+9483A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397306 | ||||||
| chr12:33397430
|
C | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(208): Show | 227 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1077+9359G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397430 | ||||||
| chr12:33397433
|
T | A | 4 | a0001c0001t0006g0032a0001c0001t0006g0040a0001c0001t0006g0041others(1): Show | 4 | HG02055.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+9356A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397433 | ||||||
| chr12:33397602
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+9187G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397602 | ||||||
| chr12:33397603
|
T | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+9186A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397603 | ||||||
| chr12:33397624
|
C | G | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1077+9165G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397624 | ||||||
| chr12:33397831
|
T | C | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+8958A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397831 | ||||||
| chr12:33398015
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1077+8774T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398015 | ||||||
| chr12:33398151
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1077+8638G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398151 | ||||||
| chr12:33398240
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(127): Show | 141 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1077+8549C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398240 | ||||||
| chr12:33398241
|
C | T | 1 | a0001c0001t0002g0184 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1077+8548G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398241 | ||||||
| chr12:33398284
|
C | T | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+8505G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398284 | ||||||
| chr12:33398285
|
G | A | 1 | a0001c0002t0004g0270 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1077+8504C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398285 | ||||||
| chr12:33398350
|
A | T | 3 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0217 | 5 | HG00597.hp1 HG02071.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+8439T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398350 | ||||||
| chr12:33398372
|
G | A | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+8417C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398372 | ||||||
| chr12:33398373
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+8416G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398373 | ||||||
| chr12:33398445
|
G | A | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1077+8344C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398445 | ||||||
| chr12:33398464
|
G | A | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1077+8325C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398464 | ||||||
| chr12:33398579
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0018g0027 | 2 | NA18968.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1077+8210T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398579 | ||||||
| chr12:33398628
|
C | T | 1 | a0001c0001t0005g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1077+8161G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398628 | ||||||
| chr12:33398723
|
AC | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(208): Show | 227 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.1077+8065delG | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398723 | ||||||
| chr12:33398843
|
T | C | 2 | a0001c0001t0009g0006a0001c0001t0009g0044 | 3 | HG01891.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1077+7946A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398843 | ||||||
| chr12:33398893
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1077+7896C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398893 | ||||||
| chr12:33398906
|
G | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 276 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1077+7883C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398906 | ||||||
| chr12:33398911
|
A | G | 12 | a0001c0003t0005g0131a0001c0003t0005g0137a0001c0003t0005g0138others(9): Show | 12 | HG00639.hp2 HG00733.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1077+7878T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398911 | ||||||
| chr12:33398983
|
G | A | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1077+7806C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398983 | ||||||
| chr12:33399682
|
A | G | 2 | a0001c0001t0009g0006a0001c0001t0009g0044 | 3 | HG01891.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1077+7107T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33399682 | ||||||
| chr12:33399698
|
T | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+7091A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33399698 | ||||||
| chr12:33399779
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1077+7010A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33399779 | ||||||
| chr12:33400051
|
C | A | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+6738G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400051 | ||||||
| chr12:33400264
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(127): Show | 141 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1077+6525C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400264 | ||||||
| chr12:33400414
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077+6375G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400414 | ||||||
| chr12:33400513
|
A | G | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+6276T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400513 | ||||||
| chr12:33400578
|
C | CA | 35 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(32): Show | 38 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1077+6210dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400578 | ||||||
| chr12:33400589
|
A | AAT | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(145): Show | 159 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.1077+6199_1077+620 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400589 | ||||||
| chr12:33400589
|
A | AT | 73 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(70): Show | 78 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1077+6199dupA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400589 | ||||||
| chr12:33400639
|
A | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 276 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1077+6150T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400639 | ||||||
| chr12:33400717
|
T | C | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+6072A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400717 | ||||||
| chr12:33400761
|
C | T | 14 | a0001c0001t0002g0003a0001c0001t0002g0128a0001c0001t0002g0146others(11): Show | 16 | HG00597.hp2 HG00621.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+6028G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400761 | ||||||
| chr12:33400837
|
C | T | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1077+5952G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400837 | ||||||
| chr12:33400843
|
C | T | 1 | a0001c0001t0006g0031 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1077+5946G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400843 | ||||||
| chr12:33400846
|
T | C | 13 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0265others(10): Show | 15 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+5943A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400846 | ||||||
| chr12:33400932
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 276 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.1077+5857C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33400932 | ||||||
| chr12:33401026
|
C | CA | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(107): Show | 120 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1077+5762dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33401026 | ||||||
| chr12:33401026
|
CA | C | 16 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(13): Show | 16 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+5762delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33401026 | ||||||
| chr12:33401146
|
T | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+5643A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33401146 | ||||||
| chr12:33401362
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+5427A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33401362 | ||||||
| chr12:33401522
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1077+5267T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33401522 | ||||||
| chr12:33402329
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(292): Show | 319 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.1077+4460T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402329 | ||||||
| chr12:33402534
|
A | C | 35 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(32): Show | 39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1077+4255T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402534 | ||||||
| chr12:33402618
|
C | G | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+4171G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402618 | ||||||
| chr12:33402787
|
C | T | 25 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(22): Show | 27 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.1077+4002G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402787 | ||||||
| chr12:33402849
|
C | T | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+3940G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402849 | ||||||
| chr12:33402910
|
G | C | 2 | a0001c0002t0004g0271a0001c0002t0004g0273 | 2 | NA18970.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1077+3879C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402910 | ||||||
| chr12:33402937
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+3852T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402937 | ||||||
| chr12:33402952
|
T | A | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1077+3837A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402952 | ||||||
| chr12:33402972
|
A | G | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1077+3817T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33402972 | ||||||
