| geneid | 100131897 |
|---|---|
| ensemblid | ENSG00000204767.4 |
| hgncid | 37271 |
| symbol | INSYN2B |
| name | inhibitory synaptic factor family member 2B |
| refseq_nuc | NM_001129891.3 |
| refseq_prot | NP_001123363.1 |
| ensembl_nuc | ENST00000377365.4 |
| ensembl_prot | ENSP00000366582.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 169861303 |
| end | 169980495 |
| strand | - |
| ver | v1.2 |
| region | chr5:169861303-169980495 |
| region5000 | chr5:169856303-169985495 |
| regionname0 | INSYN2B_chr5_169861303_169980495 |
| regionname5000 | INSYN2B_chr5_169856303_169985495 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 535 | 176 | 52 | 17 | 87 | 5 | 14 | 69 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002 | 0/1 | 535 | 133 | 38 | 34 | 34 | 11 | 15 | 24 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0003 | 0/0 | 535 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0004 | 0/0 | 535 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0005 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0006 | 0/0 | 535 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1608 | 176 | 52 | 17 | 87 | 5 | 14 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0002 | 0/1 | 1608 | 131 | 38 | 33 | 34 | 11 | 14 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0003 | 0/0 | 1608 | 5 | 0 | 0 | 0 | 0 | 5 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0004 | 0/0 | 1608 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0005 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0006 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0007 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| c0008 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4109 | 90 | 5 | 32 | 31 | 11 | 10 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0002 | 1/0 | 4108 | 75 | 6 | 4 | 55 | 3 | 6 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0003 | 0/0 | 4108 | 59 | 39 | 5 | 10 | 1 | 4 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0004 | 0/0 | 4108 | 33 | 5 | 7 | 13 | 0 | 8 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0005 | 0/0 | 4109 | 13 | 12 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0006 | 0/0 | 4109 | 13 | 0 | 1 | 9 | 1 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0007 | 0/0 | 4109 | 9 | 9 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0008 | 0/0 | 4109 | 4 | 4 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0009 | 0/0 | 4108 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0010 | 0/0 | 4108 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0011 | 0/0 | 4109 | 2 | 0 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0012 | 0/0 | 4108 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0013 | 0/0 | 4109 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0014 | 0/0 | 4108 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0015 | 0/0 | 4109 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0016 | 0/0 | 4108 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0017 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0018 | 0/0 | 4109 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0019 | 0/0 | 4109 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0020 | 0/0 | 4109 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0021 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0022 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0023 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0024 | 0/0 | 4108 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| t0025 | 0/0 | 4109 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1608 | 176 | 52 | 17 | 87 | 5 | 14 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002 | 0/1 | 1608 | 131 | 38 | 33 | 34 | 11 | 14 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0005 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0007 | 0/0 | 1608 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0003c0003 | 0/0 | 1608 | 5 | 0 | 0 | 0 | 0 | 5 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0004c0004 | 0/0 | 1608 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0005c0008 | 0/0 | 1608 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0006c0006 | 0/0 | 1608 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5716 | 17 | 0 | 1 | 11 | 1 | 4 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0002 | 1/0 | 5715 | 73 | 6 | 4 | 53 | 3 | 6 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0003 | 0/0 | 5715 | 54 | 36 | 5 | 8 | 1 | 4 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0004 | 0/0 | 5715 | 22 | 2 | 7 | 13 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0007 | 0/0 | 5716 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0009 | 0/0 | 5715 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0010 | 0/0 | 5715 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0012 | 0/0 | 5715 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0021 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0001c0001t0022 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0001 | 0/1 | 5716 | 71 | 5 | 29 | 20 | 10 | 6 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0002 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0003 | 0/0 | 5715 | 3 | 3 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0004 | 0/0 | 5715 | 5 | 3 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0005 | 0/0 | 5716 | 13 | 12 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0006 | 0/0 | 5716 | 13 | 0 | 1 | 9 | 1 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0007 | 0/0 | 5716 | 7 | 7 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0008 | 0/0 | 5716 | 4 | 4 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0011 | 0/0 | 5716 | 2 | 0 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0013 | 0/0 | 5716 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0014 | 0/0 | 5715 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0015 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0016 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0017 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0018 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0019 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0020 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0023 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0024 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0002t0025 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0005t0001 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0002c0007t0004 | 0/0 | 5715 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0003c0003t0004 | 0/0 | 5715 | 5 | 0 | 0 | 0 | 0 | 5 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0004c0004t0002 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0004c0004t0003 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0005c0008t0003 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| a0006c0006t0001 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | copy fasta | chr5 | 169856303 | 169985495 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0009g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0021g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0022g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0011g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0013g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0016g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0017g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0018g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0019g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0020g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0023g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0024g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0025g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0005t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0007t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0004c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0004c0004t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0005c0008t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0006c0006t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0248 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0263 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0149 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0250 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0238 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00323 | hp1 | a0002 | c0002 | t0006 | g0196 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0252 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0246 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00609 | hp2 | a0005 | c0008 | t0003 | g0113 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00621 | hp1 | a0004 | c0004 | t0002 | g0271 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00621 | hp2 | a0002 | c0002 | t0015 | g0275 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00639 | hp2 | a0002 | c0002 | t0005 | g0309 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0266 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01106 | hp2 | a0002 | c0005 | t0001 | g0174 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01109 | hp2 | a0002 | c0002 | t0014 | g0092 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0255 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01433 | hp1 | a0002 | c0002 | t0006 | g0081 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0153 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01934 | hp1 | a0002 | c0002 | t0020 | g0298 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0229 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01993 | hp2 | a0006 | c0006 | t0001 | g0148 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0124 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02056 | hp2 | a0002 | c0002 | t0016 | g0280 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0074 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0261 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0042 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02257 | hp1 | a0002 | c0002 | t0007 | g0243 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02257 | hp2 | a0002 | c0002 | t0005 | g0218 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02451 | hp2 | a0002 | c0002 | t0007 | g0314 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02572 | hp1 | a0002 | c0002 | t0024 | g0316 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02572 | hp2 | a0002 | c0002 | t0005 | g0098 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02615 | hp1 | a0002 | c0002 | t0008 | g0078 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0108 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0006 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02717 | hp1 | a0002 | c0002 | t0005 | g0308 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02735 | hp1 | a0003 | c0003 | t0004 | g0260 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0106 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02738 | hp1 | a0002 | c0002 | t0004 | g0159 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0055 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02886 | hp1 | a0002 | c0002 | t0008 | g0303 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02886 | hp2 | a0002 | c0002 | t0025 | g0315 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02895 | hp2 | a0002 | c0002 | t0007 | g0230 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02922 | hp1 | a0002 | c0002 | t0005 | g0024 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02922 | hp2 | a0002 | c0002 | t0007 | g0011 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02965 | hp1 | a0002 | c0002 | t0005 | g0310 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02970 | hp2 | a0002 | c0002 | t0005 | g0014 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0193 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03017 | hp2 | a0003 | c0003 | t0004 | g0179 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03098 | hp1 | a0002 | c0002 | t0008 | g0234 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0151 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0231 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0158 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03195 | hp1 | a0002 | c0002 | t0017 | g0109 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03209 | hp1 | a0002 | c0002 | t0007 | g0013 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03453 | hp1 | a0002 | c0002 | t0023 | g0076 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03486 | hp1 | a0002 | c0002 | t0005 | g0017 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0133 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03491 | hp2 | a0002 | c0002 | t0011 | g0001 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03492 | hp2 | a0002 | c0002 | t0011 | g0001 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03540 | hp1 | a0002 | c0002 | t0005 | g0301 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03654 | hp1 | a0003 | c0003 | t0004 | g0208 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03704 | hp1 | a0002 | c0002 | t0018 | g0095 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03710 | hp1 | a0002 | c0002 | t0019 | g0270 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0088 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03927 | hp1 | a0002 | c0007 | t0004 | g0075 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03927 | hp2 | a0003 | c0003 | t0004 | g0269 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03942 | hp2 | a0003 | c0003 | t0004 | g0296 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04228 | hp2 | a0002 | c0002 | t0006 | g0285 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | CHB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0102 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18939 | hp2 | a0002 | c0002 | t0013 | g0059 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18950 | hp2 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18954 | hp1 | a0002 | c0002 | t0006 | g0198 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18957 | hp1 | a0002 | c0002 | t0013 | g0147 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18967 | hp2 | a0002 | c0002 | t0006 | g0278 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18986 | hp2 | a0002 | c0002 | t0006 | g0048 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18995 | hp2 | a0001 | c0001 | t0009 | g0295 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19001 | hp2 | a0002 | c0002 | t0006 | g0066 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19002 | hp1 | a0002 | c0002 | t0006 | g0099 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19004 | hp1 | a0002 | c0002 | t0006 | g0064 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19043 | hp2 | a0002 | c0002 | t0005 | g0077 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19066 | hp1 | a0004 | c0004 | t0003 | g0299 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19068 | hp1 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19088 | hp1 | a0002 | c0002 | t0006 | g0067 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0232 | AFR | ASW | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ASW | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0209 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0201 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0126 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0156 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0223 | SAS | GIH | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20905 | hp2 | a0002 | c0002 | t0006 | g0120 | SAS | GIH | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02486 | hp2 | a0002 | c0002 | t0007 | g0302 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0094 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02559 | hp2 | a0001 | c0001 | t0022 | g0305 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03471 | hp1 | a0002 | c0002 | t0005 | g0025 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG06807 | hp1 | a0002 | c0002 | t0007 | g0306 | AFR | USA | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG06807 | hp2 | a0002 | c0002 | t0008 | g0313 | AFR | USA | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | USA | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | USA | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA21309 | hp1 | a0002 | c0002 | t0004 | g0018 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0205 | REF | REF | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0116 | REF | REF | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:169882985
|
G | T | 1 | a0003 | 5 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
missense_variant | MODERATE | c.914C>A | p.Ser305Tyr | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 2051/5715 | 914/1608 | 305/535 | chr5 | 169882985 | ||
| chr5:169883180
|
C | T | 1 | a0004 | 2 | HG00621.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.719G>A | p.Arg240His | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 1856/5715 | 719/1608 | 240/535 | chr5 | 169883180 | ||
| chr5:169883209
|
A | C | 3 | a0002a0003a0006 | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
missense_variant | MODERATE | c.690T>G | p.Ser230Arg | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 1827/5715 | 690/1608 | 230/535 | chr5 | 169883209 | ||
| chr5:169883403
|
C | G | 1 | a0006 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.496G>C | p.Val166Leu | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 1633/5715 | 496/1608 | 166/535 | chr5 | 169883403 | ||
| chr5:169883753
|
G | A | 1 | a0005 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.146C>T | p.Thr49Ile | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 1283/5715 | 146/1608 | 49/535 | chr5 | 169883753 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:169864309
|
G | A | 2 | a0002c0007a0003c0003 | 6 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(3): Show |
synonymous_variant | LOW | c.1572C>T | p.Thr524Thr | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2709/5715 | 1572/1608 | 524/535 | chr5 | 169864309 | ||
| chr5:169883602
|
A | T | 1 | a0002c0005 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.297T>A | p.Thr99Thr | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 1434/5715 | 297/1608 | 99/535 | chr5 | 169883602 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:169861313
|
A | C | 1 | a0002c0002t0011 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2960T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2960 | chr5 | 169861313 | |||||
| chr5:169861374
|
C | G | 7 | a0001c0001t0007a0002c0002t0005a0002c0002t0006others(4): Show | 39 | HG00323.hp1 HG00639.hp2 HG01433.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2899G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2899 | chr5 | 169861374 | |||||
| chr5:169861421
|
G | A | 1 | a0001c0001t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2852C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2852 | chr5 | 169861421 | |||||
| chr5:169861632
|
C | T | 1 | a0001c0001t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2641G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2641 | chr5 | 169861632 | |||||
| chr5:169861728
|
A | G | 10 | a0001c0001t0001a0001c0001t0021a0002c0002t0001others(7): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2545T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2545 | chr5 | 169861728 | |||||
| chr5:169861938
|
C | CT | 10 | a0001c0001t0001a0001c0001t0021a0002c0002t0001others(7): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2334 | chr5 | 169861938 | |||||
| chr5:169862027
|
C | G | 1 | a0002c0002t0013 | 2 | NA18939.hp2 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2246G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2246 | chr5 | 169862027 | |||||
| chr5:169862186
|
G | C | 1 | a0002c0002t0016 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2087 | chr5 | 169862186 | |||||
| chr5:169862202
|
T | C | 8 | a0001c0001t0001a0002c0002t0001a0002c0002t0011others(5): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2071A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2071 | chr5 | 169862202 | |||||
| chr5:169862231
|
C | T | 1 | a0002c0002t0020 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2042G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 2042 | chr5 | 169862231 | |||||
| chr5:169862506
|
G | GA | 7 | a0001c0001t0007a0002c0002t0005a0002c0002t0006others(4): Show | 39 | HG00323.hp1 HG00639.hp2 HG01433.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1766dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 1766 | chr5 | 169862506 | |||||
| chr5:169862558
|
T | C | 1 | a0001c0001t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1715A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 1715 | chr5 | 169862558 | |||||
| chr5:169862631
|
G | C | 9 | a0001c0001t0001a0001c0001t0021a0002c0002t0001others(6): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1642C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 1642 | chr5 | 169862631 | |||||
| chr5:169862737
|
T | G | 1 | a0001c0001t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 1536 | chr5 | 169862737 | |||||
| chr5:169862827
|
A | G | 1 | a0002c0002t0018 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1446T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 1446 | chr5 | 169862827 | |||||
| chr5:169863114
|
C | A | 1 | a0001c0001t0010 | 2 | HG02451.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1159G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 1159 | chr5 | 169863114 | |||||
| chr5:169863310
|
C | T | 1 | a0002c0002t0017 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 963 | chr5 | 169863310 | |||||
| chr5:169863349
|
G | A | 6 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(3): Show | 63 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*924C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 924 | chr5 | 169863349 | |||||
| chr5:169863374
|
A | G | 1 | a0002c0002t0016 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 899 | chr5 | 169863374 | |||||
| chr5:169863459
|
C | G | 1 | a0001c0001t0009 | 2 | HG02155.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*814G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 814 | chr5 | 169863459 | |||||
| chr5:169863555
|
G | A | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 718 | chr5 | 169863555 | |||||
| chr5:169863890
|
T | C | 1 | a0002c0002t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 383 | chr5 | 169863890 | |||||
| chr5:169863988
|
T | A | 32 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*285A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 285 | chr5 | 169863988 | |||||
| chr5:169864184
|
A | G | 6 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(3): Show | 63 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*89T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 89 | chr5 | 169864184 | |||||
| chr5:169864263
|
C | A | 7 | a0001c0001t0007a0001c0001t0012a0002c0002t0005others(4): Show | 40 | HG00323.hp1 HG00639.hp2 HG01433.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*10G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 4/4 | 10 | chr5 | 169864263 | |||||
| chr5:169884097
|
C | T | 1 | a0002c0002t0014 | 1 | HG01109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-199G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 199 | chr5 | 169884097 | |||||
| chr5:169884603
|
C | T | 3 | a0002c0002t0005a0002c0002t0024a0002c0002t0025 | 15 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-705G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 705 | chr5 | 169884603 | |||||
| chr5:169884736
|
G | A | 2 | a0002c0002t0006a0002c0002t0013 | 15 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-838C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/4 | 838 | chr5 | 169884736 | |||||
| chr5:169980436
|
G | A | 2 | a0002c0002t0024a0002c0002t0025 | 2 | HG02572.hp1 HG02886.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-1078C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/4 | chr5 | 169980436 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:169864601
|
C | T | 44 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(41): Show | 44 | HG00323.hp2 HG01069.hp1 HG01981.hp1 others(41): Show |
intron_variant | MODIFIER | c.1422-142G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169864601 | ||||||
| chr5:169864801
|
A | T | 3 | a0001c0001t0003g0252a0001c0001t0003g0262a0001c0001t0003g0272 | 3 | HG00323.hp2 HG01981.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1422-342T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169864801 | ||||||
| chr5:169864966
|
C | T | 1 | a0002c0002t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1422-507G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169864966 | ||||||
| chr5:169865012
|
C | G | 1 | a0002c0002t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1422-553G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169865012 | ||||||
| chr5:169865044
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1422-585C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169865044 | ||||||
| chr5:169865182
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1422-723G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169865182 | ||||||
| chr5:169865626
|
G | A | 3 | a0001c0001t0002g0143a0001c0001t0002g0183a0001c0001t0002g0184 | 3 | NA18994.hp2 NA19060.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1422-1167C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169865626 | ||||||
| chr5:169866011
|
GGCAGGGC others(54): Show |
G | 13 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0082others(10): Show | 13 | HG01981.hp2 HG02486.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1422-1613_1422-155 others(65): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866011 | ||||||
| chr5:169866098
|
A | AG | 27 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0038others(24): Show | 27 | HG00673.hp1 HG01081.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1422-1640dupC | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866098 | ||||||
| chr5:169866098
|
A | AGGGGGCC others(55): Show |
1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1422-1640_1422-163 others(66): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866098 | ||||||
| chr5:169866131
|
G | A | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1422-1672C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866131 | ||||||
| chr5:169866218
|
G | A | 1 | a0001c0001t0022g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1422-1759C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866218 | ||||||
| chr5:169866219
|
C | G | 3 | a0002c0002t0004g0108a0002c0002t0017g0109a0002c0002t0023g0076 | 3 | HG02622.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1422-1760G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866219 | ||||||
| chr5:169866375
|
G | C | 92 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1422-1916C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866375 | ||||||
| chr5:169866379
|
A | T | 3 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0239 | 3 | NA18747.hp1 NA18975.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1422-1920T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866379 | ||||||
| chr5:169866482
|
G | A | 25 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0038others(22): Show | 25 | HG00673.hp1 HG01081.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1422-2023C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866482 | ||||||
| chr5:169866606
|
C | T | 1 | a0002c0002t0001g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1422-2147G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866606 | ||||||
| chr5:169866782
|
T | C | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1422-2323A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169866782 | ||||||
| chr5:169867102
|
C | T | 1 | a0002c0002t0025g0315 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1422-2643G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867102 | ||||||
| chr5:169867168
|
C | T | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1422-2709G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867168 | ||||||
| chr5:169867330
|
A | T | 1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1422-2871T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867330 | ||||||
| chr5:169867407
|
CTCTG | C | 156 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(153): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1422-2952_1422-294 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867407 | ||||||
| chr5:169867435
|
G | A | 118 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(115): Show | 119 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(116): Show |
intron_variant | MODIFIER | c.1422-2976C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867435 | ||||||
| chr5:169867447
|
A | ATCTG | 103 | a0001c0001t0002g0012a0001c0001t0002g0034a0001c0001t0002g0035others(100): Show | 103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1422-2992_1422-298 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867447 | ||||||
| chr5:169867447
|
A | G | 211 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1422-2988T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867447 | ||||||
| chr5:169867591
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1422-3132C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867591 | ||||||
| chr5:169867610
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1422-3151A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867610 | ||||||
| chr5:169867625
|
CATCT | C | 234 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.1422-3170_1422-316 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867625 | ||||||
| chr5:169867696
|
T | C | 2 | a0002c0002t0004g0055a0002c0002t0017g0109 | 2 | HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1422-3237A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867696 | ||||||
| chr5:169867772
|
C | G | 63 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1422-3313G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867772 | ||||||
| chr5:169867855
|
A | T | 1 | a0001c0001t0003g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1422-3396T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867855 | ||||||
| chr5:169867904
|
T | C | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1422-3445A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169867904 | ||||||
| chr5:169868038
|
A | G | 3 | a0002c0002t0001g0186a0002c0002t0001g0187a0002c0002t0001g0205 | 3 | HG01070.hp2 HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1422-3579T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169868038 | ||||||
| chr5:169868333
|
T | C | 3 | a0001c0001t0022g0305a0002c0002t0008g0078a0002c0002t0008g0234 | 3 | HG02559.hp2 HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1422-3874A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169868333 | ||||||
| chr5:169868576
|
T | C | 1 | a0002c0002t0005g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1422-4117A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169868576 | ||||||
| chr5:169868773
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0060 | 2 | NA18982.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1422-4314T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169868773 | ||||||
| chr5:169868818
|
G | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1422-4359C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169868818 | ||||||
| chr5:169869075
|
T | C | 1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1422-4616A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869075 | ||||||
| chr5:169869424
|
A | T | 6 | a0002c0002t0001g0149a0002c0002t0001g0150a0002c0002t0001g0194others(3): Show | 6 | HG00140.hp1 HG00639.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.1422-4965T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869424 | ||||||
| chr5:169869560
|
CCTTATAA others(28): Show |
C | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1422-5136_1422-510 others(39): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869560 | ||||||
| chr5:169869697
|
C | G | 1 | a0002c0002t0014g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1422-5238G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869697 | ||||||
| chr5:169869817
|
C | T | 29 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0188others(26): Show | 29 | HG01081.hp2 HG01255.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1422-5358G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869817 | ||||||
| chr5:169869847
|
C | G | 1 | a0001c0001t0003g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1422-5388G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869847 | ||||||
| chr5:169869912
|
C | T | 6 | a0002c0007t0004g0075a0003c0003t0004g0179a0003c0003t0004g0208others(3): Show | 6 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422-5453G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869912 | ||||||
| chr5:169869916
|
A | G | 1 | a0002c0002t0005g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1422-5457T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869916 | ||||||
| chr5:169869953
|
G | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085 | 3 | NA18969.hp2 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1422-5494C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169869953 | ||||||
| chr5:169870022
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1422-5563G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870022 | ||||||
| chr5:169870532
|
A | G | 1 | a0001c0001t0002g0071 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1422-6073T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870532 | ||||||
| chr5:169870567
|
G | T | 238 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1422-6108C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870567 | ||||||
| chr5:169870575
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1422-6116G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870575 | ||||||
| chr5:169870648
|
A | G | 79 | a0001c0001t0001g0167a0001c0001t0001g0197a0002c0002t0001g0004others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.1422-6189T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870648 | ||||||
| chr5:169870657
|
G | T | 13 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0082others(10): Show | 13 | HG01981.hp2 HG02486.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.1422-6198C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870657 | ||||||
| chr5:169870706
|
A | T | 6 | a0002c0002t0006g0002a0002c0002t0006g0048a0002c0002t0006g0064others(3): Show | 7 | NA18950.hp2 NA18954.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.1422-6247T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870706 | ||||||
| chr5:169870707
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1422-6248G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870707 | ||||||
| chr5:169870722
|
T | C | 1 | a0002c0002t0004g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1422-6263A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870722 | ||||||
| chr5:169870901
|
T | TATAC | 79 | a0001c0001t0001g0167a0001c0001t0001g0197a0002c0002t0001g0004others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.1422-6446_1422-644 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870901 | ||||||
| chr5:169870906
|
A | G | 60 | a0001c0001t0007g0022a0002c0002t0001g0209a0002c0002t0001g0244others(57): Show | 61 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1422-6447T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169870906 | ||||||
| chr5:169871001
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1422-6542C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871001 | ||||||
| chr5:169871047
|
A | G | 1 | a0005c0008t0003g0113 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1422-6588T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871047 | ||||||
| chr5:169871119
|
C | G | 12 | a0002c0002t0005g0006a0002c0002t0005g0014a0002c0002t0005g0017others(9): Show | 12 | HG02257.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1422-6660G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871119 | ||||||
| chr5:169871217
|
C | T | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1422-6758G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871217 | ||||||
| chr5:169871260
|
A | G | 1 | a0001c0001t0002g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1422-6801T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871260 | ||||||
| chr5:169871355
|
G | C | 1 | a0001c0001t0002g0134 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1422-6896C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871355 | ||||||
| chr5:169871558
|
G | A | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1422-7099C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871558 | ||||||
| chr5:169871571
|
A | G | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1422-7112T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871571 | ||||||
| chr5:169871582
|
A | C | 1 | a0002c0002t0014g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1422-7123T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871582 | ||||||
| chr5:169871651
|
T | G | 238 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1422-7192A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871651 | ||||||
| chr5:169872038
|
A | G | 233 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1422-7579T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872038 | ||||||
| chr5:169872100
|
G | A | 1 | a0001c0001t0003g0274 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1422-7641C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872100 | ||||||
| chr5:169872559
|
T | C | 15 | a0002c0002t0005g0006a0002c0002t0005g0014a0002c0002t0005g0017others(12): Show | 15 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1422-8100A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872559 | ||||||
| chr5:169872681
|
A | G | 79 | a0001c0001t0001g0167a0001c0001t0001g0197a0002c0002t0001g0004others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.1422-8222T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872681 | ||||||
| chr5:169872717
|
T | C | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1422-8258A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872717 | ||||||
| chr5:169872725
|
C | T | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1422-8266G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872725 | ||||||
| chr5:169872964
|
A | G | 14 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(11): Show | 14 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1421+8404T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169872964 | ||||||
| chr5:169873057
|
T | C | 1 | a0002c0002t0007g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1421+8311A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169873057 | ||||||
| chr5:169873203
|
C | T | 2 | a0002c0002t0008g0313a0002c0002t0016g0280 | 2 | HG02056.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1421+8165G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169873203 | ||||||
| chr5:169873346
|
C | T | 29 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0188others(26): Show | 29 | HG01081.hp2 HG01255.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1421+8022G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169873346 | ||||||
| chr5:169873688
|
T | C | 1 | a0002c0002t0020g0298 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1421+7680A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169873688 | ||||||
| chr5:169873828
