Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MAQQN others(530): Show |
chr5 | 169856303 | 169985495 |
| a0002 | 0/1 | 535 | 133 | 38 | 34 | 34 | 11 | 15 | 24 | INSYN2B_chr5_169856303_169985495 | INSYN2B | MAQQN others(530): Show |
chr5 | 169856303 | 169985495 |
| a0003 | 0/0 | 535 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | MAQQN others(530): Show |
chr5 | 169856303 | 169985495 |
| a0004 | 0/0 | 535 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | MAQQN others(530): Show |
chr5 | 169856303 | 169985495 |
| a0005 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | MAQQN others(530): Show |
chr5 | 169856303 | 169985495 |
| a0006 | 0/0 | 535 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | MAQQN others(530): Show |
chr5 | 169856303 | 169985495 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1605 | 176 | 52 | 17 | 87 | 5 | 14 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0002c0002 | 0/1 | 1605 | 131 | 38 | 33 | 34 | 11 | 14 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0002c0005 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0002c0007 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0003c0003 | 0/0 | 1605 | 5 | 0 | 0 | 0 | 0 | 5 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0004c0004 | 0/0 | 1605 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0005c0008 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
chr5 | 169856303 | 169985495 | ||
| a0006c0006 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | ATGGC others(1600): Show |
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 | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0002 | 1/0 | 5715 | 73 | 6 | 4 | 53 | 3 | 6 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0003 | 0/0 | 5715 | 54 | 36 | 5 | 8 | 1 | 4 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0004 | 0/0 | 5715 | 22 | 2 | 7 | 13 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0007 | 0/0 | 5716 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0009 | 0/0 | 5715 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0010 | 0/0 | 5715 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0012 | 0/0 | 5715 | 2 | 2 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0021 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0001c0001t0022 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0001 | 0/1 | 5716 | 71 | 5 | 29 | 20 | 10 | 6 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0002 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0003 | 0/0 | 5715 | 3 | 3 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0004 | 0/0 | 5715 | 5 | 3 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0005 | 0/0 | 5716 | 13 | 12 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0006 | 0/0 | 5716 | 13 | 0 | 1 | 9 | 1 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0007 | 0/0 | 5716 | 7 | 7 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0008 | 0/0 | 5716 | 4 | 4 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0011 | 0/0 | 5716 | 2 | 0 | 0 | 0 | 0 | 2 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0013 | 0/0 | 5716 | 2 | 0 | 0 | 2 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0014 | 0/0 | 5715 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0015 | 0/0 | 5716 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0016 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0017 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0018 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0019 | 0/0 | 5716 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0020 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0023 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0024 | 0/0 | 5715 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0002c0002t0025 | 0/0 | 5716 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0005t0001 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| a0002c0007t0004 | 0/0 | 5715 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0003c0003t0004 | 0/0 | 5715 | 5 | 0 | 0 | 0 | 0 | 5 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0004c0004t0002 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0004c0004t0003 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0005c0008t0003 | 0/0 | 5715 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5710): Show |
chr5 | 169856303 | 169985495 |
| a0006c0006t0001 | 0/0 | 5716 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | GTCTT others(5711): Show |
chr5 | 169856303 | 169985495 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0001g0283 | 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 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0080 | 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 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0115 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0154 | 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 |
| a0001c0001t0002g0162 | 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 |
| a0001c0001t0002g0165 | 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 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0169 | 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 |
| a0001c0001t0002g0171 | 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 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0250 | 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 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0022 | 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 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0052 | 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 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0003g0301 | 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 |
| a0001c0001t0003g0313 | 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 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0009g0234 | 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 |
| a0001c0001t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0001c0001t0021g0255 | 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 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0113 | 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 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 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 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | 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 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0243 | 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 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0003g0066 | 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 |
| a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0002c0002t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0005g0302 | 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 |
| a0002c0002t0005g0312 | 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 |
| a0002c0002t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0006g0273 | 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 |
| a0002c0002t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0007g0300 | 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 |
| a0002c0002t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0008g0265 | 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 |
| a0002c0002t0008g0310 | 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 |
| a0002c0002t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0013g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0014g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0015g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0016g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0018g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0019g0235 | 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 |
| a0002c0002t0023g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0024g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0002t0025g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0005t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0002c0007t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0003c0003t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0004c0004t0002g0236 | 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 |
| a0005c0008t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| a0006c0006t0001g0194 | 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 | g0282 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0296 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0196 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0284 | EUR | GBR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0275 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0206 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00323 | hp1 | a0002 | c0002 | t0006 | g0203 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0278 | EUR | FIN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00609 | hp2 | a0005 | c0008 | t0003 | g0106 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00621 | hp1 | a0004 | c0004 | t0002 | g0236 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00621 | hp2 | a0002 | c0002 | t0015 | g0240 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0112 | 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 | g0022 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0229 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0200 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01106 | hp2 | a0002 | c0005 | t0001 | g0217 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01109 | hp2 | a0002 | c0002 | t0014 | g0053 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | PUR | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0109 | 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 | g0127 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0241 | 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 | g0211 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0289 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0208 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01433 | hp1 | a0002 | c0002 | t0006 | g0036 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0202 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0155 | EUR | IBS | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0116 | 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 | g0124 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG01993 | hp2 | a0006 | c0006 | t0001 | g0194 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0212 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02056 | hp2 | a0002 | c0002 | t0016 | g0242 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0027 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0098 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | CDX | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02257 | hp1 | a0002 | c0002 | t0007 | g0274 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02257 | hp2 | a0002 | c0002 | t0005 | g0186 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0210 | 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 | g0146 | AMR | PEL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0197 | 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 | g0311 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02572 | hp1 | a0002 | c0002 | t0024 | g0315 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02572 | hp2 | a0002 | c0002 | t0005 | g0058 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02615 | hp1 | a0002 | c0002 | t0008 | g0033 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02622 | hp1 | a0002 | c0002 | t0004 | g0099 | 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 | g0057 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0167 | 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 | g0153 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0314 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02735 | hp1 | a0003 | c0003 | t0004 | g0286 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02735 | hp2 | a0002 | c0002 | t0004 | g0088 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02738 | hp1 | a0002 | c0002 | t0004 | g0095 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0067 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0060 | 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 | g0316 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02895 | hp2 | a0002 | c0002 | t0007 | g0263 | 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 | g0268 | 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 | g0312 | 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 | g0175 | 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 | g0082 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0195 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0295 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03017 | hp2 | a0003 | c0003 | t0004 | g0159 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03098 | hp1 | a0002 | c0002 | t0008 | g0265 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0198 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0030 | 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 | g0100 | AFR | ESN | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0256 | 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 | g0269 | 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 | g0037 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03453 | hp1 | a0002 | c0002 | t0023 | g0031 | 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 | g0158 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0089 | 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 | g0302 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | GWD | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | MSL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03654 | hp1 | a0003 | c0003 | t0004 | g0104 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0051 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03704 | hp1 | a0002 | c0002 | t0018 | g0055 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03710 | hp1 | a0002 | c0002 | t0019 | g0235 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | PJL | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03927 | hp1 | a0002 | c0007 | t0004 | g0029 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03927 | hp2 | a0003 | c0003 | t0004 | g0233 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG03942 | hp2 | a0003 | c0003 | t0004 | g0239 | SAS | BEB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0182 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0081 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | STU | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG04228 | hp2 | a0002 | c0002 | t0006 | g0273 | 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 | g0072 | EAS | CHB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | CHB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0066 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18939 | hp2 | a0002 | c0002 | t0013 | g0073 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0094 | 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 | g0083 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18954 | hp1 | a0002 | c0002 | t0006 | g0042 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18957 | hp1 | a0002 | c0002 | t0013 | g0193 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18967 | hp2 | a0002 | c0002 | t0006 | g0252 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0166 | 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 | g0092 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18986 | hp2 | a0002 | c0002 | t0006 | g0137 