Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55752 |
| ensemblid | ENSG00000138758.12 |
| hgncid | 25589 |
| symbol | SEPTIN11 |
| name | septin 11 |
| refseq_nuc | NM_018243.4 |
| refseq_prot | NP_060713.1 |
| ensembl_nuc | ENST00000264893.11 |
| ensembl_prot | ENSP00000264893.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 76949752 |
| end | 77038615 |
| strand | + |
| ver | v1.2 |
| region | chr4:76949752-77038615 |
| region5000 | chr4:76944752-77043615 |
| regionname0 | SEPTIN11_chr4_76949752_77038615 |
| regionname5000 | SEPTIN11_chr4_76944752_77043615 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 429 | 368 | 81 | 58 | 171 | 14 | 42 | 131 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | MAVAV others(424): Show |
chr4 | 76944752 | 77043615 |
| a0002 | 0/0 | 429 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | MAVAV others(424): Show |
chr4 | 76944752 | 77043615 |
| a0003 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | MAVAV others(424): Show |
chr4 | 76944752 | 77043615 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1287 | 368 | 81 | 58 | 171 | 14 | 42 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | ATGGC others(1282): Show |
chr4 | 76944752 | 77043615 | ||
| a0002c0003 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | ATGGC others(1282): Show |
chr4 | 76944752 | 77043615 | ||
| a0003c0002 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | ATGGC others(1282): Show |
chr4 | 76944752 | 77043615 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5545 | 88 | 21 | 13 | 34 | 4 | 16 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0002 | 0/0 | 5545 | 77 | 3 | 14 | 50 | 3 | 7 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0003 | 0/1 | 5545 | 38 | 8 | 9 | 13 | 2 | 5 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0004 | 1/0 | 5545 | 30 | 3 | 7 | 13 | 2 | 4 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0005 | 0/0 | 5545 | 27 | 0 | 6 | 13 | 2 | 6 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0006 | 0/0 | 5545 | 24 | 9 | 3 | 12 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0007 | 0/0 | 5539 | 24 | 2 | 1 | 21 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5534): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0008 | 0/0 | 5541 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5536): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0009 | 0/0 | 5545 | 5 | 5 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0010 | 0/0 | 5539 | 5 | 0 | 3 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5534): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0011 | 0/0 | 5545 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0012 | 0/0 | 5545 | 4 | 1 | 1 | 0 | 0 | 2 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0013 | 0/0 | 5545 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0014 | 0/0 | 5539 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5534): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0015 | 0/0 | 5545 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0016 | 0/0 | 5545 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0017 | 0/0 | 5545 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0018 | 0/0 | 5545 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0019 | 0/0 | 5540 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5535): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0020 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0021 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0022 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0023 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0024 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0025 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0026 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0027 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0028 | 0/0 | 5545 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0029 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5534): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0030 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0031 | 0/0 | 5545 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0032 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0033 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0034 | 0/0 | 5545 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0035 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0036 | 0/0 | 5545 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0037 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5536): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0038 | 0/0 | 5539 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5534): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0039 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5534): Show |
chr4 | 76944752 | 77043615 |
| a0001c0001t0040 | 0/0 | 5545 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| a0002c0003t0008 | 0/0 | 5541 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5536): Show |
chr4 | 76944752 | 77043615 |
| a0003c0002t0005 | 0/0 | 5545 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | GAGCA others(5540): Show |
chr4 | 76944752 | 77043615 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0007g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0010g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0010g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0010g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0011g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0011g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0011g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0012g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0012g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0014g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0014g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0015g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0015g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0016g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0016g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0018g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0018g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0019g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0019g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0020g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0022g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0023g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0024g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0025g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0026g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0027g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0028g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0029g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0030g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0031g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0032g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0033g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0034g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0035g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0036g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0037g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0038g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0039g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0001c0001t0040g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0002c0003t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| a0003c0002t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | GBR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0021 | EUR | GBR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | GBR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | GBR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0309 | EUR | FIN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | FIN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0047 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00544 | hp2 | a0001 | c0001 | t0007 | g0171 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00673 | hp1 | a0001 | c0001 | t0030 | g0134 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | CHS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0033 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0322 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0221 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01109 | hp1 | a0001 | c0001 | t0012 | g0242 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0194 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0175 | AMR | PUR | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01257 | hp2 | a0001 | c0001 | t0034 | g0125 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0197 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0019 | EUR | IBS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0198 | EUR | IBS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0200 | EUR | IBS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01884 | hp1 | a0001 | c0001 | t0038 | g0101 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0086 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01891 | hp2 | a0002 | c0003 | t0008 | g0237 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01943 | hp1 | a0001 | c0001 | t0010 | g0035 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01975 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0050 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0185 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02015 | hp2 | a0001 | c0001 | t0015 | g0054 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02055 | hp2 | a0001 | c0001 | t0027 | g0264 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02056 | hp1 | a0001 | c0001 | t0016 | g0274 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0181 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02132 | hp2 | a0001 | c0001 | t0011 | g0041 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0084 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02148 | hp1 | a0001 | c0001 | t0010 | g0036 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | CDX | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CDX | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02165 | hp1 | a0001 | c0001 | t0011 | g0048 | EAS | CDX | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CDX | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02258 | hp1 | a0001 | c0001 | t0036 | g0206 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02258 | hp2 | a0001 | c0001 | t0013 | g0097 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0065 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0098 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0085 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0232 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0073 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02738 | hp2 | a0001 | c0001 | t0028 | g0222 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0243 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02818 | hp2 | a0001 | c0001 | t0018 | g0162 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0063 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02965 | hp1 | a0001 | c0001 | t0033 | g0167 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0099 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0029 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03017 | hp1 | a0001 | c0001 | t0012 | g0220 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03017 | hp2 | a0001 | c0001 | t0031 | g0105 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0245 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0092 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0231 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0241 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03453 | hp1 | a0001 | c0001 | t0014 | g0100 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03453 | hp2 | a0001 | c0001 | t0026 | g0313 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03486 | hp2 | a0001 | c0001 | t0018 | g0161 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0317 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0236 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03654 | hp2 | a0001 | c0001 | t0012 | g0132 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0216 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0165 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0215 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0258 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | BEB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0214 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0217 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | STU | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18522 | hp1 | a0001 | c0001 | t0014 | g0093 | AFR | YRI | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18522 | hp2 | a0001 | c0001 | t0024 | g0315 | AFR | YRI | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0304 | EAS | CHB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CHB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0169 | EAS | CHB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18943 | hp2 | a0001 | c0001 | t0007 | g0191 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0170 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0042 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18951 | hp2 | a0001 | c0001 | t0005 | g0224 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18960 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18962 | hp2 | a0001 | c0001 | t0016 | g0284 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18970 | hp1 | a0001 | c0001 | t0010 | g0089 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0178 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18990 | hp1 | a0001 | c0001 | t0010 | g0288 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18990 | hp2 | a0001 | c0001 | t0032 | g0193 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18998 | hp2 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19003 | hp2 | a0001 | c0001 | t0039 | g0188 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19004 | hp2 | a0001 | c0001 | t0007 | g0192 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0030 | AFR | LWK | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0064 | AFR | LWK | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | LWK | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19043 | hp2 | a0001 | c0001 | t0022 | g0028 | AFR | LWK | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19055 | hp2 | a0003 | c0002 | t0005 | g0225 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0044 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19064 | hp1 | a0001 | c0001 | t0035 | g0113 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19072 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19076 | hp1 | a0001 | c0001 | t0015 | g0055 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0226 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19087 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0062 | AFR | YRI | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ASW | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ASW | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0332 | EUR | TSI | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA20752 | hp2 | a0001 | c0001 | t0040 | g0154 | EUR | TSI | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | GIH | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | GIH | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0078 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02559 | hp1 | a0001 | c0001 | t0037 | g0163 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03471 | hp1 | a0001 | c0001 | t0019 | g0166 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG06807 | hp1 | a0001 | c0001 | t0029 | g0261 | AFR | USA | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0146 | AFR | USA | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0257 | REF | REF | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0201 | REF | REF | SEPTIN11_chr4_76944752_77043615 | SEPTIN11 | chr4 | 76944752 | 77043615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:77005780 | A | T | 1 | a0002 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.322A>T | p.Ile108Leu | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/10 | 474/5545 | 322/1290 | 108/429 | chr4 | 77005780 | |||
| chr4:77020591 | C | G | 1 | a0003 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.874C>G | p.Arg292Gly | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/10 | 1026/5545 | 874/1290 | 292/429 | chr4 | 77020591 | |||
| chr4:77020592 | G | C | 1 | a0003 | 1 | NA19055.hp2 | missense_variant | MODERATE | c.875G>C | p.Arg292Pro | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/10 | 1027/5545 | 875/1290 | 292/429 | chr4 | 77020592 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76949781 | G | C | 1 | a0001c0001t0020 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-123G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/10 | 123 | chr4 | 76949781 | ||||||
| chr4:76949786 | C | T | 1 | a0001c0001t0040 | 1 | NA20752.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/10 | 118 | chr4 | 76949786 | ||||||
| chr4:76949863 | T | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
5_prime_UTR_variant | MODIFIER | c.-41T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/10 | 41 | chr4 | 76949863 | ||||||
| chr4:77034590 | GTTTTA | G | 10 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(7): Show |
44 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*98_*102delATTTT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 98 | INFO_REALIGN_3_PRIME | chr4 | 77034590 | |||||
| chr4:77034601 | T | C | 1 | a0001c0001t0015 | 2 | HG02015.hp2 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*89T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 89 | chr4 | 77034601 | ||||||
| chr4:77034807 | C | T | 4 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0014 others(1): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*295C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 295 | chr4 | 77034807 | ||||||
| chr4:77034873 | C | T | 1 | a0001c0001t0011 | 4 | HG02132.hp2 HG02165.hp1 NA19010.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*361C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 361 | chr4 | 77034873 | ||||||
| chr4:77035015 | A | G | 1 | a0001c0001t0036 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 503 | chr4 | 77035015 | ||||||
| chr4:77035146 | A | G | 1 | a0001c0001t0035 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*634A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 634 | chr4 | 77035146 | ||||||
| chr4:77035274 | T | A | 1 | a0001c0001t0017 | 2 | HG02451.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*762T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 762 | chr4 | 77035274 | ||||||
| chr4:77035295 | T | A | 10 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(7): Show |
44 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*783T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 783 | chr4 | 77035295 | ||||||
| chr4:77035558 | A | G | 1 | a0001c0001t0028 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1046A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1046 | chr4 | 77035558 | ||||||
| chr4:77035834 | C | T | 2 | a0001c0001t0029 a0001c0001t0038 |
2 | HG01884.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1322C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1322 | chr4 | 77035834 | ||||||
| chr4:77036037 | G | A | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | HG02970.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1525G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1525 | chr4 | 77036037 | ||||||
| chr4:77036094 | C | T | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1582C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1582 | chr4 | 77036094 | ||||||
| chr4:77036096 | A | T | 3 | a0001c0001t0008 a0001c0001t0037 a0002c0003t0008 |
7 | HG01891.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1584A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1584 | chr4 | 77036096 | ||||||
| chr4:77036136 | T | G | 4 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0014 others(1): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1624T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1624 | chr4 | 77036136 | ||||||
| chr4:77036195 | T | C | 1 | a0001c0001t0009 | 5 | HG02280.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1683T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 1683 | chr4 | 77036195 | ||||||
| chr4:77036580 | T | G | 1 | a0001c0001t0023 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2068T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2068 | chr4 | 77036580 | ||||||
| chr4:77036650 | C | CT | 3 | a0001c0001t0008 a0001c0001t0037 a0002c0003t0008 |
7 | HG01891.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2148dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2149 | INFO_REALIGN_3_PRIME | chr4 | 77036650 | |||||
| chr4:77036660 | T | A | 6 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0021 others(3): Show |
35 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2148T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2148 | chr4 | 77036660 | ||||||
| chr4:77036661 | A | T | 9 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(6): Show |
43 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2149A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2149 | chr4 | 77036661 | ||||||
| chr4:77036662 | A | T | 6 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0014 others(3): Show |
35 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2150A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2150 | chr4 | 77036662 | ||||||
| chr4:77036757 | CT | C | 10 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(7): Show |
44 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2252delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2252 | INFO_REALIGN_3_PRIME | chr4 | 77036757 | |||||
| chr4:77036840 | A | G | 1 | a0001c0001t0034 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2328A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2328 | chr4 | 77036840 | ||||||
| chr4:77036977 | G | A | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(32): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*2465G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2465 | chr4 | 77036977 | ||||||
| chr4:77037049 | C | T | 1 | a0001c0001t0033 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2537C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2537 | chr4 | 77037049 | ||||||
| chr4:77037148 | G | A | 9 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0011 others(6): Show |
67 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2636G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2636 | chr4 | 77037148 | ||||||
| chr4:77037174 | G | A | 1 | a0001c0001t0026 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2662 | chr4 | 77037174 | ||||||
| chr4:77037232 | C | T | 3 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0039 |
30 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2720C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2720 | chr4 | 77037232 | ||||||
| chr4:77037337 | G | A | 1 | a0001c0001t0019 | 2 | HG03471.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2825G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2825 | chr4 | 77037337 | ||||||
| chr4:77037358 | C | CA | 4 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0037 others(1): Show |
9 | HG01891.hp2 HG02145.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2858dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 2859 | INFO_REALIGN_3_PRIME | chr4 | 77037358 | |||||
| chr4:77037612 | A | G | 36 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(33): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*3100A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 3100 | chr4 | 77037612 | ||||||
| chr4:77037900 | A | G | 1 | a0001c0001t0018 | 2 | HG02818.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3388A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 3388 | chr4 | 77037900 | ||||||