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1421+7540C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169873828 | ||||||
| chr5:169873833
|
A | G | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+7535T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169873833 | ||||||
| chr5:169874024
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0188others(26): Show | 29 | HG01081.hp2 HG01255.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.1421+7344C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874024 | ||||||
| chr5:169874054
|
G | A | 7 | a0002c0002t0007g0011a0002c0002t0007g0013a0002c0002t0007g0230others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1421+7314C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874054 | ||||||
| chr5:169874060
|
A | G | 2 | a0002c0002t0008g0313a0002c0002t0016g0280 | 2 | HG02056.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1421+7308T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874060 | ||||||
| chr5:169874130
|
C | T | 1 | a0002c0002t0008g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1421+7238G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874130 | ||||||
| chr5:169874131
|
G | A | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1421+7237C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874131 | ||||||
| chr5:169874311
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1421+7057C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874311 | ||||||
| chr5:169874392
|
G | A | 3 | a0001c0001t0003g0015a0001c0001t0003g0096a0001c0001t0003g0237 | 3 | HG02055.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1421+6976C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874392 | ||||||
| chr5:169874410
|
C | CA | 84 | a0001c0001t0001g0167a0001c0001t0001g0197a0001c0001t0002g0065others(81): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.1421+6957dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874410 | ||||||
| chr5:169874410
|
CA | C | 133 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(130): Show | 134 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.1421+6957delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874410 | ||||||
| chr5:169874554
|
T | C | 1 | a0002c0002t0023g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1421+6814A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874554 | ||||||
| chr5:169874587
|
G | A | 3 | a0001c0001t0003g0252a0001c0001t0003g0262a0001c0001t0003g0272 | 3 | HG00323.hp2 HG01981.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1421+6781C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874587 | ||||||
| chr5:169874590
|
T | A | 126 | a0001c0001t0001g0197a0002c0002t0001g0004a0002c0002t0001g0028others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.1421+6778A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874590 | ||||||
| chr5:169874800
|
G | A | 2 | a0002c0002t0001g0231a0002c0002t0008g0303 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1421+6568C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874800 | ||||||
| chr5:169874891
|
AG | A | 66 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(63): Show | 66 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1421+6476delC | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169874891 | ||||||
| chr5:169875097
|
A | G | 5 | a0003c0003t0004g0179a0003c0003t0004g0208a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1421+6271T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169875097 | ||||||
| chr5:169875185
|
T | TA | 33 | a0002c0002t0003g0158a0002c0002t0004g0108a0002c0002t0005g0006others(30): Show | 34 | HG00323.hp1 HG00639.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.1421+6182dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169875185 | ||||||
| chr5:169875349
|
C | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+6019G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169875349 | ||||||
| chr5:169875438
|
G | C | 1 | a0001c0001t0010g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1421+5930C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169875438 | ||||||
| chr5:169875755
|
G | A | 1 | a0001c0001t0003g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1421+5613C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169875755 | ||||||
| chr5:169875813
|
G | A | 1 | a0002c0002t0004g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1421+5555C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169875813 | ||||||
| chr5:169876015
|
G | A | 4 | a0002c0002t0001g0045a0002c0002t0001g0121a0002c0002t0001g0161others(1): Show | 4 | HG01106.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1421+5353C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876015 | ||||||
| chr5:169876099
|
C | T | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1421+5269G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876099 | ||||||
| chr5:169876151
|
C | G | 1 | a0002c0002t0001g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1421+5217G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876151 | ||||||
| chr5:169876207
|
C | A | 1 | a0001c0001t0002g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1421+5161G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876207 | ||||||
| chr5:169876479
|
C | G | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1421+4889G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876479 | ||||||
| chr5:169876582
|
G | T | 2 | a0002c0002t0019g0270a0002c0007t0004g0075 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1421+4786C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876582 | ||||||
| chr5:169876600
|
C | T | 30 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0167others(27): Show | 30 | HG00597.hp2 HG01081.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1421+4768G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169876600 | ||||||
| chr5:169877033
|
G | C | 1 | a0002c0002t0001g0181 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1421+4335C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877033 | ||||||
| chr5:169877332
|
A | C | 2 | a0002c0002t0019g0270a0002c0007t0004g0075 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1421+4036T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877332 | ||||||
| chr5:169877368
|
G | A | 96 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(93): Show | 96 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.1421+4000C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877368 | ||||||
| chr5:169877391
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1421+3977G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877391 | ||||||
| chr5:169877408
|
G | A | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1421+3960C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877408 | ||||||
| chr5:169877555
|
A | T | 11 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0029others(8): Show | 11 | HG01261.hp1 HG01496.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1421+3813T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877555 | ||||||
| chr5:169877568
|
G | C | 15 | a0002c0002t0005g0006a0002c0002t0005g0014a0002c0002t0005g0017others(12): Show | 15 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1421+3800C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877568 | ||||||
| chr5:169877655
|
TTAGA | T | 23 | a0002c0002t0004g0055a0002c0002t0005g0006a0002c0002t0005g0014others(20): Show | 23 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.1421+3709_1421+371 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877655 | ||||||
| chr5:169877800
|
T | C | 1 | a0002c0002t0001g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1421+3568A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877800 | ||||||
| chr5:169877921
|
G | C | 93 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0029others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1421+3447C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877921 | ||||||
| chr5:169877984
|
A | G | 1 | a0001c0001t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1421+3384T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169877984 | ||||||
| chr5:169878149
|
G | A | 30 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0167others(27): Show | 30 | HG00597.hp2 HG01081.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1421+3219C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878149 | ||||||
| chr5:169878171
|
G | T | 1 | a0001c0001t0002g0281 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1421+3197C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878171 | ||||||
| chr5:169878203
|
C | T | 1 | a0002c0002t0001g0161 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1421+3165G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878203 | ||||||
| chr5:169878223
|
C | T | 16 | a0002c0002t0004g0055a0002c0002t0005g0006a0002c0002t0005g0014others(13): Show | 16 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1421+3145G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878223 | ||||||
| chr5:169878773
|
T | G | 2 | a0002c0002t0004g0106a0002c0002t0004g0159 | 2 | HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1421+2595A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878773 | ||||||
| chr5:169878822
|
G | A | 14 | a0002c0002t0006g0002a0002c0002t0006g0048a0002c0002t0006g0064others(11): Show | 15 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.1421+2546C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878822 | ||||||
| chr5:169878923
|
C | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2445G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878923 | ||||||
| chr5:169878951
|
C | T | 1 | a0003c0003t0004g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1421+2417G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169878951 | ||||||
| chr5:169879128
|
G | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+2240C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879128 | ||||||
| chr5:169879130
|
A | G | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2238T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879130 | ||||||
| chr5:169879260
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1421+2108G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879260 | ||||||
| chr5:169879277
|
G | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2091C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879277 | ||||||
| chr5:169879278
|
G | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2090C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879278 | ||||||
| chr5:169879279
|
G | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2089C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879279 | ||||||
| chr5:169879280
|
A | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2088T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879280 | ||||||
| chr5:169879283
|
A | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2085T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879283 | ||||||
| chr5:169879284
|
G | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2084C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879284 | ||||||
| chr5:169879286
|
A | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1421+2082T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879286 | ||||||
| chr5:169879655
|
A | G | 1 | a0001c0001t0004g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1421+1713T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879655 | ||||||
| chr5:169879712
|
C | T | 1 | a0002c0002t0001g0144 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1421+1656G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879712 | ||||||
| chr5:169879729
|
A | G | 7 | a0002c0002t0019g0270a0002c0007t0004g0075a0003c0003t0004g0179others(4): Show | 7 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1421+1639T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879729 | ||||||
| chr5:169879803
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1421+1565G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169879803 | ||||||
| chr5:169880071
|
T | C | 93 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0029others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1421+1297A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880071 | ||||||
| chr5:169880331
|
G | T | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1421+1037C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880331 | ||||||
| chr5:169880406
|
T | C | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1421+962A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880406 | ||||||
| chr5:169880433
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0089 | 2 | HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1421+935C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880433 | ||||||
| chr5:169880748
|
A | G | 80 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0029others(77): Show | 81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.1421+620T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880748 | ||||||
| chr5:169880789
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1421+579C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880789 | ||||||
| chr5:169880795
|
A | C | 2 | a0002c0002t0001g0194a0002c0002t0001g0204 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1421+573T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880795 | ||||||
| chr5:169880888
|
A | G | 2 | a0002c0002t0019g0270a0002c0007t0004g0075 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1421+480T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880888 | ||||||
| chr5:169880945
|
T | C | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1421+423A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880945 | ||||||
| chr5:169880964
|
G | A | 14 | a0002c0002t0006g0002a0002c0002t0006g0048a0002c0002t0006g0064others(11): Show | 15 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.1421+404C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169880964 | ||||||
| chr5:169881875
|
T | G | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1347-433A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/3 | chr5 | 169881875 | ||||||
| chr5:169881920
|
G | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1347-478C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/3 | chr5 | 169881920 | ||||||
| chr5:169882028
|
T | C | 13 | a0002c0002t0001g0209a0002c0002t0004g0106a0002c0002t0004g0159others(10): Show | 13 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1346+525A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/3 | chr5 | 169882028 | ||||||
| chr5:169882076
|
C | T | 66 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(63): Show | 66 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1346+477G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/3 | chr5 | 169882076 | ||||||
| chr5:169882217
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | NA18947.hp2 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1346+336A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 2/3 | chr5 | 169882217 | ||||||
| chr5:169884983
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-918-167C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169884983 | ||||||
| chr5:169884988
|
A | G | 237 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.-918-172T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169884988 | ||||||
| chr5:169884999
|
C | T | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-918-183G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169884999 | ||||||
| chr5:169885094
|
G | A | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-278C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885094 | ||||||
| chr5:169885104
|
C | A | 1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-918-288G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885104 | ||||||
| chr5:169885184
|
T | C | 14 | a0002c0002t0006g0002a0002c0002t0006g0048a0002c0002t0006g0064others(11): Show | 15 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.-918-368A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885184 | ||||||
| chr5:169885264
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-918-448G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885264 | ||||||
| chr5:169885290
|
A | G | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-918-474T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885290 | ||||||
| chr5:169885466
|
C | A | 1 | a0002c0002t0003g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-918-650G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885466 | ||||||
| chr5:169885491
|
T | C | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-675A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885491 | ||||||
| chr5:169885576
|
A | G | 1 | a0001c0001t0004g0283 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-918-760T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885576 | ||||||
| chr5:169885601
|
C | T | 1 | a0001c0001t0002g0037 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-918-785G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885601 | ||||||
| chr5:169885873
|
C | CA | 93 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0029others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-918-1058dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885873 | ||||||
| chr5:169886017
|
ACT | A | 16 | a0002c0002t0004g0055a0002c0002t0005g0006a0002c0002t0005g0014others(13): Show | 16 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-918-1203_-918-120 others(6): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886017 | ||||||
| chr5:169886112
|
A | G | 17 | a0002c0002t0003g0158a0002c0002t0004g0108a0002c0002t0006g0002others(14): Show | 18 | HG00323.hp1 HG01433.hp1 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-918-1296T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886112 | ||||||
| chr5:169886173
|
G | A | 1 | a0002c0002t0019g0270 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-918-1357C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886173 | ||||||
| chr5:169886215
|
A | G | 93 | a0002c0002t0001g0004a0002c0002t0001g0028a0002c0002t0001g0029others(90): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.-918-1399T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886215 | ||||||
| chr5:169886551
|
A | G | 2 | a0002c0002t0008g0313a0002c0002t0016g0280 | 2 | HG02056.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-918-1735T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886551 | ||||||
| chr5:169886652
|
C | T | 1 | a0001c0001t0002g0265 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-918-1836G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886652 | ||||||
| chr5:169886691
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-918-1875C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886691 | ||||||
| chr5:169886786
|
T | TTTTTTGC | 5 | a0003c0003t0004g0179a0003c0003t0004g0208a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-1977_-918-197 others(11): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886786 | ||||||
| chr5:169886816
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-918-2000G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886816 | ||||||
| chr5:169886854
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-918-2038A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169886854 | ||||||
| chr5:169887126
|
C | T | 15 | a0002c0002t0005g0006a0002c0002t0005g0014a0002c0002t0005g0017others(12): Show | 15 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-2310G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169887126 | ||||||
| chr5:169887239
|
C | T | 1 | a0001c0001t0002g0226 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-918-2423G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169887239 | ||||||
| chr5:169887347
|
A | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0188a0001c0001t0001g0199 | 3 | NA18963.hp1 NA18968.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-918-2531T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169887347 | ||||||
| chr5:169887599
|
T | A | 1 | a0002c0002t0014g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-918-2783A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169887599 | ||||||
| chr5:169887725
|
T | C | 16 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(13): Show | 16 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-918-2909A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169887725 | ||||||
| chr5:169887865
|
T | C | 137 | a0001c0001t0002g0155a0002c0002t0001g0004a0002c0002t0001g0028others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-918-3049A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169887865 | ||||||
| chr5:169888057
|
G | GA | 16 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(13): Show | 16 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-918-3242dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888057 | ||||||
| chr5:169888162
|
G | A | 31 | a0002c0002t0003g0158a0002c0002t0004g0108a0002c0002t0005g0006others(28): Show | 32 | HG00323.hp1 HG00639.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.-918-3346C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888162 | ||||||
| chr5:169888230
|
A | G | 16 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(13): Show | 16 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-918-3414T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888230 | ||||||
| chr5:169888231
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-918-3415T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888231 | ||||||
| chr5:169888377
|
G | A | 15 | a0001c0001t0002g0135a0002c0002t0001g0209a0002c0002t0001g0244others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-3561C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888377 | ||||||
| chr5:169888427
|
T | C | 1 | a0002c0002t0014g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-918-3611A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888427 | ||||||
| chr5:169888620
|
A | G | 41 | a0001c0001t0001g0178a0001c0001t0003g0005a0001c0001t0003g0007others(38): Show | 41 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-918-3804T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888620 | ||||||
| chr5:169888662
|
G | A | 3 | a0002c0002t0004g0055a0002c0002t0006g0081a0002c0002t0024g0316 | 3 | HG01433.hp1 HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-918-3846C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888662 | ||||||
| chr5:169888719
|
G | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-918-3903C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888719 | ||||||
| chr5:169888775
|
C | T | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-3959G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888775 | ||||||
| chr5:169888831
|
T | A | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-4015A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888831 | ||||||
| chr5:169888848
|
C | T | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-4032G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888848 | ||||||
| chr5:169888894
|
A | G | 2 | a0002c0002t0019g0270a0002c0007t0004g0075 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-918-4078T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888894 | ||||||
| chr5:169888947
|
G | A | 18 | a0002c0002t0003g0158a0002c0002t0004g0108a0002c0002t0006g0002others(15): Show | 19 | HG00323.hp1 HG01433.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.-918-4131C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169888947 | ||||||
| chr5:169889044
|
G | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0107 | 2 | HG03491.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-918-4228C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889044 | ||||||
| chr5:169889056
|
A | G | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-4240T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889056 | ||||||
| chr5:169889068
|
T | C | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-4252A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889068 | ||||||
| chr5:169889101
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-918-4285C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889101 | ||||||
| chr5:169889190
|
T | C | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-4374A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889190 | ||||||
| chr5:169889297
|
T | C | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-4481A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889297 | ||||||
| chr5:169889378
|
T | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-918-4562A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889378 | ||||||
| chr5:169889379
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-918-4563C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889379 | ||||||
| chr5:169889713
|
T | C | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-4897A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889713 | ||||||
| chr5:169889838
|
C | T | 22 | a0002c0002t0005g0006a0002c0002t0005g0014a0002c0002t0005g0017others(19): Show | 22 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.-918-5022G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889838 | ||||||
| chr5:169889873
|
A | G | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-5057T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889873 | ||||||
| chr5:169889914
|
T | C | 4 | a0001c0001t0002g0044a0001c0001t0002g0131a0001c0001t0002g0146others(1): Show | 4 | NA18967.hp1 NA18977.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-5098A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889914 | ||||||
| chr5:169889935
|
G | C | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-5119C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169889935 | ||||||
| chr5:169890001
|
AT | A | 67 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(64): Show | 67 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-918-5186delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890001 | ||||||
| chr5:169890042
|
G | A | 66 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(63): Show | 66 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-918-5226C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890042 | ||||||
| chr5:169890160
|
A | G | 6 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(3): Show | 6 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-5344T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890160 | ||||||
| chr5:169890238
|
A | G | 15 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0263others(12): Show | 15 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-5422T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890238 | ||||||
| chr5:169890608
|
T | G | 77 | a0001c0001t0002g0090a0002c0002t0001g0004a0002c0002t0001g0028others(74): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.-918-5792A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890608 | ||||||
| chr5:169890617
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-918-5801C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890617 | ||||||
| chr5:169890746
|
G | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-5930C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890746 | ||||||
| chr5:169890776
|
T | C | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-5960A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890776 | ||||||
| chr5:169890979
|
A | G | 15 | a0002c0002t0005g0006a0002c0002t0005g0014a0002c0002t0005g0017others(12): Show | 15 | HG00639.hp2 HG02257.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-918-6163T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169890979 | ||||||
| chr5:169891037
|
G | C | 10 | a0002c0002t0001g0209a0002c0002t0004g0106a0002c0002t0004g0159others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-918-6221C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891037 | ||||||
| chr5:169891177
|
A | C | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-6361T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891177 | ||||||
| chr5:169891224
|
T | C | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-6408A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891224 | ||||||
| chr5:169891263
|
G | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-6447C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891263 | ||||||
| chr5:169891290
|
C | G | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-6474G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891290 | ||||||
| chr5:169891367
|
A | G | 1 | a0001c0001t0012g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-918-6551T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891367 | ||||||
| chr5:169891390
|
G | A | 65 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-918-6574C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891390 | ||||||
| chr5:169891450
|
G | C | 1 | a0001c0001t0003g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-918-6634C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891450 | ||||||
| chr5:169891454
|
G | C | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-6638C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891454 | ||||||
| chr5:169891712
|
C | T | 4 | a0001c0001t0003g0019a0001c0001t0003g0235a0001c0001t0003g0240others(1): Show | 4 | HG02965.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-6896G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891712 | ||||||
| chr5:169891748
|
GTCAAGGC others(9): Show |
G | 1 | a0002c0002t0014g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-918-6948_-918-693 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891748 | ||||||
| chr5:169891995
|
C | CA | 7 | a0001c0001t0002g0069a0001c0001t0004g0112a0002c0002t0003g0074others(4): Show | 7 | HG00639.hp2 HG02056.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-918-7180dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891995 | ||||||
| chr5:169891995
|
CA | C | 21 | a0002c0002t0001g0045a0002c0002t0001g0121a0002c0002t0001g0161others(18): Show | 22 | HG00323.hp1 HG01106.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-918-7180delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169891995 | ||||||
| chr5:169892099
|
A | G | 4 | a0001c0001t0007g0133a0001c0001t0012g0154a0001c0001t0012g0193others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-7283T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892099 | ||||||
| chr5:169892124
|
T | C | 1 | a0002c0002t0007g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-918-7308A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892124 | ||||||
| chr5:169892334
|
A | G | 7 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0103others(4): Show | 7 | HG01981.hp2 HG02486.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-918-7518T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892334 | ||||||
| chr5:169892527
|
A | G | 1 | a0002c0002t0006g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-918-7711T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892527 | ||||||
| chr5:169892628
|
A | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0141a0001c0001t0003g0175 | 3 | HG02055.hp2 HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-918-7812T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892628 | ||||||
| chr5:169892729
|
A | G | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-7913T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892729 | ||||||
| chr5:169892934
|
C | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-8118G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892934 | ||||||
| chr5:169892935
|
C | G | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-8119G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169892935 | ||||||
| chr5:169893302
|
G | A | 234 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-918-8486C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893302 | ||||||
| chr5:169893323
|
A | T | 1 | a0001c0001t0002g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-918-8507T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893323 | ||||||
| chr5:169893362
|
G | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-8546C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893362 | ||||||
| chr5:169893363
|
G | A | 1 | a0002c0002t0001g0220 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-918-8547C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893363 | ||||||
| chr5:169893479
|
C | CT | 204 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-918-8664dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893479 | ||||||
| chr5:169893499
|
A | T | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-8683T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893499 | ||||||
| chr5:169893685
|
A | C | 126 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(123): Show | 126 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-918-8869T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893685 | ||||||
| chr5:169893698
|
A | G | 6 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-8882T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893698 | ||||||
| chr5:169893882
|
G | A | 1 | a0002c0002t0001g0030 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-918-9066C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893882 | ||||||
| chr5:169893958
|
G | T | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-918-9142C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893958 | ||||||
| chr5:169894056
|
G | A | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-918-9240C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894056 | ||||||
| chr5:169894151
|
C | T | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-9335G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894151 | ||||||
| chr5:169894224
|
C | A | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-9408G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894224 | ||||||
| chr5:169894351
|
C | T | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-9535G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894351 | ||||||
| chr5:169894412
|
T | C | 2 | a0002c0002t0008g0078a0002c0002t0008g0234 | 2 | HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-918-9596A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894412 | ||||||
| chr5:169894431
|
A | G | 1 | a0002c0002t0014g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-918-9615T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894431 | ||||||
| chr5:169894459
|
G | A | 29 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0167others(26): Show | 29 | HG00597.hp2 HG01081.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.-918-9643C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894459 | ||||||
| chr5:169894459
|
G | T | 2 | a0001c0001t0003g0279a0001c0001t0009g0042 | 2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-918-9643C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894459 | ||||||
| chr5:169894480
|
A | C | 2 | a0002c0002t0004g0055a0002c0002t0024g0316 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-918-9664T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894480 | ||||||
| chr5:169894564
|
G | C | 2 | a0002c0002t0004g0055a0002c0002t0024g0316 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-918-9748C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894564 | ||||||
| chr5:169894569
|
G | T | 4 | a0001c0001t0004g0112a0001c0001t0004g0177a0001c0001t0004g0283others(1): Show | 4 | NA18947.hp1 NA19009.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-9753C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894569 | ||||||
| chr5:169894571
|
A | T | 65 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(62): Show | 65 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-918-9755T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894571 | ||||||
| chr5:169894887
|
C | T | 2 | a0001c0001t0004g0026a0001c0001t0021g0232 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-918-10071G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894887 | ||||||
| chr5:169894954
|
G | T | 2 | a0002c0002t0004g0055a0002c0002t0024g0316 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-918-10138C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169894954 | ||||||
| chr5:169895019
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-918-10203C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895019 | ||||||
| chr5:169895193
|
A | G | 77 | a0001c0001t0002g0090a0001c0001t0002g0155a0002c0002t0001g0004others(74): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.-918-10377T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895193 | ||||||
| chr5:169895434
|
G | A | 15 | a0001c0001t0003g0003a0002c0002t0006g0002a0002c0002t0006g0048others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-10618C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895434 | ||||||
| chr5:169895441
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-918-10625C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895441 | ||||||
| chr5:169895446
|
T | C | 15 | a0001c0001t0003g0003a0002c0002t0006g0002a0002c0002t0006g0048others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-10630A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895446 | ||||||
| chr5:169895466
|
T | C | 1 | a0006c0006t0001g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-918-10650A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895466 | ||||||
| chr5:169895527
|
G | A | 17 | a0001c0001t0003g0003a0002c0002t0004g0108a0002c0002t0006g0002others(14): Show | 18 | HG00323.hp1 HG01433.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-918-10711C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895527 | ||||||
| chr5:169895557
|
C | G | 17 | a0001c0001t0003g0003a0002c0002t0004g0108a0002c0002t0006g0002others(14): Show | 18 | HG00323.hp1 HG01433.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-918-10741G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895557 | ||||||
| chr5:169895695
|
A | G | 1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-918-10879T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895695 | ||||||
| chr5:169895823
|
G | C | 2 | a0002c0002t0014g0092a0002c0002t0024g0316 | 2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-918-11007C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895823 | ||||||
| chr5:169895928
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-918-11112C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895928 | ||||||
| chr5:169895935
|
G | A | 5 | a0003c0003t0004g0179a0003c0003t0004g0208a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-11119C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169895935 | ||||||
| chr5:169896220
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-918-11404G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896220 | ||||||
| chr5:169896436
|
A | G | 2 | a0002c0002t0006g0066a0002c0002t0008g0313 | 2 | HG06807.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-918-11620T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896436 | ||||||
| chr5:169896506
|
A | C | 230 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.-918-11690T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896506 | ||||||
| chr5:169896650
|
A | G | 89 | a0001c0001t0002g0090a0001c0001t0002g0221a0001c0001t0004g0026others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-918-11834T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896650 | ||||||
| chr5:169896715
|
C | T | 222 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(219): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.-918-11899G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896715 | ||||||
| chr5:169896875
|