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18995 | hp2 | a0001 | c0001 | t0009 | g0234 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19001 | hp2 | a0002 | c0002 | t0006 | g0070 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19002 | hp1 | a0002 | c0002 | t0006 | g0059 | 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 | g0101 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19004 | hp1 | a0002 | c0002 | t0006 | g0079 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0250 | 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 | g0247 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19043 | hp2 | a0002 | c0002 | t0005 | g0032 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0152 | 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 | g0154 | 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 | g0173 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19088 | hp1 | a0002 | c0002 | t0006 | g0071 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0215 | 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 | g0313 | AFR | YRI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20129 | hp1 | a0001 | c0001 | t0021 | g0255 | 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 | g0041 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0160 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0140 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0207 | EUR | TSI | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0238 | SAS | GIH | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20905 | hp2 | a0002 | c0002 | t0006 | g0125 | SAS | GIH | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02486 | hp2 | a0002 | c0002 | t0007 | g0300 | AFR | ACB | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0054 | 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 | g0177 | 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 | g0310 | AFR | USA | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | USA | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0052 | 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 | g0179 | AFR | LWK | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0222 | REF | REF | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0115 | REF | REF | INSYN2B_chr5_169856303_169985495 | INSYN2B | chr5 | 169856303 | 169985495 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002 a0003 a0006 |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:169864309 | G | A | 2 | a0002c0007 a0003c0003 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0007 a0002c0002t0005 a0002c0002t0006 others(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 | a0001c0001t0001 a0001c0001t0021 a0002c0002t0001 others(7): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): 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 | a0001c0001t0001 a0001c0001t0021 a0002c0002t0001 others(7): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): 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 | a0001c0001t0001 a0002c0002t0001 a0002c0002t0011 others(5): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): 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 | a0001c0001t0007 a0002c0002t0005 a0002c0002t0006 others(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 | a0001c0001t0001 a0001c0001t0021 a0002c0002t0001 others(6): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): 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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): 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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): 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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(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 | a0001c0001t0007 a0001c0001t0012 a0002c0002t0005 others(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 | a0002c0002t0005 a0002c0002t0024 a0002c0002t0025 |
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 | a0002c0002t0006 a0002c0002t0013 |
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 | a0002c0002t0024 a0002c0002t0025 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:169864601 | C | T | 44 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0001c0001t0003g0237 a0001c0001t0003g0278 a0001c0001t0003g0295 |
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 | a0002c0002t0001g0140 | 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 | a0002c0002t0001g0041 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0003g0178 | 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 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0188 |
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 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0037 others(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 | a0001c0001t0004g0026 a0001c0001t0004g0043 a0001c0001t0004g0069 others(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 | a0002c0002t0017g0100 | 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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | a0002c0002t0004g0099 a0002c0002t0017g0100 a0002c0002t0023g0031 |
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 | 91 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): 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 | a0001c0001t0002g0072 a0001c0001t0002g0162 a0001c0001t0002g0226 |
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 | a0001c0001t0004g0026 a0001c0001t0004g0043 a0001c0001t0004g0069 others(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 | a0002c0002t0001g0120 | 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 | a0002c0002t0024g0315 | 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 | a0002c0002t0025g0316 | 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 | a0001c0001t0021g0255 | 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 | a0001c0001t0002g0276 | 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 | 155 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): 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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0038 a0001c0001t0002g0039 others(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 | 210 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(207): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): 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 | a0001c0001t0003g0257 | 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 | a0001c0001t0002g0133 | 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 | 233 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0002c0002t0004g0060 a0002c0002t0017g0100 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0001c0001t0003g0253 | 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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | 2 | a0002c0002t0001g0138 a0002c0002t0001g0139 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1422-3579T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169868038 | |||||||
| chr5:169868333 | T | C | 3 | a0001c0001t0022g0305 a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0005g0058 | 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 | a0001c0001t0002g0074 a0001c0001t0002g0086 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0008g0310 | 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 | a0002c0002t0001g0112 a0002c0002t0001g0196 a0002c0002t0001g0197 others(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 | a0002c0002t0017g0100 | 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 | a0002c0002t0014g0053 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0003g0301 | 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 | a0002c0007t0004g0029 a0003c0003t0004g0104 a0003c0003t0004g0159 others(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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
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 | a0002c0002t0001g0108 | 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 | a0001c0001t0002g0165 | 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 | 237 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): 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 | a0001c0001t0002g0173 | 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 | 78 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0002c0002t0001g0004 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): 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 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0037 others(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 | a0002c0002t0006g0002 a0002c0002t0006g0042 a0002c0002t0006g0059 others(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 | a0001c0001t0003g0022 | 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 | a0002c0002t0004g0099 | 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 | 78 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0002c0002t0001g0004 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): 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 | a0001c0001t0007g0021 a0002c0002t0001g0041 a0002c0002t0001g0229 others(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 | a0001c0001t0002g0168 | 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 | a0005c0008t0003g0106 | 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 | a0002c0002t0005g0006 a0002c0002t0005g0014 a0002c0002t0005g0017 others(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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0002g0167 | 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 | a0001c0001t0002g0168 | 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 | a0002c0002t0017g0100 | 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 | a0002c0002t0017g0100 | 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 | a0002c0002t0014g0053 | 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 | 237 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1422-7192A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 3/3 | chr5 | 169871651 | |||||||
| chr5:169872038 | A | G | 232 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): 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 | a0001c0001t0003g0228 | 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 | a0002c0002t0005g0006 a0002c0002t0005g0014 a0002c0002t0005g0017 others(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 | 78 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0002c0002t0001g0004 others(75): Show |
79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): 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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0008g0310 a0002c0002t0016g0242 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0002g0213 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0002c0002t0007g0011 a0002c0002t0007g0013 a0002c0002t0007g0263 others(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 | a0002c0002t0008g0310 a0002c0002t0016g0242 |
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 | a0002c0002t0024g0315 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0056 a0001c0001t0003g0272 |
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 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0001c0001t0002g0080 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0023g0031 | 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 | a0001c0001t0003g0237 a0001c0001t0003g0278 a0001c0001t0003g0295 |
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 | 125 | a0001c0001t0001g0204 a0002c0002t0001g0004 a0002c0002t0001g0044 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): 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 | a0002c0002t0001g0246 a0002c0002t0008g0303 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0003c0003t0004g0104 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0002c0002t0003g0030 a0002c0002t0004g0099 a0002c0002t0005g0006 others(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 | a0002c0002t0004g0060 | 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 | a0001c0001t0010g0198 | 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 | a0001c0001t0003g0313 | 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 | a0002c0002t0004g0088 | 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 | a0002c0002t0001g0107 a0002c0002t0001g0126 a0002c0002t0001g0127 others(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 | a0002c0002t0003g0030 | 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 | a0002c0002t0001g0120 | 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 | a0001c0001t0002g0171 | 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 | a0002c0002t0017g0100 | 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 | a0002c0002t0019g0235 a0002c0007t0004g0029 |
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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0002c0002t0001g0157 | 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 | a0002c0002t0019g0235 a0002c0007t0004g0029 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0176 | 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 | a0002c0002t0017g0100 | 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 | a0002c0002t0001g0004 a0002c0002t0001g0044 a0002c0002t0001g0045 others(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 | a0002c0002t0005g0006 a0002c0002t0005g0014 a0002c0002t0005g0017 others(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 | a0002c0002t0004g0060 a0002c0002t0005g0006 a0002c0002t0005g0014 others(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 | a0002c0002t0001g0156 | 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 | 92 | a0002c0002t0001g0004 a0002c0002t0001g0041 a0002c0002t0001g0044 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): 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 | a0001c0001t0004g0179 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0002g0254 | 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 | a0002c0002t0001g0107 | 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 | a0002c0002t0004g0060 a0002c0002t0005g0006 a0002c0002t0005g0014 others(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 | a0002c0002t0004g0088 a0002c0002t0004g0095 |
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 | a0002c0002t0006g0002 a0002c0002t0006g0036 a0002c0002t0006g0042 others(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 | a0002c0002t0004g0060 | 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 | a0003c0003t0004g0104 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0004g0060 | 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 | a0001c0001t0003g0178 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0001g0189 | 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 | a0002c0002t0019g0235 a0002c0007t0004g0029 a0003c0003t0004g0104 others(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 | a0001c0001t0001g0204 | 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 | 92 | a0002c0002t0001g0004 a0002c0002t0001g0041 a0002c0002t0001g0044 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): 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 | a0002c0002t0017g0100 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0064 |
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 | 79 | a0002c0002t0001g0004 a0002c0002t0001g0044 a0002c0002t0001g0045 others(76): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): 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 | a0001c0001t0002g0130 | 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 | a0002c0002t0001g0199 a0002c0002t0001g0209 |
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 | a0002c0002t0019g0235 a0002c0007t0004g0029 |
