Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 989 |
| ensemblid | ENSG00000122545.22 |
| hgncid | 1717 |
| symbol | SEPTIN7 |
| name | septin 7 |
| refseq_nuc | NM_001788.6 |
| refseq_prot | NP_001779.3 |
| ensembl_nuc | ENST00000350320.11 |
| ensembl_prot | ENSP00000344868.8 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 35801057 |
| end | 35907110 |
| strand | + |
| ver | v1.2 |
| region | chr7:35801057-35907110 |
| region5000 | chr7:35796057-35912110 |
| regionname0 | SEPTIN7_chr7_35801057_35907110 |
| regionname5000 | SEPTIN7_chr7_35796057_35912110 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 437 | 345 | 91 | 60 | 154 | 10 | 28 | 118 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | MSVSA others(432): Show |
chr7 | 35796057 | 35912110 |
| a0002 | 0/0 | 437 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | MSVSA others(432): Show |
chr7 | 35796057 | 35912110 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1311 | 334 | 89 | 58 | 148 | 10 | 27 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | ATGTC others(1306): Show |
chr7 | 35796057 | 35912110 | ||
| a0001c0002 | 0/0 | 1311 | 9 | 1 | 2 | 6 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | ATGTC others(1306): Show |
chr7 | 35796057 | 35912110 | ||
| a0001c0003 | 0/0 | 1311 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | ATGTC others(1306): Show |
chr7 | 35796057 | 35912110 | ||
| a0001c0004 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | ATGTC others(1306): Show |
chr7 | 35796057 | 35912110 | ||
| a0002c0005 | 0/0 | 1311 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | ATGTC others(1306): Show |
chr7 | 35796057 | 35912110 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4283 | 86 | 9 | 30 | 31 | 4 | 11 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0002 | 0/0 | 4282 | 74 | 28 | 6 | 38 | 1 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0003 | 0/0 | 4282 | 36 | 2 | 8 | 17 | 4 | 5 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0004 | 1/0 | 4284 | 16 | 15 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4279): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0005 | 0/0 | 4283 | 15 | 5 | 4 | 0 | 0 | 6 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0006 | 0/0 | 4283 | 12 | 1 | 0 | 11 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0007 | 0/0 | 4283 | 9 | 1 | 1 | 6 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0008 | 0/0 | 4284 | 9 | 9 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4279): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0009 | 0/0 | 4283 | 9 | 0 | 0 | 9 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0010 | 0/0 | 4283 | 8 | 0 | 1 | 7 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0011 | 0/0 | 4283 | 8 | 8 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0012 | 0/0 | 4283 | 8 | 0 | 0 | 8 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0013 | 0/0 | 4283 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0014 | 0/0 | 4282 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0015 | 0/0 | 4284 | 3 | 0 | 1 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4279): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0016 | 0/0 | 4283 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0017 | 0/0 | 4282 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0018 | 0/0 | 4282 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0019 | 0/0 | 4283 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0020 | 0/0 | 4283 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0021 | 0/0 | 4283 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0022 | 0/0 | 4284 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4279): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0023 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0024 | 0/0 | 4284 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4279): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0025 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0026 | 0/0 | 4284 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4279): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0027 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0028 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0029 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0030 | 0/0 | 4282 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0031 | 0/0 | 4282 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0032 | 0/0 | 4282 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0033 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0034 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0035 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0036 | 0/0 | 4283 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0037 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0038 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0001t0039 | 0/0 | 4283 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0002t0001 | 0/0 | 4283 | 9 | 1 | 2 | 6 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0001c0003t0002 | 0/0 | 4282 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| a0001c0004t0013 | 0/0 | 4283 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4278): Show |
chr7 | 35796057 | 35912110 |
| a0002c0005t0002 | 0/0 | 4282 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | AGTCG others(4277): Show |
chr7 | 35796057 | 35912110 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0004g0312 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0008g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0009g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0010g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0012g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0014g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0015g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0015g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0016g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0016g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0017g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0017g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0018g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0018g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0019g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0019g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0020g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0021g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0021g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0022g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0022g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0023g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0025g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0026g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0027g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0028g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0029g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0030g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0031g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0032g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0033g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0034g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0035g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0036g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0037g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0038g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0001t0039g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0001c0004t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| a0002c0005t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0101 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | GBR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00597 | hp2 | a0001 | c0001 | t0033 | g0061 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00609 | hp1 | a0001 | c0001 | t0012 | g0233 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0201 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01081 | hp1 | a0001 | c0001 | t0026 | g0203 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01081 | hp2 | a0001 | c0001 | t0023 | g0089 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0045 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0196 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01257 | hp1 | a0001 | c0001 | t0020 | g0008 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01258 | hp1 | a0001 | c0001 | t0020 | g0008 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01433 | hp2 | a0001 | c0001 | t0030 | g0107 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0030 | EUR | IBS | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0048 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0049 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0202 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0305 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0208 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02055 | hp1 | a0001 | c0001 | t0019 | g0308 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0209 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0257 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02129 | hp2 | a0001 | c0001 | t0016 | g0262 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02132 | hp2 | a0001 | c0001 | t0032 | g0158 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02135 | hp1 | a0001 | c0001 | t0014 | g0165 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02155 | hp1 | a0001 | c0001 | t0014 | g0130 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02155 | hp2 | a0001 | c0001 | t0021 | g0059 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02165 | hp1 | a0001 | c0001 | t0014 | g0129 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0070 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02293 | hp2 | a0001 | c0001 | t0015 | g0009 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02300 | hp1 | a0001 | c0001 | t0018 | g0121 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0218 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02615 | hp2 | a0001 | c0001 | t0011 | g0067 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0136 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02886 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0026 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0065 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0047 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03195 | hp1 | a0002 | c0005 | t0002 | g0104 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0204 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03486 | hp1 | a0001 | c0001 | t0022 | g0194 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0068 | AFR | ESN | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03540 | hp2 | a0001 | c0001 | t0019 | g0264 | AFR | GWD | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03669 | hp2 | a0001 | c0001 | t0037 | g0205 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0085 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0191 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03942 | hp2 | a0001 | c0001 | t0034 | g0259 | SAS | BEB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04115 | hp1 | a0001 | c0001 | t0031 | g0167 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0206 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0207 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | STU | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0005 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18612 | hp1 | a0001 | c0001 | t0025 | g0168 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CHB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18906 | hp2 | a0001 | c0001 | t0029 | g0037 | AFR | YRI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18940 | hp1 | a0001 | c0001 | t0028 | g0054 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18942 | hp1 | a0001 | c0001 | t0009 | g0320 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18948 | hp1 | a0001 | c0001 | t0010 | g0269 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18948 | hp2 | a0001 | c0001 | t0014 | g0105 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18949 | hp1 | a0001 | c0001 | t0018 | g0103 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18952 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18952 | hp2 | a0001 | c0001 | t0012 | g0263 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18956 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0293 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0027 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18961 | hp1 | a0001 | c0001 | t0016 | g0077 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18968 | hp1 | a0001 | c0001 | t0027 | g0145 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18969 | hp1 | a0001 | c0001 | t0036 | g0200 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18970 | hp2 | a0001 | c0001 | t0012 | g0232 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18972 | hp1 | a0001 | c0001 | t0015 | g0052 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18975 | hp2 | a0001 | c0001 | t0012 | g0064 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18978 | hp1 | a0001 | c0001 | t0015 | g0274 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18978 | hp2 | a0001 | c0001 | t0006 | g0060 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18991 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18992 | hp1 | a0001 | c0001 | t0012 | g0227 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18995 | hp1 | a0001 | c0001 | t0016 | g0326 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18995 | hp2 | a0001 | c0001 | t0017 | g0216 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18997 | hp1 | a0001 | c0001 | t0010 | g0240 