| chr4:77038003 | G | A | 1 | a0001c0001t0031 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3491G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 3491 | chr4 | 77038003 | ||||||
| chr4:77038195 | T | C | 2 | a0001c0001t0019 a0001c0001t0024 |
3 | HG03471.hp1 HG03516.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3683T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 3683 | chr4 | 77038195 | ||||||
| chr4:77038585 | C | T | 2 | a0001c0001t0025 a0001c0001t0032 |
2 | NA18990.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4073C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 4073 | chr4 | 77038585 | ||||||
| chr4:77038612 | A | G | 1 | a0001c0001t0029 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4100A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 10/10 | 4100 | chr4 | 77038612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:76950016 | CG | C | 67 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0003g0005 others(64): Show |
71 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.27+89delG | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76950016 | ||||||
| chr4:76950034 | C | CGCG | 97 | a0001c0001t0001g0025 a0001c0001t0001g0247 a0001c0001t0001g0248 others(94): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.27+114_27+116dupGC others(1): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76950034 | ||||||
| chr4:76950043 | G | C | 1 | a0001c0001t0006g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27+113G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950043 | |||||||
| chr4:76950182 | C | A | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0021g0029 others(2): Show |
5 | HG02723.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+252C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950182 | |||||||
| chr4:76950190 | T | C | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+260T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950190 | |||||||
| chr4:76950275 | G | A | 67 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0003g0005 others(64): Show |
71 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.27+345G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950275 | |||||||
| chr4:76950343 | C | G | 4 | a0001c0001t0002g0022 a0001c0001t0012g0241 a0001c0001t0012g0242 others(1): Show |
5 | HG01109.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+413C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950343 | |||||||
| chr4:76950443 | C | T | 13 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(10): Show |
13 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.27+513C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950443 | |||||||
| chr4:76950470 | T | G | 1 | a0001c0001t0003g0244 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.27+540T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950470 | |||||||
| chr4:76950517 | G | C | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0008g0245 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+587G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950517 | |||||||
| chr4:76950720 | A | G | 1 | a0001c0001t0010g0089 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.27+790A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950720 | |||||||
| chr4:76950746 | C | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0008g0245 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+816C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950746 | |||||||
| chr4:76950910 | C | T | 3 | a0001c0001t0002g0238 a0001c0001t0002g0240 a0001c0001t0004g0239 |
3 | HG00423.hp1 NA19000.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.27+980C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950910 | |||||||
| chr4:76950916 | A | G | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0008g0245 others(1): Show |
4 | HG02622.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+986A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950916 | |||||||
| chr4:76950935 | C | T | 161 | a0001c0001t0001g0025 a0001c0001t0001g0207 a0001c0001t0001g0208 others(158): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.27+1005C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76950935 | |||||||
| chr4:76951169 | C | T | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0021g0029 others(2): Show |
5 | HG02723.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+1239C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951169 | |||||||
| chr4:76951182 | C | A | 2 | a0001c0001t0002g0091 a0001c0001t0007g0090 |
2 | HG02071.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.27+1252C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951182 | |||||||
| chr4:76951204 | C | T | 1 | a0002c0003t0008g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.27+1274C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951204 | |||||||
| chr4:76951231 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.27+1301G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951231 | |||||||
| chr4:76951282 | T | C | 118 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0002g0001 others(115): Show |
133 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.27+1352T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951282 | |||||||
| chr4:76951313 | C | G | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.27+1383C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951313 | |||||||
| chr4:76951321 | G | A | 10 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0003g0031 others(7): Show |
10 | HG02622.hp2 HG02723.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.27+1391G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951321 | |||||||
| chr4:76951391 | T | A | 1 | a0001c0001t0006g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.27+1461T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951391 | |||||||
| chr4:76951605 | T | G | 7 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(4): Show |
7 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+1675T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951605 | |||||||
| chr4:76951777 | A | G | 1 | a0001c0001t0001g0337 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.27+1847A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951777 | |||||||
| chr4:76951982 | C | A | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | NA19000.hp2 NA19057.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.27+2052C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76951982 | |||||||
| chr4:76952115 | T | TGGGGGGG others(36): Show |
1 | a0001c0001t0002g0160 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.27+2188_27+2189ins others(43): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76952115 | ||||||
| chr4:76952121 | A | C | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+2191A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952121 | |||||||
| chr4:76952256 | T | C | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.27+2326T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952256 | |||||||
| chr4:76952275 | A | G | 94 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(91): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.27+2345A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952275 | |||||||
| chr4:76952288 | G | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+2358G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952288 | |||||||
| chr4:76952670 | G | C | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.27+2740G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952670 | |||||||
| chr4:76952841 | A | T | 1 | a0001c0001t0006g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.27+2911A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952841 | |||||||
| chr4:76952981 | A | G | 1 | a0001c0001t0001g0323 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.27+3051A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952981 | |||||||
| chr4:76952991 | G | A | 31 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(28): Show |
37 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.27+3061G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76952991 | |||||||
| chr4:76953210 | G | A | 1 | a0001c0001t0005g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.27+3280G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953210 | |||||||
| chr4:76953449 | T | C | 320 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(317): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.27+3519T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953449 | |||||||
| chr4:76953520 | C | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.27+3590C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953520 | |||||||
| chr4:76953540 | G | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+3610G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953540 | |||||||
| chr4:76953603 | T | C | 1 | a0001c0001t0006g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.27+3673T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953603 | |||||||
| chr4:76953712 | G | A | 96 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.27+3782G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953712 | |||||||
| chr4:76953774 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.27+3844G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953774 | |||||||
| chr4:76953879 | C | T | 1 | a0001c0001t0003g0322 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.27+3949C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76953879 | |||||||
| chr4:76954002 | A | G | 76 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(73): Show |
83 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.27+4072A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954002 | |||||||
| chr4:76954066 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.27+4136A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954066 | |||||||
| chr4:76954208 | T | C | 43 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(40): Show |
47 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.27+4278T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954208 | |||||||
| chr4:76954226 | G | A | 1 | a0001c0001t0032g0193 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.27+4296G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954226 | |||||||
| chr4:76954310 | T | G | 1 | a0001c0001t0004g0103 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+4380T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954310 | |||||||
| chr4:76954395 | A | C | 1 | a0001c0001t0001g0321 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.27+4465A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954395 | |||||||
| chr4:76954566 | G | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+4636G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954566 | |||||||
| chr4:76954746 | C | T | 14 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(11): Show |
14 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.27+4816C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954746 | |||||||
| chr4:76954765 | C | T | 22 | a0001c0001t0001g0218 a0001c0001t0005g0003 a0001c0001t0005g0019 others(19): Show |
28 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.27+4835C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76954765 | |||||||
| chr4:76954983 | AT | A | 305 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(302): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.27+5062delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76954983 | ||||||
| chr4:76955022 | A | T | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+5092A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955022 | |||||||
| chr4:76955164 | A | C | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.27+5234A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955164 | |||||||
| chr4:76955193 | G | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0025g0030 |
3 | HG02723.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.27+5263G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955193 | |||||||
| chr4:76955433 | A | T | 28 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(25): Show |
31 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.27+5503A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955433 | |||||||
| chr4:76955503 | G | A | 3 | a0001c0001t0003g0037 a0001c0001t0010g0035 a0001c0001t0010g0036 |
3 | HG01943.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.27+5573G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955503 | |||||||
| chr4:76955686 | T | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.27+5756T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955686 | |||||||
| chr4:76955808 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0032 |
2 | HG02723.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.27+5878C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76955808 | |||||||
| chr4:76956167 | T | C | 76 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(73): Show |
83 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.27+6237T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956167 | |||||||
| chr4:76956400 | C | G | 1 | a0001c0001t0005g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.27+6470C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956400 | |||||||
| chr4:76956455 | G | A | 1 | a0001c0001t0022g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.27+6525G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956455 | |||||||
| chr4:76956729 | G | T | 2 | a0001c0001t0003g0087 a0001c0001t0006g0088 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.27+6799G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956729 | |||||||
| chr4:76956910 | T | A | 1 | a0001c0001t0002g0168 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.27+6980T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956910 | |||||||
| chr4:76956962 | A | ATG | 10 | a0001c0001t0002g0205 a0001c0001t0005g0020 a0001c0001t0005g0219 others(7): Show |
11 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+7063_27+7064dup others(2): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTG | 10 | a0001c0001t0001g0061 a0001c0001t0001g0207 a0001c0001t0001g0208 others(7): Show |
11 | HG00735.hp1 HG02071.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+7061_27+7064dup others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTG | 34 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0262 others(31): Show |
39 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.27+7059_27+7064dup others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(1): Show |
26 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0266 others(23): Show |
30 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.27+7057_27+7064dup others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(3): Show |
77 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0273 others(74): Show |
84 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.27+7055_27+7064dup others(10): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(5): Show |
36 | a0001c0001t0001g0253 a0001c0001t0001g0259 a0001c0001t0001g0292 others(33): Show |
38 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.27+7053_27+7064dup others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(7): Show |
24 | a0001c0001t0001g0034 a0001c0001t0001g0254 a0001c0001t0001g0305 others(21): Show |
25 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.27+7051_27+7064dup others(14): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(9): Show |
10 | a0001c0001t0001g0255 a0001c0001t0001g0314 a0001c0001t0002g0158 others(7): Show |
10 | HG02135.hp2 HG02155.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+7049_27+7064dup others(16): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(11): Show |
4 | a0001c0001t0001g0256 a0001c0001t0001g0318 a0001c0001t0002g0159 others(1): Show |
4 | HG02717.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+7047_27+7064dup others(18): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(15): Show |
4 | a0001c0001t0001g0319 a0001c0001t0008g0083 a0001c0001t0008g0084 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+7043_27+7064dup others(22): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | A | ATGTGTGT others(17): Show |
1 | a0001c0001t0006g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.27+7041_27+7064dup others(24): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956962 | ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+7055_27+7064del others(10): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956962 | ||||||
| chr4:76956993 | T | TGTGAGA | 3 | a0001c0001t0013g0097 a0001c0001t0017g0098 a0001c0001t0017g0099 |
3 | HG02258.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.27+7064_27+7065ins others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGA | 25 | a0001c0001t0003g0037 a0001c0001t0005g0056 a0001c0001t0006g0006 others(22): Show |
27 | HG00544.hp1 HG01943.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.27+7064_27+7065ins others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(1): Show |
10 | a0001c0001t0003g0008 a0001c0001t0003g0031 a0001c0001t0003g0032 others(7): Show |
11 | HG00738.hp1 HG01884.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+7064_27+7065ins others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(3): Show |
24 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(21): Show |
27 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.27+7064_27+7065ins others(10): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0004g0102 a0001c0001t0007g0190 a0001c0001t0007g0191 |
3 | HG02559.hp2 NA18943.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.27+7064_27+7065ins others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(7): Show |
2 | a0001c0001t0007g0192 a0001c0001t0018g0161 |
2 | HG03486.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.27+7064_27+7065ins others(14): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0247 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.27+7064_27+7065ins others(18): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0018g0162 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.27+7064_27+7065ins others(18): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.27+7064_27+7065ins others(20): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956993 | TGA | T | 3 | a0001c0001t0001g0260 a0001c0001t0004g0014 a0001c0001t0004g0164 |
4 | HG00609.hp1 HG02027.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+7076_27+7077del others(2): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76956993 | ||||||
| chr4:76956995 | A | T | 219 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(216): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.27+7065A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956995 | |||||||
| chr4:76956997 | A | T | 141 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(138): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.27+7067A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956997 | |||||||
| chr4:76956999 | A | T | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.27+7069A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76956999 | |||||||
| chr4:76957001 | A | T | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.27+7071A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957001 | |||||||
| chr4:76957003 | A | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.27+7073A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957003 | |||||||
| chr4:76957005 | A | T | 129 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(126): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.27+7075A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957005 | |||||||
| chr4:76957008 | C | G | 1 | a0001c0001t0002g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.27+7078C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957008 | |||||||
| chr4:76957156 | G | C | 1 | a0001c0001t0031g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.27+7226G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957156 | |||||||
| chr4:76957239 | T | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.27+7309T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957239 | |||||||
| chr4:76957368 | G | A | 80 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.27+7438G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957368 | |||||||
| chr4:76957407 | C | T | 43 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(40): Show |
47 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.27+7477C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957407 | |||||||
| chr4:76957408 | G | A | 5 | a0001c0001t0003g0087 a0001c0001t0006g0077 a0001c0001t0006g0078 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+7478G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957408 | |||||||
| chr4:76957940 | A | G | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+8010A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76957940 | |||||||
| chr4:76958049 | A | G | 76 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(73): Show |
83 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.27+8119A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958049 | |||||||
| chr4:76958061 | A | G | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+8131A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958061 | |||||||
| chr4:76958107 | C | T | 1 | a0001c0001t0026g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27+8177C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958107 | |||||||
| chr4:76958159 | G | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.27+8229G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958159 | |||||||
| chr4:76958162 | G | A | 15 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+8232G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958162 | |||||||
| chr4:76958330 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.27+8400A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958330 | |||||||
| chr4:76958390 | C | G | 2 | a0001c0001t0002g0091 a0001c0001t0007g0090 |
2 | HG02071.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.27+8460C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958390 | |||||||
| chr4:76958594 | T | C | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.27+8664T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958594 | |||||||
| chr4:76958873 | G | A | 1 | a0001c0001t0032g0193 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.27+8943G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76958873 | |||||||
| chr4:76959040 | G | A | 96 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.27+9110G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959040 | |||||||
| chr4:76959044 | A | T | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.27+9114A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959044 | |||||||
| chr4:76959190 | G | A | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.27+9260G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959190 | |||||||
| chr4:76959229 | T | C | 1 | a0001c0001t0005g0223 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.27+9299T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959229 | |||||||
| chr4:76959251 | A | G | 1 | a0001c0001t0005g0056 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.27+9321A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959251 | |||||||
| chr4:76959253 | G | GT | 33 | a0001c0001t0001g0265 a0001c0001t0001g0303 a0001c0001t0002g0142 others(30): Show |
36 | HG00621.hp1 HG00673.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.27+9338dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76959253 | ||||||
| chr4:76959268 | TA | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0210 a0001c0001t0001g0291 others(3): Show |
7 | HG00738.hp1 HG02451.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+9343delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76959268 | ||||||
| chr4:76959269 | A | T | 202 | a0001c0001t0001g0034 a0001c0001t0001g0207 a0001c0001t0001g0208 others(199): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.27+9339A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959269 | |||||||