G | A | 4 | a0001c0001t0003g0252a0001c0001t0003g0262a0001c0001t0003g0272others(1): Show | 4 | HG00323.hp2 HG01069.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-12059C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896875 | ||||||
| chr5:169896884
|
AG | A | 62 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(59): Show | 62 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-918-12069delC | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896884 | ||||||
| chr5:169896969
|
A | T | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-12153T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896969 | ||||||
| chr5:169897053
|
A | C | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-12237T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897053 | ||||||
| chr5:169897197
|
T | C | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-12381A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897197 | ||||||
| chr5:169897352
|
C | T | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-12536G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897352 | ||||||
| chr5:169897353
|
C | T | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-12537G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897353 | ||||||
| chr5:169897483
|
T | G | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-12667A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897483 | ||||||
| chr5:169897610
|
C | T | 1 | a0002c0002t0001g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-918-12794G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897610 | ||||||
| chr5:169897612
|
A | G | 89 | a0001c0001t0002g0090a0001c0001t0002g0155a0001c0001t0002g0221others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-918-12796T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897612 | ||||||
| chr5:169897751
|
C | T | 3 | a0001c0001t0022g0305a0002c0002t0006g0066a0002c0002t0008g0313 | 3 | HG02559.hp2 HG06807.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-918-12935G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897751 | ||||||
| chr5:169897880
|
G | A | 15 | a0001c0001t0002g0044a0001c0001t0002g0131a0002c0002t0006g0002others(12): Show | 16 | HG00323.hp1 HG01433.hp1 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-13064C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897880 | ||||||
| chr5:169897958
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-918-13142C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169897958 | ||||||
| chr5:169898254
|
G | T | 10 | a0001c0001t0003g0019a0001c0001t0003g0235a0001c0001t0003g0240others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-918-13438C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898254 | ||||||
| chr5:169898528
|
A | AAAC | 3 | a0001c0001t0002g0057a0001c0001t0002g0089a0001c0001t0003g0164 | 3 | HG03688.hp1 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-918-13715_-918-13 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898528
|
A | AAACAAC | 6 | a0001c0001t0004g0112a0003c0003t0004g0179a0003c0003t0004g0208others(3): Show | 6 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-13718_-918-13 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898528
|
AAAC | A | 23 | a0001c0001t0002g0044a0001c0001t0002g0131a0001c0001t0004g0026others(20): Show | 24 | HG00323.hp1 HG01074.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-918-13715_-918-13 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898528
|
AAACAAC | A | 10 | a0001c0001t0003g0019a0001c0001t0003g0235a0001c0001t0003g0240others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-918-13718_-918-13 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898528
|
AAACAACA others(2): Show |
A | 3 | a0001c0001t0022g0305a0002c0002t0006g0066a0002c0002t0008g0313 | 3 | HG02559.hp2 HG06807.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-918-13721_-918-13 others(15): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898528
|
AAACAACA others(5): Show |
A | 74 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(71): Show | 74 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-918-13724_-918-13 others(18): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898528
|
AAACAACA others(8): Show |
A | 1 | a0002c0002t0004g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-918-13727_-918-13 others(21): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898528 | ||||||
| chr5:169898568
|
C | T | 4 | a0002c0002t0004g0055a0002c0002t0008g0078a0002c0002t0008g0234others(1): Show | 4 | HG02615.hp1 HG02818.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-13752G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898568 | ||||||
| chr5:169898590
|
G | A | 63 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-918-13774C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898590 | ||||||
| chr5:169898604
|
T | A | 2 | a0001c0001t0004g0026a0002c0002t0024g0316 | 2 | HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-918-13788A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898604 | ||||||
| chr5:169898615
|
C | T | 1 | a0002c0002t0001g0110 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-918-13799G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898615 | ||||||
| chr5:169898658
|
T | C | 63 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-918-13842A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898658 | ||||||
| chr5:169898735
|
G | A | 63 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(60): Show | 63 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-918-13919C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898735 | ||||||
| chr5:169898751
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-918-13935T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898751 | ||||||
| chr5:169898858
|
C | T | 7 | a0001c0001t0022g0305a0002c0002t0004g0055a0002c0002t0006g0066others(4): Show | 7 | HG02559.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-918-14042G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898858 | ||||||
| chr5:169898859
|
G | A | 62 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(59): Show | 62 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-918-14043C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898859 | ||||||
| chr5:169898947
|
A | T | 1 | a0002c0002t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-918-14131T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169898947 | ||||||
| chr5:169899048
|
C | T | 3 | a0001c0001t0003g0252a0001c0001t0003g0262a0001c0001t0003g0272 | 3 | HG00323.hp2 HG01981.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-918-14232G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899048 | ||||||
| chr5:169899058
|
C | T | 64 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(61): Show | 64 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-918-14242G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899058 | ||||||
| chr5:169899324
|
C | T | 1 | a0001c0001t0003g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-918-14508G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899324 | ||||||
| chr5:169899471
|
C | T | 98 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(95): Show | 99 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-918-14655G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899471 | ||||||
| chr5:169899582
|
A | C | 1 | a0001c0001t0002g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-918-14766T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899582 | ||||||
| chr5:169899598
|
G | A | 4 | a0001c0001t0003g0015a0001c0001t0003g0096a0001c0001t0003g0237others(1): Show | 4 | HG02055.hp1 HG02615.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-14782C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899598 | ||||||
| chr5:169899615
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-918-14799C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899615 | ||||||
| chr5:169899674
|
C | T | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-918-14858G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899674 | ||||||
| chr5:169899744
|
T | A | 1 | a0002c0002t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-918-14928A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899744 | ||||||
| chr5:169899801
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-918-14985C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899801 | ||||||
| chr5:169899820
|
A | G | 3 | a0001c0001t0022g0305a0002c0002t0006g0066a0002c0002t0008g0313 | 3 | HG02559.hp2 HG06807.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-918-15004T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899820 | ||||||
| chr5:169899871
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-918-15055A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899871 | ||||||
| chr5:169899872
|
T | A | 1 | a0001c0001t0002g0069 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-918-15056A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899872 | ||||||
| chr5:169899913
|
G | A | 91 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(88): Show | 91 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.-918-15097C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169899913 | ||||||
| chr5:169900191
|
C | A | 98 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(95): Show | 99 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-918-15375G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900191 | ||||||
| chr5:169900227
|
C | T | 1 | a0002c0002t0001g0033 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-918-15411G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900227 | ||||||
| chr5:169900265
|
A | C | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-15449T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900265 | ||||||
| chr5:169900576
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-918-15760A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900576 | ||||||
| chr5:169900616
|
A | T | 219 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(216): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-918-15800T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900616 | ||||||
| chr5:169900696
|
C | T | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-15880G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900696 | ||||||
| chr5:169900722
|
G | T | 37 | a0001c0001t0002g0044a0001c0001t0002g0131a0001c0001t0003g0019others(34): Show | 38 | HG00099.hp2 HG00323.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.-918-15906C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900722 | ||||||
| chr5:169900877
|
G | A | 61 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(58): Show | 61 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-918-16061C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900877 | ||||||
| chr5:169900886
|
C | T | 24 | a0001c0001t0002g0044a0001c0001t0002g0131a0001c0001t0004g0026others(21): Show | 25 | HG00323.hp1 HG01433.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.-918-16070G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900886 | ||||||
| chr5:169900941
|
G | A | 1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-918-16125C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900941 | ||||||
| chr5:169900952
|
C | T | 1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-918-16136G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169900952 | ||||||
| chr5:169901075
|
G | T | 3 | a0001c0001t0022g0305a0002c0002t0006g0066a0002c0002t0008g0313 | 3 | HG02559.hp2 HG06807.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-918-16259C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901075 | ||||||
| chr5:169901169
|
T | C | 3 | a0002c0002t0001g0142a0002c0002t0019g0270a0002c0007t0004g0075 | 3 | HG02129.hp1 HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-918-16353A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901169 | ||||||
| chr5:169901234
|
T | C | 89 | a0001c0001t0002g0090a0001c0001t0002g0221a0001c0001t0004g0027others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.-918-16418A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901234 | ||||||
| chr5:169901414
|
G | A | 12 | a0002c0002t0005g0006a0002c0002t0005g0017a0002c0002t0005g0024others(9): Show | 12 | HG00639.hp2 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-918-16598C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901414 | ||||||
| chr5:169901480
|
G | A | 61 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(58): Show | 61 | HG00323.hp2 HG00609.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-918-16664C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901480 | ||||||
| chr5:169901502
|
T | C | 1 | a0001c0001t0004g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-918-16686A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901502 | ||||||
| chr5:169901625
|
G | A | 12 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(9): Show | 12 | HG02055.hp1 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-918-16809C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901625 | ||||||
| chr5:169901984
|
A | G | 4 | a0001c0001t0003g0252a0001c0001t0003g0262a0001c0001t0003g0272others(1): Show | 4 | HG00323.hp2 HG01069.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-17168T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901984 | ||||||
| chr5:169901989
|
T | C | 1 | a0004c0004t0002g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-918-17173A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169901989 | ||||||
| chr5:169902047
|
C | G | 1 | a0002c0002t0001g0263 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-918-17231G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902047 | ||||||
| chr5:169902108
|
C | A | 3 | a0002c0002t0001g0031a0002c0002t0001g0195a0002c0002t0001g0219 | 3 | HG01074.hp1 HG01255.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-918-17292G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902108 | ||||||
| chr5:169902214
|
A | G | 1 | a0002c0002t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-918-17398T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902214 | ||||||
| chr5:169902270
|
G | C | 204 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-918-17454C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902270 | ||||||
| chr5:169902360
|
A | C | 313 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(310): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.-918-17544T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902360 | ||||||
| chr5:169902423
|
T | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0253a0001c0001t0002g0258 | 3 | HG00642.hp2 NA18952.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-918-17607A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902423 | ||||||
| chr5:169902465
|
C | T | 1 | a0002c0002t0006g0285 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-918-17649G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902465 | ||||||
| chr5:169902727
|
A | G | 88 | a0001c0001t0002g0090a0001c0001t0002g0221a0001c0001t0004g0027others(85): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-918-17911T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902727 | ||||||
| chr5:169902802
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-918-17986A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902802 | ||||||
| chr5:169902895
|
C | T | 10 | a0002c0002t0005g0006a0002c0002t0005g0017a0002c0002t0005g0024others(7): Show | 10 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-918-18079G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902895 | ||||||
| chr5:169902969
|
A | G | 1 | a0002c0002t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-918-18153T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902969 | ||||||
| chr5:169903049
|
G | A | 2 | a0002c0002t0001g0186a0002c0002t0001g0187 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-918-18233C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903049 | ||||||
| chr5:169903054
|
C | T | 2 | a0002c0002t0004g0108a0002c0002t0023g0076 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-918-18238G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903054 | ||||||
| chr5:169903096
|
C | CA | 6 | a0001c0001t0002g0290a0001c0001t0003g0003a0001c0001t0007g0133others(3): Show | 6 | HG02258.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-18281dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903096 | ||||||
| chr5:169903118
|
G | A | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-918-18302C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903118 | ||||||
| chr5:169903232
|
G | A | 131 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0178others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-918-18416C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903232 | ||||||
| chr5:169903311
|
T | TA | 55 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0167others(52): Show | 55 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-918-18496dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903311 | ||||||
| chr5:169903311
|
TA | T | 95 | a0001c0001t0002g0057a0001c0001t0002g0090a0001c0001t0002g0191others(92): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.-918-18496delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903311 | ||||||
| chr5:169903453
|
C | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-918-18637G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903453 | ||||||
| chr5:169903529
|
C | T | 1 | a0002c0002t0001g0229 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-918-18713G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903529 | ||||||
| chr5:169903658
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-918-18842T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903658 | ||||||
| chr5:169903675
|
C | G | 1 | a0001c0001t0003g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-918-18859G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903675 | ||||||
| chr5:169903680
|
G | A | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-918-18864C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903680 | ||||||
| chr5:169903694
|
C | T | 5 | a0001c0001t0003g0003a0001c0001t0007g0133a0001c0001t0012g0154others(2): Show | 5 | HG02258.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-918-18878G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903694 | ||||||
| chr5:169903695
|
G | A | 187 | a0001c0001t0001g0050a0001c0001t0001g0127a0001c0001t0001g0167others(184): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.-918-18879C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903695 | ||||||
| chr5:169903735
|
G | A | 2 | a0002c0002t0001g0091a0002c0007t0004g0075 | 2 | HG02738.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-918-18919C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903735 | ||||||
| chr5:169903827
|
G | C | 13 | a0001c0001t0003g0003a0001c0001t0003g0307a0001c0001t0007g0133others(10): Show | 13 | HG02258.hp2 HG02735.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.-918-19011C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903827 | ||||||
| chr5:169903960
|
C | T | 2 | a0001c0001t0002g0290a0002c0002t0008g0078 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-918-19144G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169903960 | ||||||
| chr5:169904047
|
C | T | 1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-918-19231G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904047 | ||||||
| chr5:169904066
|
T | C | 8 | a0001c0001t0002g0128a0001c0001t0002g0155a0001c0001t0003g0262others(5): Show | 8 | HG00280.hp2 HG01069.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-918-19250A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904066 | ||||||
| chr5:169904091
|
C | CA | 14 | a0001c0001t0001g0199a0001c0001t0002g0130a0001c0001t0002g0146others(11): Show | 14 | HG01433.hp1 HG01975.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.-918-19276dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904091 | ||||||
| chr5:169904091
|
C | CAA | 80 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(77): Show | 80 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-918-19277_-918-19 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904091 | ||||||
| chr5:169904091
|
C | CAAA | 28 | a0001c0001t0001g0127a0001c0001t0001g0167a0001c0001t0001g0249others(25): Show | 28 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-918-19278_-918-19 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904091 | ||||||
| chr5:169904091
|
CA | C | 8 | a0001c0001t0002g0072a0001c0001t0002g0239a0001c0001t0003g0252others(5): Show | 8 | HG00323.hp2 HG01168.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-918-19276delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904091 | ||||||
| chr5:169904091
|
CAAAAAAA others(5): Show |
C | 5 | a0003c0003t0004g0179a0003c0003t0004g0208a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-19287_-918-19 others(18): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904091 | ||||||
| chr5:169904187
|
T | C | 139 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(136): Show | 140 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.-918-19371A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904187 | ||||||
| chr5:169904193
|
C | A | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-918-19377G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904193 | ||||||
| chr5:169904235
|
A | G | 175 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-918-19419T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904235 | ||||||
| chr5:169904307
|
CCCTT | C | 18 | a0001c0001t0002g0180a0001c0001t0003g0007a0001c0001t0003g0008others(15): Show | 18 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.-918-19495_-918-19 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904307 | ||||||
| chr5:169904380
|
T | C | 1 | a0001c0001t0003g0233 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-918-19564A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904380 | ||||||
| chr5:169904446
|
C | A | 153 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-918-19630G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904446 | ||||||
| chr5:169904636
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-918-19820T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904636 | ||||||
| chr5:169904691
|
G | C | 11 | a0001c0001t0002g0290a0001c0001t0003g0007a0001c0001t0003g0008others(8): Show | 11 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-918-19875C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904691 | ||||||
| chr5:169904724
|
C | T | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-19908G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904724 | ||||||
| chr5:169904748
|
T | C | 3 | a0001c0001t0002g0185a0001c0001t0004g0124a0002c0002t0001g0229 | 3 | HG01975.hp2 HG02004.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-918-19932A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904748 | ||||||
| chr5:169904934
|
G | A | 80 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(77): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-918-20118C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904934 | ||||||
| chr5:169904975
|
T | A | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-20159A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904975 | ||||||
| chr5:169904995
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-20179G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169904995 | ||||||
| chr5:169905012
|
C | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-20196G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905012 | ||||||
| chr5:169905152
|
A | G | 228 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-918-20336T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905152 | ||||||
| chr5:169905221
|
A | G | 5 | a0001c0001t0002g0052a0001c0001t0002g0160a0001c0001t0002g0225others(2): Show | 5 | NA18955.hp2 NA19000.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-918-20405T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905221 | ||||||
| chr5:169905256
|
G | T | 134 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(131): Show | 135 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.-918-20440C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905256 | ||||||
| chr5:169905288
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-918-20472G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905288 | ||||||
| chr5:169905293
|
G | GT | 217 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.-918-20478dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905293 | ||||||
| chr5:169905293
|
G | GTT | 6 | a0001c0001t0002g0090a0001c0001t0002g0207a0002c0002t0001g0294others(3): Show | 6 | HG01261.hp2 HG02165.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-20479_-918-20 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905293 | ||||||
| chr5:169905293
|
GT | G | 37 | a0001c0001t0002g0128a0001c0001t0002g0155a0001c0001t0002g0290others(34): Show | 37 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.-918-20478delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905293 | ||||||
| chr5:169905299
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-918-20483A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905299 | ||||||
| chr5:169905645
|
G | C | 134 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(131): Show | 135 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.-918-20829C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905645 | ||||||
| chr5:169905658
|
A | G | 1 | a0001c0001t0003g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-918-20842T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905658 | ||||||
| chr5:169905718
|
T | C | 1 | a0002c0002t0005g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-918-20902A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905718 | ||||||
| chr5:169905725
|
G | A | 144 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-918-20909C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905725 | ||||||
| chr5:169905905
|
C | A | 1 | a0002c0002t0019g0270 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-918-21089G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905905 | ||||||
| chr5:169905954
|
T | A | 1 | a0002c0002t0001g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-918-21138A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905954 | ||||||
| chr5:169905960
|
A | G | 4 | a0001c0001t0003g0251a0002c0002t0005g0309a0002c0002t0005g0310others(1): Show | 4 | HG00639.hp2 HG02040.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-21144T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169905960 | ||||||
| chr5:169906072
|
A | G | 9 | a0001c0001t0002g0290a0001c0001t0021g0232a0002c0002t0003g0158others(6): Show | 9 | HG02615.hp1 HG02735.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.-918-21256T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906072 | ||||||
| chr5:169906117
|
C | A | 1 | a0002c0002t0005g0310 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-918-21301G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906117 | ||||||
| chr5:169906208
|
G | A | 13 | a0001c0001t0002g0049a0001c0001t0002g0185a0001c0001t0002g0268others(10): Show | 13 | HG01975.hp2 HG02004.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-918-21392C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906208 | ||||||
| chr5:169906324
|
C | T | 4 | a0001c0001t0002g0180a0002c0002t0001g0157a0002c0002t0001g0263others(1): Show | 4 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-21508G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906324 | ||||||
| chr5:169906485
|
C | T | 249 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(246): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-918-21669G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906485 | ||||||
| chr5:169906491
|
GTT | G | 11 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-918-21677_-918-21 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906491 | ||||||
| chr5:169906520
|
C | T | 6 | a0001c0001t0002g0180a0001c0001t0002g0290a0002c0002t0001g0157others(3): Show | 6 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-21704G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906520 | ||||||
| chr5:169906524
|
G | T | 4 | a0001c0001t0002g0052a0001c0001t0002g0225a0001c0001t0002g0226others(1): Show | 4 | NA18955.hp2 NA19009.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-21708C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906524 | ||||||
| chr5:169906551
|
T | C | 262 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-918-21735A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906551 | ||||||
| chr5:169906570
|
T | C | 1 | a0002c0002t0005g0310 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-918-21754A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906570 | ||||||
| chr5:169906625
|
G | C | 5 | a0002c0002t0018g0095a0003c0003t0004g0179a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-21809C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906625 | ||||||
| chr5:169906791
|
G | A | 2 | a0001c0001t0021g0232a0002c0002t0003g0158 | 2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-918-21975C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906791 | ||||||
| chr5:169906797
|
G | A | 2 | a0001c0001t0021g0232a0002c0002t0003g0158 | 2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-918-21981C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906797 | ||||||
| chr5:169906903
|
T | A | 152 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(149): Show | 153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-918-22087A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169906903 | ||||||
| chr5:169907128
|
G | A | 2 | a0001c0001t0003g0141a0001c0001t0003g0175 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-918-22312C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907128 | ||||||
| chr5:169907236
|
G | A | 3 | a0001c0001t0022g0305a0002c0002t0004g0106a0002c0002t0004g0159 | 3 | HG02559.hp2 HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-918-22420C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907236 | ||||||
| chr5:169907399
|
C | G | 1 | a0001c0001t0003g0251 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-918-22583G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907399 | ||||||
| chr5:169907534
|
G | C | 24 | a0001c0001t0003g0003a0001c0001t0003g0007a0001c0001t0003g0008others(21): Show | 24 | HG02258.hp2 HG02559.hp1 HG02572.hp2 others(21): Show |
intron_variant | MODIFIER | c.-918-22718C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907534 | ||||||
| chr5:169907635
|
A | G | 3 | a0001c0001t0002g0290a0002c0002t0008g0078a0002c0002t0024g0316 | 3 | HG02572.hp1 HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-918-22819T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907635 | ||||||
| chr5:169907841
|
TGGCATCT others(4): Show |
T | 1 | a0002c0002t0007g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-918-23036_-918-23 others(17): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907841 | ||||||
| chr5:169907884
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-918-23068G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907884 | ||||||
| chr5:169907910
|
C | T | 78 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(75): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.-918-23094G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907910 | ||||||
| chr5:169907934
|
A | G | 1 | a0002c0002t0001g0312 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-918-23118T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169907934 | ||||||
| chr5:169908102
|
A | T | 2 | a0001c0001t0002g0290a0002c0002t0008g0078 | 2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-918-23286T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908102 | ||||||
| chr5:169908125
|
A | G | 154 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-918-23309T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908125 | ||||||
| chr5:169908382
|
C | T | 261 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-918-23566G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908382 | ||||||
| chr5:169908450
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-918-23634G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908450 | ||||||
| chr5:169908566
|
T | C | 16 | a0001c0001t0002g0180a0001c0001t0003g0003a0001c0001t0003g0307others(13): Show | 16 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-23750A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908566 | ||||||
| chr5:169908622
|
A | G | 1 | a0002c0002t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-918-23806T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908622 | ||||||
| chr5:169908681
|
A | G | 4 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-23865T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908681 | ||||||
| chr5:169908713
|
CT | C | 105 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(102): Show | 106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-918-23898delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908713 | ||||||
| chr5:169908713
|
CTT | C | 138 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-918-23899_-918-23 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908713 | ||||||
| chr5:169908713
|
CTTT | C | 6 | a0001c0001t0003g0003a0001c0001t0003g0233a0001c0001t0003g0307others(3): Show | 6 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-23900_-918-23 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908713 | ||||||
| chr5:169908958
|
C | G | 145 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(142): Show | 146 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.-918-24142G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169908958 | ||||||
| chr5:169909160
|
A | G | 20 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(17): Show | 20 | HG00597.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-918-24344T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909160 | ||||||
| chr5:169909382
|
A | G | 1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-918-24566T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909382 | ||||||
| chr5:169909401
|
G | T | 1 | a0001c0001t0002g0071 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-918-24585C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909401 | ||||||
| chr5:169909460
|
A | C | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-24644T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909460 | ||||||
| chr5:169909584
|
A | G | 1 | a0001c0001t0004g0283 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-918-24768T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909584 | ||||||
| chr5:169909619
|
A | G | 168 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-918-24803T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909619 | ||||||
| chr5:169909622
|
T | A | 1 | a0001c0001t0004g0261 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-918-24806A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909622 | ||||||
| chr5:169909934
|
C | G | 4 | a0002c0002t0001g0032a0002c0002t0001g0115a0002c0002t0001g0286others(1): Show | 4 | HG00621.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-25118G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909934 | ||||||
| chr5:169909988
|
T | C | 1 | a0001c0001t0003g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-918-25172A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169909988 | ||||||
| chr5:169910173
|
G | A | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-918-25357C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910173 | ||||||
| chr5:169910281
|
C | T | 1 | a0002c0002t0005g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-918-25465G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910281 | ||||||
| chr5:169910282
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-25466C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910282 | ||||||
| chr5:169910291
|
C | T | 136 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(133): Show | 137 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.-918-25475G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910291 | ||||||
| chr5:169910359
|
A | G | 6 | a0002c0002t0001g0091a0002c0002t0018g0095a0003c0003t0004g0179others(3): Show | 6 | HG02735.hp1 HG02738.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-25543T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910359 | ||||||
| chr5:169910486
|
C | T | 6 | a0002c0002t0001g0091a0002c0002t0018g0095a0003c0003t0004g0179others(3): Show | 6 | HG02735.hp1 HG02738.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-25670G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910486 | ||||||
| chr5:169910537
|
CAGCATCC others(19): Show |
C | 2 | a0001c0001t0003g0252a0001c0001t0003g0272 | 2 | HG00323.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-918-25747_-918-25 others(32): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910537 | ||||||
| chr5:169910613
|
A | G | 16 | a0001c0001t0002g0180a0001c0001t0003g0003a0001c0001t0003g0307others(13): Show | 16 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.-918-25797T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910613 | ||||||
| chr5:169910656
|
A | G | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-918-25840T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910656 | ||||||
| chr5:169910671
|
T | C | 1 | a0001c0001t0003g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-918-25855A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910671 | ||||||
| chr5:169910681
|
C | T | 1 | a0002c0002t0008g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-918-25865G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910681 | ||||||
| chr5:169910763
|
T | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-25947A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910763 | ||||||
| chr5:169910875
|
C | A | 26 | a0001c0001t0002g0180a0001c0001t0003g0003a0001c0001t0003g0007others(23): Show | 26 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.-918-26059G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910875 | ||||||
| chr5:169910877
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-918-26061C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910877 | ||||||
| chr5:169910878
|
C | A | 2 | a0001c0001t0003g0056a0001c0001t0003g0097 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-918-26062G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169910878 | ||||||
| chr5:169911320
|
T | C | 170 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(167): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-918-26504A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169911320 | ||||||
| chr5:169911457
|
T | C | 1 | a0005c0008t0003g0113 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-918-26641A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169911457 | ||||||
| chr5:169911481
|
T | G | 143 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(140): Show | 144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-918-26665A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169911481 | ||||||
| chr5:169911811
|
G | A | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-26995C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169911811 | ||||||
| chr5:169912032
|
C | T | 130 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(127): Show | 131 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.-918-27216G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912032 | ||||||
| chr5:169912125
|
C | T | 1 | a0002c0002t0003g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-918-27309G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912125 | ||||||
