Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 151011 |
| ensemblid | ENSG00000186522.15 |
| hgncid | 14349 |
| symbol | SEPTIN10 |
| name | septin 10 |
| refseq_nuc | NM_144710.5 |
| refseq_prot | NP_653311.1 |
| ensembl_nuc | ENST00000397712.7 |
| ensembl_prot | ENSP00000380824.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 109542799 |
| end | 109613966 |
| strand | - |
| ver | v1.2 |
| region | chr2:109542799-109613966 |
| region5000 | chr2:109537799-109618966 |
| regionname0 | SEPTIN10_chr2_109542799_109613966 |
| regionname5000 | SEPTIN10_chr2_109537799_109618966 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 454 | 398 | 97 | 73 | 167 | 14 | 45 | 127 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | MASSE others(449): Show |
chr2 | 109537799 | 109618966 |
| a0002 | 0/0 | 454 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | MASSE others(449): Show |
chr2 | 109537799 | 109618966 |
| a0003 | 0/0 | 454 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | MVSSE others(449): Show |
chr2 | 109537799 | 109618966 |
| a0004 | 0/0 | 454 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | MASSE others(449): Show |
chr2 | 109537799 | 109618966 |
| a0005 | 0/0 | 454 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | MASSE others(449): Show |
chr2 | 109537799 | 109618966 |
| a0006 | 0/0 | 454 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | MASSE others(449): Show |
chr2 | 109537799 | 109618966 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1362 | 392 | 91 | 73 | 167 | 14 | 45 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0001c0002 | 0/0 | 1362 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0001c0007 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0001c0008 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0002c0003 | 0/0 | 1362 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0003c0009 | 0/0 | 1362 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGT others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0004c0005 | 0/0 | 1362 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0005c0004 | 0/0 | 1362 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 | ||
| a0006c0006 | 0/0 | 1362 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | ATGGC others(1357): Show |
chr2 | 109537799 | 109618966 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3014 | 149 | 18 | 25 | 78 | 7 | 19 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0002 | 0/0 | 3014 | 92 | 21 | 15 | 34 | 4 | 18 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0003 | 0/0 | 3014 | 64 | 1 | 24 | 36 | 0 | 3 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0004 | 0/0 | 3014 | 57 | 31 | 7 | 15 | 3 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0005 | 0/0 | 3014 | 15 | 13 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0006 | 0/0 | 3014 | 7 | 3 | 0 | 1 | 0 | 3 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0007 | 0/0 | 3014 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0008 | 0/0 | 3014 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0009 | 0/0 | 3014 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0001t0010 | 0/0 | 3014 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0002t0002 | 0/0 | 3014 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0007t0004 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0001c0008t0002 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0002c0003t0001 | 0/0 | 3014 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0003c0009t0004 | 0/0 | 3014 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0004c0005t0004 | 0/0 | 3014 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0005c0004t0006 | 0/0 | 3014 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| a0006c0006t0004 | 0/0 | 3014 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | CCCTT others(3009): Show |
chr2 | 109537799 | 109618966 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0372 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0373 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0008g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0009g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0007t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0001c0008t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0002c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0003c0009t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0004c0005t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0005c0004t0006g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| a0006c0006t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0304 | EUR | GBR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | GBR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0198 | EUR | FIN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0380 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0375 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0238 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0094 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0111 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | IBS | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0378 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0369 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0387 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0385 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0386 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02280 | hp1 | a0004 | c0005 | t0004 | g0219 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0390 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0224 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0104 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0337 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0376 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02970 | hp2 | a0001 | c0007 | t0004 | g0232 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0344 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03453 | hp1 | a0001 | c0008 | t0002 | g0089 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0161 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | ESN | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0343 | AFR | GWD | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0136 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04199 | hp2 | a0005 | c0004 | t0006 | g0160 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0134 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0342 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CHB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18963 | hp1 | a0001 | c0001 | t0008 | g0311 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0208 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18984 | hp1 | a0002 | c0003 | t0001 | g0286 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0383 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0100 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0388 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19066 | hp2 | a0001 | c0001 | t0008 | g0267 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19067 | hp1 | a0006 | c0006 | t0004 | g0194 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0379 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19078 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0073 | AFR | YRI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | ASW | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | ASW | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0184 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0327 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0384 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0105 | SAS | GIH | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0371 | SAS | GIH | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01123 | hp1 | a0003 | c0009 | t0004 | g0242 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | MSL | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | USA | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0135 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0373 | REF | REF | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0372 | REF | REF | SEPTIN10_chr2_109537799_109618966 | SEPTIN10 | chr2 | 109537799 | 109618966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:109546056 | C | T | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1343G>A | p.Arg448His | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/11 | 1482/3014 | 1343/1365 | 448/454 | chr2 | 109546056 | |||
| chr2:109546167 | C | A | 1 | a0006 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.1232G>T | p.Arg411Ile | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/11 | 1371/3014 | 1232/1365 | 411/454 | chr2 | 109546167 | |||
| chr2:109553137 | C | T | 1 | a0005 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1111G>A | p.Val371Met | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/11 | 1250/3014 | 1111/1365 | 371/454 | chr2 | 109553137 | |||
| chr2:109574615 | A | G | 1 | a0002 | 2 | NA18969.hp2 NA18984.hp1 |
missense_variant | MODERATE | c.566T>C | p.Leu189Pro | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/11 | 705/3014 | 566/1365 | 189/454 | chr2 | 109574615 | |||
| chr2:109613823 | G | A | 1 | a0003 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.5C>T | p.Ala2Val | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/11 | 144/3014 | 5/1365 | 2/454 | chr2 | 109613823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:109585212 | T | C | 1 | a0001c0007 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.327A>G | p.Thr109Thr | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/11 | 466/3014 | 327/1365 | 109/454 | chr2 | 109585212 | |||
| chr2:109585749 | T | C | 1 | a0001c0002 | 4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
synonymous_variant | LOW | c.189A>G | p.Gln63Gln | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/11 | 328/3014 | 189/1365 | 63/454 | chr2 | 109585749 | |||
| chr2:109585827 | G | A | 1 | a0001c0008 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.111C>T | p.Asn37Asn | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/11 | 250/3014 | 111/1365 | 37/454 | chr2 | 109585827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:109542880 | T | C | 1 | a0001c0001t0009 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1429A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 1429 | chr2 | 109542880 | ||||||
| chr2:109542937 | G | C | 1 | a0001c0001t0010 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1372C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 1372 | chr2 | 109542937 | ||||||
| chr2:109543299 | A | G | 1 | a0001c0001t0005 | 15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1010T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 1010 | chr2 | 109543299 | ||||||
| chr2:109543406 | C | A | 1 | a0001c0001t0003 | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*903G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 903 | chr2 | 109543406 | ||||||
| chr2:109543508 | T | A | 5 | a0001c0001t0004 a0001c0007t0004 a0003c0009t0004 others(2): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*801A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 801 | chr2 | 109543508 | ||||||
| chr2:109543529 | T | C | 1 | a0001c0001t0008 | 2 | NA18963.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*780A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 780 | chr2 | 109543529 | ||||||
| chr2:109543830 | A | G | 1 | a0001c0001t0003 | 64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*479T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 479 | chr2 | 109543830 | ||||||
| chr2:109543934 | T | C | 1 | a0001c0001t0007 | 4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*375A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 375 | chr2 | 109543934 | ||||||
| chr2:109544015 | G | A | 2 | a0001c0001t0006 a0005c0004t0006 |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*294C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 11/11 | 294 | chr2 | 109544015 | ||||||
| chr2:109613916 | A | T | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(10): Show |
246 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
5_prime_UTR_variant | MODIFIER | c.-89T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/11 | 89 | chr2 | 109613916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:109544465 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1350-141T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544465 | |||||||
| chr2:109544556 | AG | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1350-233delC | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544556 | |||||||
| chr2:109544614 | T | A | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1350-290A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544614 | |||||||
| chr2:109544615 | G | T | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1350-291C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544615 | |||||||
| chr2:109544786 | C | A | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0152 |
3 | HG02027.hp1 NA18978.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1350-462G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544786 | |||||||
| chr2:109544845 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1350-521T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544845 | |||||||
| chr2:109544868 | C | A | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1350-544G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544868 | |||||||
| chr2:109544869 | C | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1350-545G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544869 | |||||||
| chr2:109544886 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1350-562A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544886 | |||||||
| chr2:109544887 | G | A | 233 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(230): Show |
242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.1350-563C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544887 | |||||||
| chr2:109544901 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1350-577A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544901 | |||||||
| chr2:109544906 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1350-582C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544906 | |||||||
| chr2:109544927 | A | C | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1350-603T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109544927 | |||||||
| chr2:109545137 | T | A | 6 | a0001c0001t0005g0095 a0001c0001t0005g0097 a0001c0001t0005g0098 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1350-813A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545137 | |||||||
| chr2:109545272 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1349+778C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545272 | |||||||
| chr2:109545495 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1349+555G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545495 | |||||||
| chr2:109545510 | A | G | 1 | a0001c0001t0004g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1349+540T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545510 | |||||||
| chr2:109545523 | C | A | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1349+527G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545523 | |||||||
| chr2:109545565 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1349+485G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545565 | |||||||
| chr2:109545626 | T | A | 1 | a0003c0009t0004g0242 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1349+424A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545626 | |||||||
| chr2:109545649 | C | T | 2 | a0001c0001t0004g0195 a0001c0001t0004g0208 |
2 | NA18940.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1349+401G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545649 | |||||||
| chr2:109545735 | G | A | 28 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(25): Show |
28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1349+315C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545735 | |||||||
| chr2:109545782 | C | A | 5 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0001t0004g0235 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1349+268G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 10/10 | chr2 | 109545782 | |||||||
| chr2:109546247 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0316 |
2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1162-10T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546247 | |||||||
| chr2:109546262 | C | T | 2 | a0001c0001t0003g0033 a0001c0001t0003g0035 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1162-25G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546262 | |||||||
| chr2:109546299 | G | A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0001c0001t0001g0247 others(27): Show |
31 | HG00544.hp1 HG02027.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.1162-62C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546299 | |||||||
| chr2:109546317 | G | A | 3 | a0001c0001t0001g0375 a0001c0001t0001g0380 a0001c0001t0001g0384 |
3 | HG00741.hp1 HG01106.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1162-80C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546317 | |||||||
| chr2:109546499 | C | T | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162-262G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546499 | |||||||
| chr2:109546557 | A | C | 1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1162-320T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546557 | |||||||
| chr2:109546575 | A | G | 1 | a0001c0001t0004g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1162-338T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546575 | |||||||
| chr2:109546618 | A | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0055 |
2 | NA18969.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1162-381T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546618 | |||||||
| chr2:109546847 | T | C | 1 | a0001c0001t0006g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1162-610A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546847 | |||||||
| chr2:109546900 | T | G | 13 | a0001c0001t0003g0021 a0001c0001t0003g0028 a0001c0001t0003g0029 others(10): Show |
13 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1162-663A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109546900 | |||||||
| chr2:109547091 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1162-854G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547091 | |||||||
| chr2:109547113 | T | C | 37 | a0001c0001t0004g0008 a0001c0001t0004g0181 a0001c0001t0004g0182 others(34): Show |
38 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1162-876A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547113 | |||||||
| chr2:109547369 | G | GT | 104 | a0001c0001t0001g0010 a0001c0001t0001g0247 a0001c0001t0001g0252 others(101): Show |
108 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1162-1133dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547369 | |||||||
| chr2:109547369 | G | GTT | 64 | a0001c0001t0001g0333 a0001c0001t0002g0165 a0001c0001t0003g0001 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1162-1134_1162-113 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547369 | |||||||
| chr2:109547369 | GT | G | 9 | a0001c0001t0001g0324 a0001c0001t0001g0386 a0001c0001t0004g0224 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1162-1133delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547369 | |||||||
| chr2:109547770 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1162-1533T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547770 | |||||||
| chr2:109547928 | C | A | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1162-1691G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109547928 | |||||||
| chr2:109548083 | A | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1162-1846T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548083 | |||||||
| chr2:109548139 | G | GA | 335 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(332): Show |
348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.1162-1903dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548139 | |||||||
| chr2:109548177 | CA | C | 232 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(229): Show |
241 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(238): Show |
intron_variant | MODIFIER | c.1162-1941delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548177 | |||||||
| chr2:109548508 | A | C | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.1162-2271T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548508 | |||||||
| chr2:109548724 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1162-2487G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548724 | |||||||
| chr2:109548758 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1162-2521T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548758 | |||||||
| chr2:109548763 | T | G | 233 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(230): Show |
242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.1162-2526A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548763 | |||||||
| chr2:109548775 | C | CA | 17 | a0001c0001t0001g0252 a0001c0001t0001g0288 a0001c0001t0001g0289 others(14): Show |
17 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1162-2539dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | C | CAA | 82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
86 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1162-2540_1162-253 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | C | CAAA | 12 | a0001c0001t0001g0244 a0001c0001t0001g0297 a0001c0001t0001g0308 others(9): Show |
12 | HG00544.hp1 HG02056.hp2 HG03688.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162-2541_1162-253 others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | CA | C | 52 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(49): Show |
55 | HG00609.hp1 HG00735.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.1162-2539delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | CAA | C | 48 | a0001c0001t0002g0107 a0001c0001t0002g0108 a0001c0001t0002g0109 others(45): Show |
49 | HG01255.hp1 HG01256.hp2 HG01257.hp1 others(46): Show |
intron_variant | MODIFIER | c.1162-2540_1162-253 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | CAAA | C | 55 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1162-2541_1162-253 others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1162-2551_1162-253 others(17): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548775 | CAAAAAAA others(7): Show |
C | 67 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(64): Show |
71 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1162-2552_1162-253 others(18): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548775 | |||||||
| chr2:109548848 | A | G | 213 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0075 others(210): Show |
221 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(218): Show |