| chr4:76959270 | A | T | 208 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(205): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.27+9340A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959270 | |||||||
| chr4:76959284 | T | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.27+9354T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959284 | |||||||
| chr4:76959286 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.27+9356T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959286 | |||||||
| chr4:76959310 | T | C | 28 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(25): Show |
31 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.27+9380T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959310 | |||||||
| chr4:76959395 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.27+9465T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959395 | |||||||
| chr4:76959426 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.27+9496G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959426 | |||||||
| chr4:76959496 | G | T | 1 | a0001c0001t0002g0141 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.27+9566G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959496 | |||||||
| chr4:76959615 | A | C | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+9685A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959615 | |||||||
| chr4:76959694 | T | A | 94 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(91): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.27+9764T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959694 | |||||||
| chr4:76959704 | TAATC | T | 15 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+9777_27+9780del others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76959704 | ||||||
| chr4:76959739 | T | C | 76 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(73): Show |
83 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.27+9809T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959739 | |||||||
| chr4:76959953 | G | C | 1 | a0001c0001t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.27+10023G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959953 | |||||||
| chr4:76959984 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.27+10054G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76959984 | |||||||
| chr4:76960033 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.27+10103C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76960033 | |||||||
| chr4:76960157 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.27+10227C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76960157 | |||||||
| chr4:76960501 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.27+10571A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76960501 | |||||||
| chr4:76960518 | T | A | 1 | a0001c0001t0005g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.27+10588T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76960518 | |||||||
| chr4:76960554 | C | T | 320 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(317): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.27+10624C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76960554 | |||||||
| chr4:76960622 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.27+10692T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76960622 | |||||||
| chr4:76961000 | A | T | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.27+11070A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961000 | |||||||
| chr4:76961077 | A | G | 8 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+11147A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961077 | |||||||
| chr4:76961200 | T | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.27+11270T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961200 | |||||||
| chr4:76961278 | C | T | 93 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(90): Show |
104 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.27+11348C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961278 | |||||||
| chr4:76961307 | G | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.27+11377G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961307 | |||||||
| chr4:76961491 | A | G | 1 | a0001c0001t0004g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.27+11561A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961491 | |||||||
| chr4:76961536 | G | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0059 others(2): Show |
6 | HG02080.hp2 NA18957.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+11606G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961536 | |||||||
| chr4:76961625 | G | A | 1 | a0001c0001t0004g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.27+11695G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961625 | |||||||
| chr4:76961808 | C | G | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.27+11878C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76961808 | |||||||
| chr4:76962345 | G | A | 3 | a0001c0001t0001g0275 a0001c0001t0014g0092 a0001c0001t0014g0093 |
3 | HG03130.hp2 NA18522.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.27+12415G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76962345 | |||||||
| chr4:76962371 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.27+12441C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76962371 | |||||||
| chr4:76962412 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.27+12482T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76962412 | |||||||
| chr4:76962515 | C | T | 5 | a0001c0001t0003g0087 a0001c0001t0006g0077 a0001c0001t0006g0078 others(2): Show |
5 | HG02109.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+12585C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76962515 | |||||||
| chr4:76962755 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.27+12825G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76962755 | |||||||
| chr4:76963146 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.27+13216T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76963146 | |||||||
| chr4:76963513 | C | T | 3 | a0001c0001t0006g0231 a0001c0001t0006g0233 a0002c0003t0008g0237 |
3 | HG01891.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.27+13583C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76963513 | |||||||
| chr4:76963577 | A | G | 2 | a0001c0001t0015g0054 a0001c0001t0015g0055 |
2 | HG02015.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.27+13647A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76963577 | |||||||
| chr4:76964010 | G | T | 42 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(39): Show |
46 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.27+14080G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964010 | |||||||
| chr4:76964024 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.27+14094A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964024 | |||||||
| chr4:76964244 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.27+14314A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964244 | |||||||
| chr4:76964298 | A | AT | 23 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0095 others(20): Show |
26 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.27+14387dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76964298 | ||||||
| chr4:76964298 | ATT | A | 75 | a0001c0001t0001g0234 a0001c0001t0002g0168 a0001c0001t0002g0176 others(72): Show |
82 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.27+14386_27+14387d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76964298 | ||||||
| chr4:76964298 | ATTT | A | 9 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0320 others(6): Show |
9 | HG02622.hp2 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+14385_27+14387d others(5): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76964298 | ||||||
| chr4:76964298 | ATTTT | A | 127 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(124): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.27+14384_27+14387d others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76964298 | ||||||
| chr4:76964388 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.27+14458C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964388 | |||||||
| chr4:76964432 | T | C | 5 | a0001c0001t0009g0062 a0001c0001t0009g0063 a0001c0001t0009g0064 others(2): Show |
5 | HG02280.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+14502T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964432 | |||||||
| chr4:76964893 | T | C | 31 | a0001c0001t0001g0234 a0001c0001t0002g0168 a0001c0001t0002g0176 others(28): Show |
34 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.27+14963T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964893 | |||||||
| chr4:76964943 | C | G | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+15013C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76964943 | |||||||
| chr4:76965450 | C | CA | 10 | a0001c0001t0001g0303 a0001c0001t0002g0095 a0001c0001t0002g0116 others(7): Show |
12 | HG00099.hp2 HG00741.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.27+15536dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76965450 | ||||||
| chr4:76965468 | G | C | 8 | a0001c0001t0002g0133 a0001c0001t0002g0155 a0001c0001t0002g0156 others(5): Show |
8 | HG00423.hp1 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+15538G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76965468 | |||||||
| chr4:76965582 | ATACT | A | 28 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(25): Show |
31 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.27+15655_27+15658d others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76965582 | ||||||
| chr4:76965794 | T | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0135 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.27+15864T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76965794 | |||||||
| chr4:76965900 | G | T | 1 | a0001c0001t0003g0008 | 2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.27+15970G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76965900 | |||||||
| chr4:76965969 | ACTTTCTG others(15): Show |
A | 1 | a0001c0001t0001g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+16045_27+16066d others(24): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76965969 | ||||||
| chr4:76966467 | CT | C | 8 | a0001c0001t0001g0291 a0001c0001t0002g0011 a0001c0001t0002g0012 others(5): Show |
10 | HG02976.hp1 NA18612.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.27+16550delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76966467 | ||||||
| chr4:76966523 | C | T | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+16593C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76966523 | |||||||
| chr4:76966807 | T | A | 1 | a0001c0001t0026g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27+16877T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76966807 | |||||||
| chr4:76966812 | C | T | 1 | a0001c0001t0031g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.27+16882C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76966812 | |||||||
| chr4:76966829 | A | G | 1 | a0001c0001t0012g0132 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.27+16899A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76966829 | |||||||
| chr4:76966912 | T | C | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.27+16982T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76966912 | |||||||
| chr4:76967104 | C | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.27+17174C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76967104 | |||||||
| chr4:76967105 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.27+17175G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76967105 | |||||||
| chr4:76967414 | T | C | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+17484T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76967414 | |||||||
| chr4:76967740 | GTTT | G | 131 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(128): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.27+17821_27+17823d others(5): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76967740 | ||||||
| chr4:76968048 | T | C | 31 | a0001c0001t0001g0234 a0001c0001t0002g0168 a0001c0001t0002g0176 others(28): Show |
34 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.27+18118T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968048 | |||||||
| chr4:76968275 | T | A | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+18345T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968275 | |||||||
| chr4:76968346 | T | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0305 a0001c0001t0023g0304 |
3 | HG02074.hp2 HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.27+18416T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968346 | |||||||
| chr4:76968357 | T | A | 1 | a0001c0001t0026g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.27+18427T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968357 | |||||||
| chr4:76968484 | A | G | 1 | a0001c0001t0040g0154 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.27+18554A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968484 | |||||||
| chr4:76968545 | C | A | 32 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0037 others(29): Show |
36 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.27+18615C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968545 | |||||||
| chr4:76968772 | A | G | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+18842A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968772 | |||||||
| chr4:76968841 | T | C | 77 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(74): Show |
84 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.27+18911T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76968841 | |||||||
| chr4:76969063 | A | G | 4 | a0001c0001t0013g0097 a0001c0001t0014g0100 a0001c0001t0017g0098 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+19133A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969063 | |||||||
| chr4:76969235 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0332 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.27+19305G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969235 | |||||||
| chr4:76969506 | A | C | 2 | a0001c0001t0004g0102 a0001c0001t0038g0101 |
2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.27+19576A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969506 | |||||||
| chr4:76969590 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.27+19660C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969590 | |||||||
| chr4:76969640 | G | T | 34 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(31): Show |
40 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.27+19710G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969640 | |||||||
| chr4:76969663 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.27+19733C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969663 | |||||||
| chr4:76969927 | A | G | 1 | a0001c0001t0030g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.27+19997A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76969927 | |||||||
| chr4:76970016 | A | G | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.27+20086A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970016 | |||||||
| chr4:76970049 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.27+20119C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970049 | |||||||
| chr4:76970111 | T | G | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.27+20181T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970111 | |||||||
| chr4:76970209 | C | G | 1 | a0001c0001t0003g0316 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.27+20279C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970209 | |||||||
| chr4:76970347 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.27+20417G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970347 | |||||||
| chr4:76970460 | A | G | 8 | a0001c0001t0005g0003 a0001c0001t0005g0223 a0001c0001t0005g0226 others(5): Show |
11 | NA18952.hp2 NA18960.hp1 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.27+20530A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970460 | |||||||
| chr4:76970494 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.27+20564C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970494 | |||||||
| chr4:76970773 | T | C | 1 | a0001c0001t0027g0264 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.27+20843T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970773 | |||||||
| chr4:76970849 | T | C | 3 | a0001c0001t0001g0234 a0001c0001t0018g0161 a0001c0001t0018g0162 |
3 | HG02615.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.27+20919T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970849 | |||||||
| chr4:76970889 | C | T | 22 | a0001c0001t0001g0218 a0001c0001t0005g0003 a0001c0001t0005g0019 others(19): Show |
28 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.27+20959C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970889 | |||||||
| chr4:76970897 | A | G | 80 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.27+20967A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76970897 | |||||||
| chr4:76971109 | C | G | 97 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.27+21179C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971109 | |||||||
| chr4:76971244 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.27+21314A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971244 | |||||||
| chr4:76971478 | GA | G | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(12): Show |
15 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+21549delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971478 | |||||||
| chr4:76971563 | ATTAGAT | A | 78 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(75): Show |
85 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.27+21653_27+21658d others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76971563 | ||||||
| chr4:76971571 | T | C | 5 | a0001c0001t0002g0022 a0001c0001t0012g0241 a0001c0001t0012g0242 others(2): Show |
6 | HG01109.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.27+21641T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971571 | |||||||
| chr4:76971583 | TAGATTA | T | 15 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.27+21660_27+21665d others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76971583 | ||||||
| chr4:76971836 | C | T | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.27+21906C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971836 | |||||||
| chr4:76971913 | A | G | 1 | a0001c0001t0033g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.27+21983A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971913 | |||||||
| chr4:76971991 | A | G | 97 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.27+22061A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76971991 | |||||||
| chr4:76972090 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.27+22160C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972090 | |||||||
| chr4:76972214 | C | T | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.27+22284C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972214 | |||||||
| chr4:76972460 | A | G | 4 | a0001c0001t0013g0097 a0001c0001t0014g0100 a0001c0001t0017g0098 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+22530A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972460 | |||||||
| chr4:76972477 | A | C | 1 | a0001c0001t0006g0053 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.27+22547A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972477 | |||||||
| chr4:76972521 | A | G | 305 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(302): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.27+22591A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972521 | |||||||
| chr4:76972617 | C | T | 1 | a0001c0001t0014g0093 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.27+22687C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972617 | |||||||
| chr4:76972671 | G | C | 1 | a0001c0001t0004g0103 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.27+22741G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972671 | |||||||
| chr4:76972825 | G | C | 4 | a0001c0001t0013g0097 a0001c0001t0014g0100 a0001c0001t0017g0098 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+22895G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76972825 | |||||||
| chr4:76973000 | TCTC | T | 3 | a0001c0001t0002g0153 a0001c0001t0004g0103 a0001c0001t0004g0131 |
3 | HG01433.hp2 HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.27+23071_27+23073d others(5): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973000 | |||||||
| chr4:76973053 | A | T | 1 | a0001c0001t0003g0290 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.27+23123A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973053 | |||||||
| chr4:76973065 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.27+23135C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973065 | |||||||
| chr4:76973067 | G | A | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.27+23137G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973067 | |||||||
| chr4:76973097 | C | T | 2 | a0001c0001t0006g0051 a0001c0001t0006g0052 |
2 | NA18994.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.27+23167C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973097 | |||||||
| chr4:76973136 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0019g0236 |
2 | HG02698.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.27+23206G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973136 | |||||||
| chr4:76973246 | A | G | 320 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(317): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.28-23179A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973246 | |||||||
| chr4:76973324 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-23101C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973324 | |||||||
| chr4:76973535 | G | T | 97 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.28-22890G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973535 | |||||||
| chr4:76973597 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.28-22828C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973597 | |||||||
| chr4:76973624 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.28-22801C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973624 | |||||||
| chr4:76973667 | C | T | 4 | a0001c0001t0006g0086 a0001c0001t0008g0083 a0001c0001t0008g0084 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-22758C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973667 | |||||||
| chr4:76973940 | A | G | 1 | a0001c0001t0018g0162 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.28-22485A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973940 | |||||||
| chr4:76973997 | C | T | 1 | a0001c0001t0028g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.28-22428C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76973997 | |||||||
| chr4:76974043 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-22382T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76974043 | |||||||
| chr4:76974343 | T | C | 1 | a0001c0001t0022g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-22082T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76974343 | |||||||
| chr4:76974501 | A | G | 1 | a0001c0001t0010g0050 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.28-21924A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76974501 | |||||||
| chr4:76974641 | A | G | 31 | a0001c0001t0001g0234 a0001c0001t0002g0168 a0001c0001t0002g0176 others(28): Show |
34 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.28-21784A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76974641 | |||||||
| chr4:76974797 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.28-21628G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76974797 | |||||||
| chr4:76974798 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.28-21627A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76974798 | |||||||
| chr4:76975125 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-21300A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76975125 | |||||||