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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | a0002c0002t0006g0002 a0002c0002t0006g0036 a0002c0002t0006g0042 others(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 | a0002c0002t0017g0100 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0001g0041 a0002c0002t0004g0088 a0002c0002t0004g0095 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0244 a0001c0001t0001g0247 |
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 | a0001c0001t0002g0152 | 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 | 236 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): 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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | a0001c0001t0021g0255 | 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 | a0002c0002t0008g0310 | 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 | a0002c0002t0006g0002 a0002c0002t0006g0036 a0002c0002t0006g0042 others(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 | a0001c0001t0003g0267 | 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 | a0002c0002t0017g0100 | 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 | a0002c0002t0003g0027 | 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 | a0002c0002t0003g0030 | 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 | a0001c0001t0004g0259 | 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 | a0001c0001t0002g0086 | 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 | 92 | a0002c0002t0001g0004 a0002c0002t0001g0041 a0002c0002t0001g0044 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.-918-1058dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169885873 | |||||||
| chr5:169886017 | ACT | A | 16 | a0002c0002t0004g0060 a0002c0002t0005g0006 a0002c0002t0005g0014 others(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 | a0002c0002t0003g0030 a0002c0002t0004g0099 a0002c0002t0006g0002 others(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 | a0002c0002t0019g0235 | 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 | 92 | a0002c0002t0001g0004 a0002c0002t0001g0041 a0002c0002t0001g0044 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): 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 | a0002c0002t0008g0310 a0002c0002t0016g0242 |
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 | a0001c0001t0002g0224 | 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 | a0001c0001t0003g0285 | 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 | a0003c0003t0004g0104 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0001c0001t0002g0188 | 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 | a0001c0001t0002g0225 | 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 | a0002c0002t0005g0006 a0002c0002t0005g0014 a0002c0002t0005g0017 others(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 | a0001c0001t0002g0249 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 |
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 | a0002c0002t0014g0053 | 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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | 136 | a0001c0001t0002g0206 a0002c0002t0001g0004 a0002c0002t0001g0041 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): 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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0003g0030 a0002c0002t0004g0099 a0002c0002t0005g0006 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0001c0001t0002g0213 | 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 | a0001c0001t0002g0169 a0002c0002t0001g0041 a0002c0002t0001g0229 others(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 | a0002c0002t0014g0053 | 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 | a0001c0001t0001g0221 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0002c0002t0004g0060 a0002c0002t0006g0036 a0002c0002t0024g0315 |
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 | a0002c0002t0004g0060 | 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 | a0001c0001t0021g0255 | 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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0019g0235 a0002c0007t0004g0029 |
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 | a0002c0002t0003g0030 a0002c0002t0004g0099 a0002c0002t0006g0002 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0001c0001t0003g0253 | 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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0004g0060 | 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 | a0001c0001t0002g0215 | 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 | a0002c0002t0003g0030 | 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 | a0002c0002t0005g0006 a0002c0002t0005g0014 a0002c0002t0005g0017 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0001c0001t0002g0114 a0001c0001t0002g0122 a0001c0001t0002g0154 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | a0002c0002t0001g0041 a0002c0002t0001g0229 a0002c0002t0001g0277 others(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 | 76 | a0001c0001t0002g0051 a0002c0002t0001g0004 a0002c0002t0001g0044 others(73): Show |
77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): 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 | a0001c0001t0002g0141 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0005g0006 a0002c0002t0005g0014 a0002c0002t0005g0017 others(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 | a0002c0002t0001g0041 a0002c0002t0004g0088 a0002c0002t0004g0095 others(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 | a0002c0002t0003g0030 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0012g0195 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0057 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0003g0019 a0001c0001t0003g0266 a0001c0001t0003g0269 others(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 | a0002c0002t0014g0053 | 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 | a0001c0001t0002g0162 a0001c0001t0004g0103 a0002c0002t0003g0027 others(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 | a0002c0002t0001g0107 a0002c0002t0001g0126 a0002c0002t0001g0127 others(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 | a0001c0001t0007g0158 a0001c0001t0012g0195 a0001c0001t0012g0205 others(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 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0067 others(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 | a0002c0002t0006g0203 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0001c0001t0021g0255 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | 233 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0001t0002g0262 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0001g0112 | 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 | 203 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-918-8664dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169893479 | |||||||
| chr5:169893499 | A | T | 2 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(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 | a0002c0002t0001g0063 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0004g0060 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0001c0001t0021g0255 | 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 | a0002c0002t0008g0033 a0002c0002t0008g0265 |
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 | a0002c0002t0014g0053 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0003g0253 a0001c0001t0009g0098 |
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 | a0002c0002t0004g0060 a0002c0002t0024g0315 |
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 | a0002c0002t0004g0060 a0002c0002t0024g0315 |
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 | a0001c0001t0004g0103 a0001c0001t0004g0219 a0001c0001t0004g0258 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0004g0026 a0001c0001t0021g0255 |
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 | a0002c0002t0004g0060 a0002c0002t0024g0315 |
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 | a0001c0001t0003g0272 | 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 | 76 | a0001c0001t0002g0051 a0001c0001t0002g0206 a0002c0002t0001g0004 others(73): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(74): 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 | a0001c0001t0003g0003 a0002c0002t0006g0002 a0002c0002t0006g0036 others(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 | a0001c0001t0002g0206 | 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 | a0001c0001t0003g0003 a0002c0002t0006g0002 a0002c0002t0006g0036 others(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 | a0006c0006t0001g0194 | 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 | a0001c0001t0003g0003 a0002c0002t0004g0099 a0002c0002t0006g0002 others(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 | a0001c0001t0003g0003 a0002c0002t0004g0099 a0002c0002t0006g0002 others(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 | a0002c0002t0008g0310 | 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 | a0002c0002t0014g0053 a0002c0002t0024g0315 |
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 | a0001c0001t0001g0090 | 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 | a0003c0003t0004g0104 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0002c0007t0004g0029 | 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 | a0002c0002t0006g0070 a0002c0002t0008g0310 |
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 | 229 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-918-11690T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896506 | |||||||
| chr5:169896650 | A | G | 88 | a0001c0001t0002g0051 a0001c0001t0002g0134 a0001c0001t0004g0026 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.-918-11834T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169896650 | |||||||
| chr5:169896715 | C | T | 221 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(218): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): 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 | a0001c0001t0003g0237 a0001c0001t0003g0257 a0001c0001t0003g0278 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0002c0002t0001g0202 | 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 | 88 | a0001c0001t0002g0051 a0001c0001t0002g0134 a0001c0001t0002g0206 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): 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 | a0001c0001t0022g0305 a0002c0002t0006g0070 a0002c0002t0008g0310 |
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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0002c0002t0006g0002 others(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 | a0001c0001t0002g0167 | 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 | a0001c0001t0003g0019 a0001c0001t0003g0266 a0001c0001t0003g0269 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0003g0118 |
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 | a0001c0001t0004g0103 a0003c0003t0004g0104 a0003c0003t0004g0159 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0001c0001t0004g0026 others(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 | a0001c0001t0003g0019 a0001c0001t0003g0266 a0001c0001t0003g0269 others(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 | a0001c0001t0022g0305 a0002c0002t0006g0070 a0002c0002t0008g0310 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0004g0099 | 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 | a0002c0002t0004g0060 a0002c0002t0008g0033 a0002c0002t0008g0265 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0004g0026 a0002c0002t0024g0315 |
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 | a0002c0002t0001g0101 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0001g0246 | 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 | a0001c0001t0022g0305 a0002c0002t0004g0060 a0002c0002t0006g0070 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0001g0092 | 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 | a0001c0001t0003g0237 a0001c0001t0003g0278 a0001c0001t0003g0295 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0034 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0167 | 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 | a0001c0001t0003g0015 a0001c0001t0003g0056 a0001c0001t0003g0272 others(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 | a0001c0001t0001g0221 | 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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | a0002c0002t0001g0093 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0022g0305 a0002c0002t0006g0070 a0002c0002t0008g0310 |
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 | a0001c0001t0003g0022 | 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 | a0001c0001t0002g0162 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0001g0094 | 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 | a0001c0001t0021g0255 | 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 | a0001c0001t0002g0155 | 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 | 218 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): 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 | a0002c0002t0003g0030 | 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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0001c0001t0003g0019 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0122 a0001c0001t0002g0154 a0001c0001t0004g0026 others(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 | a0001c0001t0002g0173 | 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 | a0002c0002t0008g0310 | 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 | a0001c0001t0022g0305 a0002c0002t0006g0070 a0002c0002t0008g0310 |
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 | a0002c0002t0001g0192 a0002c0002t0019g0235 a0002c0007t0004g0029 |
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 | 88 | a0001c0001t0002g0051 a0001c0001t0002g0134 a0001c0001t0004g0043 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): 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 | a0002c0002t0005g0006 a0002c0002t0005g0017 a0002c0002t0005g0024 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(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 | a0001c0001t0003g0237 a0001c0001t0003g0257 a0001c0001t0003g0278 others(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 | a0004c0004t0002g0236 | 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 | a0002c0002t0001g0296 | 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 | a0002c0002t0001g0081 a0002c0002t0001g0109 a0002c0002t0001g0200 |
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 | a0002c0002t0001g0140 | 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 | 203 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(200): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-918-17454C>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169902270 | |||||||
| chr5:169902360 | A | C | 312 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(309): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0001c0001t0002g0083 a0001c0001t0002g0287 a0001c0001t0002g0292 |
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 | a0002c0002t0006g0273 | 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 | 87 | a0001c0001t0002g0051 a0001c0001t0002g0134 a0001c0001t0004g0043 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): 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 | a0001c0001t0002g0173 | 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 | a0002c0002t0005g0006 a0002c0002t0005g0017 a0002c0002t0005g0024 others(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 | a0002c0002t0001g0214 | 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 | a0002c0002t0001g0138 a0002c0002t0001g0139 |