intron_variant | MODIFIER | c.1162-2611T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548848 | |||||||
| chr2:109548930 | C | G | 233 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(230): Show |
242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.1162-2693G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548930 | |||||||
| chr2:109548995 | T | G | 1 | a0001c0001t0002g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1162-2758A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109548995 | |||||||
| chr2:109549348 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1162-3111T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549348 | |||||||
| chr2:109549819 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1161+3268T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549819 | |||||||
| chr2:109549897 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1161+3190G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549897 | |||||||
| chr2:109549909 | T | C | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1161+3178A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109549909 | |||||||
| chr2:109550057 | G | A | 13 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(10): Show |
13 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1161+3030C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550057 | |||||||
| chr2:109550073 | G | A | 60 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(57): Show |
62 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.1161+3014C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550073 | |||||||
| chr2:109550238 | T | G | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1161+2849A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550238 | |||||||
| chr2:109550319 | T | G | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+2768A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550319 | |||||||
| chr2:109550320 | T | G | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1161+2767A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550320 | |||||||
| chr2:109550344 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1161+2743C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550344 | |||||||
| chr2:109550533 | C | G | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1161+2554G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550533 | |||||||
| chr2:109550572 | C | T | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1161+2515G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550572 | |||||||
| chr2:109550673 | G | T | 1 | a0001c0008t0002g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1161+2414C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550673 | |||||||
| chr2:109550674 | A | T | 1 | a0001c0008t0002g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1161+2413T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550674 | |||||||
| chr2:109550741 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1161+2346A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550741 | |||||||
| chr2:109550804 | C | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161+2283G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109550804 | |||||||
| chr2:109551283 | T | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0265 a0001c0001t0001g0270 |
3 | HG01070.hp1 HG03486.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1161+1804A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551283 | |||||||
| chr2:109551321 | T | C | 22 | a0001c0001t0001g0010 a0001c0001t0001g0252 a0001c0001t0001g0255 others(19): Show |
23 | HG00323.hp1 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1161+1766A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551321 | |||||||
| chr2:109551432 | C | T | 20 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(17): Show |
22 | HG00609.hp1 HG01934.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.1161+1655G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551432 | |||||||
| chr2:109551460 | T | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1161+1627A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551460 | |||||||
| chr2:109551641 | T | A | 34 | a0001c0001t0004g0008 a0001c0001t0004g0181 a0001c0001t0004g0182 others(31): Show |
35 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1161+1446A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551641 | |||||||
| chr2:109551890 | G | C | 19 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0075 others(16): Show |
20 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1161+1197C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551890 | |||||||
| chr2:109551892 | G | A | 2 | a0001c0001t0004g0233 a0001c0001t0004g0237 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1161+1195C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551892 | |||||||
| chr2:109551923 | C | A | 5 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0001t0004g0235 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1161+1164G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551923 | |||||||
| chr2:109551955 | G | A | 82 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(79): Show |
85 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.1161+1132C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551955 | |||||||
| chr2:109551957 | G | A | 1 | a0005c0004t0006g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1161+1130C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551957 | |||||||
| chr2:109551976 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1161+1111C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109551976 | |||||||
| chr2:109552160 | G | T | 102 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1161+927C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552160 | |||||||
| chr2:109552202 | G | A | 1 | a0001c0001t0004g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1161+885C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552202 | |||||||
| chr2:109552398 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1161+689A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552398 | |||||||
| chr2:109552473 | T | C | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1161+614A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552473 | |||||||
| chr2:109552532 | G | A | 4 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0103 others(1): Show |
5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+555C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552532 | |||||||
| chr2:109552870 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1161+217T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552870 | |||||||
| chr2:109552960 | G | A | 2 | a0001c0001t0001g0349 a0001c0001t0001g0365 |
2 | NA18989.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1161+127C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109552960 | |||||||
| chr2:109553034 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1161+53A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109553034 | |||||||
| chr2:109553053 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1161+34T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 9/10 | chr2 | 109553053 | |||||||
| chr2:109553409 | T | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0250 |
2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1029-190A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553409 | |||||||
| chr2:109553496 | A | C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-277T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553496 | |||||||
| chr2:109553544 | C | CA | 9 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(6): Show |
9 | HG01952.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029-326dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553544 | |||||||
| chr2:109553544 | C | CAA | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029-327_1029-326d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553544 | |||||||
| chr2:109553588 | C | T | 15 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(12): Show |
16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-369G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553588 | |||||||
| chr2:109553723 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1029-504C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553723 | |||||||
| chr2:109553771 | T | C | 2 | a0001c0001t0002g0113 a0001c0001t0002g0121 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1029-552A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553771 | |||||||
| chr2:109553810 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1029-591G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109553810 | |||||||
| chr2:109554106 | T | C | 3 | a0001c0001t0004g0196 a0001c0001t0004g0203 a0001c0001t0004g0212 |
3 | NA18942.hp1 NA19062.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1029-887A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554106 | |||||||
| chr2:109554316 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1029-1097C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554316 | |||||||
| chr2:109554337 | T | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1118A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554337 | |||||||
| chr2:109554344 | T | A | 1 | a0001c0001t0002g0118 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1029-1125A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554344 | |||||||
| chr2:109554417 | T | C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1029-1198A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554417 | |||||||
| chr2:109554569 | G | A | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1350C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554569 | |||||||
| chr2:109554829 | C | G | 2 | a0001c0001t0003g0015 a0001c0001t0003g0057 |
2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1029-1610G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554829 | |||||||
| chr2:109554834 | C | A | 9 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1029-1615G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554834 | |||||||
| chr2:109554974 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1029-1755C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109554974 | |||||||
| chr2:109555042 | T | C | 2 | a0001c0001t0004g0192 a0001c0001t0004g0209 |
2 | NA18945.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1029-1823A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555042 | |||||||
| chr2:109555152 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1029-1933G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555152 | |||||||
| chr2:109555238 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0313 |
2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1029-2019T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555238 | |||||||
| chr2:109555620 | T | C | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1029-2401A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555620 | |||||||
| chr2:109555624 | G | A | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1029-2405C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555624 | |||||||
| chr2:109555707 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0002g0141 |
2 | HG02027.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1029-2488G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555707 | |||||||
| chr2:109555912 | A | C | 214 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0075 others(211): Show |
222 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(219): Show |
intron_variant | MODIFIER | c.1029-2693T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109555912 | |||||||
| chr2:109556078 | A | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0120 |
2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1029-2859T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556078 | |||||||
| chr2:109556239 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1029-3020G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556239 | |||||||
| chr2:109556244 | A | G | 71 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(68): Show |
73 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1029-3025T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556244 | |||||||
| chr2:109556519 | GAACAGAT others(16): Show |
G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00621.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.1029-3323_1029-330 others(27): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556519 | |||||||
| chr2:109556584 | C | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1029-3365G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556584 | |||||||
| chr2:109556743 | T | C | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1029-3524A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556743 | |||||||
| chr2:109556770 | TAAA | T | 3 | a0001c0001t0004g0195 a0001c0001t0004g0205 a0001c0001t0004g0208 |
3 | NA18940.hp1 NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1029-3554_1029-355 others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556770 | |||||||
| chr2:109556936 | T | C | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1029-3717A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109556936 | |||||||
| chr2:109557144 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1029-3925G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557144 | |||||||
| chr2:109557183 | A | T | 248 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1029-3964T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557183 | |||||||
| chr2:109557184 | A | T | 1 | a0001c0001t0003g0020 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1029-3965T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557184 | |||||||
| chr2:109557286 | A | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0256 a0001c0001t0001g0259 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-4067T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557286 | |||||||
| chr2:109557408 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1029-4189A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557408 | |||||||
| chr2:109557631 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1029-4412T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557631 | |||||||
| chr2:109557787 | A | G | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1029-4568T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557787 | |||||||
| chr2:109557851 | C | CT | 67 | a0001c0001t0002g0126 a0001c0001t0002g0173 a0001c0001t0003g0001 others(64): Show |
71 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1029-4633dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557851 | |||||||
| chr2:109557851 | C | CTT | 27 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(24): Show |
27 | HG00735.hp2 HG01106.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1029-4634_1029-463 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557851 | |||||||
| chr2:109557927 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1029-4708C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109557927 | |||||||
| chr2:109558100 | A | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-4881T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558100 | |||||||
| chr2:109558113 | A | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1029-4894T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558113 | |||||||
| chr2:109558190 | T | C | 1 | a0001c0001t0002g0159 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1029-4971A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558190 | |||||||
| chr2:109558293 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1029-5074G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558293 | |||||||
| chr2:109558351 | G | A | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1029-5132C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558351 | |||||||
| chr2:109558429 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1029-5210G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558429 | |||||||
| chr2:109558482 | T | C | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0002g0072 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-5263A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558482 | |||||||
| chr2:109558631 | G | A | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.1029-5412C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558631 | |||||||
| chr2:109558632 | C | T | 3 | a0001c0001t0004g0195 a0001c0001t0004g0205 a0001c0001t0004g0208 |
3 | NA18940.hp1 NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1029-5413G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558632 | |||||||
| chr2:109558642 | T | C | 4 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0103 others(1): Show |
5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029-5423A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558642 | |||||||
| chr2:109558708 | C | T | 67 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(64): Show |
69 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.1029-5489G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558708 | |||||||
| chr2:109558892 | C | CT | 70 | a0001c0001t0002g0017 a0001c0001t0002g0167 a0001c0001t0002g0168 others(67): Show |
71 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1028+5473dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558892 | |||||||
| chr2:109558949 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1028+5417C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558949 | |||||||
| chr2:109558969 | T | G | 1 | a0001c0001t0001g0356 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1028+5397A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109558969 | |||||||
| chr2:109559013 | A | G | 337 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(334): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1028+5353T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559013 | |||||||
| chr2:109559035 | G | A | 60 | a0001c0001t0001g0319 a0001c0001t0002g0006 a0001c0001t0002g0007 others(57): Show |
62 | HG00140.hp2 HG00609.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1028+5331C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559035 | |||||||
| chr2:109559054 | T | C | 3 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 |
3 | HG02135.hp2 NA18984.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1028+5312A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559054 | |||||||
| chr2:109559074 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0155 |
2 | NA18942.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1028+5292G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559074 | |||||||
| chr2:109559466 | C | A | 1 | a0001c0001t0002g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1028+4900G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559466 | |||||||
| chr2:109559909 | G | GT | 5 | a0001c0001t0004g0180 a0001c0001t0004g0191 a0001c0001t0004g0212 others(2): Show |
5 | HG02622.hp2 NA18942.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+4456_1028+445 others(5): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559909 | |||||||
| chr2:109559910 | C | T | 55 | a0001c0001t0004g0008 a0001c0001t0004g0181 a0001c0001t0004g0182 others(52): Show |
56 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1028+4456G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559910 | |||||||
| chr2:109559911 | C | CT | 130 | a0001c0001t0001g0256 a0001c0001t0001g0316 a0001c0001t0001g0323 others(127): Show |
136 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.1028+4454dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559911 | |||||||
| chr2:109559911 | C | CTT | 77 | a0001c0001t0002g0110 a0001c0001t0002g0138 a0001c0001t0002g0162 others(74): Show |
79 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1028+4453_1028+445 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559911 | |||||||
| chr2:109559911 | C | T | 5 | a0001c0001t0004g0180 a0001c0001t0004g0191 a0001c0001t0004g0212 others(2): Show |
5 | HG02622.hp2 NA18942.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+4455G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559911 | |||||||
| chr2:109559952 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1028+4414C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559952 | |||||||
| chr2:109559973 | T | C | 5 | a0001c0001t0001g0340 a0001c0001t0007g0337 a0001c0001t0007g0342 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028+4393A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559973 | |||||||
| chr2:109559989 | T | C | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028+4377A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559989 | |||||||
| chr2:109559997 | C | T | 16 | a0001c0001t0003g0002 a0001c0001t0003g0052 a0001c0001t0005g0005 others(13): Show |
18 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1028+4369G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109559997 | |||||||
| chr2:109560014 | A | G | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028+4352T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560014 | |||||||
| chr2:109560040 | C | A | 1 | a0001c0001t0001g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1028+4326G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560040 | |||||||
| chr2:109560054 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1028+4312C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560054 | |||||||
| chr2:109560077 | C | T | 1 | a0006c0006t0004g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1028+4289G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560077 | |||||||
| chr2:109560152 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0002g0158 |
2 | HG03834.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1028+4214G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560152 | |||||||
| chr2:109560210 | G | C | 22 | a0001c0001t0004g0008 a0001c0001t0004g0184 a0001c0001t0004g0188 others(19): Show |
23 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1028+4156C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560210 | |||||||
| chr2:109560211 | G | C | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1028+4155C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560211 | |||||||
| chr2:109560312 | C | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1028+4054G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560312 | |||||||
| chr2:109560408 | C | A | 15 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(12): Show |
16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1028+3958G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560408 | |||||||
| chr2:109560532 | T | C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028+3834A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560532 | |||||||
| chr2:109560672 | C | T | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1028+3694G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560672 | |||||||
| chr2:109560692 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028+3674C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560692 | |||||||