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA18997 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19001 | hp1 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19001 | hp2 | a0001 | c0001 | t0009 | g0229 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19004 | hp2 | a0001 | c0001 | t0009 | g0265 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19006 | hp1 | a0001 | c0001 | t0012 | g0063 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19009 | hp2 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19010 | hp1 | a0001 | c0001 | t0012 | g0260 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19043 | hp1 | a0001 | c0004 | t0013 | g0044 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0177 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19057 | hp2 | a0001 | c0001 | t0035 | g0226 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19059 | hp1 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19059 | hp2 | a0001 | c0001 | t0009 | g0297 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19060 | hp1 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19062 | hp2 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0241 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19067 | hp2 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19072 | hp2 | a0001 | c0001 | t0010 | g0328 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19076 | hp2 | a0001 | c0001 | t0010 | g0327 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19078 | hp2 | a0001 | c0001 | t0010 | g0238 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19081 | hp1 | a0001 | c0001 | t0021 | g0051 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19084 | hp1 | a0001 | c0001 | t0009 | g0325 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19085 | hp2 | a0001 | c0001 | t0010 | g0271 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0303 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0046 | AFR | ASW | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ASW | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20805 | hp1 | a0001 | c0001 | t0039 | g0195 | EUR | TSI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0092 | EUR | TSI | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0013 | SAS | GIH | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | GIH | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02486 | hp2 | a0001 | c0001 | t0038 | g0170 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03471 | hp1 | a0001 | c0001 | t0022 | g0193 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | USA | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0098 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | LWK | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0011 | REF | REF | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0312 | REF | REF | SEPTIN7_chr7_35796057_35912110 | SEPTIN7 | chr7 | 35796057 | 35912110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801229 | C | G | 1 | a0002 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.20C>G | p.Ser7Cys | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 173/4284 | 20/1314 | 7/437 | chr7 | 35801229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801233 | T | A | 1 | a0001c0003 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.24T>A | p.Ala8Ala | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 177/4284 | 24/1314 | 8/437 | chr7 | 35801233 | |||
| chr7:35903153 | C | T | 1 | a0001c0002 | 9 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(6): Show |
synonymous_variant | LOW | c.1212C>T | p.Phe404Phe | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/14 | 1365/4284 | 1212/1314 | 404/437 | chr7 | 35903153 | |||
| chr7:35904290 | T | C | 1 | a0001c0004 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1311T>C | p.Phe437Phe | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1464/4284 | 1311/1314 | 437/437 | chr7 | 35904290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801107 | A | C | 2 | a0001c0001t0022 a0001c0001t0039 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
5_prime_UTR_variant | MODIFIER | c.-103A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 103 | chr7 | 35801107 | ||||||
| chr7:35801198 | G | A | 1 | a0001c0001t0023 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/14 | 12 | chr7 | 35801198 | ||||||
| chr7:35904342 | T | A | 1 | a0001c0001t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 49 | chr7 | 35904342 | ||||||
| chr7:35904593 | T | C | 1 | a0001c0001t0025 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 300 | chr7 | 35904593 | ||||||
| chr7:35904636 | C | T | 1 | a0001c0001t0014 | 4 | HG02135.hp1 HG02155.hp1 HG02165.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*343C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 343 | chr7 | 35904636 | ||||||
| chr7:35904805 | GA | G | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(33): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*524delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 524 | INFO_REALIGN_3_PRIME | chr7 | 35904805 | |||||
| chr7:35904895 | T | C | 1 | a0001c0001t0027 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*602T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 602 | chr7 | 35904895 | ||||||
| chr7:35905147 | C | G | 1 | a0001c0001t0016 | 3 | HG02129.hp2 NA18961.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*854C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 854 | chr7 | 35905147 | ||||||
| chr7:35905363 | G | A | 1 | a0001c0001t0017 | 2 | HG02080.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1070G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1070 | chr7 | 35905363 | ||||||
| chr7:35905495 | C | T | 1 | a0001c0001t0021 | 2 | HG02155.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1202C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1202 | chr7 | 35905495 | ||||||
| chr7:35905522 | AT | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(12): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1239delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1239 | INFO_REALIGN_3_PRIME | chr7 | 35905522 | |||||
| chr7:35905529 | T | C | 1 | a0001c0001t0028 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1236T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1236 | chr7 | 35905529 | ||||||
| chr7:35905571 | T | G | 1 | a0001c0001t0029 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1278T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1278 | chr7 | 35905571 | ||||||
| chr7:35905574 | G | A | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(18): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1281G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1281 | chr7 | 35905574 | ||||||
| chr7:35905592 | T | C | 32 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(29): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*1299T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1299 | chr7 | 35905592 | ||||||
| chr7:35905737 | C | T | 1 | a0001c0001t0018 | 2 | HG02300.hp1 NA18949.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1444C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1444 | chr7 | 35905737 | ||||||
| chr7:35905802 | G | A | 3 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0023 |
39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1509G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1509 | chr7 | 35905802 | ||||||
| chr7:35905811 | A | G | 2 | a0001c0001t0009 a0001c0001t0035 |
10 | HG02083.hp2 NA18942.hp1 NA18957.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1518A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1518 | chr7 | 35905811 | ||||||
| chr7:35905825 | T | G | 1 | a0001c0001t0036 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1532T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1532 | chr7 | 35905825 | ||||||
| chr7:35905866 | A | T | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0016 others(1): Show |
21 | HG00609.hp1 HG02083.hp2 HG02129.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1573A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1573 | chr7 | 35905866 | ||||||
| chr7:35906106 | C | T | 1 | a0001c0001t0011 | 8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1813C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1813 | chr7 | 35906106 | ||||||
| chr7:35906243 | C | G | 6 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0021 others(3): Show |
22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1950C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 1950 | chr7 | 35906243 | ||||||
| chr7:35906325 | A | G | 1 | a0001c0001t0034 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2032A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2032 | chr7 | 35906325 | ||||||
| chr7:35906357 | T | C | 1 | a0001c0001t0019 | 2 | HG02055.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2064T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2064 | chr7 | 35906357 | ||||||
| chr7:35906411 | G | A | 6 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0021 others(3): Show |
22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2118G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2118 | chr7 | 35906411 | ||||||
| chr7:35906494 | T | C | 4 | a0001c0001t0006 a0001c0001t0021 a0001c0001t0028 others(1): Show |
16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2201T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2201 | chr7 | 35906494 | ||||||
| chr7:35906499 | A | C | 1 | a0001c0001t0020 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2206A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2206 | chr7 | 35906499 | ||||||
| chr7:35906612 | G | A | 1 | a0001c0001t0035 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2319 | chr7 | 35906612 | ||||||
| chr7:35906643 | T | C | 5 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0026 others(2): Show |
20 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2350T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2350 | chr7 | 35906643 | ||||||
| chr7:35906649 | A | G | 1 | a0001c0001t0010 | 8 | HG01934.hp1 NA18948.hp1 NA18997.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2356A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2356 | chr7 | 35906649 | ||||||
| chr7:35906660 | C | T | 1 | a0001c0001t0032 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2367C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2367 | chr7 | 35906660 | ||||||
| chr7:35906680 | G | A | 1 | a0001c0001t0030 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2387G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2387 | chr7 | 35906680 | ||||||
| chr7:35906711 | T | C | 1 | a0001c0001t0037 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2418T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2418 | chr7 | 35906711 | ||||||
| chr7:35906743 | C | G | 1 | a0001c0001t0033 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2450 | chr7 | 35906743 | ||||||
| chr7:35906818 | T | G | 1 | a0001c0001t0031 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2525T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2525 | chr7 | 35906818 | ||||||
| chr7:35906999 | T | G | 1 | a0001c0001t0008 | 9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2706T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 14/14 | 2706 | chr7 | 35906999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:35801464 | G | A | 1 | a0001c0001t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.61+194G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801464 | |||||||
| chr7:35801488 | G | A | 1 | a0001c0001t0005g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.61+218G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801488 | |||||||
| chr7:35801490 | G | A | 4 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(1): Show |
4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+220G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801490 | |||||||
| chr7:35801647 | T | G | 213 | a0001c0001t0001g0050 a0001c0001t0001g0180 a0001c0001t0001g0181 others(210): Show |
224 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.61+377T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801647 | |||||||
| chr7:35801669 | G | C | 9 | a0001c0001t0008g0018 a0001c0001t0008g0019 a0001c0001t0008g0020 others(6): Show |
9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.61+399G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801669 | |||||||
| chr7:35801687 | G | C | 148 | a0001c0001t0001g0050 a0001c0001t0002g0004 a0001c0001t0002g0006 others(145): Show |
155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.61+417G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35801687 | |||||||
| chr7:35802127 | G | A | 1 | a0001c0001t0006g0027 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.61+857G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802127 | |||||||
| chr7:35802276 | A | G | 42 | a0001c0001t0003g0002 a0001c0001t0003g0183 a0001c0001t0003g0184 others(39): Show |
46 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.61+1006A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802276 | |||||||
| chr7:35802379 | T | A | 9 | a0001c0001t0003g0002 a0001c0001t0003g0183 a0001c0001t0003g0184 others(6): Show |
11 | HG00438.hp1 HG00673.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+1109T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802379 | |||||||
| chr7:35802398 | T | G | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.61+1128T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802398 | |||||||
| chr7:35802455 | C | G | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.61+1185C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802455 | |||||||
| chr7:35802567 | A | C | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+1297A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802567 | |||||||