| chr5:169912460
|
C | T | 1 | a0002c0002t0013g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-918-27644G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912460 | ||||||
| chr5:169912554
|
T | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-27738A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912554 | ||||||
| chr5:169912621
|
A | ATG | 106 | a0001c0001t0001g0127a0001c0001t0001g0167a0001c0001t0001g0249others(103): Show | 107 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.-918-27807_-918-27 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912621 | ||||||
| chr5:169912621
|
A | ATGTG | 62 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-918-27809_-918-27 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912621 | ||||||
| chr5:169912689
|
A | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-27873T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912689 | ||||||
| chr5:169912756
|
A | T | 1 | a0002c0002t0020g0298 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-918-27940T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912756 | ||||||
| chr5:169912805
|
C | G | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-918-27989G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912805 | ||||||
| chr5:169912846
|
T | A | 11 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 11 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-918-28030A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912846 | ||||||
| chr5:169912884
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-28068C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912884 | ||||||
| chr5:169912966
|
T | C | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-918-28150A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169912966 | ||||||
| chr5:169913059
|
T | C | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-28243A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913059 | ||||||
| chr5:169913099
|
T | C | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-28283A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913099 | ||||||
| chr5:169913151
|
A | G | 147 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(144): Show | 148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.-918-28335T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913151 | ||||||
| chr5:169913263
|
G | A | 2 | a0002c0002t0005g0309a0002c0002t0005g0310 | 2 | HG00639.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-918-28447C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913263 | ||||||
| chr5:169913267
|
A | G | 9 | a0001c0001t0002g0012a0001c0001t0002g0060a0001c0001t0002g0062others(6): Show | 9 | HG02083.hp2 HG02155.hp1 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-28451T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913267 | ||||||
| chr5:169913362
|
G | C | 2 | a0001c0001t0010g0151a0002c0002t0007g0013 | 2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-918-28546C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913362 | ||||||
| chr5:169913375
|
A | T | 31 | a0001c0001t0001g0127a0001c0001t0001g0167a0001c0001t0001g0249others(28): Show | 31 | HG00597.hp2 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-918-28559T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913375 | ||||||
| chr5:169913640
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-28824C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913640 | ||||||
| chr5:169913707
|
CGCCCTCT | C | 83 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(80): Show | 83 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-918-28898_-918-28 others(13): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913707 | ||||||
| chr5:169913715
|
G | A | 13 | a0001c0001t0002g0049a0001c0001t0002g0185a0001c0001t0002g0268others(10): Show | 13 | HG01975.hp2 HG02004.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-918-28899C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913715 | ||||||
| chr5:169913761
|
G | T | 76 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-918-28945C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169913761 | ||||||
| chr5:169914272
|
A | G | 155 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(152): Show | 156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-918-29456T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914272 | ||||||
| chr5:169914333
|
T | C | 9 | a0001c0001t0002g0053a0001c0001t0004g0026a0001c0001t0010g0020others(6): Show | 9 | HG00741.hp1 HG01168.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-29517A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914333 | ||||||
| chr5:169914637
|
A | C | 6 | a0001c0001t0002g0049a0001c0001t0002g0185a0001c0001t0002g0268others(3): Show | 6 | HG01975.hp2 HG02004.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-29821T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914637 | ||||||
| chr5:169914681
|
C | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-29865G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914681 | ||||||
| chr5:169914701
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-918-29885T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914701 | ||||||
| chr5:169914735
|
T | A | 1 | a0002c0002t0007g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-918-29919A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914735 | ||||||
| chr5:169914825
|
T | G | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-30009A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914825 | ||||||
| chr5:169914886
|
A | C | 6 | a0002c0002t0001g0091a0002c0002t0018g0095a0003c0003t0004g0179others(3): Show | 6 | HG02735.hp1 HG02738.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-30070T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914886 | ||||||
| chr5:169914947
|
C | A | 90 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(87): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-918-30131G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914947 | ||||||
| chr5:169914992
|
G | C | 1 | a0003c0003t0004g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-918-30176C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169914992 | ||||||
| chr5:169915069
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085 | 3 | NA18969.hp2 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-918-30253T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915069 | ||||||
| chr5:169915104
|
C | T | 1 | a0002c0002t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-918-30288G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915104 | ||||||
| chr5:169915281
|
G | A | 168 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(165): Show | 169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-918-30465C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915281 | ||||||
| chr5:169915347
|
G | C | 93 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-918-30531C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915347 | ||||||
| chr5:169915471
|
A | G | 1 | a0005c0008t0003g0113 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-918-30655T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915471 | ||||||
| chr5:169915513
|
A | G | 150 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(147): Show | 151 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.-918-30697T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915513 | ||||||
| chr5:169915557
|
A | AAC | 23 | a0001c0001t0001g0178a0001c0001t0002g0053a0001c0001t0002g0072others(20): Show | 23 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-918-30743_-918-30 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
A | AACAC | 6 | a0001c0001t0002g0180a0001c0001t0002g0256a0001c0001t0007g0133others(3): Show | 6 | HG01168.hp1 HG01358.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-30745_-918-30 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
A | AACACAC | 5 | a0001c0001t0002g0135a0001c0001t0002g0253a0001c0001t0002g0258others(2): Show | 5 | HG00642.hp2 HG01358.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-918-30747_-918-30 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AAC | A | 18 | a0001c0001t0001g0127a0001c0001t0001g0210a0001c0001t0002g0065others(15): Show | 18 | HG01081.hp2 HG01516.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.-918-30743_-918-30 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACAC | A | 50 | a0001c0001t0001g0167a0001c0001t0001g0197a0001c0001t0001g0249others(47): Show | 50 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-918-30745_-918-30 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACACAC | A | 107 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(104): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-918-30747_-918-30 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0002g0036a0002c0002t0024g0316a0002c0002t0025g0315 | 3 | HG02572.hp1 HG02886.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.-918-30749_-918-30 others(14): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0002g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-918-30751_-918-30 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-918-30755_-918-30 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACACACA others(9): Show |
A | 1 | a0002c0002t0003g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-918-30757_-918-30 others(22): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915557
|
AACACACA others(11): Show |
A | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-918-30759_-918-30 others(24): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915557 | ||||||
| chr5:169915672
|
C | T | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-918-30856G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915672 | ||||||
| chr5:169915673
|
A | G | 6 | a0001c0001t0002g0290a0001c0001t0003g0300a0002c0002t0005g0098others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-30857T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915673 | ||||||
| chr5:169915738
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-918-30922G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915738 | ||||||
| chr5:169915742
|
C | T | 1 | a0001c0001t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-918-30926G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915742 | ||||||
| chr5:169915944
|
C | T | 6 | a0001c0001t0003g0251a0002c0002t0001g0171a0002c0002t0005g0309others(3): Show | 6 | HG00639.hp2 HG02040.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-918-31128G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169915944 | ||||||
| chr5:169916075
|
T | C | 1 | a0001c0001t0004g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-918-31259A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916075 | ||||||
| chr5:169916183
|
T | C | 15 | a0001c0001t0002g0180a0001c0001t0003g0003a0001c0001t0003g0307others(12): Show | 15 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.-918-31367A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916183 | ||||||
| chr5:169916213
|
G | A | 87 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-918-31397C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916213 | ||||||
| chr5:169916245
|
G | A | 1 | a0001c0001t0003g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-918-31429C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916245 | ||||||
| chr5:169916350
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-918-31534G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916350 | ||||||
| chr5:169916668
|
A | G | 87 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(84): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-918-31852T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916668 | ||||||
| chr5:169916689
|
C | CTG | 263 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(260): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-918-31874_-918-31 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916689 | ||||||
| chr5:169916976
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-32160T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916976 | ||||||
| chr5:169916995
|
C | T | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-32179G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169916995 | ||||||
| chr5:169917066
|
A | T | 1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-918-32250T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917066 | ||||||
| chr5:169917090
|
C | T | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-918-32274G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917090 | ||||||
| chr5:169917162
|
C | T | 1 | a0001c0001t0004g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-918-32346G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917162 | ||||||
| chr5:169917362
|
A | C | 1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-918-32546T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917362 | ||||||
| chr5:169917395
|
T | C | 1 | a0001c0001t0002g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-918-32579A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917395 | ||||||
| chr5:169917428
|
T | A | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-918-32612A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917428 | ||||||
| chr5:169917531
|
T | G | 7 | a0001c0001t0003g0251a0001c0001t0021g0232a0002c0002t0001g0171others(4): Show | 7 | HG00639.hp2 HG02040.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-918-32715A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917531 | ||||||
| chr5:169917570
|
T | C | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-918-32754A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917570 | ||||||
| chr5:169917676
|
T | C | 140 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(137): Show | 141 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-918-32860A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917676 | ||||||
| chr5:169917926
|
G | C | 2 | a0001c0001t0003g0019a0001c0001t0003g0079 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-918-33110C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917926 | ||||||
| chr5:169917940
|
C | G | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-918-33124G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917940 | ||||||
| chr5:169917947
|
T | C | 1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-918-33131A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169917947 | ||||||
| chr5:169918016
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-918-33200C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918016 | ||||||
| chr5:169918037
|
C | G | 5 | a0001c0001t0003g0251a0002c0002t0001g0171a0002c0002t0005g0309others(2): Show | 5 | HG00639.hp2 HG02040.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-33221G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918037 | ||||||
| chr5:169918077
|
T | C | 5 | a0001c0001t0003g0300a0002c0002t0005g0098a0002c0002t0005g0301others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-918-33261A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918077 | ||||||
| chr5:169918113
|
A | G | 2 | a0001c0001t0003g0141a0001c0001t0003g0175 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-918-33297T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918113 | ||||||
| chr5:169918162
|
T | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-918-33346A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918162 | ||||||
| chr5:169918175
|
A | G | 1 | a0002c0002t0001g0294 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-918-33359T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918175 | ||||||
| chr5:169918183
|
A | C | 1 | a0001c0001t0002g0069 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-918-33367T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918183 | ||||||
| chr5:169918255
|
G | A | 4 | a0001c0001t0003g0300a0002c0002t0005g0098a0002c0002t0005g0301others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-33439C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918255 | ||||||
| chr5:169918329
|
C | G | 1 | a0001c0001t0003g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-918-33513G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918329 | ||||||
| chr5:169918479
|
G | A | 2 | a0002c0002t0001g0231a0002c0002t0008g0303 | 2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-918-33663C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918479 | ||||||
| chr5:169918574
|
A | C | 1 | a0001c0001t0009g0295 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-918-33758T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918574 | ||||||
| chr5:169918631
|
G | A | 153 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(150): Show | 154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-918-33815C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918631 | ||||||
| chr5:169918635
|
A | G | 157 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-918-33819T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918635 | ||||||
| chr5:169918934
|
G | T | 3 | a0001c0001t0003g0235a0001c0001t0003g0240a0002c0002t0008g0234 | 3 | HG03098.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-918-34118C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918934 | ||||||
| chr5:169918941
|
T | C | 1 | a0002c0002t0004g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-918-34125A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918941 | ||||||
| chr5:169918944
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-34128C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169918944 | ||||||
| chr5:169919015
|
G | T | 8 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017others(5): Show | 8 | HG02258.hp2 HG02735.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.-918-34199C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919015 | ||||||
| chr5:169919018
|
A | T | 1 | a0001c0001t0002g0253 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-918-34202T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919018 | ||||||
| chr5:169919329
|
T | C | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-34513A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919329 | ||||||
| chr5:169919481
|
A | C | 4 | a0001c0001t0007g0133a0001c0001t0012g0154a0001c0001t0012g0193others(1): Show | 4 | HG02717.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-34665T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919481 | ||||||
| chr5:169919547
|
A | G | 2 | a0001c0001t0021g0232a0002c0002t0003g0158 | 2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-918-34731T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919547 | ||||||
| chr5:169919617
|
T | C | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-34801A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919617 | ||||||
| chr5:169919751
|
T | A | 1 | a0002c0002t0025g0315 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-918-34935A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919751 | ||||||
| chr5:169919782
|
AT | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0107a0002c0007t0004g0075 | 3 | HG03491.hp1 HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-918-34967delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919782 | ||||||
| chr5:169919851
|
G | A | 76 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-918-35035C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919851 | ||||||
| chr5:169919852
|
G | A | 1 | a0003c0003t0004g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-918-35036C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919852 | ||||||
| chr5:169919969
|
A | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-35153T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919969 | ||||||
| chr5:169919988
|
C | G | 89 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(86): Show | 89 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-918-35172G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169919988 | ||||||
| chr5:169920133
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-918-35317C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920133 | ||||||
| chr5:169920255
|
T | G | 162 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-918-35439A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920255 | ||||||
| chr5:169920368
|
C | T | 69 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(66): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-918-35552G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920368 | ||||||
| chr5:169920384
|
A | G | 158 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.-918-35568T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920384 | ||||||
| chr5:169920522
|
C | T | 35 | a0001c0001t0001g0111a0001c0001t0001g0178a0001c0001t0001g0276others(32): Show | 35 | HG00423.hp1 HG00621.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-918-35706G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920522 | ||||||
| chr5:169920673
|
C | G | 1 | a0002c0002t0005g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-918-35857G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920673 | ||||||
| chr5:169920853
|
A | G | 157 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-918-36037T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920853 | ||||||
| chr5:169920862
|
G | A | 157 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-918-36046C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920862 | ||||||
| chr5:169920864
|
A | ACAGG | 157 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-918-36049_-918-36 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920864 | ||||||
| chr5:169920866
|
C | G | 157 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-918-36050G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920866 | ||||||
| chr5:169920884
|
T | C | 1 | a0002c0002t0005g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-918-36068A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920884 | ||||||
| chr5:169920889
|
A | T | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-36073T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920889 | ||||||
| chr5:169920932
|
T | C | 1 | a0002c0002t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-918-36116A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169920932 | ||||||
| chr5:169921049
|
A | G | 6 | a0001c0001t0002g0290a0001c0001t0003g0300a0002c0002t0005g0098others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-36233T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921049 | ||||||
| chr5:169921144
|
C | A | 1 | a0001c0001t0002g0087 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-918-36328G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921144 | ||||||
| chr5:169921182
|
A | G | 4 | a0001c0001t0002g0180a0002c0002t0001g0157a0002c0002t0001g0263others(1): Show | 4 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-36366T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921182 | ||||||
| chr5:169921226
|
C | T | 1 | a0001c0001t0003g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-918-36410G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921226 | ||||||
| chr5:169921292
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-918-36476C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921292 | ||||||
| chr5:169921473
|
C | G | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-36657G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921473 | ||||||
| chr5:169921736
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-918-36920C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921736 | ||||||
| chr5:169921787
|
G | A | 250 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(247): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.-918-36971C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921787 | ||||||
| chr5:169921788
|
T | G | 81 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(78): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.-918-36972A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921788 | ||||||
| chr5:169921806
|
G | A | 77 | a0001c0001t0002g0035a0001c0001t0002g0037a0001c0001t0002g0047others(74): Show | 78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-918-36990C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921806 | ||||||
| chr5:169921849
|
A | T | 1 | a0002c0002t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-918-37033T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921849 | ||||||
| chr5:169921894
|
C | G | 4 | a0001c0001t0003g0300a0002c0002t0005g0098a0002c0002t0005g0301others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-37078G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921894 | ||||||
| chr5:169921899
|
A | C | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-918-37083T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921899 | ||||||
| chr5:169921918
|
A | C | 3 | a0001c0001t0021g0232a0002c0002t0023g0076a0002c0002t0024g0316 | 3 | HG02572.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-918-37102T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921918 | ||||||
| chr5:169921950
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-918-37134C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169921950 | ||||||
| chr5:169922031
|
C | A | 9 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(6): Show | 9 | HG02622.hp1 HG02630.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-37215G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922031 | ||||||
| chr5:169922128
|
A | G | 2 | a0002c0002t0001g0206a0002c0002t0006g0285 | 2 | HG02258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-918-37312T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922128 | ||||||
| chr5:169922157
|
C | G | 4 | a0001c0001t0002g0180a0002c0002t0001g0157a0002c0002t0001g0263others(1): Show | 4 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-37341G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922157 | ||||||
| chr5:169922302
|
C | G | 13 | a0001c0001t0002g0180a0001c0001t0003g0003a0001c0001t0003g0307others(10): Show | 13 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.-918-37486G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922302 | ||||||
| chr5:169922309
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-918-37493T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922309 | ||||||
| chr5:169922378
|
G | T | 2 | a0002c0002t0003g0158a0002c0002t0023g0076 | 2 | HG03139.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-918-37562C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922378 | ||||||
| chr5:169922447
|
C | G | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-918-37631G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922447 | ||||||
| chr5:169922579
|
G | T | 4 | a0001c0001t0002g0180a0002c0002t0001g0157a0002c0002t0001g0263others(1): Show | 4 | HG00099.hp2 HG01358.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-37763C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922579 | ||||||
| chr5:169922698
|
A | G | 3 | a0001c0001t0021g0232a0002c0002t0023g0076a0002c0002t0024g0316 | 3 | HG02572.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-918-37882T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922698 | ||||||
| chr5:169922831
|
G | A | 1 | a0002c0002t0007g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-918-38015C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922831 | ||||||
| chr5:169922991
|
G | A | 31 | a0001c0001t0001g0127a0001c0001t0001g0167a0001c0001t0001g0249others(28): Show | 31 | HG00597.hp2 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-918-38175C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169922991 | ||||||
| chr5:169923107
|
T | C | 1 | a0001c0001t0003g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-918-38291A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923107 | ||||||
| chr5:169923123
|
A | G | 5 | a0002c0002t0018g0095a0003c0003t0004g0179a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-38307T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923123 | ||||||
| chr5:169923132
|
G | T | 5 | a0002c0002t0018g0095a0003c0003t0004g0179a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-38316C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923132 | ||||||
| chr5:169923382
|
A | T | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-918-38566T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923382 | ||||||
| chr5:169923438
|
C | G | 1 | a0001c0001t0002g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-918-38622G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923438 | ||||||
| chr5:169923478
|
C | T | 1 | a0002c0002t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-918-38662G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923478 | ||||||
| chr5:169923483
|
G | GCA | 11 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(8): Show | 11 | HG02451.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-918-38669_-918-38 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923483 | ||||||
| chr5:169923483
|
G | GCACA | 4 | a0001c0001t0002g0065a0001c0001t0002g0290a0001c0001t0003g0300others(1): Show | 4 | HG03041.hp1 HG03540.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-38671_-918-38 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923483 | ||||||
| chr5:169923483
|
G | GCACACA | 3 | a0002c0002t0008g0078a0002c0002t0024g0316a0002c0002t0025g0315 | 3 | HG02572.hp1 HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-918-38673_-918-38 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923483 | ||||||
| chr5:169923483
|
GCA | G | 217 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(214): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.-918-38669_-918-38 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923483 | ||||||
| chr5:169923483
|
GCACA | G | 3 | a0002c0002t0007g0243a0002c0002t0007g0314a0002c0002t0023g0076 | 3 | HG02257.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-918-38671_-918-38 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923483 | ||||||
| chr5:169923511
|
A | T | 1 | a0002c0002t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-918-38695T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923511 | ||||||
| chr5:169923661
|
A | C | 5 | a0001c0001t0003g0251a0002c0002t0001g0171a0002c0002t0005g0309others(2): Show | 5 | HG00639.hp2 HG02040.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-38845T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923661 | ||||||
| chr5:169923739
|
A | G | 141 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(138): Show | 142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-918-38923T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923739 | ||||||
| chr5:169923801
|
C | A | 1 | a0001c0001t0002g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-918-38985G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923801 | ||||||
| chr5:169923963
|
T | C | 136 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(133): Show | 137 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.-918-39147A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923963 | ||||||
| chr5:169923994
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-918-39178T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169923994 | ||||||
| chr5:169924051
|
T | G | 5 | a0001c0001t0003g0251a0002c0002t0001g0171a0002c0002t0005g0309others(2): Show | 5 | HG00639.hp2 HG02040.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-39235A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924051 | ||||||
| chr5:169924130
|
T | A | 136 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(133): Show | 137 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.-918-39314A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924130 | ||||||
| chr5:169924403
|
A | G | 1 | a0002c0002t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-918-39587T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924403 | ||||||
| chr5:169924521
|
G | A | 1 | a0002c0002t0001g0169 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-918-39705C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924521 | ||||||
| chr5:169924538
|
T | A | 5 | a0002c0002t0018g0095a0003c0003t0004g0179a0003c0003t0004g0260others(2): Show | 5 | HG02735.hp1 HG03017.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-918-39722A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924538 | ||||||
| chr5:169924783
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0307a0002c0002t0005g0017 | 3 | HG02258.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-918-39967T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924783 | ||||||
| chr5:169924800
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-918-39984T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924800 | ||||||
| chr5:169924967
|
T | C | 9 | a0001c0001t0002g0291a0001c0001t0003g0016a0001c0001t0003g0093others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-918-40151A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169924967 | ||||||
| chr5:169925105
|
C | A | 1 | a0001c0001t0003g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-918-40289G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925105 | ||||||
| chr5:169925162
|
G | A | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-918-40346C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925162 | ||||||
| chr5:169925418
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-918-40602T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925418 | ||||||
| chr5:169925463
|
C | G | 1 | a0001c0001t0003g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-918-40647G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925463 | ||||||
| chr5:169925535
|
A | G | 39 | a0001c0001t0002g0291a0001c0001t0003g0008a0001c0001t0003g0009others(36): Show | 39 | HG00639.hp2 HG01109.hp2 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.-918-40719T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925535 | ||||||
| chr5:169925562
|
A | T | 5 | a0001c0001t0003g0097a0001c0001t0007g0022a0002c0002t0001g0231others(2): Show | 5 | HG02630.hp2 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-918-40746T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925562 | ||||||
| chr5:169925577
|
CT | C | 56 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0197others(53): Show | 56 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.-918-40762delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925577 | ||||||
| chr5:169925578
|
T | TA | 53 | a0001c0001t0001g0050a0001c0001t0001g0199a0001c0001t0002g0012others(50): Show | 55 | HG00280.hp1 HG01952.hp1 HG01981.hp1 others(52): Show |
intron_variant | MODIFIER | c.-918-40763_-918-40 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925578 | ||||||
| chr5:169925578
|
T | TAA | 23 | a0001c0001t0001g0167a0001c0001t0002g0052a0001c0001t0002g0134others(20): Show | 23 | HG00597.hp2 HG01168.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.-918-40763_-918-40 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925578 | ||||||
| chr5:169925578
|
T | TAAA | 7 | a0001c0001t0003g0104a0001c0001t0003g0212a0001c0001t0003g0236others(4): Show | 7 | HG01981.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-918-40763_-918-40 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925578 | ||||||
| chr5:169925578
|
TTA | T | 6 | a0001c0001t0003g0056a0001c0001t0003g0300a0001c0001t0022g0305others(3): Show | 6 | HG02559.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-40764_-918-40 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925578 | ||||||
| chr5:169925579
|
T | A | 179 | a0001c0001t0001g0050a0001c0001t0001g0167a0001c0001t0001g0178others(176): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.-918-40763A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925579 | ||||||
| chr5:169925579
|
T | TA | 43 | a0001c0001t0001g0111a0001c0001t0001g0127a0001c0001t0001g0276others(40): Show | 43 | HG00609.hp2 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-918-40764dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925579 | ||||||
| chr5:169925579
|
T | TAA | 7 | a0001c0001t0002g0137a0001c0001t0003g0175a0001c0001t0004g0112others(4): Show | 7 | HG01109.hp1 HG01978.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-918-40765_-918-40 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925579 | ||||||
| chr5:169925642
|
T | C | 5 | a0001c0001t0007g0022a0002c0002t0001g0194a0002c0002t0001g0204others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-918-40826A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925642 | ||||||
| chr5:169925658
|
C | T | 68 | a0001c0001t0001g0111a0001c0001t0001g0127a0001c0001t0001g0276others(65): Show | 68 | HG00423.hp2 HG00609.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.-918-40842G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925658 | ||||||
| chr5:169925698
|
C | T | 4 | a0001c0001t0007g0022a0002c0002t0001g0194a0002c0002t0001g0204others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-40882G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925698 | ||||||
| chr5:169925728
|
TTG | T | 283 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0107others(280): Show | 285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.-918-40914_-918-40 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925728 | ||||||
| chr5:169925822
|
G | A | 48 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0002g0035others(45): Show | 49 | HG00423.hp1 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-918-41006C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925822 | ||||||
| chr5:169925849
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-918-41033G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925849 | ||||||
| chr5:169926197
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-918-41381G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926197 | ||||||
| chr5:169926355
|
T | C | 2 | a0002c0002t0006g0002a0002c0002t0006g0099 | 3 | NA18950.hp2 NA19002.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-918-41539A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926355 | ||||||
| chr5:169926462
|
T | C | 15 | a0001c0001t0003g0019a0001c0001t0003g0093a0001c0001t0004g0026others(12): Show | 15 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-918-41646A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926462 | ||||||
| chr5:169926478
|
T | C | 1 | a0001c0001t0002g0254 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-918-41662A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926478 | ||||||
| chr5:169926497
|
G | A | 1 | a0002c0002t0001g0181 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-918-41681C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926497 | ||||||
| chr5:169926539
|
T | C | 4 | a0001c0001t0002g0053a0001c0001t0003g0073a0002c0002t0005g0017others(1): Show | 4 | HG01109.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-41723A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926539 | ||||||
| chr5:169926622
|
T | A | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-918-41806A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926622 | ||||||
| chr5:169926746
|
G | A | 1 | a0002c0002t0025g0315 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-918-41930C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926746 | ||||||
| chr5:169926753
|
T | A | 162 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0127others(159): Show | 162 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.-918-41937A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926753 | ||||||
| chr5:169926980
|
T | C | 2 | a0001c0001t0003g0019a0001c0001t0010g0020 | 2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-918-42164A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169926980 | ||||||