| chr2:109560749 | C | T | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028+3617G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560749 | |||||||
| chr2:109560796 | A | T | 1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1028+3570T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109560796 | |||||||
| chr2:109561017 | T | G | 235 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(232): Show |
244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.1028+3349A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561017 | |||||||
| chr2:109561068 | TC | T | 13 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0094 others(10): Show |
14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1028+3297delG | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561068 | |||||||
| chr2:109561145 | G | A | 1 | a0001c0001t0004g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1028+3221C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561145 | |||||||
| chr2:109561314 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1028+3052G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561314 | |||||||
| chr2:109561342 | C | T | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1028+3024G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561342 | |||||||
| chr2:109561482 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1028+2884G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561482 | |||||||
| chr2:109561724 | A | G | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1028+2642T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561724 | |||||||
| chr2:109561756 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1028+2610C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561756 | |||||||
| chr2:109561971 | TCAAGGCC others(15): Show |
T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1028+2373_1028+239 others(26): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109561971 | |||||||
| chr2:109562058 | C | A | 1 | a0001c0001t0005g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1028+2308G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562058 | |||||||
| chr2:109562110 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1028+2256C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562110 | |||||||
| chr2:109562128 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1028+2238C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562128 | |||||||
| chr2:109562169 | T | G | 1 | a0001c0001t0001g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1028+2197A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562169 | |||||||
| chr2:109562215 | AAATAAT | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1028+2145_1028+215 others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562215 | |||||||
| chr2:109562498 | G | A | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.1028+1868C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562498 | |||||||
| chr2:109562530 | TA | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1028+1835delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562530 | |||||||
| chr2:109562674 | G | A | 1 | a0001c0001t0001g0338 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1028+1692C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562674 | |||||||
| chr2:109562904 | C | T | 1 | a0001c0001t0002g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1028+1462G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562904 | |||||||
| chr2:109562906 | CA | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1028+1459delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562906 | |||||||
| chr2:109562911 | C | CT | 59 | a0001c0001t0001g0312 a0001c0001t0003g0001 a0001c0001t0003g0002 others(56): Show |
62 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1028+1454dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562911 | |||||||
| chr2:109562911 | C | CTT | 6 | a0001c0001t0003g0003 a0001c0001t0003g0024 a0001c0001t0003g0027 others(3): Show |
7 | HG01255.hp2 HG01496.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.1028+1453_1028+145 others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562911 | |||||||
| chr2:109562924 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1028+1442A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562924 | |||||||
| chr2:109562942 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0002g0130 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1028+1424C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562942 | |||||||
| chr2:109562964 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1028+1402C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109562964 | |||||||
| chr2:109563040 | A | G | 1 | a0001c0001t0001g0351 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1028+1326T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563040 | |||||||
| chr2:109563208 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1028+1158C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563208 | |||||||
| chr2:109563333 | T | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.1028+1033A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563333 | |||||||
| chr2:109563494 | C | T | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.1028+872G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563494 | |||||||
| chr2:109563653 | A | G | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.1028+713T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109563653 | |||||||
| chr2:109564020 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1028+346A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564020 | |||||||
| chr2:109564071 | G | T | 1 | a0006c0006t0004g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1028+295C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564071 | |||||||
| chr2:109564110 | CAG | C | 102 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1028+254_1028+255d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564110 | |||||||
| chr2:109564128 | C | T | 4 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0183 others(1): Show |
4 | HG02809.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1028+238G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564128 | |||||||
| chr2:109564140 | T | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1028+226A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564140 | |||||||
| chr2:109564226 | T | TA | 37 | a0001c0001t0004g0008 a0001c0001t0004g0181 a0001c0001t0004g0182 others(34): Show |
38 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.1028+139dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564226 | |||||||
| chr2:109564233 | T | A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0117 |
2 | NA18963.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1028+133A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564233 | |||||||
| chr2:109564253 | A | G | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1028+113T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564253 | |||||||
| chr2:109564361 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.1028+5G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 8/10 | chr2 | 109564361 | |||||||
| chr2:109564540 | C | CA | 5 | a0001c0001t0001g0245 a0001c0001t0001g0249 a0001c0001t0001g0272 others(2): Show |
5 | HG00423.hp2 NA18960.hp2 NA18962.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.860-7dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564540 | |||||||
| chr2:109564659 | A | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.860-125T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564659 | |||||||
| chr2:109564768 | G | C | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.860-234C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564768 | |||||||
| chr2:109564915 | G | A | 3 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.860-381C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564915 | |||||||
| chr2:109564967 | T | C | 23 | a0001c0001t0004g0008 a0001c0001t0004g0184 a0001c0001t0004g0188 others(20): Show |
24 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.860-433A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109564967 | |||||||
| chr2:109565020 | T | A | 1 | a0001c0001t0004g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.860-486A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565020 | |||||||
| chr2:109565060 | T | C | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.860-526A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565060 | |||||||
| chr2:109565074 | C | T | 6 | a0001c0001t0002g0112 a0001c0001t0002g0115 a0001c0001t0002g0124 others(3): Show |
6 | HG01516.hp2 HG01517.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.860-540G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565074 | |||||||
| chr2:109565127 | G | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-593C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565127 | |||||||
| chr2:109565239 | C | T | 337 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(334): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.859+524G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565239 | |||||||
| chr2:109565294 | A | T | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0002g0072 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+469T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565294 | |||||||
| chr2:109565390 | A | T | 1 | a0001c0001t0002g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.859+373T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565390 | |||||||
| chr2:109565412 | C | A | 1 | a0001c0001t0004g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.859+351G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565412 | |||||||
| chr2:109565432 | A | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.859+331T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565432 | |||||||
| chr2:109565433 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.859+330A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565433 | |||||||
| chr2:109565575 | T | A | 29 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(26): Show |
30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.859+188A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565575 | |||||||
| chr2:109565733 | A | G | 2 | a0001c0001t0004g0222 a0001c0001t0004g0231 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.859+30T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 7/10 | chr2 | 109565733 | |||||||
| chr2:109565885 | T | G | 2 | a0001c0001t0005g0097 a0001c0001t0005g0098 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.763-26A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109565885 | |||||||
| chr2:109565943 | ATAAT | A | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.763-88_763-85delAT others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109565943 | |||||||
| chr2:109565985 | G | A | 1 | a0001c0001t0004g0191 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.763-126C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109565985 | |||||||
| chr2:109566117 | A | T | 235 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(232): Show |
244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.763-258T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566117 | |||||||
| chr2:109566156 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.763-297A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566156 | |||||||
| chr2:109566160 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.763-301C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566160 | |||||||
| chr2:109566292 | T | G | 3 | a0001c0001t0004g0224 a0001c0001t0004g0225 a0001c0001t0004g0226 |
3 | HG02451.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.763-433A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566292 | |||||||
| chr2:109566310 | G | A | 1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.763-451C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566310 | |||||||
| chr2:109566312 | C | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.763-453G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566312 | |||||||
| chr2:109566442 | G | A | 4 | a0001c0001t0004g0192 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | NA18945.hp2 NA18962.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.763-583C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566442 | |||||||
| chr2:109566493 | T | C | 18 | a0001c0001t0004g0180 a0001c0001t0004g0218 a0001c0001t0004g0220 others(15): Show |
18 | HG00639.hp1 HG01175.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.763-634A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566493 | |||||||
| chr2:109566564 | T | C | 1 | a0001c0001t0002g0139 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.763-705A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566564 | |||||||
| chr2:109566613 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.763-754T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566613 | |||||||
| chr2:109566661 | G | A | 1 | a0001c0001t0004g0189 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.763-802C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566661 | |||||||
| chr2:109566703 | C | G | 347 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(344): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.763-844G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566703 | |||||||
| chr2:109566776 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.763-917G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566776 | |||||||
| chr2:109566896 | T | G | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.762+919A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109566896 | |||||||
| chr2:109567016 | G | GT | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.762+798dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567016 | |||||||
| chr2:109567208 | G | A | 1 | a0001c0001t0002g0123 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.762+607C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567208 | |||||||
| chr2:109567459 | C | A | 67 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(64): Show |
69 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.762+356G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567459 | |||||||
| chr2:109567463 | C | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.762+352G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567463 | |||||||
| chr2:109567696 | A | G | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.762+119T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 6/10 | chr2 | 109567696 | |||||||
| chr2:109568116 | C | T | 3 | a0001c0001t0003g0054 a0001c0001t0003g0065 a0001c0001t0003g0067 |
3 | HG00609.hp2 NA18961.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.601-140G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568116 | |||||||
| chr2:109568373 | C | CT | 68 | a0001c0001t0001g0261 a0001c0001t0001g0309 a0001c0001t0001g0317 others(65): Show |
68 | HG00639.hp1 HG00735.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.601-398dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568373 | |||||||
| chr2:109568404 | C | T | 3 | a0001c0001t0001g0375 a0001c0001t0001g0380 a0001c0001t0001g0384 |
3 | HG00741.hp1 HG01106.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.601-428G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568404 | |||||||
| chr2:109568466 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-490C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568466 | |||||||
| chr2:109568670 | G | GCCT | 337 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(334): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.601-697_601-695dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568670 | |||||||
| chr2:109568757 | G | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0315 |
2 | NA18943.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.601-781C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568757 | |||||||
| chr2:109568860 | C | T | 5 | a0001c0001t0001g0340 a0001c0001t0007g0337 a0001c0001t0007g0342 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-884G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568860 | |||||||
| chr2:109568868 | T | C | 23 | a0001c0001t0004g0180 a0001c0001t0004g0218 a0001c0001t0004g0220 others(20): Show |
23 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.601-892A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568868 | |||||||
| chr2:109568878 | T | C | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.601-902A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109568878 | |||||||
| chr2:109569192 | G | A | 12 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(9): Show |
12 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-1216C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569192 | |||||||
| chr2:109569237 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.601-1261A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569237 | |||||||
| chr2:109569300 | A | G | 2 | a0001c0001t0007g0343 a0001c0001t0007g0344 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.601-1324T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569300 | |||||||
| chr2:109569379 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0264 a0001c0001t0001g0282 others(3): Show |
7 | HG01261.hp1 HG01358.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-1403G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569379 | |||||||
| chr2:109569387 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.601-1411G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569387 | |||||||
| chr2:109569437 | T | TA | 44 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0001c0001t0001g0247 others(41): Show |
45 | HG00544.hp1 HG00639.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.601-1462dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569437 | |||||||
| chr2:109569437 | TA | T | 100 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(97): Show |
104 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(101): Show |
intron_variant | MODIFIER | c.601-1462delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569437 | |||||||
| chr2:109569437 | TAA | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-1463_601-1462d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569437 | |||||||
| chr2:109569439 | A | C | 1 | a0001c0001t0004g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.601-1463T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569439 | |||||||
| chr2:109569513 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.601-1537C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569513 | |||||||
| chr2:109569589 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.601-1613C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569589 | |||||||
| chr2:109569847 | G | GT | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.601-1872dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569847 | |||||||
| chr2:109569857 | A | G | 2 | a0001c0001t0001g0295 a0001c0001t0001g0316 |
2 | HG02080.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.601-1881T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569857 | |||||||
| chr2:109569938 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.601-1962T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109569938 | |||||||
| chr2:109570027 | C | CA | 39 | a0001c0001t0001g0266 a0001c0001t0002g0155 a0001c0001t0004g0008 others(36): Show |
40 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.601-2052dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570027 | |||||||
| chr2:109570061 | G | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.601-2085C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570061 | |||||||
| chr2:109570156 | G | A | 5 | a0001c0001t0004g0193 a0001c0001t0004g0199 a0001c0001t0004g0200 others(2): Show |
5 | HG01192.hp2 HG02451.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-2180C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570156 | |||||||
| chr2:109570175 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.601-2199A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570175 | |||||||
| chr2:109570188 | A | G | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-2212T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570188 | |||||||
| chr2:109570527 | G | GT | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(103): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.601-2552dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570527 | |||||||
| chr2:109570527 | GT | G | 35 | a0001c0001t0004g0008 a0001c0001t0004g0182 a0001c0001t0004g0183 others(32): Show |
36 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.601-2552delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570527 | |||||||
| chr2:109570605 | ACCTCCGC others(22): Show |
A | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-2658_601-2630d others(31): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570605 | |||||||
| chr2:109570781 | G | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-2805C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570781 | |||||||
| chr2:109570996 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.601-3020C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109570996 | |||||||
| chr2:109571024 | C | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.601-3048G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571024 | |||||||
| chr2:109571130 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.601-3154G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571130 | |||||||
| chr2:109571282 | C | T | 28 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(25): Show |
28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.600+3299G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571282 | |||||||
| chr2:109571290 | T | C | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.600+3291A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571290 | |||||||
| chr2:109571398 | C | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.600+3183G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571398 | |||||||
| chr2:109571523 | A | T | 1 | a0001c0001t0003g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.600+3058T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571523 | |||||||
| chr2:109571527 | C | G | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.600+3054G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571527 | |||||||
| chr2:109571588 | A | G | 1 | a0001c0001t0002g0157 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.600+2993T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571588 | |||||||
| chr2:109571645 | G | A | 233 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(230): Show |
242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.600+2936C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571645 | |||||||
| chr2:109571808 | C | A | 2 | a0001c0001t0006g0133 a0001c0001t0006g0135 |
2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.600+2773G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571808 | |||||||
| chr2:109571871 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0142 |