| chr4:76975136 | GA | G | 37 | a0001c0001t0001g0272 a0001c0001t0003g0005 a0001c0001t0003g0008 others(34): Show |
41 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(38): Show |
intron_variant | MODIFIER | c.28-21275delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76975136 | ||||||
| chr4:76975195 | T | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0266 a0001c0001t0001g0268 others(12): Show |
16 | HG01361.hp2 HG01928.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-21230T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76975195 | |||||||
| chr4:76975217 | T | G | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-21208T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76975217 | |||||||
| chr4:76975328 | A | G | 15 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(12): Show |
15 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-21097A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76975328 | |||||||
| chr4:76975428 | C | T | 4 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-20997C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76975428 | |||||||
| chr4:76975695 | GA | G | 3 | a0001c0001t0001g0330 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG00280.hp2 HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.28-20726delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76975695 | ||||||
| chr4:76975706 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-20719A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76975706 | |||||||
| chr4:76976163 | C | G | 28 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(25): Show |
31 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-20262C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76976163 | |||||||
| chr4:76976197 | G | A | 320 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(317): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.28-20228G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76976197 | |||||||
| chr4:76976560 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-19865G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76976560 | |||||||
| chr4:76976792 | G | A | 211 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(208): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.28-19633G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76976792 | |||||||
| chr4:76976902 | T | C | 1 | a0001c0001t0011g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.28-19523T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76976902 | |||||||
| chr4:76977022 | C | T | 1 | a0001c0001t0014g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-19403C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977022 | |||||||
| chr4:76977033 | A | G | 1 | a0001c0001t0026g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.28-19392A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977033 | |||||||
| chr4:76977122 | A | G | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.28-19303A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977122 | |||||||
| chr4:76977207 | CA | C | 43 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(40): Show |
47 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.28-19213delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76977207 | ||||||
| chr4:76977236 | T | C | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28-19189T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977236 | |||||||
| chr4:76977434 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-18991G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977434 | |||||||
| chr4:76977492 | C | G | 46 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(43): Show |
50 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-18933C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977492 | |||||||
| chr4:76977726 | C | CT | 15 | a0001c0001t0001g0289 a0001c0001t0001g0331 a0001c0001t0001g0333 others(12): Show |
18 | HG02055.hp1 HG02257.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.28-18683dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76977726 | ||||||
| chr4:76977726 | CT | C | 9 | a0001c0001t0001g0234 a0001c0001t0001g0272 a0001c0001t0001g0297 others(6): Show |
9 | HG02109.hp2 HG02135.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.28-18683delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76977726 | ||||||
| chr4:76977971 | A | C | 1 | a0002c0003t0008g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.28-18454A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76977971 | |||||||
| chr4:76978081 | A | T | 1 | a0001c0001t0013g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.28-18344A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978081 | |||||||
| chr4:76978613 | C | A | 1 | a0001c0001t0001g0332 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28-17812C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978613 | |||||||
| chr4:76978657 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-17768C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978657 | |||||||
| chr4:76978698 | A | G | 31 | a0001c0001t0001g0234 a0001c0001t0002g0168 a0001c0001t0002g0176 others(28): Show |
34 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.28-17727A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978698 | |||||||
| chr4:76978789 | C | T | 1 | a0001c0001t0003g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28-17636C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978789 | |||||||
| chr4:76978808 | C | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-17617C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978808 | |||||||
| chr4:76978901 | A | G | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-17524A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76978901 | |||||||
| chr4:76979093 | A | G | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-17332A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979093 | |||||||
| chr4:76979374 | T | G | 2 | a0001c0001t0006g0231 a0001c0001t0006g0233 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.28-17051T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979374 | |||||||
| chr4:76979446 | GGGC | G | 6 | a0001c0001t0002g0012 a0001c0001t0002g0106 a0001c0001t0002g0114 others(3): Show |
7 | NA18612.hp2 NA18939.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-16976_28-16974d others(5): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76979446 | ||||||
| chr4:76979725 | A | G | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-16700A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979725 | |||||||
| chr4:76979741 | C | T | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | NA18955.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.28-16684C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979741 | |||||||
| chr4:76979758 | G | A | 1 | a0001c0001t0004g0196 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.28-16667G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979758 | |||||||
| chr4:76979848 | CA | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0266 a0001c0001t0001g0281 others(3): Show |
7 | HG01884.hp1 HG02559.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-16563delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76979848 | ||||||
| chr4:76979952 | A | G | 1 | a0001c0001t0005g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.28-16473A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979952 | |||||||
| chr4:76979979 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.28-16446C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76979979 | |||||||
| chr4:76980016 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.28-16409G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980016 | |||||||
| chr4:76980103 | G | A | 320 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(317): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.28-16322G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980103 | |||||||
| chr4:76980159 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-16266T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980159 | |||||||
| chr4:76980236 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-16189G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980236 | |||||||
| chr4:76980265 | G | A | 43 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(40): Show |
47 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.28-16160G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980265 | |||||||
| chr4:76980296 | A | C | 96 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.28-16129A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980296 | |||||||
| chr4:76980297 | A | G | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28-16128A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980297 | |||||||
| chr4:76980354 | A | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-16071A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980354 | |||||||
| chr4:76980471 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.28-15954T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980471 | |||||||
| chr4:76980475 | G | A | 2 | a0001c0001t0005g0217 a0001c0001t0012g0220 |
2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.28-15950G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980475 | |||||||
| chr4:76980513 | G | A | 2 | a0001c0001t0004g0102 a0001c0001t0038g0101 |
2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.28-15912G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980513 | |||||||
| chr4:76980549 | T | A | 96 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.28-15876T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980549 | |||||||
| chr4:76980730 | A | G | 34 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(31): Show |
40 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.28-15695A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980730 | |||||||
| chr4:76980898 | T | C | 1 | a0001c0001t0038g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.28-15527T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980898 | |||||||
| chr4:76980972 | A | G | 94 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(91): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.28-15453A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76980972 | |||||||
| chr4:76981177 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-15248G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981177 | |||||||
| chr4:76981203 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.28-15222C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981203 | |||||||
| chr4:76981384 | A | C | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-15041A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981384 | |||||||
| chr4:76981409 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-15016T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981409 | |||||||
| chr4:76981435 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.28-14990A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981435 | |||||||
| chr4:76981744 | AT | A | 324 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0061 others(321): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.28-14667delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76981744 | ||||||
| chr4:76981964 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28-14461G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981964 | |||||||
| chr4:76981969 | C | A | 46 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0031 others(43): Show |
50 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.28-14456C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76981969 | |||||||
| chr4:76982029 | A | G | 28 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(25): Show |
31 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.28-14396A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982029 | |||||||
| chr4:76982042 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.28-14383G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982042 | |||||||
| chr4:76982074 | A | C | 7 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0079 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-14351A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982074 | |||||||
| chr4:76982084 | C | G | 1 | a0001c0001t0033g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-14341C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982084 | |||||||
| chr4:76982212 | C | CT | 25 | a0001c0001t0001g0218 a0001c0001t0001g0234 a0001c0001t0001g0275 others(22): Show |
31 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.28-14199dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76982212 | ||||||
| chr4:76982212 | CT | C | 6 | a0001c0001t0002g0104 a0001c0001t0002g0147 a0001c0001t0002g0205 others(3): Show |
6 | HG01943.hp1 HG02970.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-14199delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76982212 | ||||||
| chr4:76982508 | C | A | 1 | a0001c0001t0003g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28-13917C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982508 | |||||||
| chr4:76982756 | A | T | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-13669A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982756 | |||||||
| chr4:76982871 | T | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-13554T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982871 | |||||||
| chr4:76982959 | T | G | 97 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.28-13466T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982959 | |||||||
| chr4:76982994 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.28-13431A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76982994 | |||||||
| chr4:76983157 | G | A | 29 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(26): Show |
35 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.28-13268G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983157 | |||||||
| chr4:76983195 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.28-13230T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983195 | |||||||
| chr4:76983364 | G | A | 2 | a0001c0001t0004g0102 a0001c0001t0038g0101 |
2 | HG01884.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.28-13061G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983364 | |||||||
| chr4:76983547 | G | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-12878G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983547 | |||||||
| chr4:76983572 | A | G | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-12853A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983572 | |||||||
| chr4:76983635 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.28-12790T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983635 | |||||||
| chr4:76983679 | G | T | 1 | a0001c0001t0002g0126 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28-12746G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983679 | |||||||
| chr4:76983823 | C | T | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-12602C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983823 | |||||||
| chr4:76983901 | G | A | 2 | a0001c0001t0004g0197 a0001c0001t0004g0204 |
2 | HG01358.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.28-12524G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983901 | |||||||
| chr4:76983959 | A | G | 97 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.28-12466A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76983959 | |||||||
| chr4:76984018 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-12407G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984018 | |||||||
| chr4:76984045 | A | T | 32 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0037 others(29): Show |
36 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-12380A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984045 | |||||||
| chr4:76984126 | A | T | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-12299A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984126 | |||||||
| chr4:76984278 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.28-12147G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984278 | |||||||
| chr4:76984323 | T | C | 1 | a0001c0001t0006g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.28-12102T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984323 | |||||||
| chr4:76984486 | C | G | 1 | a0001c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.28-11939C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984486 | |||||||
| chr4:76984742 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.28-11683C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984742 | |||||||
| chr4:76984748 | T | C | 7 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(4): Show |
7 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-11677T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984748 | |||||||
| chr4:76984874 | C | T | 1 | a0001c0001t0006g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.28-11551C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984874 | |||||||
| chr4:76984918 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0271 |
2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.28-11507G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984918 | |||||||
| chr4:76984986 | C | T | 15 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(12): Show |
15 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.28-11439C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76984986 | |||||||
| chr4:76985088 | C | T | 1 | a0001c0001t0002g0004 | 3 | HG00741.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.28-11337C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985088 | |||||||
| chr4:76985317 | C | T | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-11108C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985317 | |||||||
| chr4:76985326 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-11099G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985326 | |||||||
| chr4:76985469 | C | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-10956C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985469 | |||||||
| chr4:76985543 | G | A | 3 | a0001c0001t0006g0231 a0001c0001t0006g0233 a0002c0003t0008g0237 |
3 | HG01891.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.28-10882G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985543 | |||||||
| chr4:76985549 | G | T | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | NA19000.hp2 NA19057.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.28-10876G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985549 | |||||||
| chr4:76985886 | C | T | 132 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(129): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.28-10539C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985886 | |||||||
| chr4:76985958 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-10467G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76985958 | |||||||
| chr4:76986151 | T | C | 1 | a0001c0001t0006g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.28-10274T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986151 | |||||||
| chr4:76986269 | A | G | 2 | a0001c0001t0002g0022 a0001c0001t0013g0243 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.28-10156A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986269 | |||||||
| chr4:76986520 | C | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-9905C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986520 | |||||||
| chr4:76986753 | AAATATTG others(3): Show |
A | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.28-9671_28-9662del others(10): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986753 | |||||||
| chr4:76986781 | A | G | 1 | a0001c0001t0006g0040 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.28-9644A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986781 | |||||||
| chr4:76986792 | T | C | 1 | a0001c0001t0004g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-9633T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986792 | |||||||
| chr4:76986912 | G | A | 1 | a0001c0001t0033g0167 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.28-9513G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76986912 | |||||||
| chr4:76987125 | G | T | 1 | a0001c0001t0039g0188 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.28-9300G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987125 | |||||||
| chr4:76987170 | T | C | 135 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(132): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.28-9255T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987170 | |||||||
| chr4:76987494 | T | G | 1 | a0001c0001t0005g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.28-8931T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987494 | |||||||
| chr4:76987495 | G | A | 1 | a0001c0001t0004g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.28-8930G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987495 | |||||||
| chr4:76987619 | T | C | 1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.28-8806T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987619 | |||||||
| chr4:76987715 | A | T | 1 | a0001c0001t0003g0008 | 2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.28-8710A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987715 | |||||||
| chr4:76987881 | C | T | 132 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(129): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.28-8544C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76987881 | |||||||
| chr4:76988054 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.28-8371G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988054 | |||||||
| chr4:76988125 | G | T | 5 | a0001c0001t0001g0260 a0001c0001t0001g0321 a0001c0001t0004g0014 others(2): Show |
6 | HG00609.hp1 HG02027.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-8300G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988125 | |||||||
| chr4:76988404 | C | T | 36 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(33): Show |
42 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.28-8021C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988404 | |||||||
| chr4:76988631 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0271 |
2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.28-7794C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988631 | |||||||
| chr4:76988667 | C | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-7758C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988667 | |||||||
| chr4:76988668 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.28-7757G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988668 | |||||||
| chr4:76988701 | T | G | 1 | a0001c0001t0002g0004 | 3 | HG00741.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.28-7724T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988701 | |||||||
| chr4:76988934 | A | G | 1 | a0001c0001t0004g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.28-7491A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76988934 | |||||||
| chr4:76989149 | A | G | 8 | a0001c0001t0003g0005 a0001c0001t0003g0039 a0001c0001t0003g0059 others(5): Show |
10 | HG02080.hp2 HG02132.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.28-7276A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989149 | |||||||
| chr4:76989377 | G | A | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-7048G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989377 | |||||||
| chr4:76989600 | G | A | 1 | a0001c0001t0003g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.28-6825G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989600 | |||||||
| chr4:76989646 | C | T | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6779C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989646 | |||||||
| chr4:76989657 | A | G | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6768A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989657 | |||||||
| chr4:76989806 | A | G | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6619A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989806 | |||||||