| chr7:35802577 | A | G | 1 | a0001c0001t0005g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.61+1307A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802577 | |||||||
| chr7:35802647 | G | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.61+1377G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802647 | |||||||
| chr7:35802694 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.61+1424A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802694 | |||||||
| chr7:35802720 | G | C | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+1450G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802720 | |||||||
| chr7:35802814 | G | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG00438.hp2 HG01346.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1544G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802814 | |||||||
| chr7:35802816 | G | A | 46 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(43): Show |
49 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.61+1546G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802816 | |||||||
| chr7:35802829 | G | C | 1 | a0001c0001t0035g0226 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.61+1559G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35802829 | |||||||
| chr7:35803044 | T | C | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+1774T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803044 | |||||||
| chr7:35803114 | A | G | 122 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0032 others(119): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.61+1844A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803114 | |||||||
| chr7:35803453 | A | T | 1 | a0001c0001t0003g0190 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.61+2183A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803453 | |||||||
| chr7:35803550 | G | A | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+2280G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803550 | |||||||
| chr7:35803710 | A | ACAAAACT others(307): Show |
1 | a0001c0001t0025g0168 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.61+2451_61+2452ins others(314): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35803710 | ||||||
| chr7:35803846 | C | T | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+2576C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803846 | |||||||
| chr7:35803880 | T | C | 10 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(7): Show |
11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+2610T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35803880 | |||||||
| chr7:35804029 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.61+2759C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804029 | |||||||
| chr7:35804275 | A | G | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.61+3005A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804275 | |||||||
| chr7:35804760 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.61+3490A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804760 | |||||||
| chr7:35804835 | G | GT | 37 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(34): Show |
40 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.61+3583dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35804835 | ||||||
| chr7:35804835 | G | GTT | 13 | a0001c0001t0002g0166 a0001c0001t0005g0013 a0001c0001t0005g0201 others(10): Show |
13 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.61+3582_61+3583dup others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35804835 | ||||||
| chr7:35804835 | G | T | 27 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 others(24): Show |
28 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.61+3565G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804835 | |||||||
| chr7:35804867 | G | A | 1 | a0001c0001t0011g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+3597G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35804867 | |||||||
| chr7:35805070 | C | T | 1 | a0001c0001t0011g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.61+3800C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805070 | |||||||
| chr7:35805177 | C | T | 3 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0004g0012 |
3 | HG02109.hp1 HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.61+3907C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805177 | |||||||
| chr7:35805230 | A | C | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+3960A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805230 | |||||||
| chr7:35805843 | A | C | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.61+4573A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35805843 | |||||||
| chr7:35806012 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+4742T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806012 | |||||||
| chr7:35806038 | C | G | 1 | a0001c0001t0032g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61+4768C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806038 | |||||||
| chr7:35806103 | G | T | 1 | a0001c0001t0009g0320 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.61+4833G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806103 | |||||||
| chr7:35806125 | G | T | 7 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(4): Show |
7 | HG00609.hp2 NA18951.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+4855G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806125 | |||||||
| chr7:35806237 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.61+4967T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806237 | |||||||
| chr7:35806290 | T | C | 1 | a0001c0001t0012g0227 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.61+5020T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806290 | |||||||
| chr7:35806350 | T | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+5080T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806350 | |||||||
| chr7:35806478 | G | A | 1 | a0001c0001t0005g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.61+5208G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806478 | |||||||
| chr7:35806498 | A | G | 118 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0032 others(115): Show |
121 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.61+5228A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806498 | |||||||
| chr7:35806517 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.61+5247G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806517 | |||||||
| chr7:35806648 | A | G | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+5378A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35806648 | |||||||
| chr7:35807173 | T | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.61+5903T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807173 | |||||||
| chr7:35807186 | C | CT | 44 | a0001c0001t0001g0319 a0001c0001t0002g0123 a0001c0001t0002g0124 others(41): Show |
44 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.61+5931dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807186 | ||||||
| chr7:35807237 | T | C | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.61+5967T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807237 | |||||||
| chr7:35807269 | C | T | 47 | a0001c0001t0002g0071 a0001c0001t0004g0003 a0001c0001t0004g0007 others(44): Show |
50 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.61+5999C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807269 | |||||||
| chr7:35807278 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.61+6008G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807278 | |||||||
| chr7:35807309 | G | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.61+6039G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807309 | |||||||
| chr7:35807313 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.61+6043A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807313 | |||||||
| chr7:35807351 | AT | A | 173 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(170): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.61+6110delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807351 | ||||||
| chr7:35807351 | ATT | A | 121 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0002g0004 others(118): Show |
128 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.61+6109_61+6110del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807351 | ||||||
| chr7:35807351 | ATTT | A | 14 | a0001c0001t0002g0028 a0001c0001t0002g0078 a0001c0001t0002g0079 others(11): Show |
14 | HG02129.hp1 HG02896.hp1 HG03239.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+6108_61+6110del others(3): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35807351 | ||||||
| chr7:35807400 | C | T | 1 | a0001c0001t0003g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61+6130C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807400 | |||||||
| chr7:35807431 | G | A | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.61+6161G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807431 | |||||||
| chr7:35807436 | G | A | 25 | a0001c0001t0002g0071 a0001c0001t0004g0003 a0001c0001t0004g0007 others(22): Show |
27 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.61+6166G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807436 | |||||||
| chr7:35807525 | C | T | 10 | a0001c0001t0002g0006 a0001c0001t0002g0116 a0001c0001t0002g0118 others(7): Show |
11 | HG00733.hp2 HG00741.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.61+6255C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807525 | |||||||
| chr7:35807606 | G | A | 151 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.61+6336G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807606 | |||||||
| chr7:35807643 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(21): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.61+6373G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807643 | |||||||
| chr7:35807861 | G | T | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+6591G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35807861 | |||||||
| chr7:35808095 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+6825G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808095 | |||||||
| chr7:35808099 | A | G | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.61+6829A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808099 | |||||||
| chr7:35808113 | A | G | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.61+6843A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808113 | |||||||
| chr7:35808210 | TCTTA | T | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+6944_61+6947del others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35808210 | ||||||
| chr7:35808377 | T | C | 151 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.61+7107T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808377 | |||||||
| chr7:35808709 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+7439G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808709 | |||||||
| chr7:35808720 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+7450C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808720 | |||||||
| chr7:35808802 | A | G | 5 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0040 others(2): Show |
5 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+7532A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808802 | |||||||
| chr7:35808941 | A | G | 1 | a0001c0001t0003g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.61+7671A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808941 | |||||||
| chr7:35808975 | G | A | 1 | a0001c0001t0008g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.61+7705G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808975 | |||||||
| chr7:35808988 | A | G | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.61+7718A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35808988 | |||||||
| chr7:35809227 | G | A | 3 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 |
3 | NA18975.hp2 NA19006.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.61+7957G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809227 | |||||||
| chr7:35809378 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.61+8108A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809378 | |||||||
| chr7:35809643 | G | A | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.61+8373G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809643 | |||||||
| chr7:35809706 | A | G | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.61+8436A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809706 | |||||||
| chr7:35809869 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+8599A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809869 | |||||||
| chr7:35809983 | A | T | 1 | a0001c0001t0001g0306 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.61+8713A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35809983 | |||||||
| chr7:35810044 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+8774T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810044 | |||||||
| chr7:35810448 | C | T | 7 | a0001c0001t0002g0071 a0001c0001t0013g0045 a0001c0001t0013g0046 others(4): Show |
7 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+9178C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810448 | |||||||
| chr7:35810569 | C | T | 1 | a0001c0001t0020g0008 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.61+9299C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810569 | |||||||
| chr7:35810612 | C | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.61+9342C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810612 | |||||||
| chr7:35810735 | T | C | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.61+9465T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810735 | |||||||
| chr7:35810771 | G | GT | 12 | a0001c0001t0001g0225 a0001c0001t0001g0304 a0001c0001t0003g0112 others(9): Show |