| chr5:169927077
|
A | G | 29 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0002g0053others(26): Show | 29 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.-918-42261T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927077 | ||||||
| chr5:169927427
|
G | A | 24 | a0001c0001t0001g0178a0001c0001t0002g0035a0001c0001t0002g0072others(21): Show | 24 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(21): Show |
intron_variant | MODIFIER | c.-918-42611C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927427 | ||||||
| chr5:169927433
|
A | C | 1 | a0002c0002t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-918-42617T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927433 | ||||||
| chr5:169927611
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-918-42795T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927611 | ||||||
| chr5:169927647
|
C | T | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-918-42831G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927647 | ||||||
| chr5:169927696
|
A | C | 3 | a0002c0002t0001g0149a0002c0002t0001g0150a0002c0002t0001g0220 | 3 | HG00140.hp1 HG00639.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-918-42880T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927696 | ||||||
| chr5:169927741
|
C | T | 4 | a0001c0001t0002g0291a0001c0001t0003g0023a0001c0001t0003g0233others(1): Show | 4 | HG02895.hp1 HG03195.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-42925G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927741 | ||||||
| chr5:169927750
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0002g0207a0002c0002t0001g0205others(1): Show | 4 | HG00323.hp1 HG01074.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.-918-42934C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927750 | ||||||
| chr5:169927773
|
C | G | 1 | a0002c0002t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-918-42957G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927773 | ||||||
| chr5:169927793
|
T | C | 1 | a0002c0002t0001g0100 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-918-42977A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927793 | ||||||
| chr5:169927808
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-918-42992C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927808 | ||||||
| chr5:169927863
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-918-43047C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927863 | ||||||
| chr5:169927916
|
C | T | 2 | a0002c0002t0018g0095a0002c0007t0004g0075 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-918-43100G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927916 | ||||||
| chr5:169927925
|
C | A | 286 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0107others(283): Show | 288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.-918-43109G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927925 | ||||||
| chr5:169928043
|
T | C | 4 | a0001c0001t0002g0053a0001c0001t0003g0073a0002c0002t0005g0017others(1): Show | 4 | HG01109.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-43227A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928043 | ||||||
| chr5:169928188
|
G | C | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-918-43372C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928188 | ||||||
| chr5:169928255
|
G | A | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-918-43439C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928255 | ||||||
| chr5:169928393
|
T | G | 7 | a0001c0001t0003g0097a0001c0001t0003g0300a0001c0001t0022g0305others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-918-43577A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928393 | ||||||
| chr5:169928513
|
C | T | 1 | a0002c0002t0020g0298 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-918-43697G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928513 | ||||||
| chr5:169928549
|
T | C | 89 | a0001c0001t0001g0111a0001c0001t0001g0127a0001c0001t0001g0249others(86): Show | 89 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-918-43733A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928549 | ||||||
| chr5:169928694
|
A | G | 1 | a0003c0003t0004g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-918-43878T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928694 | ||||||
| chr5:169928879
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-918-44063C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928879 | ||||||
| chr5:169928912
|
G | C | 2 | a0001c0001t0003g0141a0001c0001t0003g0175 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-918-44096C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169928912 | ||||||
| chr5:169929007
|
T | C | 3 | a0001c0001t0003g0300a0001c0001t0022g0305a0002c0002t0005g0301 | 3 | HG02559.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-918-44191A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929007 | ||||||
| chr5:169929143
|
C | T | 1 | a0002c0002t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-918-44327G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929143 | ||||||
| chr5:169929144
|
G | C | 4 | a0001c0001t0003g0288a0001c0001t0004g0112a0001c0001t0004g0283others(1): Show | 4 | NA18947.hp1 NA18971.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.-918-44328C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929144 | ||||||
| chr5:169929311
|
T | A | 194 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(191): Show | 194 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.-918-44495A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929311 | ||||||
| chr5:169929635
|
C | T | 1 | a0002c0002t0008g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-918-44819G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929635 | ||||||
| chr5:169929741
|
C | CA | 41 | a0001c0001t0002g0047a0001c0001t0002g0128a0001c0001t0002g0129others(38): Show | 41 | HG00099.hp2 HG00423.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.-918-44926dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929741 | ||||||
| chr5:169929741
|
C | CAAA | 6 | a0001c0001t0003g0097a0001c0001t0003g0300a0001c0001t0022g0305others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-918-44928_-918-44 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929741 | ||||||
| chr5:169929741
|
CA | C | 21 | a0001c0001t0001g0039a0001c0001t0001g0293a0001c0001t0002g0072others(18): Show | 21 | HG01106.hp2 HG01515.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-918-44926delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929741 | ||||||
| chr5:169929761
|
A | G | 1 | a0001c0001t0004g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-918-44945T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929761 | ||||||
| chr5:169929775
|
A | G | 203 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(200): Show | 203 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.-918-44959T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929775 | ||||||
| chr5:169929827
|
C | A | 220 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(217): Show | 221 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.-918-45011G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929827 | ||||||
| chr5:169929828
|
C | A | 15 | a0001c0001t0001g0167a0001c0001t0002g0060a0001c0001t0002g0062others(12): Show | 16 | HG00597.hp2 HG02083.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.-918-45012G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929828 | ||||||
| chr5:169929881
|
T | C | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-918-45065A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929881 | ||||||
| chr5:169929906
|
G | A | 201 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(198): Show | 201 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.-918-45090C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929906 | ||||||
| chr5:169929962
|
A | G | 201 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(198): Show | 201 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.-918-45146T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169929962 | ||||||
| chr5:169930090
|
C | A | 157 | a0001c0001t0001g0040a0001c0001t0001g0127a0001c0001t0001g0178others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-918-45274G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930090 | ||||||
| chr5:169930147
|
T | C | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-918-45331A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930147 | ||||||
| chr5:169930182
|
G | A | 16 | a0001c0001t0001g0167a0001c0001t0002g0060a0001c0001t0002g0062others(13): Show | 17 | HG00597.hp2 HG02083.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.-918-45366C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930182 | ||||||
| chr5:169930184
|
G | A | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-918-45368C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930184 | ||||||
| chr5:169930193
|
T | C | 1 | a0001c0001t0003g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-918-45377A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930193 | ||||||
| chr5:169930194
|
G | A | 1 | a0002c0002t0005g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-918-45378C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930194 | ||||||
| chr5:169930236
|
T | C | 177 | a0001c0001t0001g0040a0001c0001t0001g0111a0001c0001t0001g0127others(174): Show | 177 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.-918-45420A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930236 | ||||||
| chr5:169930288
|
C | G | 2 | a0001c0001t0002g0258a0001c0001t0004g0255 | 2 | HG00642.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-918-45472G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930288 | ||||||
| chr5:169930499
|
T | G | 35 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(32): Show | 35 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.-918-45683A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930499 | ||||||
| chr5:169930524
|
T | C | 1 | a0002c0002t0007g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-918-45708A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930524 | ||||||
| chr5:169930623
|
C | T | 2 | a0001c0001t0003g0096a0002c0002t0024g0316 | 2 | HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-918-45807G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930623 | ||||||
| chr5:169930773
|
C | G | 13 | a0001c0001t0002g0012a0001c0001t0002g0034a0001c0001t0002g0036others(10): Show | 13 | NA18952.hp1 NA18960.hp1 NA18968.hp2 others(10): Show |
intron_variant | MODIFIER | c.-918-45957G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169930773 | ||||||
| chr5:169931130
|
C | T | 1 | a0002c0002t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-918-46314G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931130 | ||||||
| chr5:169931149
|
A | G | 1 | a0002c0002t0008g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-918-46333T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931149 | ||||||
| chr5:169931177
|
G | A | 43 | a0001c0001t0001g0178a0001c0001t0002g0035a0001c0001t0002g0072others(40): Show | 43 | HG00423.hp1 HG00639.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.-918-46361C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931177 | ||||||
| chr5:169931391
|
G | C | 1 | a0002c0002t0001g0267 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-918-46575C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931391 | ||||||
| chr5:169931414
|
G | A | 136 | a0001c0001t0001g0127a0001c0001t0001g0178a0001c0001t0001g0249others(133): Show | 136 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-918-46598C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931414 | ||||||
| chr5:169931477
|
G | A | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-918-46661C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931477 | ||||||
| chr5:169931563
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-918-46747A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931563 | ||||||
| chr5:169931670
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(26): Show | 29 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.-918-46854T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931670 | ||||||
| chr5:169931710
|
T | C | 36 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(33): Show | 36 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.-918-46894A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931710 | ||||||
| chr5:169931715
|
C | T | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-918-46899G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931715 | ||||||
| chr5:169931879
|
A | T | 152 | a0001c0001t0001g0040a0001c0001t0001g0111a0001c0001t0001g0127others(149): Show | 152 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-918-47063T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931879 | ||||||
| chr5:169931913
|
T | C | 1 | a0001c0001t0003g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-918-47097A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169931913 | ||||||
| chr5:169932130
|
C | A | 2 | a0002c0002t0018g0095a0002c0007t0004g0075 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-918-47314G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932130 | ||||||
| chr5:169932135
|
G | A | 3 | a0001c0001t0003g0079a0002c0002t0008g0078a0002c0002t0023g0076 | 3 | HG02615.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-918-47319C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932135 | ||||||
| chr5:169932155
|
A | G | 36 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(33): Show | 36 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(33): Show |
intron_variant | MODIFIER | c.-918-47339T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932155 | ||||||
| chr5:169932408
|
G | C | 1 | a0003c0003t0004g0296 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-918-47592C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932408 | ||||||
| chr5:169932440
|
A | G | 1 | a0002c0002t0007g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-918-47624T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932440 | ||||||
| chr5:169932501
|
T | C | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-918-47685A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932501 | ||||||
| chr5:169932518
|
G | A | 28 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0002g0053others(25): Show | 28 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-918-47702C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932518 | ||||||
| chr5:169932551
|
G | A | 1 | a0002c0002t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-919+47726C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932551 | ||||||
| chr5:169932762
|
A | G | 29 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(26): Show | 29 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.-919+47515T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932762 | ||||||
| chr5:169932865
|
T | TA | 29 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(26): Show | 29 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.-919+47411dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932865 | ||||||
| chr5:169932910
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-919+47367G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932910 | ||||||
| chr5:169932912
|
C | CAAACTGT others(324): Show |
1 | a0001c0001t0010g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-919+47364_-919+47 others(337): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932912 | ||||||
| chr5:169932912
|
C | CAAACTGT others(325): Show |
2 | a0001c0001t0003g0019a0002c0002t0004g0018 | 2 | HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-919+47364_-919+47 others(338): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932912 | ||||||
| chr5:169932956
|
C | T | 29 | a0001c0001t0001g0040a0001c0001t0002g0191a0001c0001t0002g0216others(26): Show | 29 | HG00099.hp2 HG01081.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.-919+47321G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169932956 | ||||||
| chr5:169933151
|
C | G | 100 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0107others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-919+47126G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169933151 | ||||||
| chr5:169933222
|
T | C | 1 | a0002c0002t0001g0028 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-919+47055A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169933222 | ||||||
| chr5:169933271
|
T | C | 32 | a0001c0001t0001g0167a0001c0001t0002g0060a0001c0001t0002g0062others(29): Show | 33 | HG00597.hp2 HG01106.hp2 HG02083.hp1 others(30): Show |
intron_variant | MODIFIER | c.-919+47006A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169933271 | ||||||
| chr5:169933280
|
G | A | 28 | a0001c0001t0001g0178a0001c0001t0002g0035a0001c0001t0002g0072others(25): Show | 28 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.-919+46997C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169933280 | ||||||
| chr5:169933530
|
T | C | 2 | a0002c0002t0018g0095a0002c0007t0004g0075 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-919+46747A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169933530 | ||||||
| chr5:169934060
|
T | A | 1 | a0001c0001t0003g0264 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-919+46217A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934060 | ||||||
| chr5:169934183
|
C | T | 83 | a0001c0001t0001g0127a0001c0001t0001g0249a0001c0001t0001g0276others(80): Show | 83 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.-919+46094G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934183 | ||||||
| chr5:169934348
|
G | A | 2 | a0002c0002t0001g0245a0002c0002t0001g0267 | 2 | NA18952.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-919+45929C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934348 | ||||||
| chr5:169934403
|
C | A | 1 | a0001c0001t0002g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-919+45874G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934403 | ||||||
| chr5:169934516
|
A | T | 15 | a0001c0001t0003g0019a0001c0001t0003g0093a0001c0001t0004g0026others(12): Show | 15 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-919+45761T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934516 | ||||||
| chr5:169934591
|
A | G | 80 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(77): Show | 80 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-919+45686T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934591 | ||||||
| chr5:169934656
|
C | G | 62 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(59): Show | 62 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-919+45621G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934656 | ||||||
| chr5:169934681
|
T | G | 58 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(55): Show | 58 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-919+45596A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934681 | ||||||
| chr5:169934826
|
G | A | 56 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-919+45451C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934826 | ||||||
| chr5:169934856
|
T | C | 57 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(54): Show | 57 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-919+45421A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934856 | ||||||
| chr5:169934940
|
G | C | 57 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(54): Show | 57 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-919+45337C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169934940 | ||||||
| chr5:169935006
|
C | T | 57 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0035others(54): Show | 57 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-919+45271G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935006 | ||||||
| chr5:169935031
|
C | T | 7 | a0001c0001t0003g0097a0001c0001t0003g0300a0001c0001t0022g0305others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+45246G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935031 | ||||||
| chr5:169935075
|
G | A | 7 | a0001c0001t0003g0097a0001c0001t0003g0300a0001c0001t0022g0305others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+45202C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935075 | ||||||
| chr5:169935078
|
G | A | 99 | a0001c0001t0001g0039a0001c0001t0001g0050a0001c0001t0001g0107others(96): Show | 100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.-919+45199C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935078 | ||||||
| chr5:169935138
|
T | C | 1 | a0002c0002t0001g0263 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-919+45139A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935138 | ||||||
| chr5:169935209
|
G | A | 8 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0130others(5): Show | 8 | HG02083.hp1 HG02155.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.-919+45068C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935209 | ||||||
| chr5:169935236
|
G | GCAGGAAC others(6): Show |
56 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0072others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-919+45040_-919+45 others(19): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935236 | ||||||
| chr5:169935389
|
A | T | 56 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0002g0072others(53): Show | 56 | HG00099.hp2 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.-919+44888T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935389 | ||||||
| chr5:169935470
|
G | A | 26 | a0001c0001t0001g0178a0001c0001t0002g0072a0001c0001t0002g0146others(23): Show | 26 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.-919+44807C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935470 | ||||||
| chr5:169935601
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-919+44676C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935601 | ||||||
| chr5:169935668
|
T | C | 28 | a0001c0001t0001g0178a0001c0001t0002g0072a0001c0001t0002g0146others(25): Show | 28 | HG00423.hp1 HG00639.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-919+44609A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935668 | ||||||
| chr5:169935820
|
C | A | 3 | a0001c0001t0002g0221a0002c0002t0001g0186a0002c0002t0001g0187 | 3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-919+44457G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935820 | ||||||
| chr5:169935956
|
T | C | 21 | a0001c0001t0001g0167a0001c0001t0002g0060a0001c0001t0002g0062others(18): Show | 22 | HG00597.hp2 HG00673.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+44321A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169935956 | ||||||
| chr5:169936047
|
A | T | 57 | a0001c0001t0001g0167a0001c0001t0001g0197a0001c0001t0002g0060others(54): Show | 58 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.-919+44230T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936047 | ||||||
| chr5:169936265
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+44012A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936265 | ||||||
| chr5:169936273
|
G | A | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-919+44004C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936273 | ||||||
| chr5:169936282
|
C | T | 5 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(2): Show | 5 | NA18969.hp2 NA18986.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-919+43995G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936282 | ||||||
| chr5:169936349
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-919+43928T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936349 | ||||||
| chr5:169936578
|
C | CT | 20 | a0001c0001t0002g0012a0001c0001t0002g0034a0001c0001t0002g0035others(17): Show | 20 | HG02165.hp1 HG02717.hp2 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-919+43698dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936578 | ||||||
| chr5:169936578
|
C | CTT | 29 | a0001c0001t0001g0040a0001c0001t0001g0167a0001c0001t0002g0060others(26): Show | 29 | HG00099.hp2 HG00597.hp2 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.-919+43697_-919+43 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936578 | ||||||
| chr5:169936578
|
C | CTTT | 16 | a0001c0001t0002g0062a0001c0001t0002g0068a0001c0001t0002g0069others(13): Show | 17 | HG00673.hp1 HG02055.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.-919+43696_-919+43 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936578 | ||||||
| chr5:169936578
|
CT | C | 69 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0001g0210others(66): Show | 69 | HG00323.hp1 HG00423.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.-919+43698delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936578 | ||||||
| chr5:169936599
|
T | A | 1 | a0001c0001t0003g0251 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-919+43678A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936599 | ||||||
| chr5:169936633
|
A | G | 9 | a0001c0001t0001g0050a0001c0001t0002g0049a0001c0001t0002g0071others(6): Show | 9 | HG01258.hp2 HG01975.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.-919+43644T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936633 | ||||||
| chr5:169936673
|
C | T | 2 | a0001c0001t0003g0141a0001c0001t0003g0175 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-919+43604G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936673 | ||||||
| chr5:169936704
|
G | A | 6 | a0001c0001t0003g0079a0001c0001t0003g0080a0001c0001t0003g0096others(3): Show | 6 | HG02615.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-919+43573C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936704 | ||||||
| chr5:169936705
|
C | T | 67 | a0001c0001t0001g0040a0001c0001t0001g0197a0001c0001t0002g0128others(64): Show | 67 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-919+43572G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936705 | ||||||
| chr5:169936757
|
A | G | 42 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0168others(39): Show | 42 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.-919+43520T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936757 | ||||||
| chr5:169936786
|
C | T | 5 | a0001c0001t0003g0311a0002c0002t0001g0312a0002c0002t0004g0108others(2): Show | 5 | HG02622.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-919+43491G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936786 | ||||||
| chr5:169936787
|
G | A | 2 | a0002c0002t0001g0126a0002c0002t0001g0263 | 2 | HG00099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-919+43490C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936787 | ||||||
| chr5:169936809
|
T | C | 1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-919+43468A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936809 | ||||||
| chr5:169937064
|
C | T | 2 | a0002c0002t0003g0074a0002c0002t0025g0315 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-919+43213G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937064 | ||||||
| chr5:169937246
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-919+43031C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937246 | ||||||
| chr5:169937315
|
G | A | 1 | a0002c0002t0005g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-919+42962C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937315 | ||||||
| chr5:169937354
|
T | C | 2 | a0002c0002t0003g0074a0002c0002t0025g0315 | 2 | HG02145.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-919+42923A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937354 | ||||||
| chr5:169937384
|
C | A | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-919+42893G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937384 | ||||||
| chr5:169937571
|
A | G | 1 | a0002c0002t0001g0211 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-919+42706T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937571 | ||||||
| chr5:169937635
|
A | ATAT | 172 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(169): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-919+42639_-919+42 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937635 | ||||||
| chr5:169937736
|
G | A | 1 | a0001c0001t0003g0262 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-919+42541C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937736 | ||||||
| chr5:169937813
|
G | T | 28 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(25): Show | 28 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-919+42464C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937813 | ||||||
| chr5:169937856
|
C | T | 1 | a0002c0002t0013g0059 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-919+42421G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169937856 | ||||||
| chr5:169938139
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0002g0256a0001c0001t0003g0145 | 3 | NA18940.hp2 NA18984.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-919+42138G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938139 | ||||||
| chr5:169938225
|
C | CT | 9 | a0001c0001t0002g0052a0001c0001t0002g0225a0001c0001t0002g0226others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-919+42051dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938225 | ||||||
| chr5:169938275
|
G | A | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-919+42002C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938275 | ||||||
| chr5:169938354
|
G | A | 2 | a0002c0002t0007g0011a0002c0002t0008g0303 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-919+41923C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938354 | ||||||
| chr5:169938360
|
A | T | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+41917T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938360 | ||||||
| chr5:169938379
|
A | G | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+41898T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938379 | ||||||
| chr5:169938436
|
C | T | 1 | a0002c0002t0018g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-919+41841G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938436 | ||||||
| chr5:169938437
|
G | C | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+41840C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938437 | ||||||
| chr5:169938467
|
C | T | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(17): Show | 21 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+41810G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938467 | ||||||
| chr5:169938561
|
T | A | 1 | a0002c0002t0001g0045 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-919+41716A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938561 | ||||||
| chr5:169938639
|
A | G | 174 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(171): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-919+41638T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938639 | ||||||
| chr5:169938686
|
A | C | 2 | a0001c0001t0003g0104a0002c0002t0003g0102 | 2 | HG01981.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-919+41591T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938686 | ||||||
| chr5:169938706
|
G | A | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+41571C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938706 | ||||||
| chr5:169938725
|
T | A | 28 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(25): Show | 28 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.-919+41552A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938725 | ||||||
| chr5:169938800
|
CTT | C | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(17): Show | 21 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+41475_-919+41 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938800 | ||||||
| chr5:169938910
|
C | CTT | 123 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0111others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-919+41365_-919+41 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938910 | ||||||
| chr5:169938922
|
G | C | 13 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(10): Show | 13 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-919+41355C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938922 | ||||||
| chr5:169938924
|
A | G | 175 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(172): Show | 177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-919+41353T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938924 | ||||||
| chr5:169938930
|
G | T | 2 | a0001c0001t0003g0141a0001c0001t0003g0175 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-919+41347C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938930 | ||||||
| chr5:169938961
|
T | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+41316A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169938961 | ||||||
| chr5:169939070
|
A | AT | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+41206dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939070 | ||||||
| chr5:169939095
|
G | A | 1 | a0001c0001t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-919+41182C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939095 | ||||||
| chr5:169939125
|
T | C | 2 | a0002c0002t0001g0033a0002c0002t0018g0095 | 2 | HG03704.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-919+41152A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939125 | ||||||
| chr5:169939139
|
C | T | 38 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0180others(35): Show | 38 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-919+41138G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939139 | ||||||
| chr5:169939193
|
T | A | 1 | a0001c0001t0002g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-919+41084A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939193 | ||||||
| chr5:169939196
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-919+41081C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939196 | ||||||
| chr5:169939203
|
C | CT | 38 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0168others(35): Show | 38 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-919+41073dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939203 | ||||||
| chr5:169939203
|
C | CTTTTTT | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+41068_-919+41 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939203 | ||||||
| chr5:169939239
|
T | TAAAAACT others(310): Show |
1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+41037_-919+41 others(323): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939239 | ||||||
| chr5:169939503
|
A | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+40774T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939503 | ||||||
| chr5:169939544
|
G | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+40733C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939544 | ||||||
| chr5:169939577
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+40700G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939577 | ||||||
| chr5:169939587
|
A | G | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+40690T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939587 | ||||||
| chr5:169939618
|
C | T | 4 | a0001c0001t0002g0132a0002c0002t0001g0162a0002c0002t0001g0165others(1): Show | 4 | HG01433.hp2 HG01516.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-919+40659G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939618 | ||||||
| chr5:169939628
|
T | C | 1 | a0003c0003t0004g0296 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-919+40649A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939628 | ||||||
| chr5:169939684
|
G | A | 37 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0168others(34): Show | 37 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-919+40593C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939684 | ||||||
| chr5:169939702
|
A | G | 214 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(211): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.-919+40575T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939702 | ||||||
| chr5:169939803
|
T | TA | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+40473dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939803 | ||||||
| chr5:169939837
|
G | A | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+40440C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939837 | ||||||
| chr5:169939839
|
G | C | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+40438C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939839 | ||||||
| chr5:169939959
|
T | C | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+40318A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939959 | ||||||
| chr5:169939998
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+40279C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939998 | ||||||
| chr5:169940079
|
G | A | 1 | a0002c0002t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-919+40198C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940079 | ||||||
| chr5:169940116
|
T | A | 6 | a0001c0001t0002g0128a0001c0001t0002g0180a0001c0001t0003g0189others(3): Show | 6 | HG00741.hp1 HG02647.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.-919+40161A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940116 | ||||||
| chr5:169940146
|
A | G | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+40131T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940146 | ||||||
| chr5:169940191
|
G | A | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+40086C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940191 | ||||||
| chr5:169940341
|
C | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+39936G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940341 | ||||||
| chr5:169940418
|
A | G | 2 | a0001c0001t0002g0160a0001c0001t0004g0173 | 2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-919+39859T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940418 | ||||||
| chr5:169940484
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+39793A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940484 | ||||||
| chr5:169940526
|
T | A | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+39751A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940526 | ||||||
| chr5:169940690
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+39587C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940690 | ||||||
| chr5:169940970
|
C | G | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+39307G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940970 | ||||||
| chr5:169940977
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+39300G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169940977 | ||||||
| chr5:169941049
|
T | G | 125 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0127others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-919+39228A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941049 | ||||||
| chr5:169941080
|
C | T | 1 | a0002c0002t0007g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-919+39197G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941080 | ||||||
| chr5:169941210
|
G | A | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+39067C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941210 | ||||||
| chr5:169941382
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0002g0256a0001c0001t0003g0145 | 3 | NA18940.hp2 NA18984.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-919+38895A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941382 | ||||||
| chr5:169941495
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+38782T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941495 | ||||||
| chr5:169941702
|