| chr4:76989945 | T | C | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6480T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989945 | |||||||
| chr4:76989953 | G | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-6472G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989953 | |||||||
| chr4:76989996 | G | A | 8 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-6429G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76989996 | |||||||
| chr4:76990032 | TCCACAGC others(56): Show |
T | 1 | a0001c0001t0005g0223 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.28-6390_28-6328del others(63): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76990032 | ||||||
| chr4:76990055 | A | G | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-6370A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990055 | |||||||
| chr4:76990065 | C | T | 103 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(100): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.28-6360C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990065 | |||||||
| chr4:76990226 | C | T | 1 | a0001c0001t0028g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.28-6199C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990226 | |||||||
| chr4:76990228 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.28-6197A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990228 | |||||||
| chr4:76990233 | T | C | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6192T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990233 | |||||||
| chr4:76990294 | C | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0010 others(40): Show |
50 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.28-6131C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990294 | |||||||
| chr4:76990369 | G | C | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6056G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990369 | |||||||
| chr4:76990380 | G | T | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6045G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990380 | |||||||
| chr4:76990404 | G | A | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-6021G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990404 | |||||||
| chr4:76990480 | G | A | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-5945G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990480 | |||||||
| chr4:76990606 | C | G | 32 | a0001c0001t0003g0005 a0001c0001t0003g0008 a0001c0001t0003g0037 others(29): Show |
36 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.28-5819C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990606 | |||||||
| chr4:76990658 | C | T | 1 | a0001c0001t0025g0030 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28-5767C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990658 | |||||||
| chr4:76990756 | C | T | 1 | a0001c0001t0037g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.28-5669C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990756 | |||||||
| chr4:76990979 | G | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-5446G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990979 | |||||||
| chr4:76990992 | A | G | 1 | a0001c0001t0014g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-5433A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76990992 | |||||||
| chr4:76991160 | A | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-5265A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991160 | |||||||
| chr4:76991162 | T | G | 1 | a0001c0001t0003g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.28-5263T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991162 | |||||||
| chr4:76991178 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-5247A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991178 | |||||||
| chr4:76991260 | G | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-5165G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991260 | |||||||
| chr4:76991485 | T | G | 2 | a0001c0001t0003g0087 a0001c0001t0006g0088 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.28-4940T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991485 | |||||||
| chr4:76991561 | A | C | 1 | a0001c0001t0003g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-4864A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991561 | |||||||
| chr4:76991580 | A | AT | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-4845_28-4844ins others(1): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991580 | |||||||
| chr4:76991671 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.28-4754T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991671 | |||||||
| chr4:76991706 | T | C | 1 | a0001c0001t0005g0223 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.28-4719T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991706 | |||||||
| chr4:76991710 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-4715G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991710 | |||||||
| chr4:76991732 | T | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-4693T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76991732 | |||||||
| chr4:76992007 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28-4418G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992007 | |||||||
| chr4:76992043 | T | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-4382T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992043 | |||||||
| chr4:76992160 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-4265A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992160 | |||||||
| chr4:76992161 | G | T | 4 | a0001c0001t0002g0022 a0001c0001t0012g0241 a0001c0001t0012g0242 others(1): Show |
5 | HG01109.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-4264G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992161 | |||||||
| chr4:76992218 | C | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-4207C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992218 | |||||||
| chr4:76992376 | GAACTT | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0305 a0001c0001t0023g0304 |
3 | HG02074.hp2 HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.28-4046_28-4042del others(5): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76992376 | ||||||
| chr4:76992520 | C | T | 1 | a0001c0001t0006g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.28-3905C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992520 | |||||||
| chr4:76992795 | A | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-3630A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992795 | |||||||
| chr4:76992811 | T | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-3614T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992811 | |||||||
| chr4:76992881 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.28-3544A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992881 | |||||||
| chr4:76992938 | A | G | 1 | a0001c0001t0006g0047 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.28-3487A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992938 | |||||||
| chr4:76992940 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-3485G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992940 | |||||||
| chr4:76992949 | G | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0135 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.28-3476G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992949 | |||||||
| chr4:76992962 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-3463A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76992962 | |||||||
| chr4:76993025 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.28-3400G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993025 | |||||||
| chr4:76993058 | GTAT | G | 134 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(131): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.28-3364_28-3362del others(3): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76993058 | ||||||
| chr4:76993169 | G | A | 1 | a0001c0001t0002g0119 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.28-3256G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993169 | |||||||
| chr4:76993170 | A | G | 1 | a0001c0001t0002g0119 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.28-3255A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993170 | |||||||
| chr4:76993382 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-3043G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993382 | |||||||
| chr4:76993460 | C | G | 29 | a0001c0001t0001g0234 a0001c0001t0002g0168 a0001c0001t0002g0176 others(26): Show |
32 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.28-2965C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993460 | |||||||
| chr4:76993523 | G | C | 175 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(172): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.28-2902G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993523 | |||||||
| chr4:76993657 | A | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-2768A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993657 | |||||||
| chr4:76993903 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-2522G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993903 | |||||||
| chr4:76993905 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-2520G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993905 | |||||||
| chr4:76993972 | C | T | 3 | a0001c0001t0001g0321 a0001c0001t0004g0014 a0001c0001t0004g0164 |
4 | HG00609.hp1 HG02165.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-2453C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76993972 | |||||||
| chr4:76994015 | A | G | 3 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0213 |
5 | HG00099.hp2 HG00741.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-2410A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994015 | |||||||
| chr4:76994149 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-2276G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994149 | |||||||
| chr4:76994495 | G | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1930G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994495 | |||||||
| chr4:76994512 | A | G | 97 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.28-1913A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994512 | |||||||
| chr4:76994624 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1801G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994624 | |||||||
| chr4:76994776 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1649A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994776 | |||||||
| chr4:76994781 | T | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1644T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994781 | |||||||
| chr4:76994900 | C | CT | 37 | a0001c0001t0001g0307 a0001c0001t0002g0004 a0001c0001t0002g0009 others(34): Show |
41 | HG00597.hp1 HG00621.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.28-1497dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76994900 | ||||||
| chr4:76994900 | C | CTT | 9 | a0001c0001t0001g0234 a0001c0001t0002g0176 a0001c0001t0007g0173 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-1498_28-1497dup others(2): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76994900 | ||||||
| chr4:76994900 | C | CTTT | 41 | a0001c0001t0002g0168 a0001c0001t0002g0183 a0001c0001t0002g0184 others(38): Show |
45 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.28-1499_28-1497dup others(3): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76994900 | ||||||
| chr4:76994900 | C | CTTTT | 14 | a0001c0001t0002g0186 a0001c0001t0003g0008 a0001c0001t0003g0037 others(11): Show |
17 | HG00673.hp2 HG01975.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.28-1500_28-1497dup others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76994900 | ||||||
| chr4:76994900 | CT | C | 105 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0208 others(102): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.28-1497delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76994900 | ||||||
| chr4:76994900 | CTT | C | 11 | a0001c0001t0001g0025 a0001c0001t0001g0207 a0001c0001t0001g0210 others(8): Show |
12 | HG01070.hp1 HG01168.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-1498_28-1497del others(2): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76994900 | ||||||
| chr4:76994943 | A | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1482A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994943 | |||||||
| chr4:76994953 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.28-1472G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76994953 | |||||||
| chr4:76995005 | T | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1420T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995005 | |||||||
| chr4:76995085 | TA | T | 132 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(129): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.28-1325delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 76995085 | ||||||
| chr4:76995098 | A | T | 1 | a0001c0001t0005g0223 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.28-1327A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995098 | |||||||
| chr4:76995100 | A | T | 1 | a0001c0001t0006g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-1325A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995100 | |||||||
| chr4:76995120 | A | G | 1 | a0001c0001t0005g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.28-1305A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995120 | |||||||
| chr4:76995204 | AAACC | A | 5 | a0001c0001t0003g0037 a0001c0001t0006g0042 a0001c0001t0006g0045 others(2): Show |
5 | HG01975.hp1 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-1220_28-1217del others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995204 | |||||||
| chr4:76995242 | C | T | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1183C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995242 | |||||||
| chr4:76995252 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0135 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.28-1173C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995252 | |||||||
| chr4:76995297 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-1128A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995297 | |||||||
| chr4:76995400 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.28-1025T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995400 | |||||||
| chr4:76995552 | A | C | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-873A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995552 | |||||||
| chr4:76995590 | C | T | 2 | a0001c0001t0002g0091 a0001c0001t0007g0090 |
2 | HG02071.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.28-835C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995590 | |||||||
| chr4:76995712 | G | A | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-713G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995712 | |||||||
| chr4:76995941 | A | G | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.28-484A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76995941 | |||||||
| chr4:76996009 | G | A | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.28-416G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76996009 | |||||||
| chr4:76996041 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-384A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76996041 | |||||||
| chr4:76996070 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.28-355T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76996070 | |||||||
| chr4:76996305 | A | G | 133 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(130): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.28-120A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76996305 | |||||||
| chr4:76996382 | C | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.28-43C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 1/9 | chr4 | 76996382 | |||||||
| chr4:76996600 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.142+61C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76996600 | |||||||
| chr4:76996648 | C | T | 7 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0079 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.142+109C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76996648 | |||||||
| chr4:76996728 | T | G | 6 | a0001c0001t0002g0001 a0001c0001t0002g0124 a0001c0001t0002g0129 others(3): Show |
9 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+189T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76996728 | |||||||
| chr4:76996736 | A | G | 1 | a0001c0001t0028g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.142+197A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76996736 | |||||||
| chr4:76996883 | C | CT | 161 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(158): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.142+361dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 76996883 | ||||||
| chr4:76996883 | C | CTT | 32 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(29): Show |
38 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.142+360_142+361dup others(2): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 76996883 | ||||||
| chr4:76996961 | C | A | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.142+422C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76996961 | |||||||
| chr4:76996973 | A | G | 162 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.142+434A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76996973 | |||||||
| chr4:76997018 | T | C | 1 | a0001c0001t0012g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.142+479T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997018 | |||||||
| chr4:76997021 | A | G | 163 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(160): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.142+482A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997021 | |||||||
| chr4:76997042 | AT | A | 162 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.142+509delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 76997042 | ||||||
| chr4:76997131 | A | G | 6 | a0001c0001t0001g0272 a0001c0001t0001g0291 a0001c0001t0001g0300 others(3): Show |
6 | HG02896.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.142+592A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997131 | |||||||
| chr4:76997550 | C | A | 8 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(5): Show |
8 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.142+1011C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997550 | |||||||
| chr4:76997627 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.142+1088A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997627 | |||||||
| chr4:76997813 | A | G | 163 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(160): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.142+1274A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997813 | |||||||
| chr4:76997851 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.142+1312A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997851 | |||||||
| chr4:76997893 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.142+1354C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76997893 | |||||||
| chr4:76998032 | G | C | 162 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.142+1493G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998032 | |||||||
| chr4:76998112 | T | C | 162 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.142+1573T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998112 | |||||||
| chr4:76998257 | A | G | 162 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.142+1718A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998257 | |||||||
| chr4:76998362 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.142+1823T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998362 | |||||||
| chr4:76998425 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.142+1886C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998425 | |||||||
| chr4:76998532 | G | A | 2 | a0001c0001t0004g0103 a0001c0001t0004g0131 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.142+1993G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998532 | |||||||
| chr4:76998643 | C | T | 162 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(159): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.142+2104C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998643 | |||||||
| chr4:76998686 | C | T | 4 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0082 others(1): Show |
4 | HG02258.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+2147C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998686 | |||||||
| chr4:76998729 | T | G | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.142+2190T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998729 | |||||||
| chr4:76998772 | G | C | 73 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(70): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.142+2233G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76998772 | |||||||
| chr4:76999415 | A | G | 99 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0250 others(96): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.142+2876A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76999415 | |||||||
| chr4:76999571 | G | A | 1 | a0001c0001t0004g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.142+3032G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76999571 | |||||||
| chr4:76999778 | A | G | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.142+3239A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76999778 | |||||||
| chr4:76999792 | A | G | 1 | a0001c0001t0003g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.142+3253A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76999792 | |||||||
| chr4:76999852 | C | T | 37 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(34): Show |
43 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.142+3313C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 76999852 | |||||||
| chr4:77000009 | A | G | 2 | a0001c0001t0003g0024 a0001c0001t0003g0244 |
3 | HG00639.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.142+3470A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000009 | |||||||
| chr4:77000049 | C | T | 1 | a0001c0001t0008g0245 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142+3510C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000049 | |||||||
| chr4:77000154 | G | T | 4 | a0001c0001t0001g0275 a0001c0001t0001g0295 a0001c0001t0001g0306 others(1): Show |
4 | NA18942.hp1 NA18972.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+3615G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000154 | |||||||
| chr4:77000161 | A | G | 29 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(26): Show |
32 | HG00544.hp2 HG00673.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.142+3622A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000161 | |||||||
| chr4:77000291 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.142+3752A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000291 | |||||||
| chr4:77000338 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.142+3799G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000338 | |||||||
| chr4:77000391 | G | C | 1 | a0001c0001t0026g0313 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.142+3852G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000391 | |||||||
| chr4:77000457 | A | G | 1 | a0001c0001t0006g0044 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.142+3918A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000457 | |||||||
| chr4:77000712 | T | C | 1 | a0001c0001t0006g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.142+4173T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000712 | |||||||
| chr4:77000781 | G | T | 1 | a0001c0001t0014g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.142+4242G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000781 | |||||||
| chr4:77000782 | T | A | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.142+4243T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000782 | |||||||