12 | HG00438.hp2 HG00642.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.61+9514dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35810771 | ||||||
| chr7:35810923 | C | T | 5 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(2): Show |
5 | NA18949.hp2 NA18974.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+9653C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810923 | |||||||
| chr7:35810958 | G | A | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | NA18970.hp2 NA18975.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+9688G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35810958 | |||||||
| chr7:35811096 | G | A | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.61+9826G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811096 | |||||||
| chr7:35811224 | A | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+9954A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811224 | |||||||
| chr7:35811275 | C | T | 1 | a0001c0001t0004g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.61+10005C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811275 | |||||||
| chr7:35811288 | G | A | 1 | a0001c0001t0009g0229 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.61+10018G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811288 | |||||||
| chr7:35811628 | G | T | 199 | a0001c0001t0001g0181 a0001c0001t0002g0004 a0001c0001t0002g0006 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.61+10358G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811628 | |||||||
| chr7:35811639 | C | T | 1 | a0001c0001t0009g0229 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.61+10369C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811639 | |||||||
| chr7:35811707 | T | C | 37 | a0001c0001t0003g0002 a0001c0001t0003g0029 a0001c0001t0003g0030 others(34): Show |
39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.61+10437T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811707 | |||||||
| chr7:35811730 | T | G | 3 | a0001c0001t0004g0171 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02055.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.61+10460T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35811730 | |||||||
| chr7:35812104 | C | G | 2 | a0001c0001t0009g0296 a0001c0001t0009g0297 |
2 | NA19059.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.61+10834C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812104 | |||||||
| chr7:35812128 | CA | C | 180 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(177): Show |
190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.61+10872delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35812128 | ||||||
| chr7:35812142 | A | C | 9 | a0001c0001t0003g0213 a0001c0001t0004g0172 a0001c0001t0013g0045 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+10872A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812142 | |||||||
| chr7:35812143 | C | A | 11 | a0001c0001t0001g0181 a0001c0001t0003g0213 a0001c0001t0004g0172 others(8): Show |
11 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.61+10873C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812143 | |||||||
| chr7:35812153 | A | C | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.61+10883A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812153 | |||||||
| chr7:35812336 | T | C | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11066T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812336 | |||||||
| chr7:35812343 | T | A | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11073T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812343 | |||||||
| chr7:35812418 | A | T | 1 | a0001c0001t0018g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.61+11148A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812418 | |||||||
| chr7:35812452 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.61+11182T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812452 | |||||||
| chr7:35812481 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61+11211A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812481 | |||||||
| chr7:35812686 | C | T | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11416C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812686 | |||||||
| chr7:35812687 | T | C | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11417T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812687 | |||||||
| chr7:35812755 | A | T | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+11485A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35812755 | |||||||
| chr7:35813017 | G | A | 1 | a0001c0001t0012g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.61+11747G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813017 | |||||||
| chr7:35813282 | T | TAAAAACT others(289): Show |
1 | a0001c0004t0013g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.61+12025_61+12026i others(298): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35813282 | ||||||
| chr7:35813311 | C | T | 1 | a0001c0001t0008g0026 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.61+12041C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813311 | |||||||
| chr7:35813341 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.61+12071A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813341 | |||||||
| chr7:35813385 | C | T | 4 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(1): Show |
4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+12115C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813385 | |||||||
| chr7:35813398 | A | G | 1 | a0001c0001t0037g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.61+12128A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813398 | |||||||
| chr7:35813830 | A | T | 1 | a0001c0001t0005g0204 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61+12560A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813830 | |||||||
| chr7:35813875 | G | A | 1 | a0001c0001t0011g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.61+12605G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35813875 | |||||||
| chr7:35814006 | A | C | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+12736A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814006 | |||||||
| chr7:35814012 | A | C | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+12742A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814012 | |||||||
| chr7:35814055 | T | TAAAAGTT others(196): Show |
1 | a0001c0001t0005g0199 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.61+12802_61+12803i others(205): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | ||||||
| chr7:35814055 | T | TAAAAGTT others(197): Show |
6 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(3): Show |
6 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.61+12802_61+12803i others(206): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | ||||||
| chr7:35814055 | T | TAAAAGTT others(198): Show |
14 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(11): Show |
15 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.61+12802_61+12803i others(207): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | ||||||
| chr7:35814055 | T | TAAAAGTT others(199): Show |
1 | a0001c0001t0005g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.61+12802_61+12803i others(208): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814055 | ||||||
| chr7:35814120 | G | A | 9 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(6): Show |
9 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.61+12850G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814120 | |||||||
| chr7:35814340 | A | T | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 |
3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.61+13070A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814340 | |||||||
| chr7:35814355 | T | A | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.61+13085T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814355 | |||||||
| chr7:35814368 | T | C | 1 | a0001c0001t0023g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.61+13098T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814368 | |||||||
| chr7:35814428 | T | G | 1 | a0001c0001t0002g0125 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.61+13158T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814428 | |||||||
| chr7:35814487 | G | GT | 132 | a0001c0001t0001g0295 a0001c0001t0002g0004 a0001c0001t0002g0006 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.61+13224dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814487 | ||||||
| chr7:35814627 | G | GGTGATTT others(8): Show |
1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61+13358_61+13372d others(17): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814627 | ||||||
| chr7:35814792 | G | C | 1 | a0001c0001t0002g0126 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.61+13522G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814792 | |||||||
| chr7:35814902 | A | G | 199 | a0001c0001t0001g0295 a0001c0001t0002g0004 a0001c0001t0002g0006 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.61+13632A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814902 | |||||||
| chr7:35814930 | T | G | 17 | a0001c0001t0003g0002 a0001c0001t0003g0183 a0001c0001t0003g0184 others(14): Show |
19 | HG00438.hp1 HG00673.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.61+13660T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814930 | |||||||
| chr7:35814955 | A | G | 1 | a0001c0001t0024g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.61+13685A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814955 | |||||||
| chr7:35814974 | C | CA | 58 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(55): Show |
62 | HG00438.hp1 HG00597.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.61+13730dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814974 | ||||||
| chr7:35814974 | C | CAA | 6 | a0001c0001t0003g0090 a0001c0001t0003g0214 a0001c0001t0003g0215 others(3): Show |
6 | HG01358.hp1 HG02080.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+13729_61+13730d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814974 | ||||||
| chr7:35814974 | CA | C | 14 | a0001c0001t0002g0040 a0001c0001t0003g0101 a0001c0001t0003g0102 others(11): Show |
14 | HG00099.hp1 HG01167.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.61+13730delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35814974 | ||||||
| chr7:35814976 | A | C | 1 | a0001c0001t0001g0294 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.61+13706A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35814976 | |||||||
| chr7:35815108 | C | G | 10 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(7): Show |
10 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.61+13838C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815108 | |||||||
| chr7:35815129 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.61+13859T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815129 | |||||||
| chr7:35815244 | T | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0016 |
2 | HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.61+13974T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815244 | |||||||
| chr7:35815381 | G | T | 1 | a0001c0001t0002g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61+14111G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815381 | |||||||
| chr7:35815822 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.61+14552T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35815822 | |||||||
| chr7:35816030 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61+14760A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816030 | |||||||
| chr7:35816190 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.61+14920C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816190 | |||||||
| chr7:35816322 | A | G | 5 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0040 others(2): Show |
5 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+15052A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816322 | |||||||
| chr7:35816400 | T | A | 1 | a0001c0001t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.62-15092T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816400 | |||||||
| chr7:35816729 | G | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.62-14763G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816729 | |||||||
| chr7:35816746 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0001g0315 |
2 | NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.62-14746C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35816746 | |||||||
| chr7:35817008 | GT | G | 15 | a0001c0001t0001g0221 a0001c0001t0006g0001 a0001c0001t0006g0027 others(12): Show |
18 | HG00597.hp2 HG01943.hp2 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.62-14470delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35817008 | ||||||
| chr7:35817021 | T | TTTACGTT others(5): Show |
1 | a0001c0001t0009g0241 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.62-14470_62-14469i others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35817021 | ||||||
| chr7:35817024 | C | G | 1 | a0001c0001t0009g0241 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.62-14468C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817024 | |||||||
| chr7:35817126 | T | C | 1 | a0001c0001t0022g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.62-14366T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817126 | |||||||
| chr7:35817186 | A | G | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-14306A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817186 | |||||||
| chr7:35817201 | TTTTTGAT others(3): Show |
T | 8 | a0001c0001t0001g0182 a0001c0001t0011g0005 a0001c0001t0011g0065 others(5): Show |