2 | NA19000.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.600+2710T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571871 | |||||||
| chr2:109571884 | G | A | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.600+2697C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571884 | |||||||
| chr2:109571950 | A | G | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.600+2631T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109571950 | |||||||
| chr2:109572582 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.600+1999C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572582 | |||||||
| chr2:109572609 | C | CT | 45 | a0001c0001t0001g0264 a0001c0001t0001g0268 a0001c0001t0001g0272 others(42): Show |
45 | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.600+1971dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572609 | |||||||
| chr2:109572609 | CT | C | 28 | a0001c0001t0001g0339 a0001c0001t0001g0362 a0001c0001t0001g0374 others(25): Show |
29 | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.600+1971delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572609 | |||||||
| chr2:109572609 | CTTTTTTT others(4): Show |
C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.600+1961_600+1971d others(13): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572609 | |||||||
| chr2:109572653 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0252 a0001c0001t0001g0255 others(19): Show |
23 | HG00323.hp1 HG00738.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+1928C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572653 | |||||||
| chr2:109572666 | G | A | 1 | a0001c0001t0003g0062 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.600+1915C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572666 | |||||||
| chr2:109572885 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.600+1696C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109572885 | |||||||
| chr2:109573069 | G | T | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.600+1512C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573069 | |||||||
| chr2:109573343 | T | A | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.600+1238A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573343 | |||||||
| chr2:109573515 | C | T | 11 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(8): Show |
12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.600+1066G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573515 | |||||||
| chr2:109573561 | A | G | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.600+1020T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573561 | |||||||
| chr2:109573562 | A | C | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.600+1019T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573562 | |||||||
| chr2:109573785 | G | T | 1 | a0001c0001t0002g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.600+796C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573785 | |||||||
| chr2:109573959 | G | A | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.600+622C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109573959 | |||||||
| chr2:109574056 | A | C | 3 | a0001c0001t0001g0246 a0001c0001t0001g0250 a0001c0001t0001g0330 |
3 | HG03704.hp1 HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.600+525T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574056 | |||||||
| chr2:109574088 | T | C | 1 | a0001c0001t0005g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.600+493A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574088 | |||||||
| chr2:109574198 | A | G | 235 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(232): Show |
244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.600+383T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574198 | |||||||
| chr2:109574204 | C | G | 1 | a0001c0001t0002g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.600+377G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574204 | |||||||
| chr2:109574310 | G | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.600+271C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574310 | |||||||
| chr2:109574404 | C | A | 1 | a0001c0001t0004g0189 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.600+177G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574404 | |||||||
| chr2:109574443 | T | TA | 48 | a0001c0001t0001g0361 a0001c0001t0002g0006 a0001c0001t0002g0007 others(45): Show |
51 | HG00609.hp1 HG01257.hp1 HG01258.hp2 others(48): Show |
intron_variant | MODIFIER | c.600+137dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | |||||||
| chr2:109574443 | T | TAA | 39 | a0001c0001t0002g0106 a0001c0001t0002g0108 a0001c0001t0002g0109 others(36): Show |
39 | HG00735.hp2 HG01069.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.600+136_600+137dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | |||||||
| chr2:109574443 | T | TAAA | 55 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(52): Show |
59 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.600+135_600+137dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | |||||||
| chr2:109574443 | TA | T | 129 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.600+137delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | |||||||
| chr2:109574443 | TAA | T | 27 | a0001c0001t0001g0252 a0001c0001t0001g0266 a0001c0001t0001g0277 others(24): Show |
27 | HG00639.hp1 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.600+136_600+137del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | |||||||
| chr2:109574443 | TAAA | T | 35 | a0001c0001t0004g0008 a0001c0001t0004g0182 a0001c0001t0004g0183 others(32): Show |
36 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.600+135_600+137del others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574443 | |||||||
| chr2:109574448 | A | T | 3 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0231 |
3 | HG02109.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.600+133T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574448 | |||||||
| chr2:109574467 | T | A | 1 | a0001c0001t0002g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.600+114A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574467 | |||||||
| chr2:109574470 | A | T | 1 | a0001c0001t0002g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.600+111T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574470 | |||||||
| chr2:109574553 | G | C | 57 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(54): Show |
58 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.600+28C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574553 | |||||||
| chr2:109574553 | G | T | 3 | a0001c0001t0004g0224 a0001c0001t0004g0225 a0001c0001t0004g0226 |
3 | HG02451.hp2 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.600+28C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574553 | |||||||
| chr2:109574565 | C | T | 29 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(26): Show |
30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.600+16G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 5/10 | chr2 | 109574565 | |||||||
| chr2:109574908 | T | TA | 9 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(6): Show |
9 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-142dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109574908 | |||||||
| chr2:109574908 | TA | T | 4 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0103 others(1): Show |
5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-142delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109574908 | |||||||
| chr2:109574979 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.414-212A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109574979 | |||||||
| chr2:109575289 | T | C | 1 | a0001c0001t0001g0368 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.414-522A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575289 | |||||||
| chr2:109575351 | A | G | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.414-584T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575351 | |||||||
| chr2:109575372 | T | G | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.414-605A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575372 | |||||||
| chr2:109575434 | A | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.414-667T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575434 | |||||||
| chr2:109575678 | C | G | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-911G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575678 | |||||||
| chr2:109575692 | C | T | 19 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0075 others(16): Show |
20 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-925G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575692 | |||||||
| chr2:109575840 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.414-1073C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575840 | |||||||
| chr2:109575860 | T | C | 2 | a0001c0001t0004g0186 a0001c0001t0004g0187 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.414-1093A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109575860 | |||||||
| chr2:109576269 | A | AAT | 3 | a0001c0001t0001g0288 a0001c0001t0002g0084 a0001c0001t0002g0085 |
3 | HG02976.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.414-1504_414-1503d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576269 | |||||||
| chr2:109576271 | T | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.414-1504A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576271 | |||||||
| chr2:109576619 | A | T | 3 | a0001c0001t0003g0054 a0001c0001t0003g0065 a0001c0001t0003g0067 |
3 | HG00609.hp2 NA18961.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.414-1852T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576619 | |||||||
| chr2:109576781 | C | A | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.414-2014G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576781 | |||||||
| chr2:109576783 | C | G | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-2016G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576783 | |||||||
| chr2:109576808 | A | G | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-2041T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576808 | |||||||
| chr2:109576860 | A | G | 2 | a0001c0001t0004g0233 a0001c0001t0004g0237 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.414-2093T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576860 | |||||||
| chr2:109576884 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02165.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.414-2117C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576884 | |||||||
| chr2:109576967 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.414-2200A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109576967 | |||||||
| chr2:109577095 | G | A | 4 | a0001c0001t0001g0334 a0001c0001t0002g0215 a0002c0003t0001g0286 others(1): Show |
4 | HG04204.hp2 NA18969.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-2328C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577095 | |||||||
| chr2:109577314 | C | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-2547G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577314 | |||||||
| chr2:109577318 | C | T | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0002g0072 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-2551G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577318 | |||||||
| chr2:109577319 | G | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-2552C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577319 | |||||||
| chr2:109577598 | T | A | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(57): Show |
64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.414-2831A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577598 | |||||||
| chr2:109577598 | T | TA | 26 | a0001c0001t0002g0106 a0001c0001t0002g0108 a0001c0001t0002g0109 others(23): Show |
26 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.414-2832dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577598 | |||||||
| chr2:109577598 | TA | T | 7 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0345 others(4): Show |
7 | HG01168.hp2 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-2832delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577598 | |||||||
| chr2:109577613 | G | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.414-2846C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577613 | |||||||
| chr2:109577801 | T | C | 1 | a0001c0001t0004g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.414-3034A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577801 | |||||||
| chr2:109577857 | G | A | 1 | a0001c0001t0006g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.414-3090C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577857 | |||||||
| chr2:109577861 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.414-3094G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577861 | |||||||
| chr2:109577912 | C | CA | 24 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(21): Show |
24 | HG01167.hp2 HG01169.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.414-3146dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | |||||||
| chr2:109577912 | CA | C | 111 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.414-3146delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | |||||||
| chr2:109577912 | CAA | C | 81 | a0001c0001t0001g0266 a0001c0001t0001g0325 a0001c0001t0001g0334 others(78): Show |
84 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.414-3147_414-3146d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | |||||||
| chr2:109577912 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.414-3156_414-3146d others(13): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109577912 | |||||||
| chr2:109578061 | G | T | 5 | a0001c0001t0003g0019 a0001c0001t0003g0043 a0001c0001t0003g0059 others(2): Show |
5 | NA18947.hp1 NA18949.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-3294C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578061 | |||||||
| chr2:109578111 | C | G | 2 | a0001c0001t0005g0097 a0001c0001t0005g0098 |
2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.414-3344G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578111 | |||||||
| chr2:109578238 | A | G | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0315 |
3 | NA18943.hp2 NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.414-3471T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578238 | |||||||
| chr2:109578299 | G | T | 2 | a0001c0001t0004g0206 a0001c0001t0004g0241 |
2 | HG02074.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.414-3532C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578299 | |||||||
| chr2:109578466 | A | C | 61 | a0001c0001t0001g0386 a0001c0001t0004g0008 a0001c0001t0004g0180 others(58): Show |
62 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.414-3699T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578466 | |||||||
| chr2:109578542 | GA | G | 337 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(334): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.414-3776delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578542 | |||||||
| chr2:109578584 | G | T | 337 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(334): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.414-3817C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578584 | |||||||
| chr2:109578624 | C | T | 1 | a0001c0001t0001g0349 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.414-3857G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578624 | |||||||
| chr2:109578690 | C | T | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-3923G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578690 | |||||||
| chr2:109578703 | G | T | 10 | a0001c0001t0002g0006 a0001c0001t0002g0145 a0001c0001t0002g0146 others(7): Show |
11 | HG00609.hp1 HG02040.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.414-3936C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109578703 | |||||||
| chr2:109579142 | T | C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-4375A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579142 | |||||||
| chr2:109579214 | A | C | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-4447T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579214 | |||||||
| chr2:109579303 | C | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-4536G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579303 | |||||||
| chr2:109579343 | T | C | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.414-4576A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579343 | |||||||
| chr2:109579433 | G | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.414-4666C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579433 | |||||||
| chr2:109579462 | C | A | 5 | a0001c0001t0004g0008 a0001c0001t0004g0184 a0001c0001t0004g0188 others(2): Show |
6 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-4695G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579462 | |||||||
| chr2:109579653 | G | A | 1 | a0001c0001t0003g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.414-4886C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579653 | |||||||
| chr2:109579665 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.414-4898C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579665 | |||||||
| chr2:109579892 | G | A | 5 | a0001c0001t0002g0107 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | NA18963.hp2 NA18971.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.414-5125C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579892 | |||||||
| chr2:109579947 | C | G | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+5179G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579947 | |||||||
| chr2:109579994 | G | A | 27 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(24): Show |
28 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+5132C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109579994 | |||||||
| chr2:109580180 | G | T | 2 | a0002c0003t0001g0286 a0002c0003t0001g0287 |
2 | NA18969.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.413+4946C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580180 | |||||||
| chr2:109580181 | C | CA | 61 | a0001c0001t0002g0129 a0001c0001t0003g0068 a0001c0001t0004g0008 others(58): Show |
62 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.413+4944dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580181 | |||||||
| chr2:109580272 | G | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+4854C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580272 | |||||||
| chr2:109580326 | A | G | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.413+4800T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580326 | |||||||
| chr2:109580349 | C | CA | 7 | a0001c0001t0001g0375 a0001c0001t0001g0376 a0001c0001t0002g0171 others(4): Show |
7 | HG01106.hp2 HG01175.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+4776dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580349 | |||||||
| chr2:109580349 | CA | C | 200 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.413+4776delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580349 | |||||||
| chr2:109580349 | CAA | C | 52 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(49): Show |
53 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.413+4775_413+4776d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580349 | |||||||
| chr2:109580372 | G | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+4754C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580372 | |||||||
| chr2:109580474 | CA | C | 18 | a0001c0001t0004g0180 a0001c0001t0004g0218 a0001c0001t0004g0220 others(15): Show |
18 | HG00639.hp1 HG01175.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+4651delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580474 | |||||||
| chr2:109580589 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.413+4537G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580589 | |||||||
| chr2:109580632 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.413+4494T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580632 | |||||||
| chr2:109580820 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.413+4306A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580820 | |||||||
| chr2:109580875 | C | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+4251G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109580875 | |||||||
| chr2:109581105 | C | T | 1 | a0001c0001t0005g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413+4021G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581105 | |||||||
| chr2:109581274 | T | C | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+3852A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581274 | |||||||
| chr2:109581319 | C | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+3807G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581319 | |||||||
| chr2:109581339 | A | C | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.413+3787T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581339 | |||||||
| chr2:109581501 | T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.413+3625A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581501 | |||||||
| chr2:109581528 | G | GA | 71 | a0001c0001t0001g0321 a0001c0001t0001g0354 a0001c0001t0001g0355 others(68): Show |
75 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.413+3597dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581528 | |||||||
| chr2:109581761 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.413+3365G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581761 | |||||||
| chr2:109581763 | G | A | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+3363C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109581763 | |||||||
| chr2:109582007 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+3119G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582007 | |||||||
| chr2:109582046 | G | A | 205 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(202): Show |
213 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.413+3080C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582046 | |||||||
| chr2:109582075 | G | GAC | 13 | a0001c0001t0001g0354 a0001c0001t0001g0389 a0001c0001t0002g0084 others(10): Show |
14 | HG00735.hp1 HG01433.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+3049_413+3050d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | G | GACAC | 6 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(3): Show |
6 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+3047_413+3050d others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | G | GACACAC | 4 | a0001c0001t0005g0095 a0001c0001t0005g0096 a0001c0001t0005g0100 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+3045_413+3050d others(8): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GAC | G | 23 | a0001c0001t0001g0386 a0001c0001t0002g0004 a0001c0001t0002g0074 others(20): Show |