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 | a0002c0002t0004g0099 a0002c0002t0023g0031 |
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 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0007g0158 others(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 | a0002c0002t0024g0315 | 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 | 130 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0221 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): 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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0001c0001t0002g0051 a0001c0001t0002g0064 a0001c0001t0002g0134 others(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 | a0002c0007t0004g0029 | 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 | a0002c0002t0001g0243 | 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 | a0001c0001t0001g0223 | 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 | a0002c0002t0024g0315 | 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 | a0001c0001t0003g0003 a0001c0001t0007g0158 a0001c0001t0012g0195 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0002c0002t0001g0050 a0002c0007t0004g0029 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0001c0001t0007g0158 others(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 | a0001c0001t0002g0276 a0002c0002t0008g0033 |
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 | a0002c0002t0008g0310 | 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 | a0001c0001t0002g0147 a0001c0001t0002g0206 a0001c0001t0003g0257 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0151 a0001c0001t0002g0152 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0223 others(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 | a0001c0001t0002g0166 a0001c0001t0002g0226 a0001c0001t0003g0278 others(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 | a0003c0003t0004g0104 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0005t0001g0217 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0167 a0001c0001t0003g0007 a0001c0001t0003g0008 others(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 | a0001c0001t0003g0264 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0152 | 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 | a0001c0001t0002g0276 a0001c0001t0003g0007 a0001c0001t0003g0008 others(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 | a0001c0001t0021g0255 | 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 | a0001c0001t0002g0130 a0001c0001t0004g0132 a0002c0002t0001g0243 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0001c0001t0021g0255 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0105 a0001c0001t0002g0150 a0001c0001t0002g0249 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0313 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0051 a0001c0001t0002g0211 a0002c0002t0001g0231 others(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 | a0001c0001t0002g0147 a0001c0001t0002g0206 a0001c0001t0002g0276 others(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 | a0001c0001t0002g0206 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0253 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0019g0235 | 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 | a0002c0002t0001g0109 | 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 | a0001c0001t0003g0285 a0002c0002t0005g0309 a0002c0002t0005g0312 others(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 | a0001c0001t0002g0276 a0001c0001t0021g0255 a0002c0002t0003g0030 others(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 | a0002c0002t0005g0312 | 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 | a0001c0001t0002g0130 a0001c0001t0002g0142 a0001c0001t0002g0232 others(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 | a0001c0001t0002g0167 a0002c0002t0001g0208 a0002c0002t0001g0296 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0167 a0001c0001t0002g0276 a0002c0002t0001g0208 others(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 | a0001c0001t0002g0150 a0001c0001t0002g0249 a0001c0001t0002g0250 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0005g0312 | 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 | a0002c0002t0018g0055 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0001c0001t0021g0255 a0002c0002t0003g0030 |
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 | a0001c0001t0021g0255 a0002c0002t0003g0030 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0001c0001t0022g0305 a0002c0002t0004g0088 a0002c0002t0004g0095 |
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 | a0001c0001t0003g0285 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0008 others(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 | a0001c0001t0002g0276 a0002c0002t0008g0033 a0002c0002t0024g0315 |
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 | a0001c0001t0002g0147 | 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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0002c0002t0001g0314 | 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 | a0001c0001t0002g0276 a0002c0002t0008g0033 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0002g0167 a0001c0001t0003g0003 a0001c0001t0003g0307 others(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 | a0002c0002t0001g0246 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0051 a0001c0001t0002g0064 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0264 a0001c0001t0003g0307 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0008g0310 | 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 | a0001c0001t0002g0165 | 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 | a0002c0002t0003g0030 | 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 | a0001c0001t0004g0259 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0004g0294 | 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 | a0002c0002t0001g0093 a0002c0002t0001g0113 a0002c0002t0001g0245 others(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 | a0002c0005t0001g0217 | 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 | a0002c0002t0005g0302 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0001g0050 a0002c0002t0018g0055 a0003c0003t0004g0159 others(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 | a0002c0002t0001g0050 a0002c0002t0018g0055 a0003c0003t0004g0159 others(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 | a0001c0001t0003g0237 a0001c0001t0003g0278 |
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 | a0001c0001t0002g0167 a0001c0001t0003g0003 a0001c0001t0003g0307 others(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 | a0002c0002t0024g0315 | 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 | a0001c0001t0003g0253 | 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 | a0002c0002t0008g0033 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0002g0167 a0001c0001t0003g0003 a0001c0001t0003g0007 others(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 | a0001c0001t0002g0276 | 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 | a0001c0001t0003g0057 a0001c0001t0003g0062 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0005c0008t0003g0106 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0021g0255 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0003g0027 | 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 | a0002c0002t0013g0193 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0002c0002t0003g0030 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0005g0309 a0002c0002t0005g0312 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0010g0198 a0002c0002t0007g0013 |
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 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0223 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0142 a0001c0001t0002g0232 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0153 a0001c0001t0004g0026 a0001c0001t0010g0020 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0142 a0001c0001t0002g0232 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0002g0232 | 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 | a0002c0002t0007g0300 | 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 | a0002c0002t0003g0030 | 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 | a0002c0002t0001g0050 a0002c0002t0018g0055 a0003c0003t0004g0159 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0003c0003t0004g0104 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
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 | a0002c0002t0001g0081 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0005c0008t0003g0106 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0038 a0001c0001t0002g0153 others(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 | a0001c0001t0002g0167 a0001c0001t0002g0290 a0001c0001t0007g0158 others(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 | a0001c0001t0002g0169 a0001c0001t0002g0287 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0145 a0001c0001t0002g0080 others(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 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0001c0001t0001g0223 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0083 a0002c0002t0024g0315 a0002c0002t0025g0316 |
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 | a0001c0001t0002g0211 | 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 | a0001c0001t0002g0051 | 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 | a0002c0002t0003g0027 | 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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0002c0002t0024g0315 | 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 | a0001c0001t0002g0276 a0001c0001t0003g0301 a0002c0002t0005g0058 others(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 | a0001c0001t0002g0133 | 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 | a0001c0001t0004g0179 | 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 | a0001c0001t0003g0285 a0002c0002t0001g0214 a0002c0002t0005g0309 others(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 | a0001c0001t0002g0167 a0001c0001t0003g0003 a0001c0001t0003g0307 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0001c0001t0002g0188 | 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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0021g0255 | 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 | a0001c0001t0002g0173 | 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 | a0002c0002t0017g0100 | 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 | a0001c0001t0004g0119 | 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 | a0001c0001t0002g0276 | 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 | a0001c0001t0002g0290 | 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 | a0002c0002t0024g0315 | 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 | a0001c0001t0003g0285 a0001c0001t0021g0255 a0002c0002t0001g0214 others(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 | a0001c0001t0021g0255 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0019 a0001c0001t0003g0034 |
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 | a0001c0001t0002g0051 | 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 | a0001c0001t0002g0276 | 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 | a0001c0001t0003g0253 | 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 | a0001c0001t0003g0285 a0002c0002t0001g0214 a0002c0002t0005g0309 others(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 | a0001c0001t0003g0301 a0002c0002t0005g0058 a0002c0002t0005g0302 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0002c0002t0004g0060 | 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 | a0002c0002t0001g0231 | 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 | a0001c0001t0002g0162 | 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 | a0001c0001t0003g0301 a0002c0002t0005g0058 a0002c0002t0005g0302 others(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 | a0001c0001t0003g0177 | 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 | a0002c0002t0001g0246 a0002c0002t0008g0303 |
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 | a0001c0001t0009g0234 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0266 a0001c0001t0003g0269 a0002c0002t0008g0265 |
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 | a0002c0002t0004g0088 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 others(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 | a0001c0001t0002g0287 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0007g0158 a0001c0001t0012g0195 a0001c0001t0012g0205 others(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 | a0001c0001t0021g0255 a0002c0002t0003g0030 |
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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0025g0316 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0002c0007t0004g0029 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0003c0003t0004g0233 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0278 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | 34 | a0001c0001t0001g0102 a0001c0001t0001g0221 a0001c0001t0001g0244 others(31): Show |
34 | HG00423.hp1 HG00621.hp2 HG00642.hp2 others(31): 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 | a0002c0002t0005g0058 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0001g0238 | 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 | a0001c0001t0002g0276 a0001c0001t0003g0301 a0002c0002t0005g0058 others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0002g0167 a0002c0002t0001g0208 a0002c0002t0001g0296 others(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 | a0001c0001t0002g0064 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0001g0157 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0064 a0001c0001t0002g0086 others(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 | a0002c0002t0001g0174 | 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 | a0001c0001t0003g0301 a0002c0002t0005g0058 a0002c0002t0005g0302 others(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 | a0001c0001t0002g0051 | 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 | a0001c0001t0021g0255 a0002c0002t0023g0031 a0002c0002t0024g0315 |
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 | a0001c0001t0002g0165 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0001g0210 a0002c0002t0006g0273 |
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 | a0001c0001t0002g0167 a0002c0002t0001g0208 a0002c0002t0001g0296 others(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 | a0001c0001t0002g0167 a0001c0001t0003g0003 a0001c0001t0003g0307 others(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 | a0001c0001t0002g0051 | 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 | a0002c0002t0003g0030 a0002c0002t0023g0031 |
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 | a0001c0001t0002g0051 | 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 | a0001c0001t0002g0167 a0002c0002t0001g0208 a0002c0002t0001g0296 others(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 | a0001c0001t0021g0255 a0002c0002t0023g0031 a0002c0002t0024g0315 |