9 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-14284_62-14275d others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35817201 | ||||||
| chr7:35817252 | T | G | 1 | a0001c0001t0011g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.62-14240T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817252 | |||||||
| chr7:35817269 | A | G | 1 | a0001c0001t0010g0240 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.62-14223A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817269 | |||||||
| chr7:35817315 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.62-14177A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817315 | |||||||
| chr7:35817317 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.62-14175T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817317 | |||||||
| chr7:35817499 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.62-13993C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817499 | |||||||
| chr7:35817536 | C | T | 1 | a0001c0001t0012g0232 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.62-13956C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817536 | |||||||
| chr7:35817571 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.62-13921A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817571 | |||||||
| chr7:35817589 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.62-13903G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817589 | |||||||
| chr7:35817609 | A | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0146 |
2 | NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.62-13883A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817609 | |||||||
| chr7:35817615 | A | G | 36 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(33): Show |
40 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.62-13877A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817615 | |||||||
| chr7:35817928 | A | T | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 |
3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.62-13564A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35817928 | |||||||
| chr7:35818006 | C | T | 1 | a0001c0001t0014g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.62-13486C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818006 | |||||||
| chr7:35818094 | A | G | 1 | a0001c0001t0027g0145 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.62-13398A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818094 | |||||||
| chr7:35818460 | A | C | 2 | a0001c0001t0003g0091 a0001c0001t0003g0115 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.62-13032A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818460 | |||||||
| chr7:35818577 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-12915G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818577 | |||||||
| chr7:35818769 | T | A | 1 | a0001c0001t0020g0008 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.62-12723T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818769 | |||||||
| chr7:35818798 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.62-12694A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818798 | |||||||
| chr7:35818884 | G | A | 3 | a0001c0001t0001g0235 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | NA18979.hp1 NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.62-12608G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35818884 | |||||||
| chr7:35819054 | G | A | 208 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(205): Show |
219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.62-12438G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819054 | |||||||
| chr7:35819071 | A | G | 8 | a0001c0001t0002g0128 a0001c0001t0002g0140 a0001c0001t0002g0141 others(5): Show |
8 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.62-12421A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819071 | |||||||
| chr7:35819109 | C | T | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-12383C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819109 | |||||||
| chr7:35819137 | G | A | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-12355G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819137 | |||||||
| chr7:35819399 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0224 |
2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.62-12093C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819399 | |||||||
| chr7:35819409 | T | A | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-12083T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819409 | |||||||
| chr7:35819460 | AGTTGGTT others(6): Show |
A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-12027_62-12015d others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35819460 | ||||||
| chr7:35819496 | T | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-11996T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819496 | |||||||
| chr7:35819521 | G | A | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-11971G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819521 | |||||||
| chr7:35819535 | G | A | 1 | a0001c0001t0004g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.62-11957G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819535 | |||||||
| chr7:35819629 | C | T | 2 | a0001c0001t0004g0173 a0001c0001t0004g0176 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.62-11863C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819629 | |||||||
| chr7:35819704 | A | G | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-11788A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819704 | |||||||
| chr7:35819756 | C | G | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.62-11736C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819756 | |||||||
| chr7:35819867 | C | T | 2 | a0001c0001t0004g0003 a0001c0001t0004g0031 |
3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62-11625C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35819867 | |||||||
| chr7:35820051 | A | G | 121 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0032 others(118): Show |
124 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.62-11441A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820051 | |||||||
| chr7:35820082 | C | T | 208 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(205): Show |
219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.62-11410C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820082 | |||||||
| chr7:35820570 | T | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-10922T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820570 | |||||||
| chr7:35820619 | T | C | 47 | a0001c0001t0002g0071 a0001c0001t0004g0003 a0001c0001t0004g0007 others(44): Show |
50 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(47): Show |
intron_variant | MODIFIER | c.62-10873T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820619 | |||||||
| chr7:35820657 | A | G | 1 | a0001c0001t0012g0232 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.62-10835A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820657 | |||||||
| chr7:35820755 | GT | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-10729delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35820755 | ||||||
| chr7:35820756 | T | G | 6 | a0001c0001t0004g0171 a0001c0001t0004g0173 a0001c0001t0004g0174 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-10736T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820756 | |||||||
| chr7:35820949 | A | G | 173 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(170): Show |
181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.62-10543A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35820949 | |||||||
| chr7:35821066 | G | GT | 130 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(127): Show |
134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.62-10419dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35821066 | ||||||
| chr7:35821106 | G | A | 1 | a0001c0001t0011g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.62-10386G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821106 | |||||||
| chr7:35821154 | C | G | 173 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(170): Show |
181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.62-10338C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821154 | |||||||
| chr7:35821247 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.62-10245G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821247 | |||||||
| chr7:35821352 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62-10140C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821352 | |||||||
| chr7:35821399 | A | G | 2 | a0001c0001t0003g0090 a0001c0001t0023g0089 |
2 | HG01081.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.62-10093A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821399 | |||||||
| chr7:35821749 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.62-9743C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821749 | |||||||
| chr7:35821765 | A | T | 10 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(7): Show |
11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-9727A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821765 | |||||||
| chr7:35821952 | G | A | 1 | a0002c0005t0002g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.62-9540G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821952 | |||||||
| chr7:35821959 | C | T | 1 | a0001c0002t0001g0300 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.62-9533C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35821959 | |||||||
| chr7:35822061 | C | T | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-9431C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822061 | |||||||
| chr7:35822189 | C | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.62-9303C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822189 | |||||||
| chr7:35822512 | C | T | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-8980C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822512 | |||||||
| chr7:35822534 | G | A | 151 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.62-8958G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822534 | |||||||
| chr7:35822610 | C | T | 2 | a0001c0001t0021g0051 a0001c0001t0021g0059 |
2 | HG02155.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.62-8882C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822610 | |||||||
| chr7:35822699 | G | A | 208 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(205): Show |
219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.62-8793G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822699 | |||||||
| chr7:35822745 | C | A | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-8747C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35822745 | |||||||
| chr7:35823359 | G | A | 1 | a0001c0001t0002g0152 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.62-8133G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823359 | |||||||
| chr7:35823448 | G | T | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-8044G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823448 | |||||||
| chr7:35823491 | G | A | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.62-8001G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823491 | |||||||
| chr7:35823624 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0313 |
3 | HG00735.hp2 HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.62-7868C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823624 | |||||||
| chr7:35823861 | C | CT | 7 | a0001c0001t0003g0214 a0001c0001t0004g0171 a0001c0001t0004g0173 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-7622dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35823861 | ||||||
| chr7:35823869 | T | G | 3 | a0001c0001t0014g0105 a0001c0001t0014g0129 a0001c0001t0014g0130 |
3 | HG02155.hp1 HG02165.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.62-7623T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823869 | |||||||
| chr7:35823870 | T | G | 81 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0032 others(78): Show |
82 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.62-7622T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35823870 | |||||||
| chr7:35824037 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.62-7455C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824037 | |||||||
| chr7:35824068 | T | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-7424T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824068 | |||||||
| chr7:35824596 | A | G | 1 | a0001c0002t0001g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.62-6896A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824596 | |||||||
| chr7:35824684 | C | G | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.62-6808C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824684 | |||||||
| chr7:35824751 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.62-6741G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35824751 | |||||||
| chr7:35825319 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-6173A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825319 | |||||||
| chr7:35825442 | A | T | 9 | a0001c0001t0002g0088 a0001c0001t0002g0128 a0001c0001t0002g0140 others(6): Show |
9 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-6050A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825442 | |||||||
| chr7:35825626 | C | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.62-5866C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825626 | |||||||
| chr7:35825678 | A | G | 2 | a0001c0001t0002g0138 a0001c0001t0002g0139 |
2 | HG02071.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.62-5814A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825678 | |||||||
| chr7:35825967 | G | C | 1 | a0001c0001t0002g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.62-5525G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35825967 | |||||||