| chr4:77000797 | C | T | 93 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0234 others(90): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.142+4258C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77000797 | |||||||
| chr4:77001003 | A | G | 1 | a0001c0001t0016g0274 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.142+4464A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001003 | |||||||
| chr4:77001106 | G | A | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0020g0232 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.143-4495G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001106 | |||||||
| chr4:77001191 | T | C | 1 | a0001c0001t0003g0024 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.143-4410T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001191 | |||||||
| chr4:77001232 | A | G | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.143-4369A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001232 | |||||||
| chr4:77001350 | CT | C | 183 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(180): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.143-4237delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 77001350 | ||||||
| chr4:77001443 | A | G | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.143-4158A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001443 | |||||||
| chr4:77001538 | C | T | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.143-4063C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001538 | |||||||
| chr4:77001597 | G | A | 3 | a0001c0001t0007g0173 a0001c0001t0007g0174 a0001c0001t0007g0175 |
3 | HG01243.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.143-4004G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001597 | |||||||
| chr4:77001711 | T | C | 142 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(139): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.143-3890T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001711 | |||||||
| chr4:77001806 | G | T | 38 | a0001c0001t0003g0008 a0001c0001t0003g0031 a0001c0001t0003g0032 others(35): Show |
41 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.143-3795G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001806 | |||||||
| chr4:77001855 | C | G | 1 | a0001c0001t0003g0072 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.143-3746C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001855 | |||||||
| chr4:77001856 | A | G | 1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.143-3745A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77001856 | |||||||
| chr4:77002178 | T | C | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.143-3423T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002178 | |||||||
| chr4:77002437 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0210 |
2 | HG00735.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.143-3164G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002437 | |||||||
| chr4:77002485 | G | C | 141 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.143-3116G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002485 | |||||||
| chr4:77002525 | G | A | 75 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(72): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.143-3076G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002525 | |||||||
| chr4:77002766 | G | GT | 13 | a0001c0001t0002g0094 a0001c0001t0002g0121 a0001c0001t0003g0039 others(10): Show |
13 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.143-2824dupT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 77002766 | ||||||
| chr4:77002778 | GT | G | 11 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
11 | HG00735.hp1 HG01106.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.143-2822delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002778 | |||||||
| chr4:77002814 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.143-2787C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002814 | |||||||
| chr4:77002878 | G | A | 95 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0234 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.143-2723G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002878 | |||||||
| chr4:77002989 | C | G | 7 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0019g0166 others(4): Show |
7 | HG01884.hp1 HG02723.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-2612C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77002989 | |||||||
| chr4:77003190 | A | G | 1 | a0001c0001t0005g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143-2411A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77003190 | |||||||
| chr4:77003256 | G | T | 36 | a0001c0001t0003g0008 a0001c0001t0003g0031 a0001c0001t0003g0032 others(33): Show |
39 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.143-2345G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77003256 | |||||||
| chr4:77003263 | A | G | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.143-2338A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77003263 | |||||||
| chr4:77003412 | A | G | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.143-2189A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77003412 | |||||||
| chr4:77003744 | G | T | 1 | a0001c0001t0001g0331 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.143-1857G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77003744 | |||||||
| chr4:77004063 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.143-1538C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004063 | |||||||
| chr4:77004073 | G | C | 143 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.143-1528G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004073 | |||||||
| chr4:77004165 | T | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0332 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.143-1436T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004165 | |||||||
| chr4:77004229 | T | C | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.143-1372T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004229 | |||||||
| chr4:77004653 | T | G | 55 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(52): Show |
63 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.143-948T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004653 | |||||||
| chr4:77004731 | G | A | 95 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0234 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.143-870G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004731 | |||||||
| chr4:77004750 | G | T | 95 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0234 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.143-851G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004750 | |||||||
| chr4:77004791 | C | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.143-810C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004791 | |||||||
| chr4:77004845 | C | A | 1 | a0001c0001t0007g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.143-756C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004845 | |||||||
| chr4:77004958 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.143-643G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77004958 | |||||||
| chr4:77005158 | A | T | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.143-443A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77005158 | |||||||
| chr4:77005299 | A | G | 1 | a0001c0001t0016g0284 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.143-302A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77005299 | |||||||
| chr4:77005389 | T | G | 1 | a0001c0001t0007g0179 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.143-212T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77005389 | |||||||
| chr4:77005597 | G | T | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.143-4G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 2/9 | chr4 | 77005597 | |||||||
| chr4:77005873 | A | C | 1 | a0001c0001t0004g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.338+77A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77005873 | |||||||
| chr4:77005941 | CTCTGAGA others(5): Show |
C | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0020g0232 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.338+155_338+166del others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 77005941 | ||||||
| chr4:77006149 | T | C | 1 | a0001c0001t0003g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.338+353T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006149 | |||||||
| chr4:77006192 | G | A | 141 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.338+396G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006192 | |||||||
| chr4:77006385 | A | G | 68 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(65): Show |
77 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.338+589A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006385 | |||||||
| chr4:77006398 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.338+602C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006398 | |||||||
| chr4:77006414 | T | A | 1 | a0001c0001t0004g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.338+618T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006414 | |||||||
| chr4:77006818 | A | G | 1 | a0001c0001t0004g0239 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.338+1022A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006818 | |||||||
| chr4:77006899 | C | G | 7 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0106 others(4): Show |
9 | NA18612.hp2 NA18939.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.338+1103C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006899 | |||||||
| chr4:77006959 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.338+1163G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77006959 | |||||||
| chr4:77007200 | A | G | 16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0003g0067 others(13): Show |
16 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.338+1404A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77007200 | |||||||
| chr4:77007205 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.338+1409C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77007205 | |||||||
| chr4:77007240 | A | T | 1 | a0001c0001t0022g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.338+1444A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77007240 | |||||||
| chr4:77007312 | C | T | 75 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(72): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.338+1516C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77007312 | |||||||
| chr4:77007412 | A | T | 1 | a0001c0001t0001g0337 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.338+1616A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77007412 | |||||||
| chr4:77007542 | A | G | 1 | a0001c0001t0006g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.338+1746A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77007542 | |||||||
| chr4:77008031 | C | T | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.338+2235C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77008031 | |||||||
| chr4:77008063 | C | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.338+2267C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77008063 | |||||||
| chr4:77008584 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.338+2788A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77008584 | |||||||
| chr4:77008587 | T | C | 1 | a0001c0001t0009g0062 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.338+2791T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77008587 | |||||||
| chr4:77008743 | A | T | 17 | a0001c0001t0002g0022 a0001c0001t0003g0080 a0001c0001t0003g0081 others(14): Show |
18 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.338+2947A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77008743 | |||||||
| chr4:77008906 | A | C | 2 | a0001c0001t0003g0087 a0001c0001t0006g0088 |
2 | HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.339-2829A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77008906 | |||||||
| chr4:77009778 | G | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.339-1957G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77009778 | |||||||
| chr4:77010288 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0221 |
3 | HG01070.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.339-1447C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010288 | |||||||
| chr4:77010349 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0305 a0001c0001t0023g0304 |
3 | HG02074.hp2 HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.339-1386A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010349 | |||||||
| chr4:77010467 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.339-1268T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010467 | |||||||
| chr4:77010472 | T | A | 2 | a0001c0001t0001g0234 a0001c0001t0004g0102 |
2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.339-1263T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010472 | |||||||
| chr4:77010708 | G | T | 1 | a0001c0001t0007g0175 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.339-1027G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010708 | |||||||
| chr4:77010745 | T | C | 1 | a0001c0001t0004g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.339-990T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010745 | |||||||
| chr4:77010814 | GC | G | 62 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0259 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.339-920delC | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77010814 | |||||||
| chr4:77011039 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.339-696C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77011039 | |||||||
| chr4:77011058 | T | G | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.339-677T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77011058 | |||||||
| chr4:77011193 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.339-542G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77011193 | |||||||
| chr4:77011523 | G | C | 5 | a0001c0001t0002g0022 a0001c0001t0012g0241 a0001c0001t0012g0242 others(2): Show |
6 | HG01109.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.339-212G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77011523 | |||||||
| chr4:77011563 | A | G | 1 | a0001c0001t0004g0127 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.339-172A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77011563 | |||||||
| chr4:77011626 | A | G | 5 | a0001c0001t0009g0062 a0001c0001t0009g0063 a0001c0001t0009g0064 others(2): Show |
5 | HG02280.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.339-109A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 3/9 | chr4 | 77011626 | |||||||
| chr4:77012007 | T | G | 1 | a0001c0001t0002g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.525+86T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012007 | |||||||
| chr4:77012085 | CAAAAATA others(4): Show |
C | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.525+169_525+179del others(11): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 77012085 | ||||||
| chr4:77012096 | TAAAAC | T | 35 | a0001c0001t0003g0008 a0001c0001t0003g0031 a0001c0001t0003g0032 others(32): Show |
38 | HG00544.hp1 HG00738.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.525+186_525+190del others(5): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 77012096 | ||||||
| chr4:77012101 | C | T | 1 | a0001c0001t0019g0236 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.525+180C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012101 | |||||||
| chr4:77012325 | A | G | 1 | a0001c0001t0006g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.525+404A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012325 | |||||||
| chr4:77012414 | C | A | 1 | a0001c0001t0013g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.525+493C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012414 | |||||||
| chr4:77012433 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.525+512G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012433 | |||||||
| chr4:77012491 | C | T | 1 | a0001c0001t0006g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.525+570C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012491 | |||||||
| chr4:77012515 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.525+594A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012515 | |||||||
| chr4:77012589 | G | A | 56 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(53): Show |
64 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.525+668G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012589 | |||||||
| chr4:77012870 | C | T | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.525+949C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012870 | |||||||
| chr4:77012876 | G | T | 1 | a0001c0001t0007g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.525+955G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012876 | |||||||
| chr4:77012906 | C | G | 10 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG00735.hp1 HG01106.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+985C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77012906 | |||||||
| chr4:77013011 | C | T | 4 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(1): Show |
4 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1090C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013011 | |||||||
| chr4:77013018 | G | A | 26 | a0001c0001t0003g0008 a0001c0001t0006g0006 a0001c0001t0006g0033 others(23): Show |
29 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.525+1097G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013018 | |||||||
| chr4:77013279 | T | C | 76 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(73): Show |
87 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.525+1358T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013279 | |||||||
| chr4:77013398 | C | T | 1 | a0001c0001t0005g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.526-1458C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013398 | |||||||
| chr4:77013418 | GT | G | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0038 others(1): Show |
4 | HG02723.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-1434delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 77013418 | ||||||
| chr4:77013559 | G | A | 1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.526-1297G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013559 | |||||||
| chr4:77013624 | G | C | 1 | a0001c0001t0006g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.526-1232G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013624 | |||||||
| chr4:77013750 | G | A | 62 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0259 others(59): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.526-1106G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013750 | |||||||
| chr4:77013914 | C | T | 142 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(139): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.526-942C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013914 | |||||||
| chr4:77013956 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.526-900G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77013956 | |||||||
| chr4:77014115 | A | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.526-741A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014115 | |||||||
| chr4:77014294 | C | G | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.526-562C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014294 | |||||||
| chr4:77014360 | T | C | 3 | a0001c0001t0001g0330 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG00280.hp2 HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.526-496T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014360 | |||||||
| chr4:77014384 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.526-472G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014384 | |||||||
| chr4:77014516 | A | G | 1 | a0001c0001t0006g0042 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.526-340A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014516 | |||||||
| chr4:77014656 | T | C | 2 | a0001c0001t0006g0051 a0001c0001t0006g0052 |
2 | NA18994.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.526-200T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014656 | |||||||
| chr4:77014661 | CA | C | 158 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(155): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.526-181delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 77014661 | ||||||
| chr4:77014663 | A | C | 1 | a0001c0001t0005g0216 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.526-193A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014663 | |||||||
| chr4:77014678 | G | A | 1 | a0001c0001t0005g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.526-178G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014678 | |||||||
| chr4:77014686 | A | C | 1 | a0001c0001t0006g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.526-170A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014686 | |||||||
| chr4:77014713 | C | CA | 95 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0234 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.526-142dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 77014713 | ||||||
| chr4:77014734 | T | C | 19 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(16): Show |
22 | HG00408.hp1 HG02129.hp2 HG03491.hp2 others(19): Show |
intron_variant | MODIFIER | c.526-122T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014734 | |||||||
| chr4:77014786 | C | T | 1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.526-70C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 4/9 | chr4 | 77014786 | |||||||
| chr4:77015351 | G | C | 1 | a0001c0001t0037g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.687+334G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77015351 | |||||||
| chr4:77015376 | A | G | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.687+359A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77015376 | |||||||
| chr4:77015426 | A | G | 1 | a0001c0001t0010g0288 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.687+409A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77015426 | |||||||
| chr4:77015472 | C | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.687+455C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77015472 | |||||||
| chr4:77015680 | A | C | 1 | a0001c0001t0006g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.687+663A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77015680 | |||||||
| chr4:77015725 | G | A | 28 | a0001c0001t0002g0168 a0001c0001t0002g0176 a0001c0001t0002g0183 others(25): Show |
31 | HG00544.hp2 HG01243.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.687+708G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77015725 | |||||||
| chr4:77016068 | G | C | 5 | a0001c0001t0002g0022 a0001c0001t0012g0241 a0001c0001t0012g0242 others(2): Show |
6 | HG01109.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1051G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016068 | |||||||
| chr4:77016079 | A | C | 1 | a0001c0001t0001g0310 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.687+1062A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016079 | |||||||
| chr4:77016131 | A | C | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687+1114A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016131 | |||||||
| chr4:77016170 | A | G | 11 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0108 others(8): Show |
13 | HG00609.hp2 HG00733.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.687+1153A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016170 | |||||||
| chr4:77016258 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.687+1241T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016258 | |||||||
| chr4:77016367 | G | A | 180 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(177): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.687+1350G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016367 | |||||||