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 | a0002c0002t0007g0300 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0223 others(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 | a0002c0002t0018g0055 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0002c0002t0018g0055 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0001c0001t0002g0051 | 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 | a0001c0001t0002g0290 | 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 | a0002c0002t0001g0108 | 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 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0080 a0001c0001t0002g0276 a0001c0001t0003g0301 others(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 | a0002c0002t0008g0033 a0002c0002t0024g0315 a0002c0002t0025g0316 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0007g0274 a0002c0002t0007g0311 a0002c0002t0023g0031 |
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 | a0002c0002t0001g0081 | 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 | a0001c0001t0003g0285 a0002c0002t0001g0214 a0002c0002t0005g0309 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0130 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0181 | 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 | a0001c0001t0003g0285 a0002c0002t0001g0214 a0002c0002t0005g0309 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0002t0001g0284 | 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 | a0002c0002t0001g0212 | 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 | a0002c0002t0018g0055 a0003c0003t0004g0159 a0003c0003t0004g0233 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0307 a0002c0002t0005g0017 |
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 | a0001c0001t0002g0064 | 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 | a0001c0001t0002g0256 a0001c0001t0003g0016 a0001c0001t0003g0052 others(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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0001c0001t0003g0182 | 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 | a0001c0001t0003g0065 | 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 | a0001c0001t0002g0256 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0057 a0001c0001t0007g0021 a0002c0002t0001g0246 others(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 | 55 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0204 others(52): Show |
55 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.-918-40762delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169925577 | |||||||
| chr5:169925578 | T | TA | 53 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0002g0012 others(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 | a0001c0001t0001g0148 a0001c0001t0002g0085 a0001c0001t0002g0150 others(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 | a0001c0001t0003g0068 a0001c0001t0003g0176 a0001c0001t0003g0266 others(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 | a0001c0001t0003g0062 a0001c0001t0003g0301 a0001c0001t0022g0305 others(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 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0223 others(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 | a0001c0001t0002g0171 a0001c0001t0003g0218 a0001c0001t0004g0103 others(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 | a0001c0001t0007g0021 a0002c0002t0001g0199 a0002c0002t0001g0209 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0223 others(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 | a0001c0001t0007g0021 a0002c0002t0001g0199 a0002c0002t0001g0209 others(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 | 282 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(279): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): 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 | a0001c0001t0001g0148 a0001c0001t0001g0221 a0001c0001t0002g0074 others(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 | a0001c0001t0002g0064 | 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 | a0002c0002t0006g0002 a0002c0002t0006g0059 |
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 | a0001c0001t0003g0019 a0001c0001t0003g0052 a0001c0001t0004g0026 others(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 | a0001c0001t0002g0288 | 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 | a0002c0002t0001g0157 | 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 | a0001c0001t0002g0153 a0001c0001t0003g0028 a0002c0002t0005g0017 others(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 | a0002c0002t0017g0100 | 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 | a0002c0002t0025g0316 | 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 | 161 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0145 others(158): Show |
161 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(158): 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 | a0001c0001t0003g0019 a0001c0001t0010g0020 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0002g0153 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0097 a0001c0001t0002g0163 others(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 | a0002c0002t0001g0238 | 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 | a0001c0001t0001g0102 | 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 | a0002c0002t0003g0030 | 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 | a0002c0002t0001g0112 a0002c0002t0001g0196 a0002c0002t0001g0197 |
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 | a0001c0001t0002g0256 a0001c0001t0003g0023 a0001c0001t0003g0264 others(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 | 3 | a0001c0001t0001g0204 a0001c0001t0002g0211 a0002c0002t0006g0203 |
3 | HG00323.hp1 HG01074.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-918-42934C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169927750 | |||||||
| chr5:169927773 | C | G | 1 | a0002c0002t0001g0238 | 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 | a0002c0002t0001g0061 | 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 | a0001c0001t0003g0067 | 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 | a0001c0001t0002g0166 | 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 | a0002c0002t0018g0055 a0002c0007t0004g0029 |
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 | 285 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(282): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): 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 | a0001c0001t0002g0153 a0001c0001t0003g0028 a0002c0002t0005g0017 others(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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0002c0005t0001g0217 | 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 | a0001c0001t0003g0057 a0001c0001t0003g0301 a0001c0001t0022g0305 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0145 a0001c0001t0001g0223 others(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 | a0003c0003t0004g0286 | 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 | a0001c0001t0002g0142 | 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 | a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0001c0001t0003g0301 a0001c0001t0022g0305 a0002c0002t0005g0302 |
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 | a0002c0002t0001g0081 | 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 | a0001c0001t0003g0260 a0001c0001t0004g0103 a0001c0001t0004g0258 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0002g0105 a0001c0001t0002g0114 a0001c0001t0002g0129 others(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 | a0001c0001t0003g0057 a0001c0001t0003g0301 a0001c0001t0022g0305 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0223 a0001c0001t0002g0166 others(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 | a0001c0001t0004g0087 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0148 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0145 a0001c0001t0001g0221 others(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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0001c0001t0001g0148 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0005t0001g0217 | 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 | a0002c0002t0005g0058 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0145 others(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 | a0001c0001t0002g0292 a0001c0001t0004g0289 |
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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0001c0001t0003g0056 a0002c0002t0024g0315 |
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 | a0001c0001t0002g0012 a0001c0001t0002g0083 a0001c0001t0002g0084 others(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 | a0002c0002t0001g0214 | 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 | a0001c0001t0001g0221 a0001c0001t0002g0097 a0001c0001t0002g0163 others(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 | a0002c0002t0001g0230 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0221 a0001c0001t0001g0223 others(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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0002c0002t0017g0100 | 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 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0145 others(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 | a0002c0002t0018g0055 a0002c0007t0004g0029 |
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 | a0001c0001t0003g0034 a0002c0002t0008g0033 a0002c0002t0023g0031 |
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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0003c0003t0004g0239 | 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 | a0002c0002t0007g0274 | 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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0002g0153 others(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 | a0002c0002t0001g0284 | 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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0001c0001t0003g0068 | 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 | a0001c0001t0003g0019 a0002c0002t0004g0018 |
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 | a0001c0001t0001g0091 a0001c0001t0002g0180 a0001c0001t0002g0185 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0002c0002t0001g0045 | 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 | a0001c0001t0001g0148 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0097 a0001c0001t0002g0163 others(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 | a0002c0002t0018g0055 a0002c0007t0004g0029 |
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 | a0001c0001t0003g0227 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0223 a0001c0001t0001g0244 others(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 | a0002c0002t0001g0230 a0002c0002t0001g0279 |
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 | a0001c0001t0002g0049 | 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 | a0001c0001t0003g0019 a0001c0001t0003g0052 a0001c0001t0004g0026 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0001c0001t0003g0057 a0001c0001t0003g0301 a0001c0001t0022g0305 others(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 | a0001c0001t0003g0057 a0001c0001t0003g0301 a0001c0001t0022g0305 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0002c0002t0001g0296 | 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 | a0001c0001t0002g0074 a0001c0001t0002g0076 a0001c0001t0002g0151 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0163 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0221 a0001c0001t0002g0163 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0166 others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0166 others(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 | a0001c0001t0002g0134 a0002c0002t0001g0138 a0002c0002t0001g0139 |
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 | a0001c0001t0001g0148 a0001c0001t0002g0072 a0001c0001t0002g0074 others(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 | 56 | a0001c0001t0001g0148 a0001c0001t0001g0204 a0001c0001t0002g0072 others(53): Show |
57 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(54): 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 | a0002c0007t0004g0029 | 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 | a0002c0005t0001g0217 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0083 a0001c0001t0002g0085 others(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 | a0001c0001t0001g0091 a0001c0001t0001g0148 a0001c0001t0002g0074 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0076 a0001c0001t0002g0151 others(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 | 68 | a0001c0001t0001g0116 a0001c0001t0001g0204 a0001c0001t0001g0221 others(65): Show |
68 | HG00323.hp1 HG00423.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.-919+43698delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936578 | |||||||
| chr5:169936599 | T | A | 1 | a0001c0001t0003g0285 | 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 | a0001c0001t0001g0143 a0001c0001t0002g0142 a0001c0001t0002g0165 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0056 others(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 | 66 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0001c0001t0002g0134 others(63): Show |
66 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.-919+43572G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169936705 | |||||||
| chr5:169936757 | A | G | 41 | a0001c0001t0001g0204 a0001c0001t0002g0134 a0001c0001t0002g0147 others(38): Show |
41 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(38): 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 | a0001c0001t0003g0313 a0002c0002t0001g0314 a0002c0002t0004g0099 others(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 | a0002c0002t0001g0140 a0002c0002t0001g0296 |
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 | a0001c0001t0002g0276 | 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 | a0002c0002t0003g0027 a0002c0002t0025g0316 |
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 | a0001c0001t0002g0165 | 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 | a0002c0002t0005g0054 | 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 | a0002c0002t0003g0027 a0002c0002t0025g0316 |
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 | a0002c0005t0001g0217 | 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 | a0002c0002t0001g0183 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0295 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0013g0073 | 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 | a0001c0001t0001g0221 a0001c0001t0002g0290 a0001c0001t0003g0190 |
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 | a0001c0001t0002g0150 a0001c0001t0002g0249 a0001c0001t0002g0250 others(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 | a0002c0002t0004g0060 | 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 | a0002c0002t0007g0011 a0002c0002t0008g0303 |
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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0002t0018g0055 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0002t0001g0127 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0068 a0002c0002t0003g0066 |
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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0004g0179 | 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 | a0002c0002t0001g0094 a0002c0002t0018g0055 |
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 | 37 | a0001c0001t0001g0204 a0001c0001t0002g0147 a0001c0001t0002g0167 others(34): Show |
37 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(34): 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 | a0001c0001t0002g0180 | 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 | a0001c0001t0002g0180 | 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 | 37 | a0001c0001t0001g0204 a0001c0001t0002g0147 a0001c0001t0002g0152 others(34): Show |