24 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+3049_413+3050d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GACAC | G | 33 | a0001c0001t0001g0253 a0001c0001t0001g0352 a0001c0001t0001g0362 others(30): Show |
35 | HG00597.hp2 HG00609.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.413+3047_413+3050d others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GACACAC | G | 9 | a0001c0001t0001g0313 a0001c0001t0001g0327 a0001c0001t0001g0336 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+3045_413+3050d others(8): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GACACACA others(1): Show |
G | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.413+3043_413+3050d others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GACACACA others(3): Show |
G | 54 | a0001c0001t0001g0249 a0001c0001t0001g0272 a0001c0001t0001g0274 others(51): Show |
55 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.413+3041_413+3050d others(12): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GACACACA others(5): Show |
G | 7 | a0001c0001t0001g0295 a0001c0001t0001g0316 a0001c0001t0001g0338 others(4): Show |
7 | HG01109.hp1 HG02080.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+3039_413+3050d others(14): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582075 | GACACACA others(7): Show |
G | 69 | a0001c0001t0001g0346 a0001c0001t0001g0355 a0001c0001t0001g0358 others(66): Show |
73 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.413+3037_413+3050d others(16): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582075 | |||||||
| chr2:109582110 | A | ACACT | 3 | a0001c0001t0002g0108 a0001c0001t0002g0124 a0001c0001t0002g0128 |
3 | HG01981.hp1 HG02886.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.413+3012_413+3015d others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582110 | |||||||
| chr2:109582110 | A | ACT | 16 | a0001c0001t0002g0106 a0001c0001t0002g0110 a0001c0001t0002g0111 others(13): Show |
16 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+3015_413+3016i others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582110 | |||||||
| chr2:109582110 | A | T | 7 | a0001c0001t0002g0107 a0001c0001t0002g0109 a0001c0001t0002g0112 others(4): Show |
7 | HG01516.hp2 HG01517.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+3016T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582110 | |||||||
| chr2:109582184 | A | T | 1 | a0001c0001t0004g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.413+2942T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582184 | |||||||
| chr2:109582218 | C | T | 6 | a0001c0001t0003g0002 a0001c0001t0003g0026 a0001c0001t0003g0052 others(3): Show |
7 | HG02080.hp2 HG02135.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+2908G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582218 | |||||||
| chr2:109582304 | C | T | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+2822G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582304 | |||||||
| chr2:109582389 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.413+2737C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582389 | |||||||
| chr2:109582466 | C | T | 4 | a0001c0001t0007g0337 a0001c0001t0007g0342 a0001c0001t0007g0343 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+2660G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582466 | |||||||
| chr2:109582520 | C | T | 2 | a0001c0001t0004g0186 a0001c0001t0004g0187 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.413+2606G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582520 | |||||||
| chr2:109582873 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.413+2253C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582873 | |||||||
| chr2:109582922 | T | A | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+2204A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582922 | |||||||
| chr2:109582976 | T | C | 1 | a0001c0001t0001g0369 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.413+2150A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582976 | |||||||
| chr2:109582985 | A | C | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+2141T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109582985 | |||||||
| chr2:109583040 | A | C | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.413+2086T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583040 | |||||||
| chr2:109583175 | TTAAAC | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+1946_413+1950d others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583175 | |||||||
| chr2:109583292 | T | G | 1 | a0001c0001t0005g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.413+1834A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583292 | |||||||
| chr2:109583355 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.413+1771A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583355 | |||||||
| chr2:109583389 | G | A | 27 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(24): Show |
28 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+1737C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583389 | |||||||
| chr2:109583440 | A | G | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.413+1686T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583440 | |||||||
| chr2:109583592 | G | C | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+1534C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583592 | |||||||
| chr2:109583643 | T | A | 3 | a0001c0001t0004g0218 a0001c0001t0004g0220 a0001c0001t0004g0221 |
3 | HG02109.hp1 HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.413+1483A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583643 | |||||||
| chr2:109583751 | C | T | 12 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(9): Show |
12 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+1375G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583751 | |||||||
| chr2:109583807 | T | A | 7 | a0001c0001t0004g0224 a0001c0001t0004g0225 a0001c0001t0004g0226 others(4): Show |
7 | HG01175.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1319A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109583807 | |||||||
| chr2:109584008 | C | G | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.413+1118G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584008 | |||||||
| chr2:109584011 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.413+1115A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584011 | |||||||
| chr2:109584122 | G | A | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0335 |
3 | NA18945.hp1 NA18956.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.413+1004C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584122 | |||||||
| chr2:109584203 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.413+923C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584203 | |||||||
| chr2:109584215 | G | A | 10 | a0001c0001t0002g0017 a0001c0001t0002g0167 a0001c0001t0002g0168 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+911C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584215 | |||||||
| chr2:109584301 | A | AC | 336 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(333): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.413+824dupG | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584301 | |||||||
| chr2:109584323 | A | C | 1 | a0001c0001t0004g0199 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.413+803T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584323 | |||||||
| chr2:109584474 | C | CA | 161 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0312 others(158): Show |
168 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(165): Show |
intron_variant | MODIFIER | c.413+651dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | |||||||
| chr2:109584474 | C | CAA | 59 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0075 others(56): Show |
61 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.413+650_413+651dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | |||||||
| chr2:109584474 | C | CAAA | 15 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0081 others(12): Show |
15 | HG01192.hp2 HG01884.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+649_413+651dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | |||||||
| chr2:109584474 | CA | C | 7 | a0001c0001t0001g0256 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
7 | HG00323.hp1 HG01192.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+651delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584474 | |||||||
| chr2:109584611 | C | T | 12 | a0001c0001t0001g0346 a0001c0001t0001g0358 a0001c0001t0001g0359 others(9): Show |
12 | HG00544.hp2 HG01243.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+515G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584611 | |||||||
| chr2:109584840 | T | A | 1 | a0001c0001t0001g0384 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.413+286A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584840 | |||||||
| chr2:109584844 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.413+282G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109584844 | |||||||
| chr2:109585107 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.413+19T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 4/10 | chr2 | 109585107 | |||||||
| chr2:109585493 | G | C | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.218-172C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585493 | |||||||
| chr2:109585530 | A | G | 5 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0001t0004g0235 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+191T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585530 | |||||||
| chr2:109585541 | T | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0313 |
2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.217+180A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585541 | |||||||
| chr2:109585547 | G | T | 2 | a0001c0001t0004g0186 a0001c0001t0004g0187 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.217+174C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 3/10 | chr2 | 109585547 | |||||||
| chr2:109585942 | T | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-104A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109585942 | |||||||
| chr2:109585978 | G | A | 15 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(12): Show |
16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-140C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109585978 | |||||||
| chr2:109586336 | G | T | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.100-498C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586336 | |||||||
| chr2:109586390 | G | C | 2 | a0001c0001t0006g0161 a0005c0004t0006g0160 |
2 | HG03490.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.100-552C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586390 | |||||||
| chr2:109586405 | C | T | 10 | a0001c0001t0002g0017 a0001c0001t0002g0167 a0001c0001t0002g0168 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-567G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586405 | |||||||
| chr2:109586426 | CT | C | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(57): Show |
64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.100-589delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586426 | |||||||
| chr2:109586586 | A | G | 1 | a0001c0001t0005g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-748T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586586 | |||||||
| chr2:109586589 | C | A | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-751G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586589 | |||||||
| chr2:109586658 | T | C | 6 | a0001c0001t0002g0017 a0001c0001t0004g0233 a0001c0001t0004g0234 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-820A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586658 | |||||||
| chr2:109586995 | C | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-1157G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109586995 | |||||||
| chr2:109587180 | A | G | 12 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0224 others(9): Show |
12 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-1342T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587180 | |||||||
| chr2:109587312 | T | A | 1 | a0001c0001t0002g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-1474A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587312 | |||||||
| chr2:109587390 | T | C | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1552A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587390 | |||||||
| chr2:109587406 | T | C | 75 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.100-1568A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587406 | |||||||
| chr2:109587684 | C | T | 81 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(78): Show |
84 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(81): Show |
intron_variant | MODIFIER | c.100-1846G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587684 | |||||||
| chr2:109587837 | T | C | 4 | a0001c0001t0004g0193 a0001c0001t0004g0200 a0001c0001t0004g0201 others(1): Show |
4 | HG01192.hp2 HG02451.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-1999A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587837 | |||||||
| chr2:109587913 | C | CA | 32 | a0001c0001t0001g0276 a0001c0001t0001g0314 a0001c0001t0001g0332 others(29): Show |
32 | HG00639.hp1 HG01109.hp1 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.100-2076dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587913 | |||||||
| chr2:109587932 | A | G | 35 | a0001c0001t0004g0008 a0001c0001t0004g0181 a0001c0001t0004g0182 others(32): Show |
36 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.100-2094T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587932 | |||||||
| chr2:109587957 | G | A | 65 | a0001c0001t0002g0145 a0001c0001t0003g0001 a0001c0001t0003g0002 others(62): Show |
69 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.100-2119C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109587957 | |||||||
| chr2:109588094 | T | C | 28 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(25): Show |
28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-2256A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588094 | |||||||
| chr2:109588125 | C | T | 15 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(12): Show |
16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-2287G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588125 | |||||||
| chr2:109588336 | G | C | 1 | a0001c0001t0001g0315 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.100-2498C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588336 | |||||||
| chr2:109588533 | G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100-2695C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588533 | |||||||
| chr2:109588727 | G | A | 1 | a0001c0001t0005g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.100-2889C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588727 | |||||||
| chr2:109588813 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-2975A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588813 | |||||||
| chr2:109588850 | T | TA | 67 | a0001c0001t0002g0077 a0001c0001t0002g0109 a0001c0001t0002g0125 others(64): Show |
69 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.100-3013dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588850 | |||||||
| chr2:109588850 | T | TAA | 56 | a0001c0001t0001g0321 a0001c0001t0002g0145 a0001c0001t0003g0001 others(53): Show |
60 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.100-3014_100-3013d others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588850 | |||||||
| chr2:109588850 | TA | T | 131 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(128): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-3013delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588850 | |||||||
| chr2:109588870 | C | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-3032G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109588870 | |||||||
| chr2:109589102 | G | T | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0002g0072 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3264C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589102 | |||||||
| chr2:109589106 | T | G | 57 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(54): Show |
58 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-3268A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589106 | |||||||
| chr2:109589180 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-3342A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589180 | |||||||
| chr2:109589258 | T | C | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(57): Show |
64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.100-3420A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589258 | |||||||
| chr2:109589339 | C | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-3501G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589339 | |||||||
| chr2:109589736 | C | CA | 59 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(56): Show |
60 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.99+3314dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589736 | |||||||
| chr2:109589741 | A | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.99+3310T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589741 | |||||||
| chr2:109589825 | C | T | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3226G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589825 | |||||||
| chr2:109589970 | G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.99+3081C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109589970 | |||||||
| chr2:109590029 | CATATATA others(23): Show |
C | 3 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0135 |
3 | HG02647.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+2992_99+3021del others(30): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590029 | |||||||
| chr2:109590035 | T | TAC | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+3014_99+3015dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590035 | |||||||
| chr2:109590035 | TACACACA others(25): Show |
T | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+2984_99+3015del others(32): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590035 | |||||||
| chr2:109590041 | CAT | C | 13 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0094 others(10): Show |
14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+3008_99+3009del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590041 | |||||||
| chr2:109590041 | CATATATA others(27): Show |
C | 5 | a0001c0001t0006g0134 a0001c0001t0006g0136 a0001c0001t0006g0137 others(2): Show |
5 | HG02015.hp2 HG03490.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2976_99+3009del others(34): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590041 | |||||||
| chr2:109590048 | ATGTGTG | A | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2997_99+3002del others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590048 | |||||||
| chr2:109590073 | C | T | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2978G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590073 | |||||||
| chr2:109590078 | A | ATG | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+2972_99+2973ins others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590078 | |||||||
| chr2:109590078 | ATATGTAT others(21): Show |
A | 2 | a0001c0001t0001g0253 a0001c0001t0002g0076 |
2 | HG00597.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.99+2945_99+2972del others(28): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590078 | |||||||
| chr2:109590108 | A | ATG | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+2941_99+2942dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590108 | |||||||
| chr2:109590129 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.99+2922G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590129 | |||||||
| chr2:109590392 | T | C | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+2659A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590392 | |||||||
| chr2:109590424 | CT | C | 65 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(62): Show |
67 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+2626delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590424 | |||||||
| chr2:109590571 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+2480T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590571 | |||||||
| chr2:109590683 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99+2368G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590683 | |||||||
| chr2:109590762 | C | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+2289G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109590762 | |||||||
| chr2:109591046 | T | C | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0329 |
3 | HG00621.hp2 NA18612.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.99+2005A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591046 | |||||||
| chr2:109591085 | C | T | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+1966G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591085 | |||||||
| chr2:109591191 | A | G | 1 | a0001c0001t0003g0046 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99+1860T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591191 | |||||||
| chr2:109591365 | C | T | 5 | a0001c0001t0004g0193 a0001c0001t0004g0199 a0001c0001t0004g0200 others(2): Show |
5 | HG01192.hp2 HG02451.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1686G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591365 | |||||||
| chr2:109591409 | C | G | 1 | a0001c0001t0002g0178 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+1642G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591409 | |||||||
| chr2:109591629 | G | T | 1 | a0001c0001t0002g0215 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.99+1422C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591629 | |||||||
| chr2:109591714 | C | T | 235 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(232): Show |
244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.99+1337G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591714 | |||||||
| chr2:109591734 | G | A | 235 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(232): Show |
244 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(241): Show |
intron_variant | MODIFIER | c.99+1317C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591734 | |||||||
| chr2:109591755 | G | A | 1 | a0001c0001t0004g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.99+1296C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591755 | |||||||
| chr2:109591856 | C | T | 4 | a0001c0001t0007g0337 a0001c0001t0007g0342 a0001c0001t0007g0343 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1195G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591856 | |||||||
| chr2:109591858 | C | T | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1193G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591858 | |||||||
| chr2:109591934 | T | A | 60 | a0001c0001t0004g0008 a0001c0001t0004g0180 a0001c0001t0004g0181 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.99+1117A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591934 | |||||||
