Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MSFHK others(518): Show |
chr12 | 33369238 | 33444819 |
| a0002 | 0/0 | 523 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | MSFHK others(518): Show |
chr12 | 33369238 | 33444819 |
| a0003 | 0/0 | 523 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | MSFHK others(518): Show |
chr12 | 33369238 | 33444819 |
| a0004 | 0/0 | 523 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SYT10_chr12_33369238_33444819 | SYT10 | MSFHK others(518): Show |
chr12 | 33369238 | 33444819 |
| a0005 | 0/0 | 523 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | MSFHK others(518): Show |
chr12 | 33369238 | 33444819 |
| a0006 | 0/0 | 523 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | MSFHK others(518): Show |
chr12 | 33369238 | 33444819 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1569 | 238 | 61 | 42 | 112 | 3 | 18 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0001c0002 | 0/0 | 1569 | 38 | 7 | 19 | 10 | 1 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0001c0003 | 0/0 | 1569 | 13 | 0 | 6 | 1 | 2 | 4 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0001c0004 | 0/0 | 1569 | 10 | 8 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0001c0005 | 0/0 | 1569 | 8 | 7 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0001c0006 | 0/0 | 1569 | 4 | 1 | 0 | 0 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0001c0012 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0002c0008 | 0/0 | 1569 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0003c0007 | 0/0 | 1569 | 2 | 2 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0004c0009 | 0/0 | 1569 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0005c0011 | 0/0 | 1569 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
chr12 | 33369238 | 33444819 | ||
| a0006c0010 | 0/0 | 1569 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ATGAG others(1564): Show |
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 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0002 | 0/1 | 4461 | 73 | 7 | 7 | 48 | 1 | 9 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0003 | 1/0 | 4461 | 40 | 5 | 15 | 14 | 2 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0005 | 0/0 | 4461 | 9 | 9 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0006 | 0/0 | 4461 | 10 | 9 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0007 | 0/0 | 4461 | 5 | 4 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0009 | 0/0 | 4461 | 4 | 4 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0011 | 0/0 | 4461 | 4 | 1 | 1 | 0 | 0 | 2 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0014 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0016 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0017 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0018 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0020 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0021 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0022 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0023 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0024 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0025 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0026 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0027 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0028 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0030 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0001t0033 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0002t0004 | 0/0 | 4461 | 37 | 7 | 18 | 10 | 1 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0002t0031 | 0/0 | 4461 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0003t0005 | 0/0 | 4461 | 11 | 0 | 6 | 0 | 2 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0003t0019 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0003t0029 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0004t0001 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0004t0005 | 0/0 | 4461 | 8 | 8 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0005t0010 | 0/0 | 4461 | 3 | 3 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0005t0012 | 0/0 | 4461 | 3 | 3 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0005t0015 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0005t0032 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0006t0008 | 0/0 | 4461 | 4 | 1 | 0 | 0 | 0 | 3 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0001c0012t0005 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0002c0008t0013 | 0/0 | 4461 | 2 | 1 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0003c0007t0010 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0003c0007t0015 | 0/0 | 4461 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0004c0009t0002 | 0/0 | 4461 | 2 | 0 | 0 | 2 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0005c0011t0001 | 0/0 | 4461 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| a0006c0010t0004 | 0/0 | 4461 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | ACTCC others(4456): Show |
chr12 | 33369238 | 33444819 |
| actghapid | grch38/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 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0056 | 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 |
| a0001c0001t0001g0061 | 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 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0083 | 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 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0089 | 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 | 1/0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0014g0085 | 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 |
| a0001c0001t0021g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0022g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0001c0001t0023g0062 | 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 |
| a0001c0003t0005g0084 | 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 |
| a0002c0008t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0002c0008t0013g0115 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0004c0009t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0004c0009t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0005c0011t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| a0006c0010t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0075 | 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 | g0079 | 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 | g0070 | 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 | g0245 | 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 | a0002 | 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 | g0244 | 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 | g0246 | AMR | CLM | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0071 | 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 | g0066 | 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 | g0062 | 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 | g0077 | EAS | KHV | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0058 | 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 | g0087 | 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 | g0061 | 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 | g0073 | 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 | g0072 | 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 | g0069 | 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 | a0005 | c0011 | t0001 | g0057 | 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 | g0080 | 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 | g0052 | SAS | PJL | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| HG03688 | hp1 | a0001 | c0003 | t0005 | g0084 | 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 | g0243 | 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 | g0055 | 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 | g0085 | EAS | CHB | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0063 | 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 | g0076 | 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 | g0056 | 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 | g0081 | 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 | g0082 | 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 | g0089 | 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 | g0088 | 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 | g0068 | 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 | g0060 | 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 | g0086 | 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 | g0083 | 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 | g0074 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0242 | 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 | g0053 | 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 | g0065 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0054 | 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 | a0004 | 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 | g0241 | 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 | g0059 | 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 | a0006 | c0010 | t0004 | g0286 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| NA19086 | hp2 | a0004 | 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 | g0078 | 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 | a0002 | 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 | a0001 | c0001 | t0002 | g0178 | REF | REF | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0240 | REF | REF | SYT10_chr12_33369238_33444819 | SYT10 | chr12 | 33369238 | 33444819 |
| view | 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 | a0002 | 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 | a0006 | 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 | a0005 | 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 | a0004 | 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 |
| view | 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 | a0001c0002 a0001c0003 a0001c0012 others(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 | a0002c0008 | 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 | a0001c0004 a0001c0012 |
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 | a0001c0002 a0001c0005 a0003c0007 others(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 | a0001c0002 a0001c0005 a0003c0007 others(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 |
| view | 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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(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 | a0002c0008t0013 | 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 | a0001c0001t0024 a0001c0001t0033 |
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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(36): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0016 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(36): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0021 a0001c0005t0012 |
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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0005t0010 a0001c0005t0012 a0003c0007t0010 |
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 | a0001c0002t0004 a0001c0002t0031 a0001c0005t0015 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(26): Show |
221 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(218): 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 |
| view | 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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0117 a0001c0001t0005g0118 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0081 a0001c0001t0001g0218 others(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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(118): Show |
132 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(129): 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 | a0001c0001t0005g0043 a0001c0001t0005g0117 a0001c0001t0005g0118 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0117 a0001c0001t0005g0118 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0263 a0001c0002t0004g0264 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0026g0112 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0144 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0103 a0001c0001t0002g0176 a0001c0001t0002g0179 |
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 | a0001c0001t0001g0091 a0001c0001t0003g0224 a0001c0001t0003g0243 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0132 a0001c0001t0005g0117 others(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 | a0001c0001t0006g0040 a0001c0001t0007g0030 a0001c0001t0030g0226 others(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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0049 a0001c0001t0001g0068 a0001c0001t0001g0072 others(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 | a0001c0001t0001g0066 a0001c0001t0001g0105 a0001c0001t0001g0108 others(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 | a0001c0001t0002g0172 a0001c0001t0002g0173 a0001c0001t0003g0004 others(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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0120 a0001c0001t0005g0121 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0086 others(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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0001t0002g0010 a0001c0001t0002g0129 a0001c0001t0002g0130 |
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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(251): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0265 others(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 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(251): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | 85 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0012 others(82): Show |
92 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(89): 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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0117 a0001c0001t0005g0118 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0007g0030 a0001c0001t0030g0226 a0001c0004t0005g0208 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0117 a0001c0001t0005g0118 others(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 | 90 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0012 others(87): Show |
97 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(94): 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 | a0001c0001t0007g0030 a0001c0001t0030g0226 a0001c0004t0005g0208 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0007g0005 a0001c0001t0007g0028 a0001c0001t0007g0029 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 47 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0013 others(44): Show |
50 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(47): 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 | a0004c0009t0002g0201 | 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 | a0001c0002t0004g0282 a0001c0002t0004g0289 a0001c0002t0004g0290 others(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 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0026g0112 |
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 | 107 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0013 others(104): Show |
115 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(112): 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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0175 a0001c0001t0002g0204 |
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 | a0001c0001t0007g0030 a0001c0001t0030g0226 a0001c0004t0005g0208 others(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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0001t0001g0069 | 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 | a0001c0001t0002g0171 a0001c0001t0002g0196 a0001c0001t0002g0198 |
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 | a0001c0001t0002g0013 a0001c0001t0002g0190 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(136): Show |