| chr7:35826409 | A | T | 8 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0004g0171 others(5): Show |
8 | HG00673.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-5083A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826409 | |||||||
| chr7:35826416 | A | T | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-5076A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826416 | |||||||
| chr7:35826512 | T | C | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-4980T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826512 | |||||||
| chr7:35826555 | T | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.62-4937T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826555 | |||||||
| chr7:35826765 | C | T | 6 | a0001c0001t0004g0171 a0001c0001t0004g0173 a0001c0001t0004g0174 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.62-4727C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826765 | |||||||
| chr7:35826766 | T | G | 42 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(39): Show |
46 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.62-4726T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826766 | |||||||
| chr7:35826828 | T | C | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-4664T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826828 | |||||||
| chr7:35826901 | C | T | 1 | a0001c0001t0005g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.62-4591C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35826901 | |||||||
| chr7:35827024 | C | T | 10 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(7): Show |
11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-4468C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827024 | |||||||
| chr7:35827070 | C | T | 1 | a0001c0001t0026g0203 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.62-4422C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827070 | |||||||
| chr7:35827187 | T | A | 1 | a0001c0001t0001g0306 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.62-4305T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827187 | |||||||
| chr7:35827321 | G | GT | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-4169dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35827321 | ||||||
| chr7:35827525 | C | T | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3967C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827525 | |||||||
| chr7:35827552 | G | A | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-3940G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827552 | |||||||
| chr7:35827567 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0007g0117 |
2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.62-3925T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827567 | |||||||
| chr7:35827687 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-3805C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827687 | |||||||
| chr7:35827796 | A | T | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.62-3696A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827796 | |||||||
| chr7:35827891 | T | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-3601T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827891 | |||||||
| chr7:35827987 | A | G | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.62-3505A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35827987 | |||||||
| chr7:35828058 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.62-3434C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828058 | |||||||
| chr7:35828252 | T | G | 46 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(43): Show |
49 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(46): Show |
intron_variant | MODIFIER | c.62-3240T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828252 | |||||||
| chr7:35828265 | C | G | 1 | a0001c0001t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.62-3227C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828265 | |||||||
| chr7:35828400 | A | T | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62-3092A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828400 | |||||||
| chr7:35828454 | C | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.62-3038C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828454 | |||||||
| chr7:35828545 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.62-2947A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828545 | |||||||
| chr7:35828676 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0010g0305 |
2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.62-2816C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828676 | |||||||
| chr7:35828712 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.62-2780C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828712 | |||||||
| chr7:35828821 | C | T | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-2671C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828821 | |||||||
| chr7:35828836 | C | G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0029 a0001c0001t0003g0030 others(34): Show |
39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.62-2656C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828836 | |||||||
| chr7:35828873 | G | T | 1 | a0001c0001t0002g0155 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.62-2619G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35828873 | |||||||
| chr7:35829086 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.62-2406C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829086 | |||||||
| chr7:35829128 | C | CT | 47 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0221 others(44): Show |
51 | HG00438.hp2 HG00738.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.62-2340dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTT | 9 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(6): Show |
10 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-2343_62-2340dup others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTT | 10 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0080 others(7): Show |
10 | HG01433.hp2 HG02895.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.62-2344_62-2340dup others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTT | 47 | a0001c0001t0002g0006 a0001c0001t0002g0028 a0001c0001t0002g0073 others(44): Show |
50 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.62-2345_62-2340dup others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT | 31 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0078 others(28): Show |
31 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.62-2346_62-2340dup others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(1): Show |
10 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0088 others(7): Show |
10 | HG00733.hp2 HG01175.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.62-2347_62-2340dup others(8): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0002g0087 a0001c0001t0002g0109 a0001c0001t0002g0110 others(4): Show |
7 | HG00099.hp1 HG01081.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-2349_62-2340dup others(10): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0115 |
3 | HG01106.hp1 HG02293.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.62-2350_62-2340dup others(11): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0001c0001t0003g0102 others(1): Show |
4 | HG00642.hp2 HG01167.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-2351_62-2340dup others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0098 a0001c0001t0003g0169 a0001c0001t0003g0213 |
3 | HG01192.hp2 HG02738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.62-2352_62-2340dup others(13): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0091 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.62-2353_62-2340dup others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0003g0099 a0001c0001t0003g0100 |
2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.62-2354_62-2340dup others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0003g0029 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.62-2361_62-2340dup others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0003g0030 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.62-2362_62-2340dup others(23): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | CT | C | 8 | a0001c0001t0001g0182 a0001c0001t0001g0246 a0001c0001t0001g0247 others(5): Show |
8 | HG00099.hp2 HG01099.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2340delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | CTT | C | 15 | a0001c0001t0002g0032 a0001c0001t0004g0173 a0001c0001t0004g0174 others(12): Show |
15 | HG02258.hp2 HG02572.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.62-2341_62-2340del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829128 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0245 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.62-2349_62-2340del others(10): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35829128 | ||||||
| chr7:35829257 | A | T | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.62-2235A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829257 | |||||||
| chr7:35829328 | G | C | 7 | a0001c0001t0011g0005 a0001c0001t0011g0065 a0001c0001t0011g0067 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2164G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829328 | |||||||
| chr7:35829380 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.62-2112A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829380 | |||||||
| chr7:35829394 | G | A | 3 | a0001c0001t0003g0210 a0001c0001t0003g0211 a0001c0001t0003g0214 |
3 | NA19060.hp2 NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.62-2098G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829394 | |||||||
| chr7:35829502 | C | G | 1 | a0001c0001t0004g0003 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62-1990C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829502 | |||||||
| chr7:35829545 | A | T | 1 | a0001c0001t0004g0003 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62-1947A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829545 | |||||||
| chr7:35829742 | A | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.62-1750A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829742 | |||||||
| chr7:35829911 | G | T | 1 | a0001c0001t0003g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.62-1581G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829911 | |||||||
| chr7:35829916 | G | A | 1 | a0001c0001t0001g0306 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.62-1576G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829916 | |||||||
| chr7:35829925 | C | T | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1567C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829925 | |||||||
| chr7:35829936 | C | T | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-1556C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35829936 | |||||||
| chr7:35830042 | C | T | 40 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(37): Show |
40 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.62-1450C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830042 | |||||||
| chr7:35830043 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(21): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.62-1449G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830043 | |||||||
| chr7:35830241 | T | A | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.62-1251T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830241 | |||||||
| chr7:35830337 | A | T | 1 | a0001c0001t0030g0107 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.62-1155A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830337 | |||||||
| chr7:35830447 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0276 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.62-1045G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830447 | |||||||
| chr7:35830613 | GTCATGGA others(12): Show |
G | 1 | a0001c0003t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.62-877_62-859delCA others(17): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | 35830613 | ||||||
| chr7:35830732 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.62-760T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830732 | |||||||
| chr7:35830776 | T | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.62-716T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830776 | |||||||
| chr7:35830903 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.62-589A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35830903 | |||||||
| chr7:35831190 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.62-302G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35831190 | |||||||
| chr7:35831448 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.62-44G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 1/13 | chr7 | 35831448 | |||||||
| chr7:35831616 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+120C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35831616 | |||||||
| chr7:35832038 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+542A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832038 | |||||||
| chr7:35832098 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.66+602C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832098 | |||||||
| chr7:35832124 | A | C | 5 | a0001c0001t0003g0002 a0001c0001t0003g0185 a0001c0001t0003g0186 others(2): Show |
7 | NA18954.hp2 NA18956.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+628A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832124 | |||||||
| chr7:35832246 | G | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67-552G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832246 | |||||||
| chr7:35832276 | A | G | 2 | a0001c0001t0002g0125 a0001c0001t0002g0146 |