| chr12:33403014
|
T | C | 1 | a0003c0007t0015g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1077+3775A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403014 | ||||||
| chr12:33403078
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1077+3711T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403078 | ||||||
| chr12:33403233
|
CT | C | 15 | a0001c0001t0002g0003a0001c0001t0002g0128a0001c0001t0002g0147others(12): Show | 17 | HG00597.hp2 HG00621.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077+3555delA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403233 | ||||||
| chr12:33403233
|
CTT | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(203): Show | 220 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.1077+3554_1077+355 others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403233 | ||||||
| chr12:33403398
|
A | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 9 | HG01175.hp2 HG02280.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1077+3391T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403398 | ||||||
| chr12:33403422
|
G | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(157): Show | 171 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.1077+3367C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403422 | ||||||
| chr12:33403483
|
C | G | 1 | a0001c0001t0002g0184 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1077+3306G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403483 | ||||||
| chr12:33403716
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1077+3073C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403716 | ||||||
| chr12:33403782
|
A | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+3007T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403782 | ||||||
| chr12:33403785
|
C | T | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+3004G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403785 | ||||||
| chr12:33403789
|
A | AT | 6 | a0001c0001t0033g0296a0001c0005t0010g0219a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+2999dupA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403789 | ||||||
| chr12:33403789
|
AT | A | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1077+2999delA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403789 | ||||||
| chr12:33403926
|
A | T | 1 | a0001c0002t0004g0265 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1077+2863T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33403926 | ||||||
| chr12:33404119
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1077+2670A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404119 | ||||||
| chr12:33404123
|
C | T | 13 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1077+2666G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404123 | ||||||
| chr12:33404135
|
C | G | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1077+2654G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404135 | ||||||
| chr12:33404204
|
T | G | 10 | a0001c0001t0030g0226a0001c0004t0005g0208a0001c0004t0005g0210others(7): Show | 10 | HG01192.hp1 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+2585A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404204 | ||||||
| chr12:33404211
|
T | C | 1 | a0001c0002t0004g0272 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1077+2578A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404211 | ||||||
| chr12:33404225
|
T | G | 2 | a0001c0001t0009g0006a0001c0001t0009g0044 | 3 | HG01891.hp2 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1077+2564A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404225 | ||||||
| chr12:33404289
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+2500G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404289 | ||||||
| chr12:33404422
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(1): Show | 4 | HG02451.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+2367C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404422 | ||||||
| chr12:33404470
|
C | T | 1 | a0001c0001t0003g0015 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1077+2319G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404470 | ||||||
| chr12:33404477
|
C | T | 4 | a0001c0001t0002g0100a0001c0001t0002g0101a0002c0009t0002g0201others(1): Show | 4 | HG00408.hp2 HG02083.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+2312G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404477 | ||||||
| chr12:33404672
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+2117T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404672 | ||||||
| chr12:33404835
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1077+1954T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404835 | ||||||
| chr12:33404916
|
CCAAA | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+1869_1077+187 others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33404916 | ||||||
| chr12:33405018
|
TA | T | 11 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(8): Show | 11 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1077+1770delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33405018 | ||||||
| chr12:33405125
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1077+1664A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33405125 | ||||||
| chr12:33405312
|
G | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(70): Show | 81 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1077+1477C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33405312 | ||||||
| chr12:33405785
|
A | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+1004T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33405785 | ||||||
| chr12:33405833
|
T | C | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+956A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33405833 | ||||||
| chr12:33405859
|
G | GA | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(219): Show | 238 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.1077+929dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33405859 | ||||||
| chr12:33406335
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1077+454G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406335 | ||||||
| chr12:33406462
|
A | G | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1077+327T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406462 | ||||||
| chr12:33406540
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+249C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406540 | ||||||
| chr12:33406589
|
C | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+200G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406589 | ||||||
| chr12:33406644
|
A | G | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.1077+145T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406644 | ||||||
| chr12:33406658
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.1077+131A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406658 | ||||||
| chr12:33406738
|
T | C | 14 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(11): Show | 15 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1077+51A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406738 | ||||||
| chr12:33407821
|
G | A | 13 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.510-465C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33407821 | ||||||
| chr12:33407834
|
T | C | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.510-478A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33407834 | ||||||
| chr12:33407843
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.510-487G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33407843 | ||||||
| chr12:33407859
|
C | T | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-503G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33407859 | ||||||
| chr12:33407938
|
A | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 276 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.510-582T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33407938 | ||||||
| chr12:33408185
|
A | T | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.510-829T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408185 | ||||||
| chr12:33408221
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.510-865T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408221 | ||||||
| chr12:33408227
|
A | C | 5 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0135others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-871T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408227 | ||||||
| chr12:33408441
|
T | C | 2 | a0001c0001t0005g0120a0001c0001t0005g0121 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.510-1085A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408441 | ||||||
| chr12:33408461
|
T | A | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.510-1105A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408461 | ||||||
| chr12:33408534
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.510-1178C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408534 | ||||||
| chr12:33408594
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.510-1238G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408594 | ||||||
| chr12:33408723
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.510-1367G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408723 | ||||||
| chr12:33408808
|
C | CTGACAAT others(17): Show |
7 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(4): Show | 8 | HG02970.hp2 HG03098.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-1476_510-1453d others(26): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408808 | ||||||
| chr12:33408842
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.510-1486G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408842 | ||||||
| chr12:33408936
|
A | T | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.510-1580T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408936 | ||||||
| chr12:33408973
|
C | T | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.510-1617G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33408973 | ||||||
| chr12:33409031
|
G | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-1675C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409031 | ||||||
| chr12:33409071
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-1715G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409071 | ||||||
| chr12:33409093
|
A | C | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-1737T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409093 | ||||||