37 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.-919+41073dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939203 | |||||||
| chr5:169939203 | C | CTTTTTT | 18 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0155 a0002c0002t0001g0111 a0002c0002t0001g0124 others(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 | a0003c0003t0004g0239 | 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 | 36 | a0001c0001t0001g0204 a0001c0001t0002g0147 a0001c0001t0002g0152 others(33): Show |
36 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-919+40593C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169939684 | |||||||
| chr5:169939702 | A | G | 213 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(210): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0007t0004g0029 | 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 | a0002c0002t0001g0246 | 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 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0003g0182 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0105 a0001c0001t0004g0216 |
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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0145 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0290 a0001c0001t0003g0190 |
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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0056 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0244 a0001c0001t0002g0288 |
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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0256 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0215 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0155 a0002c0002t0001g0111 a0002c0002t0001g0124 others(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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0225 a0001c0001t0003g0228 |
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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0003g0218 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0162 a0001c0001t0003g0077 others(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 | 37 | a0001c0001t0001g0204 a0001c0001t0002g0147 a0001c0001t0002g0152 others(34): Show |
37 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(34): 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 | a0002c0007t0004g0029 | 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 | a0002c0002t0001g0046 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0051 a0001c0001t0003g0007 others(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 | a0002c0002t0001g0156 | 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 | 38 | a0001c0001t0001g0204 a0001c0001t0002g0147 a0001c0001t0002g0152 others(35): Show |
38 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(35): 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 | a0002c0007t0004g0029 | 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 | a0002c0002t0001g0187 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0002c0002t0005g0032 others(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 | a0001c0001t0002g0167 | 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 | a0001c0001t0001g0145 | 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 | a0002c0007t0004g0029 | 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 | 254 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(251): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): 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 | a0001c0001t0002g0129 a0002c0002t0001g0174 |
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 | a0001c0001t0003g0019 a0001c0001t0004g0026 a0001c0001t0010g0020 others(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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0141 | 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 | a0001c0001t0002g0114 a0001c0001t0002g0136 a0001c0001t0002g0213 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0001g0091 a0002c0002t0001g0081 a0002c0002t0001g0296 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0084 | 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 | 253 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(250): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): 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 | a0001c0001t0003g0301 a0001c0001t0022g0305 a0002c0002t0005g0058 others(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 | a0001c0001t0021g0255 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0021g0255 | 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 | a0001c0001t0004g0103 | 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 | a0001c0001t0001g0102 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0004g0219 | 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 | a0001c0001t0002g0191 | 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 | a0001c0001t0007g0021 | 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 | a0004c0004t0002g0236 | 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 | a0001c0001t0003g0019 a0001c0001t0004g0026 a0001c0001t0010g0020 others(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 | a0002c0002t0007g0011 a0002c0002t0008g0303 |
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 | a0002c0002t0008g0265 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0096 | 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 | a0002c0002t0001g0050 | 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 | a0002c0002t0001g0123 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0001g0091 | 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 | 254 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0145 others(251): Show |
256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): 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 | a0001c0001t0021g0255 | 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 | a0001c0001t0002g0173 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0145 others(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 | a0001c0001t0001g0148 | 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 | 40 | a0001c0001t0001g0204 a0001c0001t0002g0147 a0001c0001t0002g0152 others(37): Show |
40 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(37): 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 | a0002c0002t0002g0261 | 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 | 79 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0012 others(76): Show |
79 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.-919+31980dupT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169948296 | |||||||
| chr5:169948391 | C | T | 4 | a0001c0001t0002g0166 a0001c0001t0004g0164 a0002c0002t0001g0101 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0110 a0001c0001t0003g0176 a0001c0001t0003g0177 others(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 | a0002c0007t0004g0029 | 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 | a0002c0002t0002g0261 | 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 | a0001c0001t0002g0191 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0051 a0001c0001t0003g0022 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0002t0002g0261 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0002t0005g0058 | 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 | a0002c0002t0004g0088 a0002c0002t0004g0095 |
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 | a0001c0001t0002g0206 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0002t0004g0060 | 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 | a0002c0002t0001g0093 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0001c0001t0003g0052 | 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 | a0001c0001t0003g0264 | 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 | a0001c0001t0002g0211 | 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 | a0002c0002t0003g0027 | 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 | a0001c0001t0002g0167 | 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 | a0002c0002t0001g0161 | 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 | a0001c0001t0002g0152 | 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 | a0002c0002t0005g0054 | 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 | a0002c0002t0001g0138 | 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 | a0002c0002t0001g0139 | 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 | a0002c0002t0006g0203 | 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 | a0001c0001t0001g0204 | 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(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 | a0002c0002t0001g0183 | 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 | a0001c0001t0004g0179 | 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 | a0003c0003t0004g0159 | 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 | a0002c0002t0001g0041 | 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 | a0002c0002t0001g0140 | 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 | a0002c0002t0007g0300 | 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 | a0002c0002t0001g0210 | 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 | a0001c0001t0003g0182 | 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 | a0001c0001t0003g0181 | 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 | a0001c0001t0002g0147 | 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 | a0001c0001t0007g0158 | 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 | a0001c0001t0012g0195 | 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 | a0001c0001t0012g0205 | 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 | a0001c0001t0003g0177 | 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 | a0001c0001t0003g0176 | 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 | a0001c0001t0003g0178 | 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 | a0002c0002t0001g0246 | 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 | a0002c0002t0001g0296 | 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 | a0002c0002t0001g0187 | 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 | a0001c0001t0003g0065 | 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 | a0002c0002t0003g0066 | 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 | a0001c0001t0003g0067 | 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 | a0001c0001t0003g0266 | 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 | a0002c0002t0001g0082 | 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 | a0001c0001t0003g0268 | 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 | a0001c0001t0003g0269 | 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 | a0001c0001t0003g0270 | 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 | a0002c0002t0004g0088 | 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 | a0002c0002t0001g0081 | 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 | a0001c0001t0003g0271 | 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 | a0001c0001t0003g0267 | 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 | a0001c0001t0003g0068 | 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 | a0002c0002t0008g0265 | 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 | a0002c0002t0007g0274 | 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 | a0002c0002t0004g0095 | 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 | a0001c0001t0003g0272 | 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 | a0001c0001t0002g0097 | 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 | a0002c0002t0001g0093 | 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 | a0001c0001t0002g0086 | 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 | a0001c0001t0002g0083 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0215 | 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 | a0001c0001t0009g0098 | 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 | a0002c0002t0001g0231 | 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 | a0001c0001t0004g0087 | 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 | a0001c0001t0002g0276 | 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 | a0001c0001t0002g0085 | 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 | a0001c0001t0002g0232 | 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 | a0001c0001t0002g0173 | 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 | a0001c0001t0002g0084 | 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 | a0002c0002t0018g0055 | 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 | a0001c0001t0003g0218 | 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 | a0001c0001t0003g0175 | 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 | a0002c0002t0003g0030 | 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 | a0001c0001t0002g0096 | 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 | a0001c0001t0002g0188 | 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 | a0001c0001t0003g0037 | 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 | a0001c0001t0002g0191 | 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 | a0002c0002t0002g0261 | 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 | a0001c0001t0002g0163 | 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 | a0002c0002t0008g0310 | 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 | a0002c0002t0013g0193 | 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 | a0001c0001t0003g0062 | 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 | a0002c0002t0007g0311 | 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 | a0002c0002t0005g0186 | 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 | a0002c0002t0001g0189 | 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0003g0190 | 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 | a0001c0001t0002g0290 | 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 | a0002c0002t0001g0192 | 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 | a0002c0002t0005g0312 | 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 | a0002c0002t0005g0058 | 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 | a0001c0001t0003g0057 | 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 | a0002c0002t0005g0302 | 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 | a0001c0001t0003g0301 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0091 | 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 | a0002c0002t0001g0280 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0191 | 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 | a0001c0001t0002g0131 a0005c0008t0003g0106 |
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 | a0003c0003t0004g0286 | 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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0002c0002t0007g0263 | 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 | a0001c0001t0003g0313 | 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 | a0001c0001t0003g0056 | 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 | a0002c0002t0001g0189 | 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 | a0001c0001t0002g0173 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0163 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | a0002c0002t0001g0187 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0002g0185 a0001c0001t0004g0201 a0002c0002t0001g0157 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0185 a0001c0001t0004g0201 a0002c0002t0001g0157 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0091 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 | 110 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0001c0001t0001g0221 others(107): Show |