| chr2:109591975 | C | A | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1076G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109591975 | |||||||
| chr2:109592070 | T | C | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+981A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592070 | |||||||
| chr2:109592262 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.99+789G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592262 | |||||||
| chr2:109592276 | G | A | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+775C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592276 | |||||||
| chr2:109592294 | G | A | 1 | a0001c0001t0001g0370 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.99+757C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592294 | |||||||
| chr2:109592395 | G | A | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(57): Show |
64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.99+656C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592395 | |||||||
| chr2:109592419 | T | C | 2 | a0001c0001t0002g0112 a0001c0001t0002g0130 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.99+632A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592419 | |||||||
| chr2:109592427 | C | T | 8 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+624G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592427 | |||||||
| chr2:109592428 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.99+623C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592428 | |||||||
| chr2:109592629 | A | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0078 |
3 | HG02615.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+422T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592629 | |||||||
| chr2:109592637 | G | A | 2 | a0001c0001t0002g0126 a0001c0001t0002g0131 |
2 | HG01255.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.99+414C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592637 | |||||||
| chr2:109592705 | G | C | 1 | a0001c0001t0003g0018 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.99+346C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592705 | |||||||
| chr2:109592887 | A | AT | 11 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(8): Show |
12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+163dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 2/10 | chr2 | 109592887 | |||||||
| chr2:109593396 | G | T | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.31-277C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593396 | |||||||
| chr2:109593409 | C | CTTTTTT | 21 | a0001c0001t0004g0180 a0001c0001t0004g0218 a0001c0001t0004g0220 others(18): Show |
21 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-296_31-291dupAA others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | |||||||
| chr2:109593409 | C | CTTTTTTT | 33 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(30): Show |
33 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-297_31-291dupAA others(5): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | |||||||
| chr2:109593409 | C | CTTTTTTT others(1): Show |
143 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(140): Show |
151 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.31-298_31-291dupAA others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | |||||||
| chr2:109593409 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0139 a0001c0001t0002g0162 a0001c0001t0003g0022 others(3): Show |
6 | HG01192.hp2 HG03225.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-299_31-291dupAA others(7): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | |||||||
| chr2:109593409 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-300_31-291dupAA others(8): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593409 | |||||||
| chr2:109593474 | C | T | 146 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(143): Show |
153 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.31-355G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593474 | |||||||
| chr2:109593847 | A | T | 1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31-728T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593847 | |||||||
| chr2:109593893 | C | G | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-774G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593893 | |||||||
| chr2:109593894 | G | C | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-775C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593894 | |||||||
| chr2:109593907 | T | A | 2 | a0002c0003t0001g0286 a0002c0003t0001g0287 |
2 | NA18969.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.31-788A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109593907 | |||||||
| chr2:109594120 | T | C | 4 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0103 others(1): Show |
5 | HG02572.hp2 HG03209.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-1001A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594120 | |||||||
| chr2:109594135 | A | C | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-1016T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594135 | |||||||
| chr2:109594149 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(11): Show |
15 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-1030C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594149 | |||||||
| chr2:109594271 | TA | T | 206 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(203): Show |
214 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.31-1153delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594271 | |||||||
| chr2:109594285 | C | T | 15 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(12): Show |
16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-1166G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594285 | |||||||
| chr2:109594382 | C | T | 30 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(27): Show |
30 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-1263G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594382 | |||||||
| chr2:109594796 | T | C | 2 | a0001c0001t0004g0233 a0001c0001t0004g0237 |
2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.31-1677A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594796 | |||||||
| chr2:109594814 | T | C | 29 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(26): Show |
30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-1695A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594814 | |||||||
| chr2:109594921 | T | A | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-1802A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594921 | |||||||
| chr2:109594922 | C | T | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-1803G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109594922 | |||||||
| chr2:109595012 | G | A | 128 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(125): Show |
134 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.31-1893C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595012 | |||||||
| chr2:109595015 | C | T | 13 | a0001c0001t0005g0005 a0001c0001t0005g0093 a0001c0001t0005g0094 others(10): Show |
14 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-1896G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595015 | |||||||
| chr2:109595096 | G | A | 233 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(230): Show |
242 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(239): Show |
intron_variant | MODIFIER | c.31-1977C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595096 | |||||||
| chr2:109595178 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.31-2059G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595178 | |||||||
| chr2:109595280 | G | A | 3 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0062 |
3 | HG02135.hp2 NA18984.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.31-2161C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595280 | |||||||
| chr2:109595380 | T | C | 16 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(13): Show |
16 | HG01175.hp1 HG01891.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-2261A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595380 | |||||||
| chr2:109595495 | T | C | 31 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.31-2376A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595495 | |||||||
| chr2:109595788 | T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-2669A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595788 | |||||||
| chr2:109595877 | A | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00621.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.31-2758T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595877 | |||||||
| chr2:109595966 | T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-2847A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109595966 | |||||||
| chr2:109596192 | C | G | 23 | a0001c0001t0004g0180 a0001c0001t0004g0218 a0001c0001t0004g0220 others(20): Show |
23 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-3073G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596192 | |||||||
| chr2:109596194 | G | A | 1 | a0006c0006t0004g0194 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.31-3075C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596194 | |||||||
| chr2:109596243 | TTTAATAT others(5): Show |
T | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-3136_31-3125del others(12): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596243 | |||||||
| chr2:109596333 | A | C | 60 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(57): Show |
61 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.31-3214T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596333 | |||||||
| chr2:109596356 | G | A | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-3237C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596356 | |||||||
| chr2:109596474 | G | A | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.31-3355C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596474 | |||||||
| chr2:109596510 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.31-3391C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596510 | |||||||
| chr2:109596574 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.31-3455C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596574 | |||||||
| chr2:109596649 | C | T | 1 | a0001c0001t0003g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.31-3530G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596649 | |||||||
| chr2:109596662 | T | C | 27 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(24): Show |
27 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-3543A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596662 | |||||||
| chr2:109596733 | T | C | 2 | a0001c0001t0004g0216 a0001c0001t0004g0217 |
2 | HG01109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.31-3614A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596733 | |||||||
| chr2:109596806 | G | C | 3 | a0001c0001t0001g0260 a0001c0001t0001g0319 a0001c0001t0001g0390 |
3 | HG00140.hp2 HG02300.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.31-3687C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596806 | |||||||
| chr2:109596822 | TGA | T | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0002g0072 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-3705_31-3704del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109596822 | |||||||
| chr2:109597278 | A | G | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(141): Show |
151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.31-4159T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597278 | |||||||
| chr2:109597337 | A | G | 2 | a0001c0001t0005g0094 a0001c0001t0005g0102 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.31-4218T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597337 | |||||||
| chr2:109597436 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.31-4317C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597436 | |||||||
| chr2:109597575 | TAC | T | 28 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(25): Show |
30 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-4458_31-4457del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597575 | |||||||
| chr2:109597805 | C | A | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.31-4686G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597805 | |||||||
| chr2:109597829 | G | T | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-4710C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597829 | |||||||
| chr2:109597884 | G | C | 1 | a0001c0001t0004g0203 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-4765C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597884 | |||||||
| chr2:109597885 | C | T | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(141): Show |
151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.31-4766G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597885 | |||||||
| chr2:109597940 | C | T | 30 | a0001c0001t0001g0013 a0001c0001t0001g0346 a0001c0001t0001g0347 others(27): Show |
31 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.31-4821G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109597940 | |||||||
| chr2:109598067 | T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-4948A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598067 | |||||||
| chr2:109598304 | G | A | 5 | a0001c0001t0001g0244 a0001c0001t0001g0261 a0001c0001t0001g0278 others(2): Show |
5 | HG00544.hp1 NA18939.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-5185C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598304 | |||||||
| chr2:109598428 | A | G | 2 | a0001c0001t0004g0186 a0001c0001t0004g0187 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.31-5309T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598428 | |||||||
| chr2:109598528 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.31-5409T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598528 | |||||||
| chr2:109598532 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.31-5413T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598532 | |||||||
| chr2:109598806 | G | A | 1 | a0001c0001t0001g0390 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.31-5687C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598806 | |||||||
| chr2:109598812 | G | A | 1 | a0001c0001t0006g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31-5693C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598812 | |||||||
| chr2:109598838 | C | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.31-5719G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598838 | |||||||
| chr2:109598856 | G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-5737C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598856 | |||||||
| chr2:109598901 | A | T | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.31-5782T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598901 | |||||||
| chr2:109598942 | T | TG | 4 | a0001c0001t0004g0192 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | NA18945.hp2 NA18962.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-5824dupC | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109598942 | |||||||
| chr2:109599090 | T | A | 5 | a0001c0001t0001g0340 a0001c0001t0007g0337 a0001c0001t0007g0342 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-5971A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599090 | |||||||
| chr2:109599269 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.31-6150G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599269 | |||||||
| chr2:109599448 | A | G | 2 | a0001c0001t0001g0356 a0001c0001t0001g0357 |
2 | HG01109.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.31-6329T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599448 | |||||||
| chr2:109599458 | C | CA | 41 | a0001c0001t0001g0322 a0001c0001t0001g0330 a0001c0001t0001g0332 others(38): Show |
42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.31-6340dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599458 | |||||||
| chr2:109599552 | T | A | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(141): Show |
151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.31-6433A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599552 | |||||||
| chr2:109599590 | G | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0063 a0001c0001t0003g0064 |
3 | NA18947.hp1 NA18971.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.31-6471C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599590 | |||||||
| chr2:109599774 | C | T | 207 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(204): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.31-6655G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599774 | |||||||
| chr2:109599963 | G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-6844C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109599963 | |||||||
| chr2:109600148 | A | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.31-7029T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600148 | |||||||
| chr2:109600190 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.31-7071A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600190 | |||||||
| chr2:109600318 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.31-7199G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600318 | |||||||
| chr2:109600538 | G | GA | 15 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0336 others(12): Show |
15 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-7420dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600538 | |||||||
| chr2:109600549 | A | C | 4 | a0001c0001t0004g0218 a0001c0001t0004g0220 a0001c0001t0004g0221 others(1): Show |
4 | HG00639.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7430T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600549 | |||||||
| chr2:109600553 | C | A | 4 | a0001c0001t0007g0337 a0001c0001t0007g0342 a0001c0001t0007g0343 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-7434G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600553 | |||||||
| chr2:109600842 | C | A | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-7723G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600842 | |||||||
| chr2:109600986 | C | T | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-7867G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600986 | |||||||
| chr2:109600995 | GA | G | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-7877delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109600995 | |||||||
| chr2:109601049 | C | T | 29 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(26): Show |
30 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.31-7930G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601049 | |||||||
| chr2:109601095 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.31-7976G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601095 | |||||||
| chr2:109601178 | G | C | 1 | a0001c0001t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-8059C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601178 | |||||||
| chr2:109601198 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-8079G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601198 | |||||||
| chr2:109601273 | G | A | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-8154C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601273 | |||||||
| chr2:109601581 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.31-8462G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601581 | |||||||
| chr2:109601594 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-8475T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601594 | |||||||
| chr2:109601757 | C | A | 5 | a0001c0001t0004g0233 a0001c0001t0004g0234 a0001c0001t0004g0235 others(2): Show |
5 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-8638G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601757 | |||||||
| chr2:109601765 | TA | T | 85 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0002g0166 others(82): Show |
90 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.31-8647delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601765 | |||||||
| chr2:109601810 | G | C | 63 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-8691C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601810 | |||||||
| chr2:109601911 | A | C | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-8792T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601911 | |||||||
| chr2:109601956 | C | T | 4 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0262 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-8837G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601956 | |||||||
| chr2:109601961 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.31-8842G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109601961 | |||||||
| chr2:109602201 | TTA | T | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-9084_31-9083del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602201 | |||||||
| chr2:109602306 | AATTAAG | A | 63 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-9193_31-9188del others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602306 | |||||||
| chr2:109602328 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG00323.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.31-9209A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602328 | |||||||
| chr2:109602503 | C | T | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-9384G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602503 | |||||||
| chr2:109602636 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.31-9517A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602636 | |||||||
| chr2:109602647 | C | A | 4 | a0001c0001t0002g0112 a0001c0001t0002g0128 a0001c0001t0002g0129 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9528G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602647 | |||||||
| chr2:109602680 | T | TA | 12 | a0001c0001t0001g0251 a0001c0001t0001g0389 a0001c0001t0002g0167 others(9): Show |
12 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-9562dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602680 | |||||||
| chr2:109602680 | TA | T | 45 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0284 others(42): Show |
48 | HG00323.hp2 HG00609.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.31-9562delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602680 | |||||||
| chr2:109602681 | A | T | 3 | a0001c0001t0002g0106 a0001c0001t0002g0119 a0001c0001t0002g0120 |
3 | HG00735.hp2 HG01106.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.31-9562T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602681 | |||||||
| chr2:109602897 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.31-9778C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602897 | |||||||
| chr2:109602901 | C | CA | 84 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(81): Show |
87 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.31-9783dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | |||||||