| chr12:33409125
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-1769C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409125 | ||||||
| chr12:33409234
|
C | T | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-1878G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409234 | ||||||
| chr12:33409236
|
A | G | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-1880T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409236 | ||||||
| chr12:33409518
|
C | CT | 38 | a0001c0001t0001g0055a0001c0001t0002g0003a0001c0001t0002g0052others(35): Show | 40 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.510-2163dupA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409518 | ||||||
| chr12:33409518
|
C | CTT | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-2164_510-2163d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409518 | ||||||
| chr12:33409518
|
CT | C | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-2163delA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409518 | ||||||
| chr12:33409600
|
G | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-2244C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409600 | ||||||
| chr12:33409608
|
G | C | 2 | a0001c0001t0005g0120a0001c0001t0005g0121 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.510-2252C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409608 | ||||||
| chr12:33409856
|
A | AAGC | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-2501_510-2500i others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409856 | ||||||
| chr12:33409869
|
G | A | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.510-2513C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409869 | ||||||
| chr12:33409923
|
C | G | 35 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(32): Show | 39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.510-2567G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409923 | ||||||
| chr12:33410009
|
C | A | 3 | a0001c0002t0004g0292a0001c0002t0004g0293a0001c0002t0004g0294 | 3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.510-2653G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410009 | ||||||
| chr12:33410181
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(144): Show | 158 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.510-2825A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410181 | ||||||
| chr12:33410236
|
G | A | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-2880C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410236 | ||||||
| chr12:33410354
|
A | G | 1 | a0003c0007t0015g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510-2998T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410354 | ||||||
| chr12:33410363
|
A | G | 36 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(33): Show | 39 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.510-3007T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410363 | ||||||
| chr12:33410398
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.510-3042T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410398 | ||||||
| chr12:33410454
|
G | C | 35 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(32): Show | 39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.510-3098C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410454 | ||||||
| chr12:33410527
|
G | A | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.510-3171C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410527 | ||||||
| chr12:33410532
|
T | TATC | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-3179_510-3177d others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410532 | ||||||
| chr12:33410534
|
T | C | 11 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0269others(8): Show | 13 | HG01256.hp2 HG01258.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.510-3178A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410534 | ||||||
| chr12:33410580
|
G | A | 1 | a0001c0002t0004g0273 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.510-3224C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410580 | ||||||
| chr12:33410632
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.510-3276C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410632 | ||||||
| chr12:33410672
|
G | C | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-3316C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410672 | ||||||
| chr12:33410717
|
G | A | 3 | a0001c0005t0010g0219a0003c0007t0010g0220a0003c0007t0015g0277 | 3 | HG03098.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-3361C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410717 | ||||||
| chr12:33410722
|
T | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-3366A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410722 | ||||||
| chr12:33410738
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-3382A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410738 | ||||||
| chr12:33410997
|
A | T | 1 | a0001c0002t0004g0285 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.510-3641T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33410997 | ||||||
| chr12:33411288
|
CATA | C | 35 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(32): Show | 39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.510-3935_510-3933d others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411288 | ||||||
| chr12:33411416
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.510-4060T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411416 | ||||||
| chr12:33411506
|
TAAC | T | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-4153_510-4151d others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411506 | ||||||
| chr12:33411531
|
C | T | 6 | a0001c0001t0003g0015a0001c0001t0003g0229a0001c0001t0003g0234others(3): Show | 7 | HG00735.hp1 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-4175G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411531 | ||||||
| chr12:33411533
|
A | G | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.510-4177T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411533 | ||||||
| chr12:33411653
|
T | C | 16 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(13): Show | 17 | HG00738.hp1 HG00741.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.510-4297A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411653 | ||||||
| chr12:33411770
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.510-4414G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411770 | ||||||
| chr12:33411959
|
T | C | 2 | a0001c0001t0002g0127a0001c0001t0002g0207 | 2 | HG00738.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.510-4603A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33411959 | ||||||
| chr12:33412009
|
A | G | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510-4653T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412009 | ||||||
| chr12:33412130
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(144): Show | 158 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.510-4774G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412130 | ||||||
| chr12:33412208
|
G | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 9 | HG01175.hp2 HG02280.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-4852C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412208 | ||||||
| chr12:33412209
|
A | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 9 | HG01175.hp2 HG02280.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-4853T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412209 | ||||||
| chr12:33412235
|
CT | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-4880delA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412235 | ||||||
| chr12:33412312
|
T | C | 1 | a0001c0003t0005g0145 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.510-4956A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412312 | ||||||
| chr12:33412362
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-5006A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412362 | ||||||
| chr12:33412391
|
TA | T | 38 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(35): Show | 41 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-5036delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412391 | ||||||
| chr12:33412541
|
G | A | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-5185C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412541 | ||||||
| chr12:33412722
|
C | A | 5 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(2): Show | 5 | HG00738.hp1 HG02145.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-5366G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412722 | ||||||
| chr12:33412751
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-5395G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412751 | ||||||
| chr12:33412914
|
CA | C | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0004t0001g0094others(1): Show | 4 | HG03831.hp1 NA18955.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-5559delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33412914 | ||||||
| chr12:33413059
|
G | C | 35 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(32): Show | 39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.510-5703C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413059 | ||||||
| chr12:33413178
|
C | T | 16 | a0001c0001t0002g0109a0001c0001t0002g0122a0001c0001t0002g0123others(13): Show | 17 | HG00738.hp1 HG00741.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.510-5822G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413178 | ||||||
| chr12:33413199
|
A | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-5843T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413199 | ||||||
| chr12:33413200
|
C | T | 1 | a0001c0002t0004g0261 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.510-5844G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413200 | ||||||
| chr12:33413201
|
A | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(292): Show | 319 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(316): Show |
intron_variant | MODIFIER | c.510-5845T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413201 | ||||||
| chr12:33413335
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.510-5979G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413335 | ||||||
| chr12:33413416
|
C | T | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-6060G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413416 | ||||||
| chr12:33413548
|
T | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(254): Show | 276 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(273): Show |
intron_variant | MODIFIER | c.510-6192A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413548 | ||||||
| chr12:33413626
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | NA18953.hp1 NA18963.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.510-6270A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413626 | ||||||
| chr12:33413695
|
G | C | 2 | a0001c0005t0012g0014a0001c0005t0012g0222 | 3 | HG02970.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.510-6339C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413695 | ||||||
| chr12:33413708
|
G | A | 35 | a0001c0001t0002g0003a0001c0001t0002g0052a0001c0001t0002g0054others(32): Show | 39 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.510-6352C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413708 | ||||||
| chr12:33413720
|
T | C | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.510-6364A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413720 | ||||||
| chr12:33413737
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.510-6381A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413737 | ||||||
| chr12:33413780
|
G | A | 2 | a0001c0001t0005g0135a0001c0001t0020g0134 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.510-6424C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413780 | ||||||
| chr12:33413915
|
G | C | 10 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0035others(7): Show | 10 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-6559C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413915 | ||||||
| chr12:33413946
|
A | G | 1 | a0001c0001t0003g0233 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.510-6590T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33413946 | ||||||
| chr12:33414039
|
A | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-6683T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414039 | ||||||
| chr12:33414199
|
A | T | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-6843T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414199 | ||||||
| chr12:33414217
|
T | G | 1 | a0001c0001t0002g0113 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.510-6861A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414217 | ||||||
| chr12:33414233
|
T | C | 5 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG02818.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-6877A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414233 | ||||||
| chr12:33414345
|
C | G | 5 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG02818.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-6989G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414345 | ||||||
| chr12:33414411
|
C | T | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-7055G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414411 | ||||||
| chr12:33414513
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.510-7157C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414513 | ||||||
| chr12:33414535
|
G | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(218): Show | 237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.510-7179C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414535 | ||||||
| chr12:33415027
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.510-7671G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415027 | ||||||
| chr12:33415263
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(217): Show | 236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.510-7907A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415263 | ||||||
| chr12:33415555
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510-8199T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415555 | ||||||
| chr12:33415616
|
A | C | 2 | a0001c0002t0004g0292a0001c0002t0004g0293 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.510-8260T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415616 | ||||||
| chr12:33415703
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510-8347T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415703 | ||||||
| chr12:33415790
|
A | C | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-8434T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415790 | ||||||
| chr12:33415881
|
T | C | 1 | a0001c0001t0005g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-8525A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415881 | ||||||
| chr12:33415909
|
A | G | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(209): Show | 227 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.510-8553T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415909 | ||||||
| chr12:33415968
|
C | T | 97 | a0001c0001t0001g0096a0001c0001t0001g0105a0001c0001t0001g0106others(94): Show | 100 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.510-8612G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415968 | ||||||
| chr12:33415972
|
T | C | 5 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119others(2): Show | 5 | HG02818.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-8616A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415972 | ||||||
| chr12:33416071
|
ACACCATT others(56): Show |
A | 38 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(35): Show | 41 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-8778_510-8716d others(65): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416071 | ||||||
| chr12:33416139
|
G | GGTAA | 38 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(35): Show | 41 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-8784_510-8783i others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416139 | ||||||
| chr12:33416237
|
C | A | 44 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(41): Show | 48 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.510-8881G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416237 | ||||||
| chr12:33416583
|
C | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(69): Show | 80 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.510-9227G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416583 | ||||||
| chr12:33416714
|
G | A | 1 | a0001c0005t0010g0223 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.510-9358C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416714 | ||||||
| chr12:33416798
|
A | G | 3 | a0001c0001t0007g0005a0001c0001t0007g0028a0001c0001t0007g0029 | 4 | HG00741.hp1 HG02109.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+9340T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416798 | ||||||
| chr12:33416818
|
G | A | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.509+9320C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33416818 | ||||||
| chr12:33417086
|
G | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(80): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.509+9052C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417086 | ||||||
| chr12:33417146
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+8992A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417146 | ||||||
| chr12:33417303
|
T | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+8835A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417303 | ||||||
| chr12:33417442
|
C | T | 3 | a0001c0001t0005g0117a0001c0001t0005g0118a0001c0001t0005g0119 | 3 | HG02818.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.509+8696G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417442 | ||||||
| chr12:33417611
|
G | C | 14 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(11): Show | 15 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.509+8527C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417611 | ||||||
| chr12:33417648
|
G | C | 14 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(11): Show | 15 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.509+8490C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417648 | ||||||
| chr12:33417671
|
G | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+8467C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417671 | ||||||
| chr12:33417672
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+8466A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417672 | ||||||
| chr12:33417787
|
A | G | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+8351T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417787 | ||||||
| chr12:33417797
|
TGAGGGTG others(7): Show |
T | 1 | a0001c0012t0005g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.509+8327_509+8340d others(16): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417797 | ||||||
| chr12:33417921
|
T | C | 1 | a0001c0002t0004g0284 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.509+8217A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417921 | ||||||
| chr12:33417968
|
G | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+8170C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33417968 | ||||||
| chr12:33418408
|
T | C | 2 | a0001c0001t0005g0135a0001c0001t0020g0134 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+7730A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33418408 | ||||||
| chr12:33418548
|
G | A | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+7590C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33418548 | ||||||
| chr12:33418619
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.509+7519G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33418619 | ||||||
| chr12:33418711
|
C | T | 9 | a0001c0004t0005g0208a0001c0004t0005g0210a0001c0004t0005g0211others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+7427G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33418711 | ||||||
| chr12:33418837
|
C | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0095 | 2 | NA18998.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.509+7301G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33418837 | ||||||
| chr12:33418940
|
A | G | 1 | a0001c0002t0004g0263 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+7198T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33418940 | ||||||
| chr12:33419054
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.509+7084G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419054 | ||||||
| chr12:33419083
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.509+7055G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419083 | ||||||
| chr12:33419277
|
T | G | 1 | a0001c0001t0006g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509+6861A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419277 | ||||||