| chr4:77016479 | T | C | 1 | a0001c0001t0031g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.687+1462T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016479 | |||||||
| chr4:77016494 | G | GTA | 5 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
5 | HG01361.hp2 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+1486_687+1487d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016494 | ||||||
| chr4:77016599 | CATATATA others(11): Show |
C | 3 | a0001c0001t0014g0100 a0001c0001t0015g0054 a0001c0001t0015g0055 |
3 | HG02015.hp2 HG03453.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.687+1614_687+1631d others(20): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016599 | ||||||
| chr4:77016611 | T | C | 6 | a0001c0001t0001g0278 a0001c0001t0001g0285 a0001c0001t0001g0292 others(3): Show |
6 | HG01981.hp1 HG04115.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1594T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016611 | |||||||
| chr4:77016611 | T | TAC | 82 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0234 others(79): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.687+1598_687+1599d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016611 | ||||||
| chr4:77016613 | C | T | 4 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0149 others(1): Show |
4 | NA18954.hp1 NA18960.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1596C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016613 | |||||||
| chr4:77016615 | C | CACATATA others(15): Show |
5 | a0001c0001t0001g0259 a0001c0001t0001g0321 a0001c0001t0004g0014 others(2): Show |
6 | HG00609.hp1 HG02165.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1599_687+1600i others(24): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016615 | C | CACATATA others(17): Show |
1 | a0001c0001t0001g0263 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.687+1599_687+1600i others(26): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016615 | C | CAT | 78 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0324 others(75): Show |
87 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.687+1612_687+1613d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016615 | C | CATAT | 16 | a0001c0001t0002g0022 a0001c0001t0002g0115 a0001c0001t0003g0008 others(13): Show |
18 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.687+1610_687+1613d others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016615 | C | CATATATA others(3): Show |
1 | a0001c0001t0019g0166 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.687+1604_687+1613d others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016615 | C | CATATATA others(23): Show |
1 | a0001c0001t0002g0157 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.687+1610_687+1639d others(32): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016615 | CATATATA others(13): Show |
C | 24 | a0001c0001t0006g0006 a0001c0001t0006g0033 a0001c0001t0006g0040 others(21): Show |
26 | HG00544.hp1 HG00738.hp1 HG01943.hp1 others(23): Show |
intron_variant | MODIFIER | c.687+1614_687+1633d others(22): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016615 | ||||||
| chr4:77016617 | T | C | 51 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(48): Show |
57 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.687+1600T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016617 | |||||||
| chr4:77016629 | T | C | 1 | a0001c0001t0005g0226 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.687+1612T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016629 | |||||||
| chr4:77016629 | T | TATAC | 29 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(26): Show |
34 | HG00408.hp1 HG00609.hp2 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.687+1613_687+1614i others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016629 | ||||||
| chr4:77016629 | T | TATACAC | 6 | a0001c0001t0002g0108 a0001c0001t0002g0117 a0001c0001t0002g0135 others(3): Show |
6 | HG00733.hp1 HG01106.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.687+1613_687+1614i others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016629 | ||||||
| chr4:77016629 | T | TATACACA others(23): Show |
2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.687+1613_687+1614i others(32): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016629 | ||||||
| chr4:77016629 | T | TATACACA others(25): Show |
1 | a0001c0001t0002g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.687+1613_687+1614i others(34): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016629 | ||||||
| chr4:77016629 | T | TATATAC | 4 | a0001c0001t0006g0086 a0001c0001t0008g0083 a0001c0001t0008g0084 others(1): Show |
4 | HG01884.hp2 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1613_687+1614i others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016629 | ||||||
| chr4:77016631 | C | T | 10 | a0001c0001t0001g0263 a0001c0001t0002g0148 a0001c0001t0003g0008 others(7): Show |
11 | HG02572.hp2 HG02723.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.687+1614C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016631 | |||||||
| chr4:77016633 | C | CACACACA others(3): Show |
1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.687+1617_687+1618i others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACACATA others(3): Show |
3 | a0001c0001t0003g0031 a0001c0001t0003g0038 a0001c0001t0025g0030 |
3 | HG02723.hp2 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.687+1617_687+1618i others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(3): Show |
5 | a0001c0001t0001g0329 a0001c0001t0001g0332 a0001c0001t0004g0102 others(2): Show |
5 | HG02559.hp2 HG02698.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.687+1617_687+1618i others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(41): Show |
1 | a0001c0001t0008g0245 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.687+1617_687+1618i others(50): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(33): Show |
1 | a0001c0001t0008g0246 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.687+1617_687+1618i others(42): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(11): Show |
1 | a0001c0001t0001g0328 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.687+1617_687+1618i others(20): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(13): Show |
2 | a0001c0001t0001g0333 a0001c0001t0001g0336 |
2 | HG02109.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.687+1617_687+1618i others(22): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(15): Show |
3 | a0001c0001t0001g0325 a0001c0001t0001g0335 a0001c0001t0004g0165 |
3 | HG00280.hp2 HG00733.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.687+1617_687+1618i others(24): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(17): Show |
5 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0330 others(2): Show |
5 | HG00639.hp2 HG03453.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+1617_687+1618i others(26): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CACATATA others(21): Show |
1 | a0001c0001t0001g0334 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.687+1617_687+1618i others(30): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CAT | 4 | a0001c0001t0002g0094 a0001c0001t0004g0195 a0001c0001t0004g0199 others(1): Show |
4 | HG02132.hp1 NA18967.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1638_687+1639d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATAT | 4 | a0001c0001t0001g0295 a0001c0001t0001g0306 a0001c0001t0001g0307 others(1): Show |
4 | HG03516.hp1 NA18972.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1634_687+1639d others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(13): Show |
4 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(1): Show |
4 | HG01361.hp2 HG01928.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.687+1623_687+1624i others(22): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.687+1628_687+1639d others(14): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0293 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.687+1626_687+1639d others(16): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(9): Show |
5 | a0001c0001t0001g0275 a0001c0001t0001g0298 a0001c0001t0001g0319 others(2): Show |
5 | HG00735.hp2 HG03654.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+1624_687+1639d others(18): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(11): Show |
11 | a0001c0001t0001g0025 a0001c0001t0001g0262 a0001c0001t0001g0266 others(8): Show |
13 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.687+1622_687+1639d others(20): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(13): Show |
33 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0256 others(30): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.687+1620_687+1639d others(22): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(15): Show |
9 | a0001c0001t0001g0034 a0001c0001t0001g0251 a0001c0001t0001g0252 others(6): Show |
9 | HG00621.hp1 HG02129.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.687+1618_687+1639d others(24): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(41): Show |
1 | a0001c0001t0001g0250 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.687+1639_687+1640i others(50): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | CATATATA others(57): Show |
1 | a0001c0001t0001g0276 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.687+1639_687+1640i others(66): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016633 | ||||||
| chr4:77016633 | C | T | 38 | a0001c0001t0001g0263 a0001c0001t0002g0009 a0001c0001t0002g0011 others(35): Show |
41 | HG00408.hp1 HG00733.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.687+1616C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016633 | |||||||
| chr4:77016635 | T | C | 49 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(46): Show |
56 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.687+1618T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016635 | |||||||
| chr4:77016637 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.687+1620T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016637 | |||||||
| chr4:77016637 | T | TATATATA others(9): Show |
6 | a0001c0001t0001g0285 a0001c0001t0001g0292 a0001c0001t0005g0214 others(3): Show |
6 | HG03017.hp1 HG03927.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.687+1633_687+1634i others(18): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016637 | ||||||
| chr4:77016639 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.687+1622T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016639 | |||||||
| chr4:77016639 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0211 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.687+1631_687+1632i others(14): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016639 | ||||||
| chr4:77016639 | T | TATATATA others(7): Show |
39 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(36): Show |
45 | HG00099.hp2 HG00735.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.687+1633_687+1634i others(16): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016639 | ||||||
| chr4:77016645 | T | TATATATA others(47): Show |
1 | a0001c0001t0001g0303 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.687+1639_687+1640i others(56): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016645 | ||||||
| chr4:77016655 | T | C | 3 | a0001c0001t0018g0161 a0001c0001t0018g0162 a0001c0001t0026g0313 |
3 | HG02818.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.687+1638T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016655 | |||||||
| chr4:77016657 | C | T | 60 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0259 others(57): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.687+1640C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016657 | |||||||
| chr4:77016659 | C | CAT | 3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0005g0217 |
3 | HG01106.hp2 HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.687+1657_687+1658d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016659 | ||||||
| chr4:77016659 | C | CATAT | 3 | a0001c0001t0019g0236 a0001c0001t0021g0029 a0001c0001t0022g0028 |
3 | HG02970.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.687+1655_687+1658d others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016659 | ||||||
| chr4:77016661 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.687+1644T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77016661 | |||||||
| chr4:77016802 | CA | C | 75 | a0001c0001t0001g0324 a0001c0001t0002g0001 a0001c0001t0002g0004 others(72): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.687+1793delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77016802 | ||||||
| chr4:77017064 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.687+2047G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77017064 | |||||||
| chr4:77017100 | A | G | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.688-2065A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77017100 | |||||||
| chr4:77017657 | T | C | 143 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.688-1508T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77017657 | |||||||
| chr4:77017662 | G | C | 1 | a0001c0001t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.688-1503G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77017662 | |||||||
| chr4:77017732 | G | A | 143 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.688-1433G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77017732 | |||||||
| chr4:77017893 | T | C | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.688-1272T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77017893 | |||||||
| chr4:77018040 | C | T | 107 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(104): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.688-1125C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018040 | |||||||
| chr4:77018045 | A | G | 15 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(12): Show |
15 | HG00735.hp1 HG01106.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.688-1120A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018045 | |||||||
| chr4:77018158 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.688-1007G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018158 | |||||||
| chr4:77018178 | GCCAGCAC others(13): Show |
G | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.688-971_688-952del others(20): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77018178 | ||||||
| chr4:77018209 | C | G | 4 | a0001c0001t0001g0291 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02145.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-956C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018209 | |||||||
| chr4:77018209 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.688-956C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018209 | |||||||
| chr4:77018225 | C | T | 1 | a0001c0001t0031g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.688-940C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018225 | |||||||
| chr4:77018226 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.688-939G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018226 | |||||||
| chr4:77018233 | A | G | 30 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(27): Show |
30 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.688-932A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018233 | |||||||
| chr4:77018246 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.688-919C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018246 | |||||||
| chr4:77018251 | C | T | 1 | a0001c0001t0006g0046 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.688-914C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018251 | |||||||
| chr4:77018257 | T | C | 1 | a0001c0001t0010g0050 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.688-908T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018257 | |||||||
| chr4:77018266 | C | T | 4 | a0001c0001t0003g0071 a0001c0001t0007g0016 a0001c0001t0007g0017 others(1): Show |
6 | NA18946.hp1 NA18978.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.688-899C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018266 | |||||||
| chr4:77018280 | T | C | 3 | a0001c0001t0021g0029 a0001c0001t0022g0028 a0001c0001t0029g0261 |
3 | HG02970.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.688-885T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018280 | |||||||
| chr4:77018310 | A | G | 2 | a0001c0001t0004g0198 a0001c0001t0004g0200 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.688-855A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018310 | |||||||
| chr4:77018316 | G | T | 1 | a0001c0001t0017g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.688-849G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018316 | |||||||
| chr4:77018321 | T | C | 2 | a0001c0001t0004g0198 a0001c0001t0004g0200 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.688-844T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018321 | |||||||
| chr4:77018369 | A | G | 1 | a0001c0001t0003g0290 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.688-796A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018369 | |||||||
| chr4:77018371 | C | T | 1 | a0001c0001t0006g0033 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.688-794C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018371 | |||||||
| chr4:77018403 | C | T | 1 | a0001c0001t0028g0222 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.688-762C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018403 | |||||||
| chr4:77018427 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.688-738C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018427 | |||||||
| chr4:77018428 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.688-737A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018428 | |||||||
| chr4:77018428 | A | T | 1 | a0001c0001t0001g0273 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.688-737A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018428 | |||||||
| chr4:77018436 | G | A | 6 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0038 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.688-729G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018436 | |||||||
| chr4:77018444 | A | G | 64 | a0001c0001t0001g0025 a0001c0001t0001g0266 a0001c0001t0001g0281 others(61): Show |
74 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.688-721A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018444 | |||||||
| chr4:77018448 | C | CA | 8 | a0001c0001t0005g0215 a0001c0001t0007g0090 a0001c0001t0007g0177 others(5): Show |
8 | HG03927.hp1 NA18944.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-702dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77018448 | ||||||
| chr4:77018448 | CA | C | 107 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(104): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.688-702delA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77018448 | ||||||
| chr4:77018571 | G | A | 206 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0207 others(203): Show |
221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.688-594G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018571 | |||||||
| chr4:77018704 | G | GTCT | 214 | a0001c0001t0001g0337 a0001c0001t0002g0001 a0001c0001t0002g0004 others(211): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.688-459_688-457dup others(3): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 77018704 | ||||||
| chr4:77018856 | A | G | 29 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(26): Show |
32 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.688-309A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018856 | |||||||
| chr4:77018880 | C | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0038 |
3 | HG02723.hp2 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.688-285C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018880 | |||||||
| chr4:77018888 | T | C | 1 | a0001c0001t0038g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.688-277T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77018888 | |||||||
| chr4:77019007 | G | A | 48 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0259 others(45): Show |
50 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.688-158G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77019007 | |||||||
| chr4:77019021 | G | A | 1 | a0001c0001t0005g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.688-144G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77019021 | |||||||
| chr4:77019102 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.688-63C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77019102 | |||||||
| chr4:77019135 | G | T | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.688-30G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 5/9 | chr4 | 77019135 | |||||||
| chr4:77019265 | T | A | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.784+4T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77019265 | |||||||
| chr4:77019407 | G | A | 1 | a0001c0001t0018g0162 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.784+146G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77019407 | |||||||
| chr4:77019608 | A | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.784+347A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77019608 | |||||||
| chr4:77019851 | G | T | 1 | a0001c0001t0001g0277 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.784+590G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77019851 | |||||||
| chr4:77020109 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0106 a0001c0001t0002g0114 others(4): Show |
8 | NA18612.hp2 NA18939.hp1 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.785-393A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77020109 | |||||||
| chr4:77020229 | G | T | 61 | a0001c0001t0003g0008 a0001c0001t0005g0003 a0001c0001t0005g0019 others(58): Show |
70 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.785-273G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77020229 | |||||||
| chr4:77020478 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.785-24C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 6/9 | chr4 | 77020478 | |||||||
| chr4:77021007 | C | G | 2 | a0001c0001t0002g0124 a0001c0001t0002g0160 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.953+337C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021007 | |||||||
| chr4:77021050 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.953+380G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021050 | |||||||
| chr4:77021211 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0305 a0001c0001t0023g0304 |
3 | HG02074.hp2 HG02129.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.953+541G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021211 | |||||||
| chr4:77021234 | GTGGAGAC others(6): Show |
G | 1 | a0003c0002t0005g0225 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.953+567_953+579del others(13): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77021234 | ||||||
| chr4:77021237 | G | A | 58 | a0001c0001t0003g0008 a0001c0001t0005g0003 a0001c0001t0005g0019 others(55): Show |
67 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.953+567G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021237 | |||||||
| chr4:77021250 | T | A | 1 | a0003c0002t0005g0225 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.953+580T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021250 | |||||||
| chr4:77021287 | C | T | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.953+617C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021287 | |||||||
| chr4:77021358 | C | T | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0038 others(1): Show |
4 | HG02723.hp2 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+688C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77021358 | |||||||
| chr4:77022018 | T | C | 59 | a0001c0001t0003g0008 a0001c0001t0005g0003 a0001c0001t0005g0019 others(56): Show |
68 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.953+1348T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022018 | |||||||
| chr4:77022029 | G | A | 3 | a0001c0001t0009g0062 a0001c0001t0009g0063 a0001c0001t0009g0064 |