150 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(147): 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 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0048 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1078-2821G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388112 | |||||||
| chr12:33388121 | TA | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(189): Show |
208 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.1078-2831delT | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388121 | |||||||
| chr12:33388167 | T | A | 49 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(168): Show |
184 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.1078-3037C>T | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33388328 | |||||||
| chr12:33388335 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(168): Show |
184 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(181): 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 | a0001c0001t0001g0070 | 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 | a0001c0001t0002g0010 a0001c0001t0002g0129 a0001c0001t0002g0130 others(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 | a0001c0001t0001g0065 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0005g0043 a0001c0001t0005g0117 a0001c0001t0005g0118 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(251): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0003g0244 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(167): Show |
184 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(181): 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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 others(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 | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(125): Show |
139 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(136): 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 | a0001c0001t0002g0055 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0086 others(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 | a0001c0001t0005g0043 a0001c0001t0006g0031 a0001c0001t0006g0032 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0044 a0001c0001t0009g0116 |
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 | a0001c0001t0002g0053 | 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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): 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 | a0001c0001t0005g0120 a0001c0001t0005g0121 |
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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1078-5946dupA | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33391236 | |||||||
| chr12:33391242 | A | T | 60 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0269 others(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 | a0001c0001t0001g0071 | 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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(135): Show |
149 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(146): 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 | a0001c0001t0030g0226 a0001c0004t0005g0208 a0001c0004t0005g0210 others(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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
209 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.1078-7129C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392420 | |||||||
| chr12:33392581 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(191): Show |
210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.1078-7290A>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33392581 | |||||||
| chr12:33392673 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(192): Show |
211 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(208): 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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0051 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0048 others(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 | 23 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0144 others(20): Show |
24 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(21): 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 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(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 | a0001c0001t0001g0167 a0001c0001t0002g0102 a0001c0001t0002g0113 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0118 a0001c0001t0005g0120 others(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 | a0001c0001t0005g0034 a0001c0001t0005g0117 a0001c0001t0005g0119 others(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 | a0001c0001t0002g0055 a0001c0001t0002g0147 a0001c0001t0007g0005 others(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 | a0001c0001t0002g0157 a0001c0001t0007g0028 a0001c0001t0028g0148 others(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 | a0001c0001t0002g0149 a0001c0001t0002g0150 a0001c0002t0004g0264 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0087 a0001c0001t0002g0153 a0001c0001t0002g0154 others(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 | a0001c0001t0002g0086 a0001c0001t0002g0128 a0001c0001t0002g0155 |
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 | a0001c0001t0002g0088 | 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 | a0001c0001t0003g0004 a0001c0001t0003g0224 a0001c0001t0003g0235 others(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 | a0001c0001t0009g0044 a0001c0001t0009g0116 a0001c0003t0005g0137 others(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 | a0001c0002t0004g0269 a0001c0002t0004g0272 a0001c0003t0005g0131 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0265 others(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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0003g0246 | 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 | a0001c0001t0022g0052 | 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 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0044 a0001c0001t0009g0116 |
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 | a0001c0001t0002g0087 | 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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-8700A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33393991 | |||||||
| chr12:33394032 | C | T | 47 | a0001c0001t0002g0010 a0001c0001t0002g0012 a0001c0001t0002g0013 others(44): Show |
50 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(47): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0023g0062 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0096 a0001c0001t0001g0097 |
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 | a0001c0001t0030g0226 a0001c0004t0005g0208 a0001c0004t0005g0210 others(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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-9015T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33394306 | |||||||
| chr12:33394460 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
275 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(272): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0002g0088 | 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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0001g0080 | 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 | a0001c0001t0002g0055 | 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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(243): Show |
265 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(262): 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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0002t0004g0271 a0001c0002t0004g0273 |
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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): 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 | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(195): Show |
214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(206): Show |