2 | NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.67-522A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832276 | |||||||
| chr7:35832424 | T | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-374T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832424 | |||||||
| chr7:35832527 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.67-271A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 2/13 | chr7 | 35832527 | |||||||
| chr7:35832941 | G | A | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+41G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35832941 | |||||||
| chr7:35832994 | T | C | 1 | a0001c0001t0007g0136 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.169+94T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35832994 | |||||||
| chr7:35833082 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.169+182C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833082 | |||||||
| chr7:35833089 | T | C | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.169+189T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833089 | |||||||
| chr7:35833207 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+307C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833207 | |||||||
| chr7:35833318 | A | C | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.169+418A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833318 | |||||||
| chr7:35833337 | C | G | 1 | a0001c0001t0001g0314 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.169+437C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833337 | |||||||
| chr7:35833444 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169+544T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833444 | |||||||
| chr7:35833503 | A | G | 2 | a0001c0001t0002g0071 a0001c0001t0002g0143 |
2 | HG02132.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.169+603A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833503 | |||||||
| chr7:35833695 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+795A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833695 | |||||||
| chr7:35833773 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+873C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833773 | |||||||
| chr7:35833930 | G | A | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+1030G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833930 | |||||||
| chr7:35833973 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.169+1073A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35833973 | |||||||
| chr7:35834113 | G | A | 9 | a0001c0001t0008g0018 a0001c0001t0008g0019 a0001c0001t0008g0020 others(6): Show |
9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+1213G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834113 | |||||||
| chr7:35834231 | A | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+1331A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834231 | |||||||
| chr7:35834492 | A | C | 1 | a0001c0001t0002g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169+1592A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834492 | |||||||
| chr7:35834519 | A | G | 1 | a0001c0001t0039g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.169+1619A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834519 | |||||||
| chr7:35834633 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0001g0275 |
2 | HG00558.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.169+1733A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834633 | |||||||
| chr7:35834650 | T | C | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+1750T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834650 | |||||||
| chr7:35834660 | G | T | 17 | a0001c0001t0003g0002 a0001c0001t0003g0183 a0001c0001t0003g0184 others(14): Show |
19 | HG00438.hp1 HG00673.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.169+1760G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834660 | |||||||
| chr7:35834681 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.169+1781A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834681 | |||||||
| chr7:35834701 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.169+1801A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834701 | |||||||
| chr7:35834706 | CACTT | C | 6 | a0001c0001t0006g0001 a0001c0001t0006g0053 a0001c0001t0006g0055 others(3): Show |
9 | NA18942.hp2 NA18944.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+1810_169+1813d others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35834706 | ||||||
| chr7:35834855 | T | G | 1 | a0001c0001t0010g0327 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.169+1955T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834855 | |||||||
| chr7:35834886 | A | C | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+1986A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834886 | |||||||
| chr7:35834946 | T | C | 1 | a0001c0001t0021g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.169+2046T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35834946 | |||||||
| chr7:35835181 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.169+2281G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835181 | |||||||
| chr7:35835318 | C | G | 209 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(206): Show |
220 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.169+2418C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835318 | |||||||
| chr7:35835379 | T | C | 3 | a0001c0001t0004g0171 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02055.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.169+2479T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835379 | |||||||
| chr7:35835893 | TG | T | 3 | a0001c0001t0003g0210 a0001c0001t0003g0211 a0001c0001t0003g0214 |
3 | NA19060.hp2 NA19068.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.169+2994delG | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835893 | |||||||
| chr7:35835904 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169+3004A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35835904 | |||||||
| chr7:35836211 | C | G | 1 | a0001c0001t0003g0101 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.169+3311C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836211 | |||||||
| chr7:35836286 | A | G | 1 | a0001c0001t0005g0202 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.169+3386A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836286 | |||||||
| chr7:35836699 | G | C | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3799G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836699 | |||||||
| chr7:35836885 | A | G | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+3985A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35836885 | |||||||
| chr7:35836933 | GTAACT | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+4039_169+4043d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35836933 | ||||||
| chr7:35837062 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.169+4162A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837062 | |||||||
| chr7:35837419 | CAGGAT | C | 8 | a0001c0001t0002g0128 a0001c0001t0002g0140 a0001c0001t0002g0141 others(5): Show |
8 | HG00558.hp1 HG00597.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+4522_169+4526d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35837419 | ||||||
| chr7:35837507 | GAAT | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+4613_169+4615d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35837507 | ||||||
| chr7:35837764 | C | G | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169+4864C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837764 | |||||||
| chr7:35837791 | G | A | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169+4891G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837791 | |||||||
| chr7:35837831 | A | G | 4 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(1): Show |
4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+4931A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837831 | |||||||
| chr7:35837930 | G | T | 2 | a0001c0001t0001g0279 a0001c0001t0001g0294 |
2 | HG00733.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.169+5030G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837930 | |||||||
| chr7:35837980 | C | T | 7 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(4): Show |
10 | NA18942.hp2 NA18944.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+5080C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35837980 | |||||||
| chr7:35838031 | C | T | 7 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 others(4): Show |
7 | HG01433.hp2 HG02486.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5131C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838031 | |||||||
| chr7:35838240 | C | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0180 others(85): Show |
91 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.169+5340C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838240 | |||||||
| chr7:35838244 | C | A | 34 | a0001c0001t0001g0050 a0001c0001t0001g0239 a0001c0001t0001g0244 others(31): Show |
35 | HG00558.hp2 HG01081.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.169+5344C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838244 | |||||||
| chr7:35838244 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.169+5344C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838244 | |||||||
| chr7:35838248 | C | A | 14 | a0001c0001t0001g0239 a0001c0001t0001g0244 a0001c0001t0004g0007 others(11): Show |
15 | HG01346.hp1 HG02071.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+5348C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838248 | |||||||
| chr7:35838252 | C | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0175 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.169+5352C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838252 | |||||||
| chr7:35838256 | C | A | 1 | a0001c0001t0004g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.169+5356C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838256 | |||||||
| chr7:35838274 | TTCCTTCC others(53): Show |
T | 1 | a0001c0001t0002g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.169+5378_169+5437d others(62): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838274 | ||||||
| chr7:35838278 | TTCCTTCC others(41): Show |
T | 1 | a0001c0001t0003g0093 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.169+5382_169+5429d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838278 | ||||||
| chr7:35838278 | TTCCTTCC others(45): Show |
T | 4 | a0001c0001t0002g0041 a0001c0001t0002g0140 a0001c0001t0002g0150 others(1): Show |
4 | HG02622.hp2 NA18954.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5382_169+5433d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838278 | ||||||
| chr7:35838278 | TTCCTTCC others(49): Show |
T | 7 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0039 others(4): Show |
7 | HG02258.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5382_169+5437d others(58): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838278 | ||||||
| chr7:35838282 | TTCCTTCC others(37): Show |
T | 4 | a0001c0001t0002g0073 a0001c0001t0002g0160 a0001c0001t0002g0161 others(1): Show |
4 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5386_169+5429d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838282 | ||||||
| chr7:35838282 | TTCCTTCC others(41): Show |
T | 7 | a0001c0001t0002g0084 a0001c0001t0002g0148 a0001c0001t0002g0154 others(4): Show |
7 | HG01952.hp1 HG02155.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5386_169+5433d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838282 | ||||||
| chr7:35838282 | TTCCTTCC others(45): Show |
T | 23 | a0001c0001t0002g0071 a0001c0001t0002g0122 a0001c0001t0002g0126 others(20): Show |
23 | HG00597.hp1 HG02027.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.169+5386_169+5437d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838282 | ||||||
| chr7:35838284 | CCTTCCTT others(72): Show |
C | 4 | a0001c0001t0002g0081 a0001c0001t0002g0106 a0001c0001t0030g0107 others(1): Show |
4 | HG01433.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+5386_169+5464d others(81): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838284 | ||||||
| chr7:35838286 | TTCCTTCC others(25): Show |
T | 1 | a0001c0001t0001g0329 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.169+5390_169+5421d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | ||||||
| chr7:35838286 | TTCCTTCC others(29): Show |
T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.169+5390_169+5425d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | ||||||
| chr7:35838286 | TTCCTTCC others(33): Show |
T | 2 | a0001c0001t0001g0181 a0001c0001t0002g0162 |
2 | HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.169+5390_169+5429d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | ||||||
| chr7:35838286 | TTCCTTCC others(37): Show |
T | 6 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(3): Show |
6 | HG00609.hp2 NA18973.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5390_169+5433d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | ||||||
| chr7:35838286 | TTCCTTCC others(41): Show |
T | 31 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0032 others(28): Show |
33 | HG00558.hp1 HG01243.hp2 HG02129.hp1 others(30): Show |
intron_variant | MODIFIER | c.169+5390_169+5437d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | ||||||
| chr7:35838286 | TTCCTTCC others(45): Show |
T | 1 | a0001c0001t0002g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.169+5390_169+5441d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838286 | ||||||
| chr7:35838290 | TTCCTTCC others(17): Show |
T | 1 | a0001c0001t0001g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169+5394_169+5417d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838290 | TTCCTTCC others(25): Show |