3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.953+1359G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022029 | |||||||
| chr4:77022262 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.953+1592C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022262 | |||||||
| chr4:77022544 | A | G | 2 | a0001c0001t0008g0245 a0001c0001t0008g0246 |
2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.953+1874A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022544 | |||||||
| chr4:77022545 | C | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(102): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.953+1875C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022545 | |||||||
| chr4:77022686 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.953+2016T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022686 | |||||||
| chr4:77022881 | C | CT | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.953+2211_953+2212i others(3): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022881 | |||||||
| chr4:77022884 | T | TGGGACAG others(7): Show |
30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.953+2214_953+2215i others(16): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022884 | |||||||
| chr4:77022885 | T | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.953+2215T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022885 | |||||||
| chr4:77022887 | G | A | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.953+2217G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022887 | |||||||
| chr4:77022891 | T | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.953+2221T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77022891 | |||||||
| chr4:77023215 | G | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0265 a0001c0001t0001g0273 others(2): Show |
5 | HG00621.hp1 HG02056.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.953+2545G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77023215 | |||||||
| chr4:77023216 | A | T | 1 | a0001c0001t0038g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.953+2546A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77023216 | |||||||
| chr4:77023269 | T | TAC | 9 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0310 others(6): Show |
9 | HG00733.hp2 HG00738.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.953+2631_953+2632d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023269 | T | TACAC | 21 | a0001c0001t0002g0145 a0001c0001t0005g0214 a0001c0001t0007g0016 others(18): Show |
23 | HG01243.hp1 HG01243.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.953+2629_953+2632d others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023269 | T | TACACAC | 100 | a0001c0001t0001g0323 a0001c0001t0002g0001 a0001c0001t0002g0004 others(97): Show |
118 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.953+2627_953+2632d others(8): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023269 | T | TACACACA others(1): Show |
23 | a0001c0001t0002g0091 a0001c0001t0002g0130 a0001c0001t0002g0139 others(20): Show |
23 | HG00544.hp1 HG00544.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.953+2625_953+2632d others(10): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023269 | TAC | T | 8 | a0001c0001t0001g0276 a0001c0001t0001g0309 a0001c0001t0004g0102 others(5): Show |
8 | HG00280.hp1 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.953+2631_953+2632d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023269 | TACACACA others(1): Show |
T | 31 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0012 others(28): Show |
37 | HG00099.hp1 HG00408.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.953+2625_953+2632d others(10): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023269 | TACACACA others(3): Show |
T | 23 | a0001c0001t0002g0022 a0001c0001t0003g0031 a0001c0001t0003g0032 others(20): Show |
24 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.953+2623_953+2632d others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77023269 | ||||||
| chr4:77023302 | A | ACACAACA others(3): Show |
1 | a0003c0002t0005g0225 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.953+2632_953+2633i others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77023302 | |||||||
| chr4:77023302 | A | ACACACAC others(3): Show |
1 | a0001c0001t0002g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.953+2632_953+2633i others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77023302 | |||||||
| chr4:77023669 | T | A | 2 | a0001c0001t0018g0161 a0001c0001t0018g0162 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.953+2999T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77023669 | |||||||
| chr4:77023972 | C | G | 11 | a0001c0001t0008g0083 a0001c0001t0008g0084 a0001c0001t0008g0085 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.953+3302C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77023972 | |||||||
| chr4:77024017 | C | T | 104 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(101): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.953+3347C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77024017 | |||||||
| chr4:77024079 | T | C | 30 | a0001c0001t0003g0008 a0001c0001t0006g0006 a0001c0001t0006g0033 others(27): Show |
33 | HG00544.hp1 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.953+3409T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77024079 | |||||||
| chr4:77024090 | A | G | 218 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(215): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.953+3420A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77024090 | |||||||
| chr4:77024414 | GGACCCAG others(16): Show |
G | 1 | a0001c0001t0014g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.953+3750_953+3772d others(25): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77024414 | ||||||
| chr4:77024613 | G | A | 1 | a0001c0001t0003g0008 | 2 | NA18984.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.953+3943G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77024613 | |||||||
| chr4:77024856 | T | C | 1 | a0001c0001t0027g0264 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.954-3773T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77024856 | |||||||
| chr4:77025113 | AT | A | 105 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(102): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.954-3514delT | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77025113 | ||||||
| chr4:77025229 | A | G | 11 | a0001c0001t0008g0083 a0001c0001t0008g0084 a0001c0001t0008g0085 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.954-3400A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025229 | |||||||
| chr4:77025295 | G | A | 2 | a0001c0001t0015g0054 a0001c0001t0015g0055 |
2 | HG02015.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.954-3334G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025295 | |||||||
| chr4:77025316 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.954-3313C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025316 | |||||||
| chr4:77025384 | A | T | 2 | a0001c0001t0019g0166 a0001c0001t0019g0236 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.954-3245A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025384 | |||||||
| chr4:77025420 | G | A | 1 | a0001c0001t0029g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.954-3209G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025420 | |||||||
| chr4:77025481 | C | T | 1 | a0001c0001t0014g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.954-3148C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025481 | |||||||
| chr4:77025544 | C | CA | 44 | a0001c0001t0002g0001 a0001c0001t0002g0124 a0001c0001t0002g0129 others(41): Show |
50 | HG00544.hp2 HG00597.hp2 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.954-3072dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77025544 | ||||||
| chr4:77025558 | G | A | 1 | a0001c0001t0012g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.954-3071G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025558 | |||||||
| chr4:77025664 | C | T | 59 | a0001c0001t0003g0008 a0001c0001t0005g0003 a0001c0001t0005g0019 others(56): Show |
68 | HG00099.hp2 HG00544.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.954-2965C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025664 | |||||||
| chr4:77025709 | A | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0094 a0001c0001t0002g0111 others(1): Show |
5 | NA18957.hp1 NA18978.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-2920A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77025709 | |||||||
| chr4:77026000 | T | C | 41 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(38): Show |
44 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.954-2629T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026000 | |||||||
| chr4:77026014 | G | T | 1 | a0001c0001t0003g0070 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.954-2615G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026014 | |||||||
| chr4:77026093 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.954-2536C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026093 | |||||||
| chr4:77026273 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.954-2356G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026273 | |||||||
| chr4:77026332 | A | G | 7 | a0001c0001t0008g0083 a0001c0001t0008g0084 a0001c0001t0008g0085 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.954-2297A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026332 | |||||||
| chr4:77026352 | T | C | 8 | a0001c0001t0001g0272 a0001c0001t0001g0291 a0001c0001t0001g0297 others(5): Show |
8 | HG02572.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.954-2277T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026352 | |||||||
| chr4:77026403 | A | C | 4 | a0001c0001t0001g0234 a0001c0001t0001g0267 a0001c0001t0004g0102 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.954-2226A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026403 | |||||||
| chr4:77026449 | T | A | 9 | a0001c0001t0008g0083 a0001c0001t0008g0084 a0001c0001t0008g0085 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.954-2180T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026449 | |||||||
| chr4:77026466 | C | T | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0096 |
3 | NA19000.hp2 NA19057.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.954-2163C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026466 | |||||||
| chr4:77026594 | G | A | 4 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(1): Show |
4 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.954-2035G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026594 | |||||||
| chr4:77026623 | A | T | 2 | a0001c0001t0029g0261 a0001c0001t0038g0101 |
2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.954-2006A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026623 | |||||||
| chr4:77026711 | A | G | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.954-1918A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026711 | |||||||
| chr4:77026911 | A | G | 1 | a0001c0001t0021g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.954-1718A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77026911 | |||||||
| chr4:77027102 | C | T | 2 | a0001c0001t0029g0261 a0001c0001t0038g0101 |
2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.954-1527C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77027102 | |||||||
| chr4:77027411 | C | T | 1 | a0001c0001t0007g0174 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.954-1218C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77027411 | |||||||
| chr4:77027493 | C | T | 2 | a0001c0001t0004g0014 a0001c0001t0004g0164 |
3 | HG00609.hp1 HG02165.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.954-1136C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77027493 | |||||||
| chr4:77027856 | A | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0039 |
3 | NA18968.hp2 NA18972.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.954-773A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77027856 | |||||||
| chr4:77027861 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.954-768A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77027861 | |||||||
| chr4:77027943 | G | A | 40 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0090 others(37): Show |
42 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.954-686G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77027943 | |||||||
| chr4:77027960 | T | TA | 101 | a0001c0001t0002g0184 a0001c0001t0003g0008 a0001c0001t0005g0003 others(98): Show |
113 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.954-668dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 77027960 | ||||||
| chr4:77028102 | C | T | 4 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0003g0071 others(1): Show |
4 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.954-527C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028102 | |||||||
| chr4:77028125 | A | G | 29 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0090 others(26): Show |
31 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.954-504A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028125 | |||||||
| chr4:77028258 | C | A | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.954-371C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028258 | |||||||
| chr4:77028418 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.954-211G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028418 | |||||||
| chr4:77028457 | T | C | 2 | a0001c0001t0029g0261 a0001c0001t0038g0101 |
2 | HG01884.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.954-172T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028457 | |||||||
| chr4:77028535 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.954-94A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028535 | |||||||
| chr4:77028563 | A | T | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.954-66A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028563 | |||||||
| chr4:77028565 | G | A | 2 | a0001c0001t0014g0092 a0001c0001t0014g0093 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.954-64G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028565 | |||||||
| chr4:77028606 | C | T | 1 | a0001c0001t0035g0113 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.954-23C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028606 | |||||||
| chr4:77028618 | A | T | 1 | a0001c0001t0004g0164 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.954-11A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 7/9 | chr4 | 77028618 | |||||||
| chr4:77028844 | TGGTCCAA | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(102): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1086+85_1086+91del others(7): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77028844 | ||||||
| chr4:77029109 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1086+348A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029109 | |||||||
| chr4:77029229 | T | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1086+468T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029229 | |||||||
| chr4:77029264 | C | A | 14 | a0001c0001t0003g0067 a0001c0001t0003g0068 a0001c0001t0003g0069 others(11): Show |
14 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1086+503C>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029264 | |||||||
| chr4:77029335 | A | AGT | 3 | a0001c0001t0004g0195 a0001c0001t0006g0049 a0001c0001t0019g0236 |
3 | HG02055.hp1 HG03516.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1086+593_1086+594d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77029335 | ||||||
| chr4:77029335 | A | AGTGT | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG00733.hp2 HG03471.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+591_1086+594d others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77029335 | ||||||
| chr4:77029335 | AGT | A | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1086+593_1086+594d others(4): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77029335 | ||||||
| chr4:77029767 | T | C | 56 | a0001c0001t0002g0152 a0001c0001t0005g0003 a0001c0001t0005g0019 others(53): Show |
65 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1086+1006T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029767 | |||||||
| chr4:77029767 | T | TAC | 5 | a0001c0001t0008g0083 a0001c0001t0008g0084 a0001c0001t0008g0085 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1087-1002_1087-100 others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77029767 | ||||||
| chr4:77029781 | C | CACACACA others(1): Show |
29 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0090 others(26): Show |
31 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(28): Show |
intron_variant | MODIFIER | c.1087-1001_1087-100 others(12): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77029781 | ||||||
| chr4:77029782 | A | G | 6 | a0001c0001t0002g0022 a0001c0001t0003g0080 a0001c0001t0003g0081 others(3): Show |
7 | HG02258.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1087-1001A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029782 | |||||||
| chr4:77029789 | T | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1087-994T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029789 | |||||||
| chr4:77029803 | CACACATA others(7): Show |
C | 2 | a0001c0001t0021g0029 a0001c0001t0022g0028 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1087-968_1087-955d others(16): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 77029803 | ||||||
| chr4:77029834 | A | G | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1087-949A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029834 | |||||||
| chr4:77029854 | A | G | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1087-929A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029854 | |||||||
| chr4:77029990 | G | C | 1 | a0001c0001t0005g0020 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1087-793G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77029990 | |||||||
| chr4:77030071 | A | AT | 41 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(38): Show |
44 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1087-712_1087-711i others(3): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77030071 | |||||||
| chr4:77030149 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1087-634G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77030149 | |||||||
| chr4:77030243 | G | A | 31 | a0001c0001t0003g0235 a0001c0001t0007g0015 a0001c0001t0007g0016 others(28): Show |
34 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(31): Show |
intron_variant | MODIFIER | c.1087-540G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77030243 | |||||||
| chr4:77030598 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1087-185T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77030598 | |||||||
| chr4:77030712 | C | G | 2 | a0001c0001t0019g0166 a0001c0001t0019g0236 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1087-71C>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 8/9 | chr4 | 77030712 | |||||||
| chr4:77031033 | T | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1274+63T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031033 | |||||||
| chr4:77031127 | T | A | 7 | a0001c0001t0008g0083 a0001c0001t0008g0084 a0001c0001t0008g0085 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1274+157T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031127 | |||||||
| chr4:77031221 | G | T | 1 | a0001c0001t0003g0322 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1274+251G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031221 | |||||||
| chr4:77031389 | T | G | 217 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(214): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1274+419T>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031389 | |||||||
| chr4:77031445 | A | T | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1274+475A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031445 | |||||||
| chr4:77031539 | T | C | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1274+569T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031539 | |||||||
| chr4:77031769 | A | C | 2 | a0001c0001t0019g0166 a0001c0001t0019g0236 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1274+799A>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031769 | |||||||
| chr4:77031779 | C | T | 31 | a0001c0001t0003g0070 a0001c0001t0007g0015 a0001c0001t0007g0016 others(28): Show |
34 | HG00544.hp2 HG00621.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1274+809C>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031779 | |||||||
| chr4:77031856 | G | A | 15 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG00280.hp2 HG00639.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1274+886G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77031856 | |||||||
| chr4:77032193 | C | CTT | 41 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(38): Show |
44 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1274+1224_1274+122 others(6): Show |
SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 77032193 | ||||||
| chr4:77032317 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1274+1347A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77032317 | |||||||
| chr4:77032320 | G | T | 1 | a0001c0001t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1274+1350G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77032320 | |||||||
| chr4:77032321 | A | T | 1 | a0001c0001t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1274+1351A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77032321 | |||||||
| chr4:77032505 | G | T | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1274+1535G>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77032505 | |||||||
| chr4:77032689 | T | C | 1 | a0001c0001t0024g0315 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1274+1719T>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77032689 | |||||||
| chr4:77032757 | G | A | 2 | a0001c0001t0019g0166 a0001c0001t0019g0236 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1275-1740G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77032757 | |||||||
| chr4:77033063 | A | G | 1 | a0001c0001t0004g0199 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1275-1434A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77033063 | |||||||
| chr4:77033159 | G | GA | 53 | a0001c0001t0002g0022 a0001c0001t0003g0031 a0001c0001t0003g0032 others(50): Show |
57 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.1275-1327dupA | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 77033159 | ||||||
| chr4:77033367 | A | T | 1 | a0001c0001t0003g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1275-1130A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77033367 | |||||||
| chr4:77033437 | G | A | 30 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0007g0017 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.1275-1060G>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77033437 | |||||||
| chr4:77033915 | A | T | 1 | a0001c0001t0001g0295 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1275-582A>T | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77033915 | |||||||
| chr4:77033956 | A | G | 1 | a0001c0001t0004g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1275-541A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77033956 | |||||||
| chr4:77033978 | T | A | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1275-519T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77033978 | |||||||
| chr4:77034052 | T | A | 12 | a0001c0001t0002g0022 a0001c0001t0003g0031 a0001c0001t0003g0032 others(9): Show |
13 | HG02055.hp2 HG02258.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1275-445T>A | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77034052 | |||||||
| chr4:77034359 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1275-138G>C | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77034359 | |||||||
| chr4:77034450 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1275-47A>G | SEPTIN11 | ENSG00000138758.12 | transcript | ENST00000264893.11 | protein_coding | 9/9 | chr4 | 77034450 |