| chr2:109602901 | C | CAA | 60 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0003g0001 others(57): Show |
64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.31-9784_31-9783dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | |||||||
| chr2:109602901 | C | CAAA | 15 | a0001c0001t0003g0065 a0001c0001t0005g0005 a0001c0001t0005g0092 others(12): Show |
16 | HG01257.hp1 HG01258.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-9785_31-9783dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | |||||||
| chr2:109602901 | CA | C | 47 | a0001c0001t0001g0262 a0001c0001t0001g0265 a0001c0001t0001g0266 others(44): Show |
48 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.31-9783delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109602901 | |||||||
| chr2:109603039 | C | CCAG | 9 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(6): Show |
10 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-9923_31-9921dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603039 | |||||||
| chr2:109603090 | C | A | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-9971G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603090 | |||||||
| chr2:109603091 | A | C | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-9972T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603091 | |||||||
| chr2:109603094 | A | T | 11 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(8): Show |
12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9975T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603094 | |||||||
| chr2:109603246 | T | A | 16 | a0001c0001t0001g0247 a0001c0001t0001g0280 a0001c0001t0001g0331 others(13): Show |
17 | HG01167.hp1 HG01192.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-10127A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603246 | |||||||
| chr2:109603482 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.30+10316C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603482 | |||||||
| chr2:109603491 | A | G | 346 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(343): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.30+10307T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603491 | |||||||
| chr2:109603524 | C | A | 1 | a0001c0007t0004g0232 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.30+10274G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603524 | |||||||
| chr2:109603535 | G | A | 101 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.30+10263C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603535 | |||||||
| chr2:109603542 | TA | T | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+10255delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603542 | |||||||
| chr2:109603758 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.30+10040A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603758 | |||||||
| chr2:109603832 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.30+9966C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109603832 | |||||||
| chr2:109604110 | C | T | 11 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(8): Show |
12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+9688G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604110 | |||||||
| chr2:109604123 | C | T | 13 | a0001c0001t0003g0021 a0001c0001t0003g0028 a0001c0001t0003g0029 others(10): Show |
13 | HG00733.hp1 HG00738.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+9675G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604123 | |||||||
| chr2:109604139 | G | A | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(141): Show |
151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.30+9659C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604139 | |||||||
| chr2:109604148 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.30+9650G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604148 | |||||||
| chr2:109604161 | C | CA | 64 | a0001c0001t0001g0250 a0001c0001t0001g0333 a0001c0001t0001g0347 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.30+9636dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604161 | |||||||
| chr2:109604161 | C | CAA | 8 | a0001c0001t0002g0077 a0001c0001t0004g0196 a0001c0001t0004g0233 others(5): Show |
8 | HG01167.hp1 HG01884.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+9635_30+9636dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604161 | |||||||
| chr2:109604161 | C | CAAA | 28 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0074 others(25): Show |
29 | HG00735.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.30+9634_30+9636dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604161 | |||||||
| chr2:109604330 | G | A | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+9468C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604330 | |||||||
| chr2:109604374 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0282 |
2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.30+9424T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604374 | |||||||
| chr2:109604383 | A | AAGGGGAG others(3): Show |
4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0171 others(1): Show |
4 | HG00735.hp1 HG01433.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(3): Show |
126 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(123): Show |
131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.30+9405_30+9414dup others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(8): Show |
15 | a0001c0001t0002g0213 a0001c0001t0005g0005 a0001c0001t0005g0092 others(12): Show |
16 | HG01257.hp1 HG01257.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(15): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(13): Show |
41 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0004g0008 others(38): Show |
42 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(20): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(18): Show |
18 | a0001c0001t0004g0180 a0001c0001t0004g0195 a0001c0001t0004g0218 others(15): Show |
18 | HG00639.hp1 HG01175.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(25): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(23): Show |
1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(30): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(33): Show |
29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(40): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(28): Show |
99 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(96): Show |
103 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.30+9414_30+9415ins others(35): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(29): Show |
1 | a0001c0001t0003g0020 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(36): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(23): Show |
1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(30): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604383 | A | AAGGGGAG others(14): Show |
1 | a0001c0001t0004g0196 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.30+9414_30+9415ins others(21): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604383 | |||||||
| chr2:109604389 | A | G | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+9409T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604389 | |||||||
| chr2:109604394 | C | A | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9404G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604394 | |||||||
| chr2:109604395 | G | C | 1 | a0001c0001t0002g0141 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.30+9403C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604395 | |||||||
| chr2:109604396 | G | A | 1 | a0001c0001t0007g0344 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.30+9402C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604396 | |||||||
| chr2:109604399 | C | A | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9399G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604399 | |||||||
| chr2:109604406 | A | G | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9392T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604406 | |||||||
| chr2:109604407 | A | G | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9391T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604407 | |||||||
| chr2:109604408 | A | G | 1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9390T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604408 | |||||||
| chr2:109604410 | G | GGGGCGGG others(9): Show |
1 | a0001c0001t0004g0214 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.30+9387_30+9388ins others(16): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604410 | |||||||
| chr2:109604449 | G | A | 4 | a0001c0002t0002g0070 a0001c0002t0002g0071 a0001c0002t0002g0072 others(1): Show |
4 | HG02145.hp1 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9349C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604449 | |||||||
| chr2:109604466 | C | T | 1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+9332G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604466 | |||||||
| chr2:109604482 | T | A | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+9316A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604482 | |||||||
| chr2:109604607 | G | A | 2 | a0001c0001t0007g0343 a0001c0001t0007g0344 |
2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.30+9191C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604607 | |||||||
| chr2:109604759 | G | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0077 others(8): Show |
12 | HG01167.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+9039C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109604759 | |||||||
| chr2:109605005 | A | G | 1 | a0001c0001t0003g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.30+8793T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605005 | |||||||
| chr2:109605110 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+8688C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605110 | |||||||
| chr2:109605193 | G | T | 8 | a0001c0001t0006g0016 a0001c0001t0006g0133 a0001c0001t0006g0134 others(5): Show |
8 | HG02015.hp2 HG02647.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+8605C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605193 | |||||||
| chr2:109605289 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.30+8509C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605289 | |||||||
| chr2:109605454 | G | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+8344C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605454 | |||||||
| chr2:109605480 | T | TA | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+8317dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605480 | |||||||
| chr2:109605629 | A | G | 3 | a0001c0001t0004g0222 a0001c0001t0004g0223 a0001c0001t0004g0231 |
3 | HG02109.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.30+8169T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605629 | |||||||
| chr2:109605766 | T | C | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(141): Show |
151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.30+8032A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605766 | |||||||
| chr2:109605976 | C | A | 1 | a0001c0001t0002g0110 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+7822G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109605976 | |||||||
| chr2:109606127 | G | A | 207 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(204): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.30+7671C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606127 | |||||||
| chr2:109606139 | G | A | 1 | a0001c0001t0006g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.30+7659C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606139 | |||||||
| chr2:109606232 | T | C | 8 | a0001c0001t0005g0005 a0001c0001t0005g0092 a0001c0001t0005g0093 others(5): Show |
9 | HG01257.hp1 HG01258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+7566A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606232 | |||||||
| chr2:109606282 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+7516C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606282 | |||||||
| chr2:109606308 | C | T | 1 | a0001c0001t0006g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.30+7490G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606308 | |||||||
| chr2:109606309 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+7489C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606309 | |||||||
| chr2:109606320 | C | CAGGAGA | 26 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(23): Show |
26 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.30+7472_30+7477dup others(6): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606320 | |||||||
| chr2:109606324 | A | G | 1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+7474T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606324 | |||||||
| chr2:109606339 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+7459G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606339 | |||||||
| chr2:109606393 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.30+7405C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606393 | |||||||
| chr2:109606440 | G | T | 1 | a0001c0001t0004g0195 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.30+7358C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606440 | |||||||
| chr2:109606582 | T | C | 1 | a0001c0001t0004g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.30+7216A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606582 | |||||||
| chr2:109606642 | TA | T | 337 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(334): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.30+7155delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606642 | |||||||
| chr2:109606672 | C | CT | 15 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0340 others(12): Show |
15 | HG00621.hp1 HG00673.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+7125dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | C | CTT | 30 | a0001c0001t0002g0204 a0001c0001t0002g0213 a0001c0001t0004g0008 others(27): Show |
31 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.30+7124_30+7125dup others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | C | CTTT | 18 | a0001c0001t0002g0190 a0001c0001t0004g0180 a0001c0001t0004g0181 others(15): Show |
18 | HG01109.hp1 HG01123.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.30+7123_30+7125dup others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | C | CTTTT | 14 | a0001c0001t0004g0186 a0001c0001t0004g0187 a0001c0001t0004g0218 others(11): Show |
14 | HG00639.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.30+7122_30+7125dup others(4): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | CT | C | 91 | a0001c0001t0001g0381 a0001c0001t0001g0382 a0001c0001t0002g0017 others(88): Show |
95 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.30+7125delA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | CTT | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0246 a0001c0001t0001g0247 others(69): Show |
76 | HG00423.hp2 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.30+7124_30+7125del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | CTTT | C | 73 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
76 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.30+7123_30+7125del others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606672 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0007g0337 a0001c0001t0007g0342 a0001c0001t0007g0343 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+7116_30+7125del others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606672 | |||||||
| chr2:109606714 | C | G | 1 | a0001c0001t0002g0167 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.30+7084G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606714 | |||||||
| chr2:109606977 | A | T | 1 | a0001c0001t0001g0347 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.30+6821T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109606977 | |||||||
| chr2:109607074 | T | G | 1 | a0001c0001t0001g0384 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.30+6724A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607074 | |||||||
| chr2:109607234 | C | T | 208 | a0001c0001t0001g0256 a0001c0001t0002g0006 a0001c0001t0002g0007 others(205): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.30+6564G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607234 | |||||||
| chr2:109607246 | T | C | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+6552A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607246 | |||||||
| chr2:109607317 | G | C | 1 | a0001c0001t0001g0012 | 2 | HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.30+6481C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607317 | |||||||
| chr2:109607480 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.30+6318C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607480 | |||||||
| chr2:109607538 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+6260G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607538 | |||||||
| chr2:109607572 | C | T | 1 | a0001c0001t0004g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.30+6226G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607572 | |||||||
| chr2:109607741 | CCT | C | 4 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0183 others(1): Show |
4 | HG02809.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+6055_30+6056del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109607741 | |||||||
| chr2:109608009 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.30+5789A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608009 | |||||||
| chr2:109608037 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.30+5761A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608037 | |||||||
| chr2:109608038 | T | C | 28 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(25): Show |
28 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.30+5760A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608038 | |||||||
| chr2:109608066 | A | ATCTATAC others(3): Show |
2 | a0001c0001t0004g0184 a0003c0009t0004g0242 |
2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.30+5731_30+5732ins others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608066 | |||||||
| chr2:109608067 | C | T | 2 | a0001c0001t0004g0184 a0003c0009t0004g0242 |
2 | HG01123.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.30+5731G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608067 | |||||||
| chr2:109608418 | G | C | 4 | a0001c0001t0007g0337 a0001c0001t0007g0342 a0001c0001t0007g0343 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+5380C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608418 | |||||||
| chr2:109608468 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+5330T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608468 | |||||||
| chr2:109608549 | G | A | 1 | a0001c0001t0003g0067 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30+5249C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608549 | |||||||
| chr2:109608776 | A | G | 1 | a0001c0001t0001g0254 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.30+5022T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608776 | |||||||
| chr2:109608836 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.30+4962T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608836 | |||||||
| chr2:109608863 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+4935G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608863 | |||||||
| chr2:109608926 | C | T | 207 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(204): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.30+4872G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109608926 | |||||||
| chr2:109609114 | C | A | 346 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(343): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.30+4684G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609114 | |||||||
| chr2:109609184 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.30+4614T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609184 | |||||||
| chr2:109609220 | T | C | 1 | a0001c0001t0001g0385 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.30+4578A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609220 | |||||||
| chr2:109609338 | GAAT | G | 144 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(141): Show |
151 | HG00597.hp1 HG00609.hp1 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.30+4457_30+4459del others(3): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609338 | |||||||
| chr2:109609358 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0250 |
2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.30+4440G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609358 | |||||||
| chr2:109609394 | T | C | 1 | a0001c0001t0001g0388 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.30+4404A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609394 | |||||||
| chr2:109609418 | G | A | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG02683.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.30+4380C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609418 | |||||||
| chr2:109609501 | G | T | 63 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(60): Show |
64 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.30+4297C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609501 | |||||||
| chr2:109609572 | C | T | 29 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0132 others(26): Show |
31 | HG00609.hp1 HG01934.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+4226G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609572 | |||||||
| chr2:109609611 | G | A | 40 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(37): Show |
41 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.30+4187C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609611 | |||||||
| chr2:109609615 | CA | C | 226 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(223): Show |
235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.30+4182delT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609615 | |||||||
| chr2:109609615 | CAA | C | 7 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
7 | HG01168.hp2 HG01257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.30+4181_30+4182del others(2): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109609615 | |||||||
| chr2:109610037 | C | G | 65 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(62): Show |
67 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.30+3761G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610037 | |||||||
| chr2:109610095 | G | GT | 67 | a0001c0001t0001g0345 a0001c0001t0002g0006 a0001c0001t0002g0007 others(64): Show |
69 | HG00597.hp1 HG00609.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.30+3702dupA | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | |||||||
| chr2:109610095 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0221 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.30+3693_30+3702dup others(10): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | |||||||