110 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(107): 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0004g0119 | 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 | a0002c0002t0004g0060 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0166 a0001c0001t0004g0164 |
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 | a0001c0001t0002g0152 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0130 | 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 | a0002c0002t0013g0193 | 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 | a0002c0002t0013g0193 | 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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0002c0002t0005g0032 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0097 others(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 | a0002c0002t0001g0296 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | 111 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0001c0001t0001g0221 others(108): Show |
111 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(108): 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 | a0002c0002t0001g0139 | 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 | a0002c0002t0005g0312 | 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 | a0002c0002t0025g0316 | 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 | a0002c0007t0004g0029 | 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 | a0002c0002t0024g0315 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0002c0002t0001g0246 | 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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0002c0002t0005g0032 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0002c0002t0001g0183 | 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 | a0001c0001t0002g0180 | 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 | a0002c0002t0001g0231 | 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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0002c0002t0001g0220 | 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 | a0001c0001t0002g0293 | 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 | a0002c0002t0001g0082 | 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 | 313 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(310): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): 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 | a0001c0001t0001g0221 a0001c0001t0002g0072 a0001c0001t0002g0074 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0173 a0001c0001t0002g0232 a0001c0001t0002g0276 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0188 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0001c0001t0002g0287 | 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 | a0001c0001t0001g0221 a0001c0001t0002g0072 a0001c0001t0002g0074 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0002g0206 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0012 a0001c0001t0002g0072 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0003g0019 a0001c0001t0010g0020 a0002c0002t0004g0018 |
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 | 256 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(253): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): 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 | a0002c0002t0001g0284 | 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 | a0002c0002t0006g0125 | 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 | a0002c0007t0004g0029 | 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 | a0002c0007t0004g0029 | 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 | 234 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(231): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-919+22048delT | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958228 | |||||||
| chr5:169958247 | C | T | 1 | a0001c0001t0004g0119 | 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 | a0001c0001t0002g0051 | 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 | a0002c0002t0001g0101 | 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 | a0001c0001t0002g0049 | 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 | a0002c0002t0007g0011 a0002c0002t0008g0303 |
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 | a0002c0002t0001g0124 a0002c0002t0006g0125 |
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 | 90 | a0001c0001t0001g0091 a0001c0001t0001g0204 a0001c0001t0002g0012 others(87): Show |
90 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.-919+21691dupA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169958585 | |||||||
| chr5:169958585 | C | CTT | 125 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(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 | a0001c0001t0002g0276 | 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 | a0002c0002t0018g0055 | 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0002g0163 a0001c0001t0002g0191 |
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 | a0001c0001t0002g0040 a0001c0001t0003g0009 a0001c0001t0003g0065 others(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 | a0001c0001t0001g0221 a0001c0001t0003g0023 a0001c0001t0003g0052 others(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 | 255 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(252): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): 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 | a0001c0001t0001g0221 a0001c0001t0002g0072 a0001c0001t0002g0074 others(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 | 81 | a0001c0001t0001g0204 a0001c0001t0002g0012 a0001c0001t0002g0083 others(78): Show |
81 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(78): 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 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(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 | 81 | a0001c0001t0001g0204 a0001c0001t0002g0012 a0001c0001t0002g0083 others(78): Show |
81 | HG00323.hp1 HG00741.hp1 HG01070.hp2 others(78): 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 | a0001c0001t0002g0211 | 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | 257 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(254): Show |
259 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(256): 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 | a0002c0002t0003g0027 a0002c0002t0007g0013 |
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 | a0002c0007t0004g0029 | 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 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 others(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 | a0001c0001t0010g0198 | 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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 |
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 | a0002c0002t0001g0246 | 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 | a0001c0001t0003g0176 | 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 | a0001c0001t0002g0049 a0001c0001t0003g0118 |
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 | a0001c0001t0002g0172 | 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 | a0001c0001t0001g0244 a0001c0001t0002g0288 |
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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0163 a0001c0001t0002g0191 others(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 | a0001c0001t0003g0028 a0002c0002t0003g0027 a0002c0002t0005g0017 others(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 | a0002c0007t0004g0029 | 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 | 255 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(252): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): 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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0003g0035 a0002c0002t0005g0032 a0002c0002t0008g0033 others(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 | a0001c0001t0003g0034 a0002c0002t0001g0199 a0002c0002t0005g0308 |
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 | a0001c0001t0002g0047 a0001c0001t0002g0051 a0001c0001t0002g0256 others(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 | a0001c0001t0001g0091 a0001c0001t0002g0153 a0001c0001t0003g0022 others(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 | a0001c0001t0002g0288 a0001c0001t0003g0008 a0001c0001t0003g0009 others(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 |
72 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0102 others(69): Show |
72 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(69): 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 | a0001c0001t0001g0283 a0001c0001t0002g0083 a0001c0001t0002g0096 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0084 a0001c0001t0002g0085 others(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 | a0001c0001t0002g0185 a0002c0002t0001g0156 a0002c0002t0001g0202 others(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 | a0001c0001t0002g0163 a0001c0001t0002g0188 a0002c0002t0005g0302 |
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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0062 others(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 | a0001c0001t0002g0191 a0001c0001t0003g0037 a0001c0001t0003g0057 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0290 a0002c0002t0001g0157 |
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 | a0002c0002t0002g0261 | 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 | a0002c0002t0013g0193 | 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 | 255 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(252): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): 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 | a0002c0007t0004g0029 | 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 | a0001c0001t0001g0148 | 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 | a0002c0002t0001g0282 | 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 | a0001c0001t0003g0065 | 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 | a0001c0001t0002g0086 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0002c0007t0004g0029 | 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 | a0001c0001t0003g0175 a0001c0001t0003g0218 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0003g0237 others(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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | a0002c0002t0001g0160 a0002c0002t0001g0275 a0002c0002t0001g0282 |
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 | a0001c0001t0002g0292 a0001c0001t0004g0289 a0002c0002t0001g0207 others(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 | a0001c0001t0002g0154 | 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 | a0001c0001t0002g0276 a0001c0001t0003g0003 a0001c0001t0003g0005 others(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 | a0002c0002t0007g0011 a0002c0002t0008g0303 |
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 | a0003c0003t0004g0159 | 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 | a0002c0002t0017g0100 a0002c0002t0024g0315 |
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 | 233 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(230): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(232): 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 | a0002c0002t0003g0030 | 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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | 173 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(170): Show |
175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): 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 | a0001c0001t0001g0221 a0001c0001t0002g0129 a0001c0001t0002g0147 others(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 | a0002c0005t0001g0217 | 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 | a0001c0001t0003g0015 a0002c0002t0001g0208 a0002c0002t0001g0220 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0129 a0001c0001t0002g0162 others(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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0002c0002t0005g0186 | 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 | a0002c0002t0005g0308 a0002c0002t0007g0263 |
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 | a0002c0002t0018g0055 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0002c0002t0006g0137 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0001g0148 a0002c0002t0001g0108 |
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 | a0001c0001t0001g0116 a0002c0002t0001g0138 a0002c0002t0001g0139 |
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 | a0002c0002t0017g0100 | 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 | a0001c0001t0003g0057 a0001c0001t0003g0062 a0002c0002t0005g0014 others(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 | a0002c0002t0018g0055 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0244 a0001c0001t0001g0247 others(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 | a0001c0001t0003g0062 a0002c0002t0005g0014 a0002c0002t0005g0186 others(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 | a0001c0001t0002g0256 a0001c0001t0021g0255 |
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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0001g0091 | 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 | a0005c0008t0003g0106 | 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 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0178 |
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 | a0001c0001t0004g0087 | 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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0002g0147 a0001c0001t0002g0167 a0001c0001t0002g0185 others(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 | a0001c0001t0002g0096 | 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 | a0002c0002t0017g0100 | 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 | a0001c0001t0002g0049 | 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 | a0002c0002t0001g0238 | 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 | 57 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0129 others(54): Show |
57 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(54): 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 | a0001c0001t0003g0057 a0001c0001t0003g0062 a0002c0002t0005g0014 others(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 | 69 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0129 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(66): 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 | a0001c0001t0001g0102 a0001c0001t0001g0110 a0001c0001t0001g0116 others(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 | a0001c0001t0003g0307 a0002c0002t0003g0030 |
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 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0283 others(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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | a0001c0001t0002g0287 | 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 | a0002c0002t0003g0030 | 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 | a0002c0002t0001g0063 | 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 | a0001c0001t0003g0313 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0002c0005t0001g0217 | 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 | a0001c0001t0002g0080 a0002c0002t0006g0079 |