225 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1077+9728C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397061 | |||||||
| chr12:33397306 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(205): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.1077+9483A>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397306 | |||||||
| chr12:33397430 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(207): Show |
226 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(223): 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 | a0001c0001t0006g0032 a0001c0001t0006g0040 a0001c0001t0006g0041 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.1077+9187G>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33397602 | |||||||
| chr12:33397603 | T | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0001g0061 | 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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
140 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(137): 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 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0217 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0001g0060 a0001c0001t0018g0027 |
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 | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(207): Show |
226 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1077+8065delG | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33398723 | |||||||
| chr12:33398843 | T | C | 2 | a0001c0001t0009g0006 a0001c0001t0009g0044 |
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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
275 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(272): 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 | a0001c0003t0005g0131 a0001c0003t0005g0137 a0001c0003t0005g0138 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0044 |
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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
140 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(137): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(144): Show |
158 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(155): 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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
275 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(272): 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 | a0001c0001t0002g0003 a0001c0001t0002g0128 a0001c0001t0002g0146 others(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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0265 others(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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
275 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(272): 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0001g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1077+5267T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33401522 | |||||||
| chr12:33402534 | A | C | 35 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0002t0004g0271 a0001c0002t0004g0273 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0128 a0001c0001t0002g0147 others(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 | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(202): Show |
219 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(216): 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 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
170 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(167): 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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0001t0033g0296 a0001c0005t0010g0219 a0001c0005t0010g0223 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0003g0246 | 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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0030g0226 a0001c0004t0005g0208 a0001c0004t0005g0210 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0044 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0004c0009t0002g0201 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(218): Show |
237 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(234): 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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.1077+249C>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 3/6 | chr12 | 33406540 | |||||||
| chr12:33406589 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
275 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(272): 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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0135 others(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 | a0001c0001t0005g0120 a0001c0001t0005g0121 |
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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.510-1675C>A | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33409031 | |||||||
| chr12:33409071 | C | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0001g0056 a0001c0001t0002g0003 a0001c0001t0002g0053 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0005g0120 a0001c0001t0005g0121 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0002t0004g0292 a0001c0002t0004g0293 a0001c0002t0004g0294 |
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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(143): Show |
157 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(154): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0269 others(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 | a0001c0005t0010g0219 a0003c0007t0010g0220 a0003c0007t0015g0277 |
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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0003g0015 a0001c0001t0003g0229 a0001c0001t0003g0234 others(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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0207 |
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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(143): Show |
157 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(154): 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 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0004t0001g0094 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0109 a0001c0001t0002g0122 a0001c0001t0002g0123 others(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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | |||||||
| chr12:33413335 | 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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(253): Show |
275 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(272): 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 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
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 | a0001c0005t0012g0014 a0001c0005t0012g0222 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0053 a0001c0001t0002g0055 others(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 | a0001c0001t0005g0135 a0001c0001t0020g0134 |
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 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0035 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): Show |
intron_variant | MODIFIER | c.510-6683T>G | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33414039 | |||||||
| chr12:33414199 | A | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 others(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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 others(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 | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
236 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(233): 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 | a0001c0001t0002g0055 | 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 | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(216): Show |
235 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(232): 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 | a0001c0002t0004g0292 a0001c0002t0004g0293 |
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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(208): Show |