T | G | 26 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(23): Show | 26 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-919+38575A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941702 | ||||||
| chr5:169941770
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+38507G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941770 | ||||||
| chr5:169941802
|
T | C | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+38475A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941802 | ||||||
| chr5:169941914
|
G | T | 26 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(23): Show | 26 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-919+38363C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941914 | ||||||
| chr5:169941923
|
C | A | 1 | a0001c0001t0003g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-919+38354G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169941923 | ||||||
| chr5:169942064
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+38213C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942064 | ||||||
| chr5:169942064
|
G | C | 1 | a0002c0002t0008g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-919+38213C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942064 | ||||||
| chr5:169942078
|
T | A | 2 | a0001c0001t0001g0276a0001c0001t0002g0254 | 2 | NA18960.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-919+38199A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942078 | ||||||
| chr5:169942131
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+38146T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942131 | ||||||
| chr5:169942306
|
A | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+37971T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942306 | ||||||
| chr5:169942359
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+37918C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942359 | ||||||
| chr5:169942402
|
G | A | 22 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(19): Show | 22 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+37875C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942402 | ||||||
| chr5:169942543
|
A | C | 1 | a0001c0001t0002g0291 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-919+37734T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942543 | ||||||
| chr5:169942686
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+37591C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942686 | ||||||
| chr5:169942714
|
G | C | 1 | a0001c0001t0002g0172 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-919+37563C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942714 | ||||||
| chr5:169942725
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+37552A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942725 | ||||||
| chr5:169942798
|
C | T | 4 | a0001c0001t0002g0132a0002c0002t0001g0162a0002c0002t0001g0165others(1): Show | 4 | HG01433.hp2 HG01516.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-919+37479G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942798 | ||||||
| chr5:169942953
|
C | G | 24 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(21): Show | 24 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-919+37324G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169942953 | ||||||
| chr5:169943080
|
G | A | 1 | a0002c0002t0001g0117 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-919+37197C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943080 | ||||||
| chr5:169943096
|
A | G | 2 | a0001c0001t0002g0273a0001c0001t0003g0274 | 2 | HG00673.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-919+37181T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943096 | ||||||
| chr5:169943139
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+37138C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943139 | ||||||
| chr5:169943147
|
T | C | 1 | a0001c0001t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-919+37130A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943147 | ||||||
| chr5:169943488
|
C | T | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+36789G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943488 | ||||||
| chr5:169943687
|
C | CTGGGATC others(11): Show |
1 | a0001c0001t0003g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-919+36572_-919+36 others(24): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943687 | ||||||
| chr5:169943779
|
G | A | 26 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(23): Show | 26 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-919+36498C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943779 | ||||||
| chr5:169943811
|
C | A | 4 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0003g0105others(1): Show | 4 | HG00673.hp1 HG02132.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+36466G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943811 | ||||||
| chr5:169943927
|
G | A | 38 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0168others(35): Show | 38 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-919+36350C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169943927 | ||||||
| chr5:169944037
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+36240C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944037 | ||||||
| chr5:169944069
|
C | T | 1 | a0002c0002t0001g0029 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-919+36208G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944069 | ||||||
| chr5:169944181
|
A | G | 31 | a0001c0001t0002g0087a0001c0001t0002g0090a0001c0001t0003g0007others(28): Show | 32 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-919+36096T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944181 | ||||||
| chr5:169944297
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-919+35980G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944297 | ||||||
| chr5:169944372
|
G | A | 39 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0168others(36): Show | 39 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.-919+35905C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944372 | ||||||
| chr5:169944599
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+35678A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944599 | ||||||
| chr5:169944663
|
AGCAAACA others(19): Show |
A | 1 | a0002c0002t0001g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-919+35588_-919+35 others(32): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944663 | ||||||
| chr5:169944710
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+35567G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944710 | ||||||
| chr5:169944757
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+35520C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944757 | ||||||
| chr5:169944774
|
C | T | 5 | a0001c0001t0003g0079a0001c0001t0003g0080a0002c0002t0005g0077others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+35503G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944774 | ||||||
| chr5:169944869
|
A | G | 1 | a0001c0001t0002g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-919+35408T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944869 | ||||||
| chr5:169944888
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-919+35389T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169944888 | ||||||
| chr5:169945128
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+35149C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945128 | ||||||
| chr5:169945189
|
G | C | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(252): Show | 257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-919+35088C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945189 | ||||||
| chr5:169945257
|
G | A | 2 | a0001c0001t0002g0129a0002c0002t0001g0140 | 2 | NA19002.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-919+35020C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945257 | ||||||
| chr5:169945265
|
A | G | 5 | a0001c0001t0003g0019a0001c0001t0004g0026a0001c0001t0010g0020others(2): Show | 5 | HG02451.hp1 HG02965.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+35012T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945265 | ||||||
| chr5:169945269
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+35008G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945269 | ||||||
| chr5:169945271
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+35006T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945271 | ||||||
| chr5:169945278
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-919+34999G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945278 | ||||||
| chr5:169945298
|
G | T | 4 | a0001c0001t0002g0047a0001c0001t0002g0163a0001c0001t0002g0170others(1): Show | 4 | HG00423.hp2 NA18977.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+34979C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945298 | ||||||
| chr5:169945333
|
CAT | C | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+34942_-919+34 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945333 | ||||||
| chr5:169945372
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+34905C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945372 | ||||||
| chr5:169945526
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+34751C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945526 | ||||||
| chr5:169945534
|
T | G | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+34743A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945534 | ||||||
| chr5:169945613
|
C | T | 5 | a0001c0001t0001g0040a0002c0002t0001g0031a0002c0002t0001g0263others(2): Show | 5 | HG00099.hp2 HG02735.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+34664G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945613 | ||||||
| chr5:169945683
|
C | G | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+34594G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945683 | ||||||
| chr5:169945747
|
G | GGGTCTCT others(13): Show |
1 | a0001c0001t0002g0183 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-919+34529_-919+34 others(26): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945747 | ||||||
| chr5:169945749
|
T | G | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(251): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-919+34528A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945749 | ||||||
| chr5:169945767
|
CT | C | 5 | a0001c0001t0003g0300a0001c0001t0022g0305a0002c0002t0005g0098others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+34509delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945767 | ||||||
| chr5:169945809
|
T | G | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-919+34468A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945809 | ||||||
| chr5:169945815
|
C | T | 18 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(15): Show | 19 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.-919+34462G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945815 | ||||||
| chr5:169945953
|
T | G | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-919+34324A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169945953 | ||||||
| chr5:169946136
|
A | T | 1 | a0001c0001t0004g0112 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-919+34141T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946136 | ||||||
| chr5:169946147
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-919+34130T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946147 | ||||||
| chr5:169946255
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+34022G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946255 | ||||||
| chr5:169946416
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+33861C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946416 | ||||||
| chr5:169946549
|
A | G | 1 | a0001c0001t0004g0177 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-919+33728T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946549 | ||||||
| chr5:169946561
|
C | T | 1 | a0002c0002t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-919+33716G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946561 | ||||||
| chr5:169946644
|
G | GAATAAGA others(21): Show |
1 | a0001c0001t0002g0146 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-919+33605_-919+33 others(34): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946644 | ||||||
| chr5:169946691
|
G | A | 1 | a0001c0001t0007g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-919+33586C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946691 | ||||||
| chr5:169946911
|
C | A | 1 | a0001c0001t0002g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-919+33366G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946911 | ||||||
| chr5:169946933
|
G | A | 1 | a0004c0004t0002g0271 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-919+33344C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169946933 | ||||||
| chr5:169947253
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-919+33024G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947253 | ||||||
| chr5:169947288
|
G | A | 5 | a0001c0001t0003g0019a0001c0001t0004g0026a0001c0001t0010g0020others(2): Show | 5 | HG02451.hp1 HG02965.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+32989C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947288 | ||||||
| chr5:169947408
|
T | C | 2 | a0002c0002t0007g0011a0002c0002t0008g0303 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-919+32869A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947408 | ||||||
| chr5:169947493
|
GCTTCCTG others(22): Show |
G | 1 | a0002c0002t0008g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-919+32755_-919+32 others(35): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947493 | ||||||
| chr5:169947511
|
C | T | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+32766G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947511 | ||||||
| chr5:169947559
|
G | T | 1 | a0001c0001t0002g0034 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-919+32718C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947559 | ||||||
| chr5:169947560
|
G | C | 1 | a0002c0002t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-919+32717C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947560 | ||||||
| chr5:169947795
|
G | A | 1 | a0002c0002t0001g0200 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-919+32482C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947795 | ||||||
| chr5:169947809
|
A | AGCATGAG others(5): Show |
1 | a0001c0001t0002g0036 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-919+32456_-919+32 others(18): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947809 | ||||||
| chr5:169947830
|
ATACAGCA others(8): Show |
A | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-919+32432_-919+32 others(21): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947830 | ||||||
| chr5:169947845
|
C | A | 255 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0127others(252): Show | 257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-919+32432G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947845 | ||||||
| chr5:169947856
|
A | T | 1 | a0001c0001t0021g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-919+32421T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947856 | ||||||
| chr5:169947858
|
G | A | 1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-919+32419C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947858 | ||||||
| chr5:169947905
|
A | G | 93 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0127others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.-919+32372T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169947905 | ||||||
| chr5:169948030
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-919+32247T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948030 | ||||||
| chr5:169948187
|
T | G | 41 | a0001c0001t0001g0197a0001c0001t0002g0128a0001c0001t0002g0168others(38): Show | 41 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.-919+32090A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948187 | ||||||
| chr5:169948240
|
T | C | 1 | a0002c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-919+32037A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948240 | ||||||
| chr5:169948296
|
T | TA | 80 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0012others(77): Show | 80 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-919+31980dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948296 | ||||||
| chr5:169948391
|
C | T | 4 | a0001c0001t0002g0072a0001c0001t0004g0070a0002c0002t0001g0110others(1): Show | 4 | HG02015.hp1 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-919+31886G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948391 | ||||||
| chr5:169948609
|
A | G | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+31668T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948609 | ||||||
| chr5:169948613
|
A | AT | 6 | a0001c0001t0001g0199a0001c0001t0003g0212a0001c0001t0003g0213others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-919+31663dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948613 | ||||||
| chr5:169948613
|
A | ATTTTTTT others(17): Show |
1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+31663_-919+31 others(30): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948613 | ||||||
| chr5:169948677
|
G | T | 1 | a0002c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-919+31600C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948677 | ||||||
| chr5:169948726
|
C | A | 1 | a0001c0001t0002g0146 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-919+31551G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948726 | ||||||
| chr5:169948836
|
TTTTTTCT others(5): Show |
T | 1 | a0001c0001t0001g0178 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-919+31429_-919+31 others(18): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948836 | ||||||
| chr5:169948944
|
T | TA | 11 | a0001c0001t0002g0087a0001c0001t0002g0090a0001c0001t0003g0021others(8): Show | 12 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.-919+31332dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948944 | ||||||
| chr5:169948954
|
C | G | 125 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0111others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-919+31323G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948954 | ||||||
| chr5:169949000
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+31277T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949000 | ||||||
| chr5:169949059
|
A | T | 1 | a0002c0002t0005g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-919+31218T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949059 | ||||||
| chr5:169949095
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+31182T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949095 | ||||||
| chr5:169949109
|
T | C | 1 | a0001c0001t0003g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-919+31168A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949109 | ||||||
| chr5:169949111
|
T | G | 1 | a0002c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-919+31166A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949111 | ||||||
| chr5:169949113
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+31164G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949113 | ||||||
| chr5:169949126
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+31151G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949126 | ||||||
| chr5:169949244
|
GGGATCCA others(5): Show |
G | 1 | a0002c0002t0005g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-919+31021_-919+31 others(18): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949244 | ||||||
| chr5:169949245
|
G | A | 2 | a0002c0002t0004g0106a0002c0002t0004g0159 | 2 | HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-919+31032C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949245 | ||||||
| chr5:169949318
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-919+30959C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949318 | ||||||
| chr5:169949407
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+30870C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949407 | ||||||
| chr5:169949415
|
A | G | 26 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(23): Show | 26 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-919+30862T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949415 | ||||||
| chr5:169949491
|
A | G | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-919+30786T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949491 | ||||||
| chr5:169949567
|
G | A | 1 | a0002c0002t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-919+30710C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949567 | ||||||
| chr5:169949627
|
T | C | 24 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(21): Show | 24 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-919+30650A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949627 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3064): Show |
1 | a0001c0001t0003g0093 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3077): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2996): Show |
1 | a0001c0001t0003g0233 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3009): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3019): Show |
1 | a0001c0001t0002g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3032): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2866): Show |
1 | a0002c0002t0003g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2879): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2804): Show |
1 | a0001c0001t0002g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2817): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2822): Show |
1 | a0002c0002t0001g0202 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2835): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3192): Show |
1 | a0001c0001t0002g0168 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3205): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3086): Show |
1 | a0002c0002t0005g0025 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3099): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2996): Show |
1 | a0002c0002t0005g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3009): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2888): Show |
1 | a0001c0001t0003g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2901): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3078): Show |
1 | a0002c0002t0001g0186 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3091): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3127): Show |
1 | a0002c0002t0001g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3140): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3097): Show |
1 | a0002c0002t0006g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3110): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3055): Show |
1 | a0002c0002t0005g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3068): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3049): Show |
1 | a0001c0001t0001g0197 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3062): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3043): Show |
1 | a0002c0002t0001g0205 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3056): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3013): Show |
1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3026): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3013): Show |
1 | a0002c0002t0001g0211 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3026): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3025): Show |
1 | a0001c0001t0004g0215 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3038): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2815): Show |
1 | a0003c0003t0004g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2828): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2803): Show |
1 | a0002c0002t0001g0209 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2816): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3032): Show |
1 | a0002c0002t0001g0126 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3045): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2990): Show |
1 | a0002c0002t0007g0302 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3003): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3070): Show |
1 | a0002c0002t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3083): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2838): Show |
1 | a0001c0001t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2851): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3066): Show |
1 | a0001c0001t0003g0217 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3079): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2814): Show |
1 | a0001c0001t0002g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2827): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2852): Show |
1 | a0001c0001t0007g0133 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2865): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2834): Show |
1 | a0001c0001t0012g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2847): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2841): Show |
1 | a0002c0002t0007g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2854): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2889): Show |
1 | a0001c0001t0012g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2902): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3013): Show |
1 | a0001c0001t0003g0213 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3026): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3019): Show |
1 | a0001c0001t0003g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3032): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3084): Show |
1 | a0001c0001t0003g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3097): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2785): Show |
1 | a0002c0002t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2798): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3159): Show |
1 | a0002c0002t0008g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3172): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3184): Show |
1 | a0002c0002t0007g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3197): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3160): Show |
1 | a0002c0002t0001g0263 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3173): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2903): Show |
1 | a0002c0002t0001g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2916): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3132): Show |
1 | a0001c0001t0003g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3145): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3215): Show |
1 | a0002c0002t0003g0102 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3228): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3125): Show |
1 | a0001c0001t0003g0103 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3138): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3167): Show |
1 | a0001c0001t0003g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3180): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3149): Show |
1 | a0002c0002t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3162): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3143): Show |
1 | a0001c0001t0003g0242 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3156): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3125): Show |
1 | a0001c0001t0003g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3138): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3071): Show |
1 | a0001c0001t0003g0292 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3084): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3107): Show |
1 | a0002c0002t0004g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3120): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3156): Show |
1 | a0002c0002t0001g0031 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3169): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3151): Show |
1 | a0001c0001t0003g0236 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3164): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3146): Show |
1 | a0001c0001t0003g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3159): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3066): Show |
1 | a0001c0001t0003g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3079): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3197): Show |
1 | a0002c0002t0008g0234 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3210): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3145): Show |
1 | a0002c0002t0007g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3158): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3154): Show |
1 | a0002c0002t0004g0159 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3167): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3129): Show |
1 | a0001c0001t0003g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3142): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2830): Show |
1 | a0001c0001t0002g0035 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2843): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2834): Show |
1 | a0001c0001t0002g0012 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2847): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2841): Show |
1 | a0002c0002t0001g0032 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2854): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2930): Show |
1 | a0001c0001t0002g0037 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2943): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2954): Show |
1 | a0001c0001t0002g0036 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2967): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2786): Show |
1 | a0001c0001t0002g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2799): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2822): Show |
1 | a0001c0001t0002g0172 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2835): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2840): Show |
1 | a0001c0001t0009g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2853): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2864): Show |
1 | a0002c0002t0001g0294 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2877): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2870): Show |
1 | a0001c0001t0004g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2883): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2798): Show |
1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2811): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2841): Show |
1 | a0001c0001t0002g0184 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2854): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2865): Show |
1 | a0001c0001t0002g0268 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2878): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2884): Show |
1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2897): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2847): Show |
1 | a0001c0001t0002g0183 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2860): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2424): Show |
1 | a0001c0001t0003g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2437): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2387): Show |
1 | a0001c0001t0004g0026 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2400): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2829): Show |
1 | a0002c0002t0018g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2842): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2800): Show |
1 | a0002c0002t0004g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2813): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2842): Show |
1 | a0001c0001t0003g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2855): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2884): Show |
1 | a0001c0001t0010g0020 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2897): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3155): Show |
1 | a0001c0001t0003g0175 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3168): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(3089): Show |
1 | a0001c0001t0003g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(3102): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2945): Show |
1 | a0001c0001t0003g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2958): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2951): Show |
1 | a0001c0001t0003g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2964): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2954): Show |
1 | a0001c0001t0003g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2967): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2424): Show |
1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2437): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2868): Show |
1 | a0001c0001t0002g0034 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2881): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949675
|
T | TCAATGTG others(2916): Show |
1 | a0001c0001t0002g0143 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-919+30601_-919+30 others(2929): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949675 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3000): Show |
1 | a0002c0002t0005g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3013): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3000): Show |
1 | a0001c0001t0003g0005 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3013): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2988): Show |
1 | a0001c0001t0003g0003 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3001): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2988): Show |
1 | a0002c0002t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3001): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2965): Show |
1 | a0001c0001t0003g0082 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(2978): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3090): Show |
1 | a0001c0001t0002g0146 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3103): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3021): Show |
1 | a0002c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3034): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3019): Show |
1 | a0001c0001t0002g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3032): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2977): Show |
1 | a0002c0002t0008g0313 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(2990): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2995): Show |
1 | a0002c0002t0013g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3008): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2987): Show |
1 | a0001c0001t0003g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3000): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3029): Show |
1 | a0002c0002t0007g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3042): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2977): Show |
1 | a0002c0002t0005g0218 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(2990): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3081): Show |
1 | a0002c0002t0001g0144 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3094): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2975): Show |
1 | a0002c0002t0005g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(2988): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3041): Show |
1 | a0001c0001t0001g0178 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3054): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3059): Show |
1 | a0001c0001t0003g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3072): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2965): Show |
1 | a0001c0001t0002g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(2978): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(3042): Show |
1 | a0002c0002t0001g0142 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(3055): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949681
|
T | TGATCTTT others(2964): Show |
1 | a0002c0002t0005g0310 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-919+30595_-919+30 others(2977): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949681 | ||||||
| chr5:169949682
|
G | GATCTTTT others(3044): Show |
1 | a0002c0002t0007g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-919+30594_-919+30 others(3057): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949682 | ||||||
| chr5:169949682
|
G | GATCTTTT others(3068): Show |
1 | a0002c0002t0005g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-919+30594_-919+30 others(3081): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949682 | ||||||
| chr5:169949682
|
G | GATCTTTT others(3038): Show |
1 | a0001c0001t0003g0097 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-919+30594_-919+30 others(3051): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949682 | ||||||
| chr5:169949682
|
G | GATCTTTT others(3049): Show |
1 | a0001c0001t0022g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-919+30594_-919+30 others(3062): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949682 | ||||||
| chr5:169949682
|
G | GATCTTTT others(3019): Show |
1 | a0002c0002t0005g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-919+30594_-919+30 others(3032): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949682 | ||||||
| chr5:169949682
|
G | GATCTTTT others(3001): Show |
1 | a0001c0001t0003g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-919+30594_-919+30 others(3014): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949682 | ||||||
| chr5:169949686
|
T | TTTTTTTT others(3112): Show |
1 | a0001c0001t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-919+30590_-919+30 others(3125): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949686 | ||||||
| chr5:169949689
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-919+30588T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949689 | ||||||
| chr5:169949848
|
T | C | 1 | a0002c0002t0001g0246 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-919+30429A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169949848 | ||||||
| chr5:169950032
|
T | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+30245A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950032 | ||||||
| chr5:169950059
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-919+30218A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950059 | ||||||
| chr5:169950142
|
A | G | 2 | a0001c0001t0002g0123a0005c0008t0003g0113 | 2 | HG00609.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-919+30135T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950142 | ||||||
| chr5:169950146
|
T | C | 1 | a0003c0003t0004g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-919+30131A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950146 | ||||||
| chr5:169950228
|
A | G | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+30049T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950228 | ||||||
| chr5:169950242
|
A | T | 1 | a0002c0002t0007g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-919+30035T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950242 | ||||||
| chr5:169950347
|
G | A | 1 | a0001c0001t0003g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-919+29930C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950347 | ||||||