| chr12:33419556
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+6582T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419556 | ||||||
| chr12:33419557
|
A | G | 1 | a0001c0001t0002g0179 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.509+6581T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419557 | ||||||
| chr12:33419603
|
T | C | 12 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0031others(9): Show | 12 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+6535A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419603 | ||||||
| chr12:33419606
|
C | T | 13 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.509+6532G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419606 | ||||||
| chr12:33419708
|
AGAT | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+6427_509+6429d others(5): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419708 | ||||||
| chr12:33419810
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.509+6328G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33419810 | ||||||
| chr12:33420056
|
G | A | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+6082C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420056 | ||||||
| chr12:33420404
|
T | C | 3 | a0001c0002t0004g0261a0001c0002t0004g0285a0001c0005t0015g0262 | 3 | HG00741.hp2 HG01346.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.509+5734A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420404 | ||||||
| chr12:33420492
|
AT | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(66): Show | 76 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.509+5645delA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420492 | ||||||
| chr12:33420493
|
T | A | 14 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0005g0043others(11): Show | 15 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.509+5645A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420493 | ||||||
| chr12:33420497
|
A | T | 1 | a0001c0001t0001g0051 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.509+5641T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420497 | ||||||
| chr12:33420539
|
C | T | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+5599G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420539 | ||||||
| chr12:33420568
|
C | T | 1 | a0001c0001t0002g0178 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.509+5570G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420568 | ||||||
| chr12:33420579
|
G | A | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+5559C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420579 | ||||||
| chr12:33420707
|
A | G | 1 | a0001c0003t0005g0158 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.509+5431T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420707 | ||||||
| chr12:33420732
|
C | T | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+5406G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420732 | ||||||
| chr12:33420788
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(68): Show | 79 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+5350A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420788 | ||||||
| chr12:33420817
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+5321G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420817 | ||||||
| chr12:33420916
|
T | A | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+5222A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420916 | ||||||
| chr12:33420995
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+5143A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33420995 | ||||||
| chr12:33421001
|
A | G | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+5137T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421001 | ||||||
| chr12:33421150
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+4988A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421150 | ||||||
| chr12:33421156
|
T | C | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.509+4982A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421156 | ||||||
| chr12:33421167
|
C | T | 3 | a0001c0001t0009g0006a0001c0001t0009g0044a0001c0002t0004g0261 | 4 | HG01346.hp1 HG01891.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+4971G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421167 | ||||||
| chr12:33421168
|
G | A | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.509+4970C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421168 | ||||||
| chr12:33421228
|
A | T | 1 | a0001c0001t0002g0177 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.509+4910T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421228 | ||||||
| chr12:33421246
|
T | C | 1 | a0001c0001t0011g0230 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+4892A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421246 | ||||||
| chr12:33421398
|
A | C | 1 | a0001c0001t0003g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.509+4740T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421398 | ||||||
| chr12:33421436
|
C | T | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+4702G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421436 | ||||||
| chr12:33421488
|
C | A | 12 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0031others(9): Show | 12 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+4650G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421488 | ||||||
| chr12:33421527
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+4611A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421527 | ||||||
| chr12:33421677
|
C | G | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+4461G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421677 | ||||||
| chr12:33421858
|
G | A | 7 | a0001c0001t0002g0010a0001c0001t0002g0129a0001c0001t0002g0130others(4): Show | 8 | HG01106.hp2 HG02300.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+4280C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33421858 | ||||||
| chr12:33422041
|
A | T | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.509+4097T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422041 | ||||||
| chr12:33422089
|
TAA | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+4047_509+4048d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422089 | ||||||
| chr12:33422616
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(68): Show | 79 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+3522T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422616 | ||||||
| chr12:33422742
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.509+3396G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422742 | ||||||
| chr12:33422743
|
G | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+3395C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422743 | ||||||
| chr12:33422788
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0204 | 2 | HG02132.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.509+3350T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422788 | ||||||
| chr12:33422878
|
A | C | 1 | a0001c0001t0003g0233 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.509+3260T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422878 | ||||||
| chr12:33422931
|
A | G | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+3207T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422931 | ||||||
| chr12:33422943
|
T | C | 3 | a0001c0002t0004g0292a0001c0002t0004g0293a0001c0002t0004g0294 | 3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.509+3195A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422943 | ||||||
| chr12:33422945
|
T | C | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+3193A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33422945 | ||||||
| chr12:33423303
|
A | AGT | 16 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(13): Show | 17 | HG00738.hp1 HG00741.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.509+2833_509+2834d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423303 | ||||||
| chr12:33423353
|
G | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+2785C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423353 | ||||||
| chr12:33423502
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.509+2636T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423502 | ||||||
| chr12:33423617
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.509+2521G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423617 | ||||||
| chr12:33423677
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.509+2461C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423677 | ||||||
| chr12:33423771
|
G | A | 14 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(11): Show | 15 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.509+2367C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423771 | ||||||
| chr12:33423920
|
T | A | 1 | a0001c0001t0006g0042 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.509+2218A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33423920 | ||||||
| chr12:33424055
|
A | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.509+2083T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424055 | ||||||
| chr12:33424117
|
A | G | 2 | a0001c0001t0024g0169a0001c0001t0033g0296 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.509+2021T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424117 | ||||||
| chr12:33424223
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+1915A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424223 | ||||||
| chr12:33424238
|
A | T | 1 | a0001c0001t0002g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.509+1900T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424238 | ||||||
| chr12:33424429
|
A | T | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+1709T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424429 | ||||||
| chr12:33424514
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+1624G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424514 | ||||||
| chr12:33424539
|
C | G | 1 | a0001c0003t0005g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.509+1599G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424539 | ||||||
| chr12:33424687
|
A | G | 1 | a0001c0001t0020g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.509+1451T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424687 | ||||||
| chr12:33424692
|
A | G | 1 | a0001c0001t0003g0254 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.509+1446T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424692 | ||||||
| chr12:33424699