| chr2:109610095 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0004g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.30+3692_30+3702dup others(11): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | |||||||
| chr2:109610095 | G | GTTTTTTT others(21): Show |
1 | a0001c0001t0004g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.30+3702_30+3703ins others(28): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | |||||||
| chr2:109610095 | G | GTTTTTTT others(22): Show |
2 | a0001c0001t0004g0239 a0004c0005t0004g0219 |
2 | HG00639.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.30+3702_30+3703ins others(29): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | |||||||
| chr2:109610095 | G | GTTTTTTT others(38): Show |
1 | a0001c0001t0004g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+3702_30+3703ins others(45): Show |
SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610095 | |||||||
| chr2:109610165 | T | C | 1 | a0001c0001t0009g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.30+3633A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610165 | |||||||
| chr2:109610192 | G | A | 64 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(61): Show |
68 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.30+3606C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610192 | |||||||
| chr2:109610254 | A | T | 4 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0183 others(1): Show |
4 | HG02809.hp2 HG03098.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+3544T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610254 | |||||||
| chr2:109610486 | G | A | 19 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0075 others(16): Show |
20 | HG01167.hp1 HG01243.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+3312C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610486 | |||||||
| chr2:109610490 | G | A | 5 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+3308C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610490 | |||||||
| chr2:109610576 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.30+3222G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610576 | |||||||
| chr2:109610981 | A | C | 8 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(5): Show |
8 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+2817T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610981 | |||||||
| chr2:109610992 | C | T | 26 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(23): Show |
26 | HG00735.hp2 HG01106.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.30+2806G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109610992 | |||||||
| chr2:109611000 | C | T | 1 | a0001c0001t0005g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.30+2798G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611000 | |||||||
| chr2:109611067 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2731G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611067 | |||||||
| chr2:109611068 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2730T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611068 | |||||||
| chr2:109611076 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2722G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611076 | |||||||
| chr2:109611078 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2720G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611078 | |||||||
| chr2:109611079 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2719T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611079 | |||||||
| chr2:109611080 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2718T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611080 | |||||||
| chr2:109611082 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2716T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611082 | |||||||
| chr2:109611083 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2715T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611083 | |||||||
| chr2:109611095 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2703G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611095 | |||||||
| chr2:109611096 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2702G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611096 | |||||||
| chr2:109611101 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2697G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611101 | |||||||
| chr2:109611102 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2696T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611102 | |||||||
| chr2:109611104 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2694G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611104 | |||||||
| chr2:109611106 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2692T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611106 | |||||||
| chr2:109611107 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2691T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611107 | |||||||
| chr2:109611108 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2690A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611108 | |||||||
| chr2:109611113 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2685G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611113 | |||||||
| chr2:109611114 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2684A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611114 | |||||||
| chr2:109611117 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2681T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611117 | |||||||
| chr2:109611119 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2679G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611119 | |||||||
| chr2:109611120 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2678T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611120 | |||||||
| chr2:109611121 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2677T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611121 | |||||||
| chr2:109611122 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2676G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611122 | |||||||
| chr2:109611123 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2675A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611123 | |||||||
| chr2:109611126 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2672T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611126 | |||||||
| chr2:109611127 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2671G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611127 | |||||||
| chr2:109611128 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2670T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611128 | |||||||
| chr2:109611130 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2668G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611130 | |||||||
| chr2:109611131 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2667G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611131 | |||||||
| chr2:109611133 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2665A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611133 | |||||||
| chr2:109611134 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2664T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611134 | |||||||
| chr2:109611137 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2661G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611137 | |||||||
| chr2:109611138 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2660G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611138 | |||||||
| chr2:109611139 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2659T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611139 | |||||||
| chr2:109611140 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2658T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611140 | |||||||
| chr2:109611141 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2657T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611141 | |||||||
| chr2:109611142 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2656T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611142 | |||||||
| chr2:109611143 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2655T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611143 | |||||||
| chr2:109611144 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2654T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611144 | |||||||
| chr2:109611145 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2653A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611145 | |||||||
| chr2:109611148 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2650G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611148 | |||||||
| chr2:109611149 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2649G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611149 | |||||||
| chr2:109611150 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2648G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611150 | |||||||
| chr2:109611152 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2646G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611152 | |||||||
| chr2:109611153 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2645T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611153 | |||||||
| chr2:109611154 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2644T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611154 | |||||||
| chr2:109611155 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2643G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611155 | |||||||
| chr2:109611156 | T | A | 1 | a0001c0001t0003g0069 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.30+2642A>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611156 | |||||||
| chr2:109611156 | T | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2642A>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611156 | |||||||
| chr2:109611314 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2484T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611314 | |||||||
| chr2:109611350 | A | C | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2448T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611350 | |||||||
| chr2:109611351 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2447G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611351 | |||||||
| chr2:109611357 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2441G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611357 | |||||||
| chr2:109611384 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2414T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611384 | |||||||
| chr2:109611385 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2413T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611385 | |||||||
| chr2:109611386 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2412T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611386 | |||||||
| chr2:109611387 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2411T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611387 | |||||||
| chr2:109611389 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2409T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611389 | |||||||
| chr2:109611391 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2407T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611391 | |||||||
| chr2:109611392 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2406T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611392 | |||||||
| chr2:109611396 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2402T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611396 | |||||||
| chr2:109611397 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2401G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611397 | |||||||
| chr2:109611398 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2400T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611398 | |||||||
| chr2:109611399 | G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2399C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611399 | |||||||
| chr2:109611401 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2397G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611401 | |||||||
| chr2:109611409 | G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2389C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611409 | |||||||
| chr2:109611410 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2388T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611410 | |||||||
| chr2:109611412 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2386G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611412 | |||||||
| chr2:109611413 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2385T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611413 | |||||||
| chr2:109611418 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2380G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611418 | |||||||
| chr2:109611424 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2374T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611424 | |||||||
| chr2:109611426 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.30+2372T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611426 | |||||||
| chr2:109611437 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2361T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611437 | |||||||
| chr2:109611459 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2339T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611459 | |||||||
| chr2:109611484 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2314T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611484 | |||||||
| chr2:109611549 | G | A | 3 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 |
3 | NA18968.hp2 NA18995.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.30+2249C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611549 | |||||||
| chr2:109611559 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2239T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611559 | |||||||
| chr2:109611560 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2238G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611560 | |||||||
| chr2:109611561 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2237G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611561 | |||||||
| chr2:109611564 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2234G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611564 | |||||||
| chr2:109611565 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2233G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611565 | |||||||
| chr2:109611567 | G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2231C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611567 | |||||||
| chr2:109611572 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2226T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611572 | |||||||
| chr2:109611581 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2217G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611581 | |||||||
| chr2:109611583 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2215G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611583 | |||||||
| chr2:109611584 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2214G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611584 | |||||||
| chr2:109611585 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2213G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611585 | |||||||
| chr2:109611589 | C | A | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2209G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611589 | |||||||
| chr2:109611590 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2208G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611590 | |||||||
| chr2:109611592 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2206G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611592 | |||||||
| chr2:109611596 | A | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2202T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611596 | |||||||
| chr2:109611597 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2201T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611597 | |||||||
| chr2:109611598 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2200T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611598 | |||||||
| chr2:109611601 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2197T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611601 | |||||||
| chr2:109611609 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2189T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611609 | |||||||
| chr2:109611630 | C | A | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2168G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611630 | |||||||
| chr2:109611632 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2166G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611632 | |||||||
| chr2:109611634 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2164G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611634 | |||||||
| chr2:109611635 | C | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2163G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611635 | |||||||
| chr2:109611637 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2161T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611637 | |||||||
| chr2:109611737 | A | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2061T>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611737 | |||||||
| chr2:109611738 | G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2060C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611738 | |||||||
| chr2:109611739 | C | G | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2059G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611739 | |||||||
| chr2:109611746 | G | T | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+2052C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611746 | |||||||
| chr2:109611753 | C | G | 38 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(35): Show |
39 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.30+2045G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611753 | |||||||
| chr2:109611931 | C | T | 60 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(57): Show |
64 | HG00597.hp1 HG00609.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.30+1867G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611931 | |||||||
| chr2:109611991 | A | G | 346 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(343): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.30+1807T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109611991 | |||||||
| chr2:109612014 | A | G | 10 | a0001c0001t0002g0017 a0001c0001t0002g0167 a0001c0001t0002g0168 others(7): Show |
10 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+1784T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612014 | |||||||
| chr2:109612050 | T | C | 1 | a0001c0001t0002g0091 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.30+1748A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612050 | |||||||
| chr2:109612072 | G | A | 65 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(62): Show |
67 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.30+1726C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612072 | |||||||
| chr2:109612238 | A | G | 1 | a0001c0001t0005g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+1560T>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612238 | |||||||
| chr2:109612307 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.30+1491G>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612307 | |||||||
| chr2:109612679 | C | A | 80 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0106 others(77): Show |
83 | HG00609.hp1 HG00735.hp2 HG01106.hp1 others(80): Show |
intron_variant | MODIFIER | c.30+1119G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612679 | |||||||
| chr2:109612755 | G | A | 1 | a0001c0001t0001g0386 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+1043C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612755 | |||||||
| chr2:109612876 | G | T | 1 | a0001c0001t0006g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+922C>A | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612876 | |||||||
| chr2:109612888 | A | C | 1 | a0001c0001t0010g0243 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.30+910T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612888 | |||||||
| chr2:109612916 | T | C | 23 | a0001c0001t0004g0180 a0001c0001t0004g0218 a0001c0001t0004g0220 others(20): Show |
23 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.30+882A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612916 | |||||||
| chr2:109612945 | T | C | 1 | a0001c0001t0004g0239 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.30+853A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109612945 | |||||||
| chr2:109613021 | C | A | 1 | a0001c0001t0004g0240 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+777G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613021 | |||||||
| chr2:109613259 | G | A | 9 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(6): Show |
9 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+539C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613259 | |||||||
| chr2:109613290 | G | GA | 8 | a0001c0001t0001g0387 a0001c0001t0001g0388 a0001c0001t0001g0389 others(5): Show |
8 | HG00741.hp2 HG01433.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+507dupT | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613290 | |||||||
| chr2:109613294 | A | C | 1 | a0001c0001t0004g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.30+504T>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613294 | |||||||
| chr2:109613318 | G | A | 64 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.30+480C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613318 | |||||||
| chr2:109613402 | G | C | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+396C>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613402 | |||||||
| chr2:109613517 | T | C | 1 | a0001c0001t0001g0390 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.30+281A>G | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613517 | |||||||
| chr2:109613551 | C | G | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+247G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613551 | |||||||
| chr2:109613670 | G | A | 1 | a0001c0001t0002g0179 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+128C>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613670 | |||||||
| chr2:109613671 | C | A | 64 | a0001c0001t0002g0190 a0001c0001t0002g0204 a0001c0001t0002g0213 others(61): Show |
65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.30+127G>T | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613671 | |||||||
| chr2:109613756 | C | G | 1 | a0001c0001t0003g0014 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.30+42G>C | SEPTIN10 | ENSG00000186522.15 | transcript | ENST00000397712.7 | protein_coding | 1/10 | chr2 | 109613756 |