| chr5:169950400
|
A | C | 1 | a0001c0001t0003g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-919+29877T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950400 | ||||||
| chr5:169950400
|
A | G | 1 | a0002c0002t0001g0144 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-919+29877T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950400 | ||||||
| chr5:169950425
|
C | A | 1 | a0001c0001t0002g0139 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-919+29852G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950425 | ||||||
| chr5:169950526
|
C | T | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+29751G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950526 | ||||||
| chr5:169950580
|
T | G | 1 | a0001c0001t0002g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-919+29697A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169950580 | ||||||
| chr5:169951037
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+29240C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951037 | ||||||
| chr5:169951307
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28970G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951307 | ||||||
| chr5:169951484
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28793A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951484 | ||||||
| chr5:169951496
|
G | A | 1 | a0002c0002t0001g0192 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-919+28781C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951496 | ||||||
| chr5:169951512
|
A | C | 1 | a0002c0002t0004g0018 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-919+28765T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951512 | ||||||
| chr5:169951512
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28765T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951512 | ||||||
| chr5:169951538
|
A | G | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+28739T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951538 | ||||||
| chr5:169951582
|
C | G | 7 | a0001c0001t0002g0191a0001c0001t0004g0152a0002c0002t0001g0153others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+28695G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951582 | ||||||
| chr5:169951628
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28649A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951628 | ||||||
| chr5:169951711
|
A | G | 7 | a0001c0001t0002g0191a0001c0001t0004g0152a0002c0002t0001g0153others(4): Show | 7 | HG01074.hp1 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+28566T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951711 | ||||||
| chr5:169951744
|
T | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28533A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951744 | ||||||
| chr5:169951795
|
G | A | 26 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(23): Show | 26 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.-919+28482C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951795 | ||||||
| chr5:169951913
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28364T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169951913 | ||||||
| chr5:169952007
|
G | T | 24 | a0001c0001t0001g0040a0001c0001t0003g0008a0001c0001t0003g0009others(21): Show | 24 | HG00099.hp2 HG01981.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-919+28270C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952007 | ||||||
| chr5:169952212
|
G | A | 111 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0001g0197others(108): Show | 111 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-919+28065C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952212 | ||||||
| chr5:169952266
|
G | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+28011C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952266 | ||||||
| chr5:169952446
|
C | T | 1 | a0001c0001t0004g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-919+27831G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952446 | ||||||
| chr5:169952474
|
T | C | 1 | a0002c0002t0004g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-919+27803A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952474 | ||||||
| chr5:169952648
|
G | A | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+27629C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952648 | ||||||
| chr5:169952696
|
T | C | 2 | a0001c0001t0002g0072a0001c0001t0004g0070 | 2 | HG02015.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.-919+27581A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952696 | ||||||
| chr5:169952729
|
T | C | 1 | a0001c0001t0002g0168 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-919+27548A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952729 | ||||||
| chr5:169952786
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+27491G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952786 | ||||||
| chr5:169952888
|
T | C | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+27389A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169952888 | ||||||
| chr5:169953053
|
G | T | 1 | a0001c0001t0002g0185 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-919+27224C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953053 | ||||||
| chr5:169953201
|
T | C | 1 | a0002c0002t0013g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-919+27076A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953201 | ||||||
| chr5:169953204
|
G | A | 1 | a0002c0002t0013g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-919+27073C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953204 | ||||||
| chr5:169953231
|
G | A | 5 | a0001c0001t0003g0079a0001c0001t0003g0080a0002c0002t0005g0077others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+27046C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953231 | ||||||
| chr5:169953332
|
C | CA | 134 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0111others(131): Show | 136 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-919+26944dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953332 | ||||||
| chr5:169953332
|
CA | C | 17 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0035others(14): Show | 17 | HG00280.hp2 HG01074.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.-919+26944delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953332 | ||||||
| chr5:169953384
|
G | A | 1 | a0002c0002t0001g0263 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-919+26893C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953384 | ||||||
| chr5:169953573
|
A | G | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02083.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+26704T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953573 | ||||||
| chr5:169953635
|
A | G | 112 | a0001c0001t0001g0040a0001c0001t0001g0178a0001c0001t0001g0197others(109): Show | 112 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-919+26642T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953635 | ||||||
| chr5:169953675
|
GGAATGGG others(23): Show |
G | 1 | a0002c0002t0001g0187 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-919+26572_-919+26 others(36): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953675 | ||||||
| chr5:169953958
|
G | A | 1 | a0002c0002t0005g0310 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-919+26319C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169953958 | ||||||
| chr5:169954028
|
T | C | 1 | a0002c0002t0025g0315 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-919+26249A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954028 | ||||||
| chr5:169954111
|
A | G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+26166T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954111 | ||||||
| chr5:169954424
|
T | A | 1 | a0002c0002t0024g0316 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-919+25853A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954424 | ||||||
| chr5:169954516
|
C | G | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(17): Show | 21 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+25761G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954516 | ||||||
| chr5:169954539
|
T | C | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+25738A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954539 | ||||||
| chr5:169954680
|
C | G | 1 | a0002c0002t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-919+25597G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954680 | ||||||
| chr5:169954682
|
G | T | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+25595C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954682 | ||||||
| chr5:169954822
|
C | T | 5 | a0001c0001t0003g0079a0001c0001t0003g0080a0002c0002t0005g0077others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+25455G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954822 | ||||||
| chr5:169954993
|
A | T | 21 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(18): Show | 21 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+25284T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169954993 | ||||||
| chr5:169955018
|
T | C | 21 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(18): Show | 21 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+25259A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955018 | ||||||
| chr5:169955034
|
A | C | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+25243T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955034 | ||||||
| chr5:169955035
|
G | C | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+25242C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955035 | ||||||
| chr5:169955151
|
T | C | 1 | a0002c0002t0001g0211 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-919+25126A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955151 | ||||||
| chr5:169955165
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-919+25112C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955165 | ||||||
| chr5:169955373
|
A | G | 1 | a0002c0002t0001g0294 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-919+24904T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955373 | ||||||
| chr5:169955433
|
C | A | 20 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(17): Show | 20 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+24844G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955433 | ||||||
| chr5:169955569
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-919+24708C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955569 | ||||||
| chr5:169955579
|
G | T | 1 | a0001c0001t0002g0259 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-919+24698C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955579 | ||||||
| chr5:169955710
|
C | T | 1 | a0002c0002t0001g0041 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-919+24567G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955710 | ||||||
| chr5:169955748
|
T | G | 314 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(311): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.-919+24529A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955748 | ||||||
| chr5:169955794
|
A | G | 42 | a0001c0001t0001g0178a0001c0001t0002g0060a0001c0001t0002g0062others(39): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-919+24483T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955794 | ||||||
| chr5:169955926
|
G | C | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+24351C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169955926 | ||||||
| chr5:169956039
|
G | GAAAA | 19 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(16): Show | 20 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+24234_-919+24 others(10): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956039 | ||||||
| chr5:169956039
|
GA | G | 7 | a0001c0001t0002g0139a0001c0001t0002g0268a0001c0001t0002g0290others(4): Show | 7 | HG03041.hp1 HG03139.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+24237delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956039 | ||||||
| chr5:169956113
|
G | C | 20 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(17): Show | 20 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+24164C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956113 | ||||||
| chr5:169956243
|
A | T | 1 | a0001c0001t0002g0143 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-919+24034T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956243 | ||||||
| chr5:169956354
|
A | G | 125 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0111others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-919+23923T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956354 | ||||||
| chr5:169956400
|
T | G | 1 | a0001c0001t0002g0253 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-919+23877A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956400 | ||||||
| chr5:169956476
|
A | G | 42 | a0001c0001t0001g0178a0001c0001t0002g0060a0001c0001t0002g0062others(39): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-919+23801T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956476 | ||||||
| chr5:169956521
|
G | A | 1 | a0002c0002t0005g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-919+23756C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956521 | ||||||
| chr5:169956875
|
G | A | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(17): Show | 21 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+23402C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956875 | ||||||
| chr5:169956909
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-919+23368C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956909 | ||||||
| chr5:169956914
|
T | C | 21 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(18): Show | 22 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.-919+23363A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169956914 | ||||||
| chr5:169957211
|
G | T | 70 | a0001c0001t0001g0178a0001c0001t0002g0012a0001c0001t0002g0034others(67): Show | 71 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.-919+23066C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957211 | ||||||
| chr5:169957226
|
G | A | 20 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(17): Show | 20 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+23051C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957226 | ||||||
| chr5:169957477
|
G | A | 13 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(10): Show | 13 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.-919+22800C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957477 | ||||||
| chr5:169957492
|
C | T | 3 | a0001c0001t0003g0019a0001c0001t0010g0020a0002c0002t0004g0018 | 3 | HG02451.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-919+22785G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957492 | ||||||
| chr5:169957539
|
T | C | 257 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(254): Show | 259 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.-919+22738A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957539 | ||||||
| chr5:169957650
|
C | T | 1 | a0002c0002t0007g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-919+22627G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957650 | ||||||
| chr5:169957652
|
C | T | 1 | a0002c0002t0001g0250 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-919+22625G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957652 | ||||||
| chr5:169957960
|
G | A | 1 | a0002c0002t0006g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-919+22317C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169957960 | ||||||
| chr5:169958094
|
G | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+22183C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958094 | ||||||
| chr5:169958162
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+22115G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958162 | ||||||
| chr5:169958228
|
CA | C | 235 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(232): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-919+22048delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958228 | ||||||
| chr5:169958247
|
C | T | 1 | a0001c0001t0004g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-919+22030G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958247 | ||||||
| chr5:169958266
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-919+22011G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958266 | ||||||
| chr5:169958276
|
A | G | 1 | a0002c0002t0001g0110 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-919+22001T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958276 | ||||||
| chr5:169958533
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-919+21744G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958533 | ||||||
| chr5:169958539
|
A | T | 2 | a0002c0002t0007g0011a0002c0002t0008g0303 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-919+21738T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958539 | ||||||
| chr5:169958568
|
T | C | 2 | a0002c0002t0001g0165a0002c0002t0006g0120 | 2 | HG01934.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-919+21709A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958568 | ||||||
| chr5:169958585
|
C | CT | 91 | a0001c0001t0001g0040a0001c0001t0001g0197a0001c0001t0002g0012others(88): Show | 91 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(88): Show |
intron_variant | MODIFIER | c.-919+21691dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958585 | ||||||
| chr5:169958585
|
C | CTT | 125 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0111others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-919+21690_-919+21 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958585 | ||||||
| chr5:169958820
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-919+21457C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958820 | ||||||
| chr5:169958826
|
A | T | 1 | a0002c0002t0018g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-919+21451T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958826 | ||||||
| chr5:169959117
|
GCATGGTG others(3): Show |
G | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+21150_-919+21 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959117 | ||||||
| chr5:169959216
|
C | A | 1 | a0002c0002t0005g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-919+21061G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959216 | ||||||
| chr5:169959373
|
G | A | 2 | a0001c0001t0002g0146a0001c0001t0002g0203 | 2 | NA18959.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-919+20904C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959373 | ||||||
| chr5:169959373
|
G | GA | 15 | a0001c0001t0002g0085a0001c0001t0003g0009a0001c0001t0003g0101others(12): Show | 15 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-919+20903dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959373 | ||||||
| chr5:169959373
|
GA | G | 14 | a0001c0001t0001g0178a0001c0001t0003g0023a0001c0001t0003g0093others(11): Show | 14 | HG02486.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-919+20903delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959373 | ||||||
| chr5:169959636
|
A | G | 256 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(253): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-919+20641T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959636 | ||||||
| chr5:169959687
|
T | C | 42 | a0001c0001t0001g0178a0001c0001t0002g0060a0001c0001t0002g0062others(39): Show | 43 | HG00423.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.-919+20590A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959687 | ||||||
| chr5:169959767
|
C | T | 82 | a0001c0001t0001g0197a0001c0001t0002g0012a0001c0001t0002g0034others(79): Show | 82 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.-919+20510G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169959767 | ||||||
| chr5:169960000
|
G | C | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(15): Show | 18 | HG01981.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-919+20277C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960000 | ||||||
| chr5:169960083
|
G | A | 82 | a0001c0001t0001g0197a0001c0001t0002g0012a0001c0001t0002g0034others(79): Show | 82 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.-919+20194C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960083 | ||||||
| chr5:169960236
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-919+20041T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960236 | ||||||
| chr5:169960532
|
A | G | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(17): Show | 21 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+19745T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960532 | ||||||
| chr5:169960657
|
G | C | 258 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(255): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-919+19620C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960657 | ||||||
| chr5:169960731
|
G | T | 2 | a0002c0002t0003g0074a0002c0002t0007g0013 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-919+19546C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960731 | ||||||
| chr5:169960803
|
T | A | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+19474A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960803 | ||||||
| chr5:169960866
|
C | T | 18 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010others(15): Show | 18 | HG01981.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-919+19411G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960866 | ||||||
| chr5:169960918
|
A | G | 1 | a0001c0001t0010g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-919+19359T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169960918 | ||||||
| chr5:169961159
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085 | 3 | NA18969.hp2 NA18986.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-919+19118T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961159 | ||||||
| chr5:169961203
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-919+19074G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961203 | ||||||
| chr5:169961232
|
C | G | 1 | a0001c0001t0003g0212 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-919+19045G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961232 | ||||||
| chr5:169961396
|
C | G | 2 | a0001c0001t0002g0089a0001c0001t0003g0164 | 2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-919+18881G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961396 | ||||||
| chr5:169961483
|
T | A | 1 | a0001c0001t0002g0138 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-919+18794A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961483 | ||||||
| chr5:169961559
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0002g0254 | 2 | NA18960.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-919+18718T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961559 | ||||||
| chr5:169961707
|
G | A | 21 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(18): Show | 21 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+18570C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961707 | ||||||
| chr5:169961853
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-919+18424G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961853 | ||||||
| chr5:169961857
|
T | G | 21 | a0001c0001t0001g0178a0001c0001t0002g0146a0001c0001t0002g0203others(18): Show | 21 | HG00423.hp1 HG00639.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+18420A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961857 | ||||||
| chr5:169961933
|
C | T | 5 | a0001c0001t0003g0073a0002c0002t0003g0074a0002c0002t0005g0017others(2): Show | 5 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+18344G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961933 | ||||||
| chr5:169961935
|
T | C | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+18342A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961935 | ||||||
| chr5:169961977
|
C | T | 256 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(253): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-919+18300G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961977 | ||||||
| chr5:169961978
|
C | CAAAAAAA | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0068others(17): Show | 21 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+18292_-919+18 others(13): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0003g0080a0002c0002t0005g0077a0002c0002t0008g0078others(1): Show | 4 | HG02615.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+18288_-919+18 others(17): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0003g0079a0002c0002t0001g0194a0002c0002t0005g0308 | 3 | HG01069.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-919+18287_-919+18 others(18): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(6): Show |
19 | a0001c0001t0002g0087a0001c0001t0002g0090a0001c0001t0002g0291others(16): Show | 20 | HG01070.hp1 HG01071.hp1 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+18286_-919+18 others(19): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(7): Show |
13 | a0001c0001t0001g0040a0001c0001t0002g0053a0001c0001t0003g0021others(10): Show | 13 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.-919+18285_-919+18 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(8): Show |
14 | a0001c0001t0002g0254a0001c0001t0003g0008a0001c0001t0003g0009others(11): Show | 14 | HG00323.hp1 HG01978.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-919+18284_-919+18 others(21): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(9): Show |
73 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0001g0111others(70): Show | 73 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.-919+18283_-919+18 others(22): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(10): Show |
51 | a0001c0001t0001g0249a0001c0001t0002g0034a0001c0001t0002g0036others(48): Show | 51 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-919+18282_-919+18 others(23): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(11): Show |
27 | a0001c0001t0002g0012a0001c0001t0002g0037a0001c0001t0002g0123others(24): Show | 27 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-919+18298_-919+18 others(24): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(12): Show |
5 | a0001c0001t0002g0191a0002c0002t0001g0054a0002c0002t0001g0153others(2): Show | 5 | HG01515.hp2 HG01952.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+18298_-919+18 others(25): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0002g0143a0001c0001t0002g0203a0002c0002t0005g0301 | 3 | HG03540.hp1 NA18959.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-919+18298_-919+18 others(26): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(14): Show |
8 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0056others(5): Show | 8 | HG00639.hp2 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-919+18298_-919+18 others(27): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(15): Show |
8 | a0001c0001t0002g0146a0001c0001t0003g0082a0001c0001t0003g0097others(5): Show | 8 | HG00423.hp1 HG02129.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-919+18298_-919+18 others(28): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(16): Show |
3 | a0001c0001t0001g0178a0001c0001t0002g0256a0002c0002t0001g0181 | 3 | HG02602.hp1 NA18940.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-919+18298_-919+18 others(29): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(17): Show |
1 | a0002c0002t0002g0289 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-919+18298_-919+18 others(30): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169961978
|
C | CAAAAAAA others(18): Show |
1 | a0002c0002t0013g0147 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-919+18298_-919+18 others(31): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169961978 | ||||||
| chr5:169962343
|
A | G | 256 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(253): Show | 258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-919+17934T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962343 | ||||||
| chr5:169962359
|
A | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+17918T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962359 | ||||||
| chr5:169962412
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-919+17865A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962412 | ||||||
| chr5:169962428
|
C | T | 1 | a0002c0002t0001g0117 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-919+17849G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962428 | ||||||
| chr5:169962455
|
G | T | 1 | a0002c0002t0001g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-919+17822C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962455 | ||||||
| chr5:169962692
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-919+17585C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962692 | ||||||
| chr5:169962835
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-919+17442C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169962835 | ||||||
| chr5:169963080
|
G | A | 123 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(120): Show | 124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-919+17197C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963080 | ||||||
| chr5:169963085
|
C | A | 1 | a0001c0001t0022g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-919+17192G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963085 | ||||||
| chr5:169963154
|
C | T | 1 | a0002c0007t0004g0075 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-919+17123G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963154 | ||||||
| chr5:169963219
|
G | A | 2 | a0001c0001t0003g0141a0001c0001t0003g0175 | 2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-919+17058C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963219 | ||||||
| chr5:169963226
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0107a0001c0001t0003g0252others(3): Show | 6 | HG00323.hp2 HG01981.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-919+17051C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963226 | ||||||
| chr5:169963458
|
C | T | 15 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(12): Show | 15 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-919+16819G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963458 | ||||||
| chr5:169963483
|
A | C | 15 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(12): Show | 15 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-919+16794T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963483 | ||||||
| chr5:169963593
|
C | T | 3 | a0002c0002t0001g0201a0002c0002t0001g0238a0002c0002t0001g0248 | 3 | HG00099.hp1 HG00280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-919+16684G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963593 | ||||||
| chr5:169963733
|
C | T | 4 | a0001c0001t0002g0258a0001c0001t0004g0255a0002c0002t0001g0156others(1): Show | 4 | HG00642.hp2 HG01358.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+16544G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963733 | ||||||
| chr5:169963763
|
A | T | 1 | a0001c0001t0002g0131 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-919+16514T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963763 | ||||||
| chr5:169963787
|
A | G | 16 | a0001c0001t0002g0290a0001c0001t0003g0003a0001c0001t0003g0005others(13): Show | 16 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-919+16490T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963787 | ||||||
| chr5:169963797
|
C | A | 2 | a0002c0002t0007g0011a0002c0002t0008g0303 | 2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-919+16480G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963797 | ||||||
| chr5:169963929
|
G | A | 1 | a0003c0003t0004g0179 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-919+16348C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169963929 | ||||||
| chr5:169964018
|
A | C | 1 | a0001c0001t0001g0297 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-919+16259T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964018 | ||||||
| chr5:169964221
|
C | T | 2 | a0002c0002t0017g0109a0002c0002t0024g0316 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-919+16056G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964221 | ||||||
| chr5:169964318
|
C | T | 234 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(231): Show | 236 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.-919+15959G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964318 | ||||||
| chr5:169964338
|
G | T | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-919+15939C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964338 | ||||||
| chr5:169964378
|
G | A | 14 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(11): Show | 14 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-919+15899C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964378 | ||||||
| chr5:169964554
|
G | A | 174 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(171): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-919+15723C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964554 | ||||||
| chr5:169964613
|
T | C | 41 | a0001c0001t0001g0178a0001c0001t0002g0069a0001c0001t0002g0071others(38): Show | 41 | HG00280.hp2 HG00423.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.-919+15664A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964613 | ||||||
| chr5:169964766
|
C | T | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-919+15511G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964766 | ||||||
| chr5:169964773
|
A | C | 5 | a0001c0001t0003g0015a0002c0002t0001g0157a0002c0002t0001g0176others(2): Show | 5 | HG01106.hp1 HG01358.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.-919+15504T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964773 | ||||||
| chr5:169964927
|
A | G | 20 | a0001c0001t0001g0178a0001c0001t0002g0069a0001c0001t0002g0071others(17): Show | 20 | HG00423.hp1 HG01261.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.-919+15350T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169964927 | ||||||
| chr5:169965077
|
C | T | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+15200G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965077 | ||||||
| chr5:169965246
|
A | G | 1 | a0002c0002t0005g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-919+15031T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965246 | ||||||
| chr5:169965288
|
G | A | 1 | a0002c0002t0005g0218 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-919+14989C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965288 | ||||||
| chr5:169965293
|
C | T | 2 | a0002c0002t0005g0308a0002c0002t0007g0230 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-919+14984G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965293 | ||||||
| chr5:169965393
|
T | C | 1 | a0002c0002t0018g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-919+14884A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965393 | ||||||
| chr5:169965516
|
A | G | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+14761T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965516 | ||||||
| chr5:169965574
|
A | C | 1 | a0002c0002t0006g0048 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-919+14703T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965574 | ||||||
| chr5:169965588
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-919+14689T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965588 | ||||||
| chr5:169965634
|
C | T | 2 | a0001c0001t0001g0167a0002c0002t0001g0114 | 2 | HG00597.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.-919+14643G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965634 | ||||||
| chr5:169965823
|
A | G | 3 | a0001c0001t0001g0210a0002c0002t0001g0186a0002c0002t0001g0187 | 3 | HG01070.hp2 HG01071.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-919+14454T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169965823 | ||||||
| chr5:169966044
|
A | G | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-919+14233T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966044 | ||||||
| chr5:169966238
|
T | A | 8 | a0001c0001t0003g0056a0001c0001t0003g0097a0002c0002t0005g0014others(5): Show | 8 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-919+14039A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966238 | ||||||
| chr5:169966261
|
G | A | 1 | a0002c0002t0018g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-919+14016C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966261 | ||||||
| chr5:169966267
|
A | G | 88 | a0001c0001t0001g0111a0001c0001t0001g0249a0001c0001t0001g0276others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-919+14010T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966267 | ||||||
| chr5:169966316
|
A | T | 1 | a0001c0001t0003g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-919+13961T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966316 | ||||||
| chr5:169966320
|
C | T | 7 | a0001c0001t0003g0056a0002c0002t0005g0014a0002c0002t0005g0218others(4): Show | 7 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+13957G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966320 | ||||||
| chr5:169966401
|
T | C | 1 | a0002c0002t0007g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-919+13876A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966401 | ||||||
| chr5:169966600
|
A | T | 2 | a0001c0001t0002g0291a0001c0001t0021g0232 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-919+13677T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966600 | ||||||
| chr5:169966622
|
C | T | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+13655G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966622 | ||||||
| chr5:169966721
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-919+13556C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966721 | ||||||
| chr5:169966871
|
T | C | 1 | a0005c0008t0003g0113 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-919+13406A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966871 | ||||||
| chr5:169966900
|
C | G | 3 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0003g0214 | 3 | HG02486.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-919+13377G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169966900 | ||||||
| chr5:169967291
|
G | A | 1 | a0001c0001t0004g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-919+12986C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967291 | ||||||
| chr5:169967316
|
C | G | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+12961G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967316 | ||||||
| chr5:169967399
|
G | A | 7 | a0001c0001t0002g0128a0001c0001t0002g0155a0001c0001t0002g0180others(4): Show | 7 | HG00280.hp2 HG01168.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+12878C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967399 | ||||||
| chr5:169967454
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-919+12823T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967454 | ||||||
| chr5:169967476
|
C | T | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-919+12801G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967476 | ||||||
| chr5:169967694
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-919+12583C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967694 | ||||||
| chr5:169967713
|
G | A | 1 | a0002c0002t0001g0223 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-919+12564C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967713 | ||||||
| chr5:169967841
|