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+1439G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424699 | ||||||
| chr12:33424747
|
A | AATAT | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+1387_509+1390d others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424747 | ||||||
| chr12:33424874
|
C | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+1264G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33424874 | ||||||
| chr12:33425003
|
T | A | 13 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.509+1135A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425003 | ||||||
| chr12:33425076
|
A | C | 1 | a0001c0001t0001g0136 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.509+1062T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425076 | ||||||
| chr12:33425265
|
T | C | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.509+873A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425265 | ||||||
| chr12:33425363
|
T | C | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+775A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425363 | ||||||
| chr12:33425433
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+705G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425433 | ||||||
| chr12:33425617
|
A | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+521T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425617 | ||||||
| chr12:33425687
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+451A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425687 | ||||||
| chr12:33425728
|
C | A | 1 | a0001c0001t0005g0043 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.509+410G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425728 | ||||||
| chr12:33425869
|
A | C | 1 | a0001c0001t0006g0036 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509+269T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425869 | ||||||
| chr12:33425888
|
C | G | 2 | a0001c0001t0005g0135a0001c0001t0020g0134 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+250G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425888 | ||||||
| chr12:33425922
|
T | A | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+216A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425922 | ||||||
| chr12:33425943
|
T | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 9 | HG01175.hp2 HG02280.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+195A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33425943 | ||||||
| chr12:33426062
|
T | TCA | 36 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0106others(33): Show | 37 | HG01081.hp1 HG01099.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.509+74_509+75dupTG | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
T | TCACA | 5 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200others(2): Show | 5 | HG01517.hp1 HG02293.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+72_509+75dupTG others(2): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
TCA | T | 4 | a0001c0001t0001g0133a0001c0001t0003g0232a0001c0001t0005g0033others(1): Show | 4 | HG00642.hp2 HG01175.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+74_509+75delTG | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
TCACA | T | 23 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(20): Show | 25 | HG00738.hp1 HG00741.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.509+72_509+75delTG others(2): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
TCACACA | T | 40 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0091others(37): Show | 43 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.509+70_509+75delTG others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
TCACACAC others(1): Show |
T | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(61): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.509+68_509+75delTG others(6): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
TCACACAC others(3): Show |
T | 1 | a0003c0007t0015g0277 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.509+66_509+75delTG others(8): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426062
|
TCACACAC others(5): Show |
T | 2 | a0001c0001t0002g0127a0001c0001t0002g0207 | 2 | HG00738.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.509+64_509+75delTG others(10): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426062 | ||||||
| chr12:33426099
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.509+39G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33426099 | ||||||
| chr12:33426524
|
A | G | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.152-29T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426524 | ||||||
| chr12:33426559
|
G | T | 1 | a0001c0001t0003g0231 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.152-64C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426559 | ||||||
| chr12:33426676
|
G | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-181C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426676 | ||||||
| chr12:33426729
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-234G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426729 | ||||||
| chr12:33426804
|
C | G | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.152-309G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426804 | ||||||
| chr12:33426814
|
G | A | 3 | a0001c0001t0007g0005a0001c0001t0007g0028a0001c0001t0007g0029 | 4 | HG00741.hp1 HG02109.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-319C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426814 | ||||||
| chr12:33426819
|
G | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0050 | 2 | NA19089.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.152-324C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426819 | ||||||
| chr12:33426853
|
A | T | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.152-358T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426853 | ||||||
| chr12:33426937
|
G | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-442C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426937 | ||||||
| chr12:33426961
|
T | C | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-466A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33426961 | ||||||
| chr12:33427054
|
A | G | 2 | a0004c0008t0013g0114a0004c0008t0013g0115 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.152-559T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33427054 | ||||||
| chr12:33427103
|
G | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-608C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33427103 | ||||||
| chr12:33427220
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(80): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.152-725T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33427220 | ||||||
| chr12:33427447
|
G | A | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-952C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33427447 | ||||||
| chr12:33427894
|
A | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-1399T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33427894 | ||||||
| chr12:33428142
|
A | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-1647T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428142 | ||||||
| chr12:33428221
|
A | C | 4 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG00738.hp1 HG02145.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-1726T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428221 | ||||||
| chr12:33428392
|
GAATGGAG others(1): Show |
G | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.152-1905_152-1898d others(10): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428392 | ||||||
| chr12:33428682
|
G | A | 46 | a0001c0001t0001g0167a0001c0002t0004g0018a0001c0002t0004g0019others(43): Show | 50 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.152-2187C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428682 | ||||||
| chr12:33428747
|
A | T | 1 | a0001c0002t0004g0282 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.152-2252T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428747 | ||||||
| chr12:33428849
|
T | C | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0004t0001g0094others(1): Show | 4 | HG03831.hp1 NA18955.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-2354A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428849 | ||||||
| chr12:33428854
|
C | T | 2 | a0001c0002t0004g0282a0001c0002t0004g0295 | 2 | HG01346.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.152-2359G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428854 | ||||||
| chr12:33428906
|
A | C | 2 | a0001c0001t0003g0229a0001c0001t0011g0230 | 2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.152-2411T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428906 | ||||||
| chr12:33428907
|
G | GA | 47 | a0001c0001t0001g0168a0001c0002t0004g0018a0001c0002t0004g0019others(44): Show | 50 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.152-2413dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428907 | ||||||
| chr12:33428907
|
G | GAA | 7 | a0001c0002t0004g0285a0001c0005t0010g0219a0001c0005t0010g0221others(4): Show | 8 | HG00741.hp2 HG02970.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.152-2414_152-2413d others(4): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428907 | ||||||
| chr12:33428907
|
GA | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(78): Show | 88 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.152-2413delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428907 | ||||||
| chr12:33428980
|
T | C | 3 | a0001c0001t0017g0026a0004c0008t0013g0114a0004c0008t0013g0115 | 3 | HG01256.hp1 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.152-2485A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33428980 | ||||||
| chr12:33429030
|
T | C | 1 | a0001c0001t0024g0169 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.152-2535A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429030 | ||||||
| chr12:33429090
|
G | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG00408.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.152-2595C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429090 | ||||||
| chr12:33429100
|
G | C | 2 | a0001c0001t0003g0247a0001c0001t0003g0248 | 2 | HG01081.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.152-2605C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429100 | ||||||
| chr12:33429182
|
G | C | 12 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0031others(9): Show | 12 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.152-2687C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429182 | ||||||