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 | a0001c0001t0003g0056 | 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 | a0002c0002t0006g0137 | 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 | a0001c0001t0003g0016 a0001c0001t0003g0264 a0001c0001t0003g0313 others(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 | a0001c0001t0007g0021 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | 60 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0129 others(57): Show |
60 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(57): 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 | a0001c0001t0002g0167 a0001c0001t0002g0185 a0001c0001t0003g0181 others(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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0083 a0001c0001t0002g0084 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | 68 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0129 others(65): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(65): 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 | a0001c0001t0003g0257 | 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 | a0003c0003t0004g0104 | 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 | 70 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0129 others(67): Show |
70 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-919+8848delA | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169971428 | |||||||
| chr5:169971428 | CTT | C | 110 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0221 | 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 | 253 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(250): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): 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 | a0001c0001t0010g0198 | 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 | 254 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): 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 | a0001c0001t0001g0110 a0001c0001t0002g0114 a0001c0001t0002g0151 others(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 | a0002c0002t0001g0107 | 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 | a0001c0001t0001g0247 a0001c0001t0002g0064 a0001c0001t0002g0281 others(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 | a0001c0001t0009g0098 a0002c0002t0001g0093 a0002c0002t0001g0094 others(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 | a0001c0001t0003g0035 a0001c0001t0003g0313 a0002c0002t0001g0063 others(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 | a0001c0001t0002g0074 a0001c0001t0002g0076 a0001c0001t0002g0080 others(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 | a0001c0001t0002g0206 a0001c0001t0003g0015 a0002c0002t0001g0208 others(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 | 54 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0129 others(51): Show |
54 | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(51): 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 | a0001c0001t0003g0301 a0002c0002t0005g0302 |
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 | a0001c0001t0002g0167 a0001c0001t0007g0158 a0002c0002t0001g0183 others(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 | a0001c0001t0002g0072 a0001c0001t0007g0021 a0001c0001t0010g0198 others(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 | a0001c0001t0004g0069 | 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 | a0001c0001t0002g0047 | 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 | a0001c0001t0002g0051 a0001c0001t0003g0022 a0001c0001t0003g0023 others(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 | a0001c0001t0003g0034 a0002c0002t0005g0032 a0002c0002t0008g0033 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0005 a0001c0001t0003g0028 a0001c0001t0003g0227 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0022g0305 |
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 | a0001c0001t0003g0266 a0001c0001t0003g0267 a0001c0001t0003g0268 others(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 | a0001c0001t0002g0012 a0001c0001t0002g0153 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0148 a0001c0001t0002g0096 a0001c0001t0002g0097 others(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 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 |
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 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0148 a0001c0001t0002g0012 a0001c0001t0002g0096 others(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 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
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 | a0002c0002t0001g0149 | 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 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0143 a0001c0001t0001g0144 others(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 | a0002c0002t0017g0100 | 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0003g0065 | 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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0003g0301 a0001c0001t0004g0026 a0002c0002t0004g0099 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0074 a0001c0001t0002g0076 others(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 | a0001c0001t0003g0264 a0002c0002t0005g0024 a0002c0002t0005g0025 others(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 | 38 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(35): Show |
38 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-919+7213G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169973064 | |||||||
| chr5:169973120 | A | G | 169 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0001g0244 others(166): Show |
169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): 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 | a0001c0001t0003g0062 a0002c0002t0005g0014 a0002c0002t0005g0186 others(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 | a0002c0002t0017g0100 | 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 | a0001c0001t0003g0065 a0001c0001t0003g0067 a0001c0001t0003g0068 others(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 | a0002c0002t0015g0240 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0002c0002t0001g0048 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | a0002c0002t0018g0055 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0283 others(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 | 38 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(35): Show |
38 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(35): 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 | a0001c0001t0001g0283 a0001c0001t0002g0038 a0001c0001t0002g0039 others(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 | a0001c0001t0003g0019 a0001c0001t0010g0020 a0002c0002t0004g0018 |
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 | a0002c0002t0017g0100 | 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 | a0002c0002t0001g0063 | 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 | 39 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(36): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-919+6269C>T | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974008 | |||||||
| chr5:169974085 | G | T | 39 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(36): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): 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 | a0001c0001t0003g0019 a0001c0001t0010g0020 a0002c0002t0004g0018 |
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 | 41 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(38): Show |
41 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.-919+6076T>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974201 | |||||||
| chr5:169974279 | A | G | 31 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(28): Show |
31 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(28): 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 | a0001c0001t0010g0198 | 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 | 50 | a0001c0001t0001g0204 a0001c0001t0002g0153 a0001c0001t0002g0167 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.-919+5885A>G | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169974392 | |||||||
| chr5:169974459 | A | G | 33 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(30): 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 | a0001c0001t0003g0003 a0001c0001t0003g0005 a0001c0001t0003g0007 others(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 | 36 | a0001c0001t0001g0204 a0001c0001t0002g0167 a0001c0001t0002g0180 others(33): Show |
36 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(33): 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 | a0001c0001t0003g0260 a0001c0001t0004g0258 a0001c0001t0004g0259 |
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 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(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 | a0001c0001t0001g0221 a0001c0001t0002g0162 a0001c0001t0002g0163 others(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 | a0002c0002t0001g0174 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0001c0001t0002g0051 others(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 | 63 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(60): Show |
63 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(60): 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 | a0002c0002t0003g0030 a0002c0002t0017g0100 |
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 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0008 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0223 a0001c0001t0001g0244 others(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 | 50 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): 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 | a0001c0001t0003g0313 | 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 | 50 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): 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 | a0002c0002t0003g0030 a0002c0002t0017g0100 |
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 | a0002c0002t0001g0101 | 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 | 252 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(249): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): 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 | a0001c0001t0001g0223 a0001c0001t0001g0244 a0001c0001t0001g0247 others(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 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0037 others(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 | a0001c0001t0002g0167 | 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 | 53 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(50): Show |
53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.-919+3521T>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976756 | |||||||
| chr5:169976772 | T | G | 50 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-919+3505A>C | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976772 | |||||||
| chr5:169976792 | C | T | 50 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-919+3485G>A | INSYN2B | ENSG00000204767.4 | transcript | ENST00000377365.4 | protein_coding | 1/3 | chr5 | 169976792 | |||||||
| chr5:169976815 | G | A | 50 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(47): Show |
50 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(47): 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 | a0001c0001t0002g0153 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | 55 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(52): 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 | a0001c0001t0002g0154 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | a0001c0001t0002g0155 | 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 | 52 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(49): Show |
52 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(49): 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 | a0002c0002t0006g0273 | 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 | a0002c0002t0001g0156 | 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 | 52 | a0001c0001t0001g0204 a0001c0001t0001g0221 a0001c0001t0002g0162 others(49): Show |
52 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(49): 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 | a0002c0002t0007g0274 | 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 | a0001c0001t0003g0313 a0002c0002t0001g0314 a0002c0002t0024g0315 |
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 | a0001c0001t0012g0195 | 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 | a0001c0001t0003g0307 a0002c0002t0005g0308 a0002c0002t0007g0306 |
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 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0002c0002t0005g0032 others(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 | a0002c0002t0003g0030 | 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 | a0001c0001t0003g0028 a0002c0002t0003g0027 a0002c0007t0004g0029 |
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 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(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 | a0001c0001t0001g0204 a0001c0001t0002g0206 a0001c0001t0004g0201 others(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 | a0002c0002t0001g0157 | 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 | 4 | a0001c0001t0002g0211 a0001c0001t0002g0276 a0002c0002t0001g0209 others(1): Show |
4 | HG01071.hp1 HG01261.hp2 HG02258.hp1 others(1): 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 | a0001c0001t0002g0134 a0002c0002t0001g0109 a0002c0002t0001g0112 others(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 | a0001c0001t0002g0163 a0002c0002t0001g0160 a0002c0002t0001g0161 others(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 | a0001c0001t0002g0167 a0001c0001t0003g0313 a0002c0002t0001g0157 others(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 | a0001c0001t0001g0116 a0001c0001t0001g0223 a0001c0001t0001g0297 others(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 | a0001c0001t0001g0110 a0001c0001t0003g0260 a0001c0001t0004g0258 others(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 | a0001c0001t0002g0256 a0001c0001t0003g0270 a0003c0003t0004g0104 |
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 | a0001c0001t0002g0064 a0001c0001t0002g0072 a0001c0001t0002g0074 others(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 | a0001c0001t0001g0221 a0001c0001t0001g0283 a0001c0001t0002g0213 others(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 | 79 | a0001c0001t0001g0110 a0001c0001t0001g0116 a0001c0001t0001g0144 others(76): Show |
79 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(76): 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 | a0001c0001t0001g0148 a0001c0001t0002g0105 a0001c0001t0002g0114 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0143 others(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 | a0001c0001t0003g0016 a0001c0001t0003g0019 a0001c0001t0003g0022 others(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 | a0001c0001t0003g0015 a0002c0002t0005g0014 |
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 | a0001c0001t0003g0304 a0002c0002t0007g0013 |
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 | a0001c0001t0002g0012 a0002c0002t0007g0011 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0244 a0001c0001t0001g0247 others(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 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0008 others(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 | a0001c0001t0003g0301 a0002c0002t0005g0302 a0002c0002t0007g0300 others(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 | a0001c0001t0003g0307 a0001c0001t0003g0313 a0002c0002t0001g0314 others(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 |