226 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.510-8553T>C | SYT10 | ENSG00000110975.8 | transcript | ENST00000228567.7 | protein_coding | 2/6 | chr12 | 33415909 | |||||||
| chr12:33415968 | C | T | 96 | a0001c0001t0001g0096 a0001c0001t0001g0105 a0001c0001t0001g0106 others(93): Show |
99 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(96): 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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0007g0005 a0001c0001t0007g0028 a0001c0001t0007g0029 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0005g0117 a0001c0001t0005g0118 a0001c0001t0005g0119 |
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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0005g0135 a0001c0001t0020g0134 |
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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0004t0005g0208 a0001c0004t0005g0210 a0001c0004t0005g0211 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0095 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0031 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0053 | 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 | a0001c0002t0004g0261 a0001c0002t0004g0285 a0001c0005t0015g0262 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0005g0043 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | |||||||
| chr12:33420579 | G | A | 6 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0044 a0001c0002t0004g0261 |
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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0031 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0129 a0001c0001t0002g0130 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0175 a0001c0001t0002g0204 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0292 a0001c0002t0004g0293 a0001c0002t0004g0294 |
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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(251): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0001t0024g0169 a0001c0001t0033g0296 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0005g0135 a0001c0001t0020g0134 |
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 | a0001c0001t0001g0011 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0105 a0001c0001t0001g0106 others(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 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 others(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 | a0001c0001t0001g0133 a0001c0001t0003g0232 a0001c0001t0005g0033 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0002g0127 a0001c0001t0002g0207 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0007g0005 a0001c0001t0007g0028 a0001c0001t0007g0029 |
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 | a0001c0001t0001g0049 a0001c0001t0002g0050 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0001g0167 a0001c0002t0004g0018 a0001c0002t0004g0019 others(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 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0004t0001g0094 others(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 | a0001c0002t0004g0282 a0001c0002t0004g0295 |
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 | a0001c0001t0003g0229 a0001c0001t0011g0230 |
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 | a0001c0001t0001g0168 a0001c0002t0004g0018 a0001c0002t0004g0019 others(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 | a0001c0002t0004g0285 a0001c0005t0010g0219 a0001c0005t0010g0221 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0017g0026 a0002c0008t0013g0114 a0002c0008t0013g0115 |
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 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
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 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0031 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0005t0010g0219 a0003c0007t0010g0220 |
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 | a0001c0002t0004g0276 a0001c0002t0004g0278 a0001c0002t0004g0279 others(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 | a0001c0002t0004g0287 a0001c0002t0004g0288 a0006c0010t0004g0286 |
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 | a0001c0001t0006g0032 a0001c0001t0006g0040 |
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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0002t0004g0292 a0001c0002t0004g0293 a0001c0002t0004g0294 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0263 a0001c0002t0004g0264 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0289 a0001c0002t0004g0290 |
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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0001t0002g0100 a0001c0001t0002g0101 |
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 | a0001c0001t0007g0005 a0001c0001t0007g0028 a0001c0001t0007g0029 |
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 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
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 | 88 | a0001c0001t0001g0195 a0001c0001t0002g0010 a0001c0001t0002g0012 others(85): Show |
95 | HG00621.hp2 HG00639.hp1 HG00642.hp1 others(92): 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 | a0001c0004t0005g0208 a0001c0004t0005g0210 a0001c0004t0005g0211 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0218 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0047 |
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 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0001c0001t0030g0226 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0129 a0001c0001t0002g0130 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(251): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0263 others(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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0011g0250 a0001c0001t0011g0251 a0001c0001t0011g0252 |
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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0001t0006g0041 a0001c0001t0006g0042 |
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 | a0001c0002t0004g0261 a0001c0005t0015g0262 |
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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(251): Show |
273 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(270): 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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0001t0005g0033 a0001c0001t0005g0034 a0001c0001t0006g0031 others(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 | a0001c0001t0003g0254 a0001c0001t0003g0255 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0004t0005g0208 a0001c0004t0005g0210 a0001c0004t0005g0211 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0001c0001t0003g0227 others(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 | a0001c0002t0004g0018 a0001c0002t0004g0019 a0001c0002t0004g0020 others(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 | a0001c0002t0004g0292 a0001c0002t0004g0293 a0001c0002t0004g0294 |
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 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(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 | a0001c0001t0002g0111 a0001c0001t0002g0113 a0001c0001t0026g0112 |
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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(203): Show |
221 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(218): 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 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
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 | a0001c0004t0005g0208 a0001c0004t0005g0210 a0001c0004t0005g0211 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | a0001c0005t0010g0219 a0001c0005t0010g0221 a0001c0005t0010g0223 others(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 | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(203): Show |
221 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(218): 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 |