| chr12:33429297
|
T | G | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-2802A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429297 | ||||||
| chr12:33429303
|
C | T | 2 | a0001c0005t0010g0219a0003c0007t0010g0220 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.152-2808G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429303 | ||||||
| chr12:33429400
|
C | T | 8 | a0001c0002t0004g0276a0001c0002t0004g0278a0001c0002t0004g0279others(5): Show | 8 | HG01433.hp1 NA18941.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-2905G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429400 | ||||||
| chr12:33429518
|
T | G | 3 | a0001c0002t0004g0287a0001c0002t0004g0288a0005c0010t0004g0286 | 3 | NA18941.hp2 NA19066.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.152-3023A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429518 | ||||||
| chr12:33429670
|
G | A | 2 | a0001c0001t0006g0032a0001c0001t0006g0040 | 2 | HG02055.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.152-3175C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429670 | ||||||
| chr12:33429701
|
A | C | 1 | a0001c0001t0002g0171 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.152-3206T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429701 | ||||||
| chr12:33429718
|
C | T | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-3223G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429718 | ||||||
| chr12:33429760
|
G | T | 3 | a0001c0002t0004g0292a0001c0002t0004g0293a0001c0002t0004g0294 | 3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.152-3265C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429760 | ||||||
| chr12:33429771
|
G | A | 1 | a0001c0001t0002g0109 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152-3276C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429771 | ||||||
| chr12:33429852
|
G | A | 38 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(35): Show | 41 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.152-3357C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33429852 | ||||||
| chr12:33430008
|
T | G | 1 | a0001c0001t0016g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.152-3513A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430008 | ||||||
| chr12:33430102
|
A | G | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.152-3607T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430102 | ||||||
| chr12:33430213
|
T | C | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.152-3718A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430213 | ||||||
| chr12:33430262
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.152-3767A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430262 | ||||||
| chr12:33430309
|
A | T | 2 | a0001c0002t0004g0263a0001c0002t0004g0264 | 2 | HG02257.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.152-3814T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430309 | ||||||
| chr12:33430427
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.152-3932G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430427 | ||||||
| chr12:33430456
|
C | T | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.152-3961G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430456 | ||||||
| chr12:33430462
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.152-3967G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430462 | ||||||
| chr12:33430502
|
C | G | 1 | a0001c0001t0002g0170 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.152-4007G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430502 | ||||||
| chr12:33430579
|
T | C | 2 | a0001c0002t0004g0289a0001c0002t0004g0290 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.152-4084A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430579 | ||||||
| chr12:33430634
|
TCAAAATG others(2): Show |
T | 4 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG00738.hp1 HG02145.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-4148_152-4140d others(11): Show |
SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430634 | ||||||
| chr12:33430853
|
T | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0101 | 2 | HG00408.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.152-4358A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430853 | ||||||
| chr12:33430866
|
A | G | 3 | a0001c0001t0007g0005a0001c0001t0007g0028a0001c0001t0007g0029 | 4 | HG00741.hp1 HG02109.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-4371T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33430866 | ||||||
| chr12:33431404
|
C | T | 1 | a0001c0001t0002g0122 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.152-4909G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33431404 | ||||||
| chr12:33431699
|
G | A | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.152-5204C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33431699 | ||||||
| chr12:33431796
|
A | G | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | NA18953.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.152-5301T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33431796 | ||||||
| chr12:33431819
|
G | A | 89 | a0001c0001t0001g0195a0001c0001t0002g0010a0001c0001t0002g0012others(86): Show | 96 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.152-5324C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33431819 | ||||||
| chr12:33431936
|
G | GA | 9 | a0001c0004t0005g0208a0001c0004t0005g0210a0001c0004t0005g0211others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-5442dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33431936 | ||||||
| chr12:33432107
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.152-5612G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432107 | ||||||
| chr12:33432190
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0218 | 2 | NA19068.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.152-5695T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432190 | ||||||
| chr12:33432219
|
A | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0047 | 3 | NA18979.hp1 NA18990.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.152-5724T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432219 | ||||||
| chr12:33432359
|
T | C | 1 | a0001c0001t0003g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.152-5864A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432359 | ||||||
| chr12:33432397
|
C | T | 3 | a0001c0001t0003g0224a0001c0001t0003g0225a0001c0001t0030g0226 | 3 | HG01192.hp1 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.152-5902G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432397 | ||||||
| chr12:33432464
|
C | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-5969G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432464 | ||||||
| chr12:33432479
|
A | T | 1 | a0001c0003t0005g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.152-5984T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432479 | ||||||
| chr12:33432530
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(142): Show | 158 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.152-6035C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432530 | ||||||
| chr12:33432640
|
A | G | 1 | a0001c0001t0005g0117 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.152-6145T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432640 | ||||||
| chr12:33432737
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0129a0001c0001t0002g0130 | 4 | HG01106.hp2 HG03491.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-6242T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432737 | ||||||
| chr12:33432894
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.152-6399G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432894 | ||||||
| chr12:33432899
|
C | G | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.152-6404G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33432899 | ||||||
| chr12:33433395
|
C | T | 1 | a0001c0001t0003g0228 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.151+5977G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433395 | ||||||
| chr12:33433576
|
C | G | 1 | a0001c0002t0004g0276 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.151+5796G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433576 | ||||||
| chr12:33433621
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.151+5751G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433621 | ||||||
| chr12:33433751
|
G | T | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.151+5621C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433751 | ||||||
| chr12:33433870
|
T | G | 1 | a0001c0001t0001g0009 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.151+5502A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433870 | ||||||
| chr12:33433926
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.151+5446T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433926 | ||||||
| chr12:33433946
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.151+5426T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33433946 | ||||||
| chr12:33434222
|
A | G | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.151+5150T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434222 | ||||||
| chr12:33434275
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.151+5097G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434275 | ||||||
| chr12:33434319
|
A | G | 20 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0263others(17): Show | 22 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.151+5053T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434319 | ||||||
| chr12:33434345
|
G | C | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.151+5027C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434345 | ||||||
| chr12:33434360
|
T | A | 3 | a0001c0001t0011g0250a0001c0001t0011g0251a0001c0001t0011g0252 | 3 | HG01358.hp1 HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.151+5012A>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434360 | ||||||
| chr12:33434420
|
T | G | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.151+4952A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434420 | ||||||
| chr12:33434437
|
G | C | 2 | a0001c0001t0006g0041a0001c0001t0006g0042 | 2 | HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.151+4935C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434437 | ||||||
| chr12:33434443
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151+4929A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434443 | ||||||