C | T | 58 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(55): Show | 58 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-919+12436G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169967841 | ||||||
| chr5:169968140
|
A | G | 8 | a0001c0001t0003g0056a0001c0001t0003g0097a0002c0002t0005g0014others(5): Show | 8 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-919+12137T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169968140 | ||||||
| chr5:169968480
|
A | T | 70 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(67): Show | 70 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-919+11797T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169968480 | ||||||
| chr5:169968576
|
G | A | 59 | a0001c0001t0001g0050a0001c0001t0001g0111a0001c0001t0001g0127others(56): Show | 59 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-919+11701C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169968576 | ||||||
| chr5:169968695
|
A | T | 2 | a0001c0001t0003g0307a0002c0002t0003g0158 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-919+11582T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169968695 | ||||||
| chr5:169968975
|
C | T | 71 | a0001c0001t0001g0249a0001c0001t0001g0276a0001c0001t0001g0277others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-919+11302G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169968975 | ||||||
| chr5:169969032
|
C | T | 13 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(10): Show | 13 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-919+11245G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969032 | ||||||
| chr5:169969155
|
G | A | 1 | a0001c0001t0002g0253 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-919+11122C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969155 | ||||||
| chr5:169969401
|
C | T | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-919+10876G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969401 | ||||||
| chr5:169969488
|
T | A | 1 | a0002c0002t0001g0030 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-919+10789A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969488 | ||||||
| chr5:169969605
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-919+10672G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969605 | ||||||
| chr5:169969706
|
G | A | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+10571C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969706 | ||||||
| chr5:169969707
|
G | GAGAACA | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+10569_-919+10 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969707 | ||||||
| chr5:169969710
|
G | GAGAGA | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+10566_-919+10 others(11): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969710 | ||||||
| chr5:169969929
|
T | C | 1 | a0002c0005t0001g0174 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-919+10348A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969929 | ||||||
| chr5:169969998
|
G | A | 2 | a0001c0001t0002g0065a0002c0002t0006g0064 | 2 | NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-919+10279C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169969998 | ||||||
| chr5:169970007
|
G | A | 1 | a0001c0001t0003g0096 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-919+10270C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169970007 | ||||||
| chr5:169970129
|
T | C | 1 | a0002c0002t0006g0048 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-919+10148A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169970129 | ||||||
| chr5:169970151
|
A | G | 1 | a0002c0002t0005g0308 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-919+10126T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169970151 | ||||||
| chr5:169970255
|
C | T | 6 | a0001c0001t0003g0016a0001c0001t0003g0233a0001c0001t0003g0311others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-919+10022G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169970255 | ||||||
| chr5:169970563
|
C | T | 1 | a0001c0001t0007g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-919+9714G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169970563 | ||||||
| chr5:169971188
|
C | CA | 11 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(8): Show | 11 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-919+9088dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971188 | ||||||
| chr5:169971188
|
C | CAAAA | 61 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-919+9085_-919+908 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971188 | ||||||
| chr5:169971188
|
C | CAAAAA | 7 | a0001c0001t0002g0180a0001c0001t0002g0191a0001c0001t0003g0189others(4): Show | 7 | HG01168.hp1 HG02109.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+9084_-919+908 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971188 | ||||||
| chr5:169971202
|
A | C | 13 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(10): Show | 13 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-919+9075T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971202 | ||||||
| chr5:169971248
|
A | G | 13 | a0001c0001t0002g0012a0001c0001t0002g0034a0001c0001t0002g0035others(10): Show | 13 | NA18939.hp1 NA18950.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.-919+9029T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971248 | ||||||
| chr5:169971255
|
C | A | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+9022G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971255 | ||||||
| chr5:169971283
|
G | A | 69 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.-919+8994C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971283 | ||||||
| chr5:169971355
|
G | A | 1 | a0001c0001t0003g0282 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-919+8922C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971355 | ||||||
| chr5:169971399
|
A | G | 1 | a0003c0003t0004g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-919+8878T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971399 | ||||||
| chr5:169971428
|
CT | C | 71 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(68): Show | 71 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-919+8848delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971428 | ||||||
| chr5:169971428
|
CTT | C | 110 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(107): Show | 112 | HG00099.hp2 HG00642.hp1 HG00673.hp1 others(109): Show |
intron_variant | MODIFIER | c.-919+8847_-919+884 others(6): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971428 | ||||||
| chr5:169971428
|
CTTT | C | 73 | a0001c0001t0001g0249a0001c0001t0001g0276a0001c0001t0001g0277others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.-919+8846_-919+884 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971428 | ||||||
| chr5:169971505
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-919+8772C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971505 | ||||||
| chr5:169971874
|
T | C | 254 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.-919+8403A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971874 | ||||||
| chr5:169971920
|
A | G | 1 | a0002c0002t0005g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-919+8357T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971920 | ||||||
| chr5:169972448
|
G | A | 1 | a0001c0001t0010g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-919+7829C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972448 | ||||||
| chr5:169972493
|
C | CATTATTA | 255 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.-919+7783_-919+778 others(11): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972493 | ||||||
| chr5:169972542
|
C | CAGAT | 13 | a0001c0001t0001g0199a0001c0001t0002g0130a0001c0001t0002g0163others(10): Show | 13 | HG00140.hp1 HG00639.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-919+7731_-919+773 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972542
|
C | CAGATAGA others(5): Show |
1 | a0002c0002t0001g0161 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-919+7723_-919+773 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972542
|
CAGAT | C | 11 | a0001c0001t0001g0277a0001c0001t0002g0057a0001c0001t0002g0247others(8): Show | 11 | HG00609.hp1 HG00621.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.-919+7731_-919+773 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972542
|
CAGATAGA others(1): Show |
C | 7 | a0001c0001t0009g0042a0002c0002t0001g0032a0002c0002t0001g0033others(4): Show | 7 | HG00099.hp2 HG02155.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+7727_-919+773 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972542
|
CAGATAGA others(5): Show |
C | 4 | a0001c0001t0003g0080a0001c0001t0003g0311a0002c0002t0001g0030others(1): Show | 4 | HG02723.hp1 HG03927.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+7723_-919+773 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972542
|
CAGATAGA others(9): Show |
C | 15 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0065others(12): Show | 16 | HG02071.hp2 HG02083.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.-919+7719_-919+773 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972542
|
CAGATAGA others(40): Show |
C | 7 | a0001c0001t0002g0155a0001c0001t0003g0015a0002c0002t0001g0157others(4): Show | 7 | HG00280.hp2 HG01358.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+7688_-919+773 others(51): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972542 | ||||||
| chr5:169972543
|
AGATAGAT others(36): Show |
A | 55 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(52): Show | 55 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-919+7691_-919+773 others(47): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972543 | ||||||
| chr5:169972546
|
T | C | 2 | a0001c0001t0003g0300a0002c0002t0005g0301 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-919+7731A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972546 | ||||||
| chr5:169972547
|
AGATAGAT others(32): Show |
A | 6 | a0001c0001t0002g0180a0001c0001t0007g0133a0002c0002t0001g0142others(3): Show | 6 | HG01106.hp1 HG01168.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-919+7691_-919+772 others(43): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972547 | ||||||
| chr5:169972570
|
TAGATAGA others(2): Show |
T | 14 | a0001c0001t0002g0068a0001c0001t0007g0022a0001c0001t0010g0151others(11): Show | 15 | HG02145.hp1 HG02559.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-919+7698_-919+770 others(13): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972570 | ||||||
| chr5:169972570
|
TAGATAGA others(13): Show |
T | 1 | a0001c0001t0004g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-919+7687_-919+770 others(24): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972570 | ||||||
| chr5:169972570
|
TAGATAGA others(17): Show |
T | 1 | a0001c0001t0002g0087 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-919+7683_-919+770 others(28): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972570 | ||||||
| chr5:169972574
|
TAGATA | T | 9 | a0001c0001t0002g0090a0001c0001t0003g0021a0001c0001t0003g0023others(6): Show | 9 | HG00642.hp1 HG02055.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+7698_-919+770 others(9): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972574 | ||||||
| chr5:169972574
|
TAGATAGA others(9): Show |
T | 5 | a0001c0001t0003g0079a0002c0002t0005g0077a0002c0002t0008g0078others(2): Show | 5 | HG01109.hp2 HG02615.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+7687_-919+770 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972574 | ||||||
| chr5:169972578
|
TA | T | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(22): Show | 25 | HG00323.hp2 HG00673.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-919+7698delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972578 | ||||||
| chr5:169972578
|
TAGATAGA others(5): Show |
T | 6 | a0001c0001t0003g0005a0001c0001t0003g0073a0001c0001t0003g0264others(3): Show | 6 | HG02572.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-919+7687_-919+769 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972578 | ||||||
| chr5:169972578
|
TAGATAGA others(9): Show |
T | 3 | a0001c0001t0003g0003a0001c0001t0003g0082a0001c0001t0022g0305 | 3 | HG02258.hp2 HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-919+7683_-919+769 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972578 | ||||||
| chr5:169972578
|
TAGATAGA others(13): Show |
T | 10 | a0001c0001t0003g0235a0001c0001t0003g0236a0001c0001t0003g0237others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-919+7679_-919+769 others(24): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972578 | ||||||
| chr5:169972579
|
A | AGAT | 6 | a0001c0001t0002g0012a0001c0001t0002g0053a0001c0001t0002g0281others(3): Show | 6 | HG02129.hp2 HG02148.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-919+7695_-919+769 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972579 | ||||||
| chr5:169972582
|
TA | T | 18 | a0001c0001t0001g0167a0001c0001t0002g0034a0001c0001t0002g0035others(15): Show | 18 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.-919+7694delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972582 | ||||||
| chr5:169972582
|
TAGATGAT others(5): Show |
T | 3 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0010 | 3 | HG02630.hp1 HG02896.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-919+7683_-919+769 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972582 | ||||||
| chr5:169972582
|
TAGATGAT others(9): Show |
T | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0085others(4): Show | 7 | HG01981.hp2 HG02818.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+7679_-919+769 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972582 | ||||||
| chr5:169972583
|
AGAT | A | 51 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(48): Show | 52 | HG00323.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.-919+7691_-919+769 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972583 | ||||||
| chr5:169972586
|
T | TA | 25 | a0001c0001t0001g0167a0001c0001t0002g0012a0001c0001t0002g0034others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-919+7690_-919+769 others(5): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972586 | ||||||
| chr5:169972586
|
T | TAGATAGA others(5): Show |
2 | a0001c0001t0002g0123a0001c0001t0002g0185 | 2 | NA19077.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-919+7690_-919+769 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972586 | ||||||
| chr5:169972586
|
T | TAGATAGA others(9): Show |
1 | a0002c0002t0001g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-919+7690_-919+769 others(20): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972586 | ||||||
| chr5:169972586
|
T | TAGATGAT others(1): Show |
7 | a0001c0001t0002g0047a0001c0001t0002g0125a0001c0001t0002g0221others(4): Show | 7 | HG00423.hp2 HG01255.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+7690_-919+769 others(12): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972586 | ||||||
| chr5:169972586
|
T | TGATA | 41 | a0001c0001t0001g0050a0001c0001t0001g0111a0001c0001t0001g0127others(38): Show | 41 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-919+7687_-919+769 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972586 | ||||||
| chr5:169972632
|
T | C | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-919+7645A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972632 | ||||||
| chr5:169972720
|
G | T | 1 | a0001c0001t0002g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-919+7557C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972720 | ||||||
| chr5:169972779
|
A | T | 1 | a0001c0001t0003g0101 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-919+7498T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972779 | ||||||
| chr5:169972786
|
G | A | 21 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(18): Show | 21 | HG00099.hp2 HG02735.hp2 HG02738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+7491C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972786 | ||||||
| chr5:169972803
|
A | G | 6 | a0001c0001t0003g0300a0001c0001t0004g0026a0002c0002t0004g0108others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-919+7474T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972803 | ||||||
| chr5:169972909
|
C | G | 20 | a0001c0001t0002g0060a0001c0001t0002g0062a0001c0001t0002g0065others(17): Show | 21 | HG00673.hp1 HG02071.hp2 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.-919+7368G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169972909 | ||||||
| chr5:169973024
|
G | A | 4 | a0001c0001t0003g0233a0002c0002t0005g0024a0002c0002t0005g0025others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+7253C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973024 | ||||||
| chr5:169973064
|
C | T | 39 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-919+7213G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973064 | ||||||
| chr5:169973120
|
A | G | 170 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0001g0249others(167): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-919+7157T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973120 | ||||||
| chr5:169973190
|
C | A | 7 | a0001c0001t0003g0056a0002c0002t0005g0014a0002c0002t0005g0218others(4): Show | 7 | HG00639.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-919+7087G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973190 | ||||||
| chr5:169973241
|
G | T | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-919+7036C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973241 | ||||||
| chr5:169973274
|
C | T | 13 | a0001c0001t0003g0101a0001c0001t0003g0103a0001c0001t0003g0104others(10): Show | 13 | HG01981.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-919+7003G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973274 | ||||||
| chr5:169973357
|
G | A | 1 | a0002c0002t0015g0275 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-919+6920C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973357 | ||||||
| chr5:169973390
|
G | T | 4 | a0001c0001t0002g0087a0001c0001t0002g0089a0002c0002t0001g0088others(1): Show | 5 | HG01070.hp1 HG03491.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-919+6887C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973390 | ||||||
| chr5:169973448
|
C | G | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+6829G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973448 | ||||||
| chr5:169973664
|
C | G | 1 | a0002c0002t0018g0095 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-919+6613G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973664 | ||||||
| chr5:169973672
|
C | T | 70 | a0001c0001t0001g0249a0001c0001t0001g0276a0001c0001t0001g0277others(67): Show | 70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-919+6605G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973672 | ||||||
| chr5:169973748
|
A | C | 39 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(36): Show | 39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-919+6529T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973748 | ||||||
| chr5:169973817
|
A | G | 38 | a0001c0001t0001g0249a0001c0001t0002g0083a0001c0001t0002g0084others(35): Show | 38 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.-919+6460T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973817 | ||||||
| chr5:169973896
|
A | G | 3 | a0001c0001t0003g0019a0001c0001t0010g0020a0002c0002t0004g0018 | 3 | HG02451.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-919+6381T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973896 | ||||||
| chr5:169973983
|
C | T | 1 | a0002c0002t0017g0109 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-919+6294G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973983 | ||||||
| chr5:169973992
|
G | T | 1 | a0002c0002t0001g0030 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-919+6285C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973992 | ||||||
| chr5:169974008
|
G | A | 40 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-919+6269C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974008 | ||||||
| chr5:169974085
|
G | T | 40 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-919+6192C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974085 | ||||||
| chr5:169974135
|
G | A | 3 | a0001c0001t0003g0019a0001c0001t0010g0020a0002c0002t0004g0018 | 3 | HG02451.hp1 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-919+6142C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974135 | ||||||
| chr5:169974201
|
A | C | 42 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(39): Show | 42 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-919+6076T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974201 | ||||||
| chr5:169974279
|
A | G | 32 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-919+5998T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974279 | ||||||
| chr5:169974364
|
A | AAAGAGAA others(5): Show |
1 | a0001c0001t0010g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-919+5912_-919+591 others(16): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974364 | ||||||
| chr5:169974392
|
T | C | 51 | a0001c0001t0001g0197a0001c0001t0002g0053a0001c0001t0002g0155others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-919+5885A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974392 | ||||||
| chr5:169974459
|
A | G | 34 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(31): Show | 34 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-919+5818T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974459 | ||||||
| chr5:169974530
|
T | A | 9 | a0001c0001t0003g0003a0001c0001t0003g0005a0001c0001t0003g0007others(6): Show | 9 | HG02258.hp2 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+5747A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974530 | ||||||
| chr5:169974553
|
C | T | 37 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0002g0180others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-919+5724G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974553 | ||||||
| chr5:169974633
|
T | G | 3 | a0001c0001t0003g0288a0001c0001t0004g0283a0001c0001t0004g0287 | 3 | NA18947.hp1 NA18971.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-919+5644A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974633 | ||||||
| chr5:169974765
|
G | A | 196 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(193): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.-919+5512C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974765 | ||||||
| chr5:169974854
|
CAT | C | 31 | a0001c0001t0001g0178a0001c0001t0002g0069a0001c0001t0002g0071others(28): Show | 31 | HG00423.hp1 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-919+5421_-919+542 others(6): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974854 | ||||||
| chr5:169974888
|
T | C | 1 | a0002c0002t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-919+5389A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974888 | ||||||
| chr5:169975061
|
C | T | 23 | a0001c0001t0002g0087a0001c0001t0002g0089a0001c0001t0002g0090others(20): Show | 24 | HG00642.hp1 HG01070.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-919+5216G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975061 | ||||||
| chr5:169975134
|
A | G | 1 | a0002c0002t0005g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-919+5143T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975134 | ||||||
| chr5:169975214
|
A | G | 64 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-919+5063T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975214 | ||||||
| chr5:169975238
|
G | A | 2 | a0002c0002t0003g0158a0002c0002t0017g0109 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-919+5039C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975238 | ||||||
| chr5:169975355
|
A | T | 8 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0008others(5): Show | 8 | HG02559.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-919+4922T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975355 | ||||||
| chr5:169975573
|
A | G | 70 | a0001c0001t0001g0111a0001c0001t0001g0249a0001c0001t0001g0276others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-919+4704T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975573 | ||||||
| chr5:169975722
|
G | A | 51 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-919+4555C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169975722 | ||||||
| chr5:169976023
|
C | T | 1 | a0001c0001t0003g0311 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-919+4254G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976023 | ||||||
| chr5:169976176
|
C | G | 51 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-919+4101G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976176 | ||||||
| chr5:169976249
|
G | A | 2 | a0002c0002t0003g0158a0002c0002t0017g0109 | 2 | HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-919+4028C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976249 | ||||||
| chr5:169976355
|
A | G | 1 | a0002c0002t0001g0110 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-919+3922T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976355 | ||||||
| chr5:169976381
|
A | G | 253 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0107others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-919+3896T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976381 | ||||||
| chr5:169976600
|
A | G | 74 | a0001c0001t0001g0249a0001c0001t0001g0276a0001c0001t0001g0277others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.-919+3677T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976600 | ||||||
| chr5:169976672
|
A | AAATGAAG others(11): Show |
4 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0082others(1): Show | 4 | HG02622.hp2 HG02647.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-919+3587_-919+360 others(22): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976672 | ||||||
| chr5:169976715
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-919+3562C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976715 | ||||||
| chr5:169976756
|
A | G | 54 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(51): Show | 54 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.-919+3521T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976756 | ||||||
| chr5:169976772
|
T | G | 51 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-919+3505A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976772 | ||||||
| chr5:169976792
|
C | T | 51 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-919+3485G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976792 | ||||||
| chr5:169976815
|
G | A | 51 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(48): Show | 51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-919+3462C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976815 | ||||||
| chr5:169976934
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-919+3343A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976934 | ||||||
| chr5:169976938
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3339G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976938 | ||||||
| chr5:169976951
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3326T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976951 | ||||||
| chr5:169976955
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3322G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976955 | ||||||
| chr5:169976965
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3312T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976965 | ||||||
| chr5:169976986
|
C | G | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3291G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976986 | ||||||
| chr5:169976987
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3290A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976987 | ||||||
| chr5:169976994
|
C | G | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3283G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976994 | ||||||
| chr5:169976998
|
A | G | 56 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(53): Show | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-919+3279T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976998 | ||||||
| chr5:169977000
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-919+3277C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977000 | ||||||
| chr5:169977001
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3276T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977001 | ||||||
| chr5:169977003
|
GTCCTGGG others(10): Show |
G | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3257_-919+327 others(21): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977003 | ||||||
| chr5:169977022
|
T | A | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3255A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977022 | ||||||
| chr5:169977034
|
C | G | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3243G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977034 | ||||||
| chr5:169977037
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3240T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977037 | ||||||
| chr5:169977038
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3239C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977038 | ||||||
| chr5:169977041
|
A | T | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3236T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977041 | ||||||
| chr5:169977048
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3229G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977048 | ||||||
| chr5:169977049
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3228G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977049 | ||||||
| chr5:169977050
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-919+3227A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977050 | ||||||
| chr5:169977084
|
C | T | 53 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-919+3193G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977084 | ||||||
| chr5:169977292
|
T | C | 1 | a0002c0002t0006g0285 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-919+2985A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977292 | ||||||
| chr5:169977374
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-919+2903C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977374 | ||||||
| chr5:169977543
|
G | A | 53 | a0001c0001t0001g0178a0001c0001t0001g0197a0001c0001t0002g0069others(50): Show | 53 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-919+2734C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977543 | ||||||
| chr5:169977642
|
T | G | 1 | a0002c0002t0007g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-919+2635A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977642 | ||||||
| chr5:169977716
|
G | A | 3 | a0001c0001t0003g0311a0002c0002t0001g0312a0002c0002t0024g0316 | 3 | HG02572.hp1 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-919+2561C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169977716 | ||||||
| chr5:169978041
|
C | T | 1 | a0001c0001t0012g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-919+2236G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978041 | ||||||
| chr5:169978048
|
G | A | 1 | a0002c0002t0007g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-919+2229C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978048 | ||||||
| chr5:169978273
|
C | T | 3 | a0001c0001t0003g0307a0002c0002t0005g0308a0002c0002t0007g0306 | 3 | HG02717.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-919+2004G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978273 | ||||||
| chr5:169978315
|
A | G | 5 | a0001c0001t0003g0079a0001c0001t0003g0080a0002c0002t0005g0077others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+1962T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978315 | ||||||
| chr5:169978321
|
A | C | 1 | a0002c0002t0003g0158 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-919+1956T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978321 | ||||||
| chr5:169978375
|
A | ATGTG | 3 | a0001c0001t0003g0073a0002c0002t0003g0074a0002c0007t0004g0075 | 3 | HG02145.hp1 HG02809.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-919+1898_-919+190 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978375 | ||||||
| chr5:169978375
|
ATG | A | 33 | a0001c0001t0002g0134a0001c0001t0002g0135a0001c0001t0002g0136others(30): Show | 33 | HG00280.hp1 HG00423.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.-919+1900_-919+190 others(6): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978375 | ||||||
| chr5:169978375
|
ATGTG | A | 14 | a0001c0001t0001g0197a0001c0001t0002g0155a0001c0001t0004g0152others(11): Show | 14 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.-919+1898_-919+190 others(8): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978375 | ||||||
| chr5:169978376
|
T | C | 1 | a0002c0002t0001g0181 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-919+1901A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978376 | ||||||
| chr5:169978387
|
GTGT | G | 5 | a0001c0001t0002g0207a0001c0001t0002g0290a0002c0002t0001g0204others(2): Show | 5 | HG01071.hp1 HG01261.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-919+1887_-919+188 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978387 | ||||||
| chr5:169978388
|
T | G | 4 | a0001c0001t0002g0221a0002c0002t0001g0219a0002c0002t0001g0220others(1): Show | 4 | HG00639.hp1 HG01081.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+1889A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978388 | ||||||
| chr5:169978389
|
GT | G | 4 | a0001c0001t0002g0203a0002c0002t0001g0201a0002c0002t0001g0202others(1): Show | 4 | HG00741.hp1 HG06807.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+1887delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978389 | ||||||
| chr5:169978389
|
GTGT | G | 7 | a0001c0001t0002g0180a0001c0001t0003g0311a0002c0002t0001g0181others(4): Show | 7 | HG00639.hp2 HG02602.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+1885_-919+188 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978389 | ||||||
| chr5:169978390
|
T | G | 21 | a0001c0001t0001g0210a0001c0001t0001g0293a0001c0001t0001g0297others(18): Show | 21 | HG00639.hp1 HG01081.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-919+1887A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978390 | ||||||
| chr5:169978390
|
T | TG | 7 | a0001c0001t0001g0199a0001c0001t0003g0288a0001c0001t0004g0287others(4): Show | 7 | NA18954.hp1 NA18964.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-919+1886dupC | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978390 | ||||||
| chr5:169978390
|
T | TGG | 3 | a0001c0001t0002g0291a0001c0001t0003g0292a0003c0003t0004g0208 | 3 | HG03195.hp2 HG03654.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-919+1886_-919+188 others(6): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978390 | ||||||
| chr5:169978390
|
TGTG | T | 19 | a0001c0001t0002g0057a0001c0001t0002g0060a0001c0001t0002g0062others(16): Show | 20 | HG00673.hp1 HG02015.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.-919+1884_-919+188 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978390 | ||||||
| chr5:169978391
|
GT | G | 32 | a0001c0001t0001g0178a0001c0001t0001g0249a0001c0001t0002g0170others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(29): Show |
intron_variant | MODIFIER | c.-919+1885delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978391 | ||||||
| chr5:169978392
|
T | G | 80 | a0001c0001t0001g0188a0001c0001t0001g0197a0001c0001t0001g0199others(77): Show | 80 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.-919+1885A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978392 | ||||||
| chr5:169978392
|
T | TG | 17 | a0001c0001t0001g0167a0001c0001t0002g0160a0001c0001t0002g0163others(14): Show | 17 | HG00597.hp1 HG00597.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-919+1884dupC | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978392 | ||||||
| chr5:169978392
|
TG | T | 37 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0050others(34): Show | 37 | HG00423.hp2 HG01258.hp1 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.-919+1884delC | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978392 | ||||||
| chr5:169978393
|
G | GTGT | 16 | a0001c0001t0003g0016a0001c0001t0003g0019a0001c0001t0003g0021others(13): Show | 17 | HG00642.hp1 HG02451.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-919+1883_-919+188 others(7): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978393 | ||||||
| chr5:169978393
|
G | T | 2 | a0001c0001t0003g0015a0002c0002t0005g0014 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-919+1884C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978393 | ||||||
| chr5:169978394
|
G | T | 2 | a0001c0001t0003g0304a0002c0002t0007g0013 | 2 | HG01255.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-919+1883C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978394 | ||||||
| chr5:169978395
|
G | T | 2 | a0001c0001t0002g0012a0002c0002t0007g0011 | 2 | HG02922.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-919+1882C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978395 | ||||||
| chr5:169978397
|
G | T | 1 | a0002c0002t0007g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-919+1880C>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978397 | ||||||
| chr5:169978439
|
G | C | 1 | a0001c0001t0001g0297 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-919+1838C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978439 | ||||||
| chr5:169978618
|
T | A | 77 | a0001c0001t0001g0249a0001c0001t0001g0276a0001c0001t0001g0277others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.-919+1659A>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978618 | ||||||
| chr5:169978897
|
T | C | 1 | a0002c0002t0020g0298 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-919+1380A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978897 | ||||||
| chr5:169978965
|
C | A | 1 | a0004c0004t0003g0299 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-919+1312G>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169978965 | ||||||
| chr5:169979012
|
A | G | 9 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0008others(6): Show | 9 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-919+1265T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169979012 | ||||||
| chr5:169979081
|
G | A | 4 | a0001c0001t0003g0300a0002c0002t0005g0301a0002c0002t0007g0302others(1): Show | 4 | HG02486.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-919+1196C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169979081 | ||||||
| chr5:169979144
|
G | A | 1 | a0001c0001t0003g0304 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-919+1133C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169979144 | ||||||
| chr5:169979229
|
A | T | 1 | a0002c0002t0001g0004 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-919+1048T>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169979229 | ||||||
| chr5:169979882
|
C | G | 1 | a0001c0001t0003g0003 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-919+395G>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169979882 | ||||||
| chr5:169980058
|
G | A | 1 | a0001c0001t0022g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-919+219C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169980058 | ||||||
| chr5:169980136
|
C | CCA | 11 | a0001c0001t0003g0307a0001c0001t0003g0311a0002c0002t0001g0312others(8): Show | 11 | HG00639.hp2 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-919+139_-919+140d others(4): Show |
INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169980136 |