| chr12:33434501
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.151+4871A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434501 | ||||||
| chr12:33434512
|
A | C | 2 | a0001c0002t0004g0261a0001c0005t0015g0262 | 2 | HG01346.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.151+4860T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434512 | ||||||
| chr12:33434720
|
G | C | 1 | a0001c0001t0009g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.151+4652C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434720 | ||||||
| chr12:33434918
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.151+4454A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434918 | ||||||
| chr12:33434942
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.151+4430C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33434942 | ||||||
| chr12:33435185
|
A | T | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+4187T>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435185 | ||||||
| chr12:33435239
|
T | C | 1 | a0001c0003t0005g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.151+4133A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435239 | ||||||
| chr12:33435425
|
G | T | 1 | a0001c0001t0002g0128 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151+3947C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435425 | ||||||
| chr12:33435453
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 274 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.151+3919A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435453 | ||||||
| chr12:33435525
|
G | T | 1 | a0001c0001t0002g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.151+3847C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435525 | ||||||
| chr12:33435598
|
T | C | 4 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(1): Show | 4 | HG00738.hp1 HG02145.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+3774A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435598 | ||||||
| chr12:33435599
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.151+3773C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435599 | ||||||
| chr12:33435619
|
G | T | 12 | a0001c0001t0005g0033a0001c0001t0005g0034a0001c0001t0006g0031others(9): Show | 12 | HG01169.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+3753C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435619 | ||||||
| chr12:33435842
|
T | C | 2 | a0001c0001t0003g0254a0001c0001t0003g0255 | 2 | NA18963.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.151+3530A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435842 | ||||||
| chr12:33435907
|
T | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(68): Show | 79 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.151+3465A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33435907 | ||||||
| chr12:33436015
|
A | G | 1 | a0001c0005t0032g0260 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.151+3357T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436015 | ||||||
| chr12:33436153
|
G | C | 1 | a0001c0001t0001g0206 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.151+3219C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436153 | ||||||
| chr12:33436289
|
A | G | 1 | a0001c0001t0006g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.151+3083T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436289 | ||||||
| chr12:33436348
|
A | G | 45 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(42): Show | 49 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.151+3024T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436348 | ||||||
| chr12:33436380
|
T | C | 13 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(10): Show | 14 | HG00738.hp1 HG00741.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.151+2992A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436380 | ||||||
| chr12:33436392
|
A | G | 9 | a0001c0004t0005g0208a0001c0004t0005g0210a0001c0004t0005g0211others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+2980T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436392 | ||||||
| chr12:33436453
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(65): Show | 75 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.151+2919A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436453 | ||||||
| chr12:33436460
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.151+2912G>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436460 | ||||||
| chr12:33436474
|
A | C | 4 | a0001c0001t0003g0224a0001c0001t0003g0225a0001c0001t0003g0227others(1): Show | 4 | HG01192.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+2898T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436474 | ||||||
| chr12:33436508
|
C | G | 39 | a0001c0002t0004g0018a0001c0002t0004g0019a0001c0002t0004g0020others(36): Show | 42 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.151+2864G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436508 | ||||||
| chr12:33436660
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.151+2712C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436660 | ||||||
| chr12:33436835
|
C | A | 1 | a0001c0001t0033g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.151+2537G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436835 | ||||||
| chr12:33436885
|
T | C | 1 | a0001c0002t0004g0291 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.151+2487A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33436885 | ||||||
| chr12:33437067
|
T | C | 1 | a0001c0001t0002g0207 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.151+2305A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437067 | ||||||
| chr12:33437144
|
T | C | 3 | a0001c0002t0004g0292a0001c0002t0004g0293a0001c0002t0004g0294 | 3 | HG01070.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.151+2228A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437144 | ||||||
| chr12:33437428
|
A | G | 17 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0124others(14): Show | 18 | HG00738.hp1 HG00741.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.151+1944T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437428 | ||||||
| chr12:33437697
|
T | C | 1 | a0001c0001t0001g0104 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.151+1675A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437697 | ||||||
| chr12:33437737
|
G | T | 3 | a0001c0001t0002g0111a0001c0001t0002g0113a0001c0001t0026g0112 | 3 | NA18995.hp2 NA19007.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.151+1635C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437737 | ||||||
| chr12:33437752
|
A | G | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+1620T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437752 | ||||||
| chr12:33437792
|
T | G | 1 | a0001c0001t0003g0256 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.151+1580A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437792 | ||||||
| chr12:33437852
|
G | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(204): Show | 222 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.151+1520C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437852 | ||||||
| chr12:33437934
|
A | G | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.151+1438T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33437934 | ||||||
| chr12:33438011
|
GC | G | 6 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+1360delG | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438011 | ||||||
| chr12:33438067
|
T | C | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+1305A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438067 | ||||||
| chr12:33438147
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(80): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.151+1225C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438147 | ||||||
| chr12:33438529
|
G | A | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.151+843C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438529 | ||||||
| chr12:33438537
|
T | C | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | NA18953.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.151+835A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438537 | ||||||
| chr12:33438722
|
T | TA | 9 | a0001c0004t0005g0208a0001c0004t0005g0210a0001c0004t0005g0211others(6): Show | 9 | HG02055.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+649dupT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438722 | ||||||
| chr12:33438723
|
A | C | 1 | a0001c0001t0017g0026 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.151+649T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438723 | ||||||
| chr12:33438931
|
A | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(80): Show | 91 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.151+441T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438931 | ||||||
| chr12:33438961
|
G | A | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+411C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33438961 | ||||||
| chr12:33439038
|
C | A | 1 | a0001c0002t0004g0295 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.151+334G>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439038 | ||||||
| chr12:33439063
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.151+309C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439063 | ||||||
| chr12:33439068
|
G | C | 6 | a0001c0005t0010g0219a0001c0005t0010g0221a0001c0005t0010g0223others(3): Show | 7 | HG02970.hp2 HG03195.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+304C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439068 | ||||||
| chr12:33439068
|
G | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(204): Show | 222 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.151+304C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439068 | ||||||
| chr12:33439075
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.151+297C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439075 | ||||||
| chr12:33439093
|
G | C | 1 | a0001c0001t0003g0259 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.151+279C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439093 | ||||||
| chr12:33439208
|
T | C | 1 | a0001c0001t0007g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151+164A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439208 | ||||||
| chr12:33439241
|
C | G | 1 | a0001c0001t0006g0031 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.151+131G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 1/6 | chr12 | 33439241 |