T | 5 | a0001c0001t0003g0210 a0001c0001t0003g0211 a0001c0001t0003g0214 others(2): Show |
5 | HG02922.hp2 NA18952.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+5394_169+5425d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838290 | TTCCTTCC others(29): Show |
T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0266 |
2 | HG03710.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.169+5394_169+5429d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838290 | TTCCTTCC others(33): Show |
T | 12 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0090 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+5394_169+5433d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838290 | TTCCTTCC others(37): Show |
T | 37 | a0001c0001t0001g0182 a0001c0001t0002g0028 a0001c0001t0002g0108 others(34): Show |
39 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.169+5394_169+5437d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838290 | TTCCTTCC others(41): Show |
T | 1 | a0001c0001t0039g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.169+5394_169+5441d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838290 | TTCCTTCC others(45): Show |
T | 1 | a0001c0001t0008g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.169+5394_169+5445d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838290 | ||||||
| chr7:35838294 | TTCCTTCC others(13): Show |
T | 3 | a0001c0001t0010g0269 a0001c0001t0010g0303 a0001c0001t0010g0327 |
3 | NA18948.hp1 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.169+5398_169+5417d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(17): Show |
T | 7 | a0001c0001t0001g0236 a0001c0001t0001g0248 a0001c0001t0001g0307 others(4): Show |
7 | HG00099.hp2 HG00408.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+5398_169+5421d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(21): Show |
T | 6 | a0001c0001t0001g0277 a0001c0001t0004g0003 a0001c0001t0004g0031 others(3): Show |
7 | HG02109.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+5398_169+5425d others(30): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(25): Show |
T | 11 | a0001c0001t0001g0223 a0001c0001t0001g0246 a0001c0001t0001g0268 others(8): Show |
11 | HG01255.hp2 HG02080.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.169+5398_169+5429d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(29): Show |
T | 4 | a0001c0001t0002g0120 a0001c0001t0003g0097 a0001c0001t0023g0089 others(1): Show |
4 | HG01081.hp2 HG02451.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5398_169+5433d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(33): Show |
T | 11 | a0001c0001t0002g0078 a0001c0001t0002g0116 a0001c0001t0002g0118 others(8): Show |
11 | HG00733.hp2 HG01884.hp2 NA18522.hp2 others(8): Show |
intron_variant | MODIFIER | c.169+5398_169+5437d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(37): Show |
T | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169+5398_169+5441d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(41): Show |
T | 3 | a0001c0001t0001g0253 a0001c0001t0013g0046 a0001c0001t0013g0049 |
3 | HG01891.hp1 NA19077.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.169+5398_169+5445d others(50): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(45): Show |
T | 1 | a0001c0001t0013g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.169+5398_169+5449d others(54): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838294 | TTCCTTCC others(49): Show |
T | 2 | a0001c0001t0012g0227 a0001c0002t0001g0301 |
2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.169+5398_169+5453d others(58): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838294 | ||||||
| chr7:35838298 | TTCCTTCC others(5): Show |
T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0313 a0001c0001t0010g0238 |
3 | HG00735.hp2 HG00741.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.169+5402_169+5413d others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(9): Show |
T | 4 | a0001c0001t0001g0330 a0001c0001t0001g0331 a0001c0001t0010g0240 others(1): Show |
4 | HG00642.hp1 HG01167.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5402_169+5417d others(18): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(13): Show |
T | 6 | a0001c0001t0001g0287 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG01106.hp2 HG01978.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+5402_169+5421d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(17): Show |
T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0282 a0001c0002t0001g0015 others(1): Show |
4 | HG01192.hp1 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5402_169+5425d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(21): Show |
T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0221 a0001c0001t0001g0222 others(17): Show |
21 | HG00438.hp2 HG00609.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.169+5402_169+5429d others(30): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(25): Show |
T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.169+5402_169+5433d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(29): Show |
T | 11 | a0001c0001t0001g0314 a0001c0001t0006g0001 a0001c0001t0006g0027 others(8): Show |
13 | HG00597.hp2 HG02155.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+5402_169+5437d others(38): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(33): Show |
T | 4 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0284 others(1): Show |
5 | HG00673.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5402_169+5441d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838298 | TTCCTTCC others(37): Show |
T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0324 |
2 | HG01517.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.169+5402_169+5445d others(46): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838298 | ||||||
| chr7:35838302 | T | C | 15 | a0001c0001t0004g0012 a0001c0001t0004g0173 a0001c0001t0004g0176 others(12): Show |
15 | HG00738.hp1 HG01081.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+5402T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838302 | |||||||
| chr7:35838302 | TTCCCTCC others(5): Show |
T | 9 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0009g0241 others(6): Show |
9 | HG00140.hp1 HG01934.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+5454_169+5465d others(14): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838302 | TTCCCTCC others(9): Show |
T | 19 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0261 others(16): Show |
19 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.169+5450_169+5465d others(18): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838302 | TTCCCTCC others(13): Show |
T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0276 a0001c0001t0009g0229 |
3 | HG02559.hp1 HG04204.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.169+5446_169+5465d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838302 | TTCCCTCC others(17): Show |
T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0234 a0001c0001t0001g0235 others(6): Show |
9 | HG00558.hp2 HG02071.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.169+5442_169+5465d others(26): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838302 | TTCCCTCC others(21): Show |
T | 2 | a0001c0001t0001g0230 a0001c0001t0003g0095 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.169+5438_169+5465d others(30): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838302 | TTCCCTCC others(25): Show |
T | 3 | a0001c0001t0001g0319 a0001c0001t0016g0077 a0001c0001t0021g0051 |
3 | HG02027.hp2 NA18961.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.169+5434_169+5465d others(34): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838302 | TTCCCTCC others(33): Show |
T | 1 | a0001c0001t0001g0254 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.169+5426_169+5465d others(42): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838302 | ||||||
| chr7:35838306 | C | T | 3 | a0001c0001t0004g0179 a0001c0001t0005g0219 a0001c0001t0005g0220 |
3 | HG01884.hp1 HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.169+5406C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838306 | |||||||
| chr7:35838308 | CCCTCCCT others(48): Show |
C | 2 | a0001c0001t0019g0264 a0001c0001t0019g0308 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.169+5436_169+5490d others(57): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838308 | ||||||
| chr7:35838310 | C | T | 1 | a0001c0001t0005g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+5410C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838310 | |||||||
| chr7:35838314 | C | T | 1 | a0001c0001t0009g0293 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.169+5414C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838314 | |||||||
| chr7:35838316 | CCCTCCCT others(40): Show |
C | 1 | a0001c0001t0013g0045 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.169+5444_169+5490d others(49): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838316 | ||||||
| chr7:35838318 | C | T | 7 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0009g0241 others(4): Show |
7 | HG00140.hp1 HG01981.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+5418C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838318 | |||||||
| chr7:35838319 | TCCCTCCC others(22): Show |
T | 11 | a0001c0001t0004g0171 a0001c0001t0005g0013 a0001c0001t0005g0191 others(8): Show |
11 | HG00738.hp1 HG01081.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+5422_169+5450d others(31): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838319 | ||||||
| chr7:35838322 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0007g0117 |
2 | HG00741.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.169+5422C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838322 | |||||||
| chr7:35838323 | TCCCTCCC others(18): Show |
T | 8 | a0001c0001t0004g0012 a0001c0001t0004g0173 a0001c0001t0004g0176 others(5): Show |
8 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+5426_169+5450d others(27): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838323 | ||||||
| chr7:35838326 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0007g0117 |
2 | HG00741.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.169+5426C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838326 | |||||||
| chr7:35838327 | TCCCTCCC others(6): Show |
T | 1 | a0001c0001t0005g0219 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.169+5430_169+5442d others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838327 | ||||||
| chr7:35838327 | TCCCTCCC others(14): Show |
T | 2 | a0001c0001t0004g0172 a0001c0001t0024g0177 |
2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.169+5430_169+5450d others(23): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838327 | ||||||
| chr7:35838330 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0276 a0001c0001t0007g0117 |
3 | HG00741.hp1 HG02135.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.169+5430C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838330 | |||||||
| chr7:35838331 | TCCCTCCC others(10): Show |
T | 1 | a0001c0001t0005g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.169+5434_169+5450d others(19): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838331 | ||||||
| chr7:35838334 | C | T | 4 | a0001c0001t0001g0230 a0001c0001t0001g0276 a0001c0001t0003g0095 others(1): Show |
4 | HG00741.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+5434C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838334 | |||||||
| chr7:35838335 | TCCCTCCC others(10): Show |
T | 1 | a0001c0001t0001g0273 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.169+5438_169+5454d others(19): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838335 | ||||||
| chr7:35838340 | CCCTCCCT others(16): Show |
C | 1 | a0001c0001t0001g0237 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.169+5466_169+5488d others(25): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838340 | ||||||
| chr7:35838347 | TC | T | 10 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0031 others(7): Show |
12 | HG01255.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+5450delC | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838347 | ||||||
| chr7:35838358 | C | A | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+5458C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838358 | |||||||
| chr7:35838360 | CCCT | C | 6 | a0001c0001t0002g0148 a0001c0001t0002g0159 a0001c0001t0005g0219 others(3): Show |
6 | HG01891.hp1 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+5466_169+5468d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838360 | ||||||
| chr7:35838362 | C | T | 49 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 others(46): Show |
52 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.169+5462C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838362 | |||||||
| chr7:35838363 | T | C | 49 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 others(46): Show |
52 | HG00140.hp2 HG00738.hp1 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.169+5463T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838363 | |||||||
| chr7:35838366 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.169+5466T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838366 | |||||||
| chr7:35838370 | TC | T | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+5473delC | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35838370 | ||||||
| chr7:35838425 | A | G | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169+5525A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838425 | |||||||
| chr7:35838482 | C | G | 1 | a0001c0001t0005g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.169+5582C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838482 | |||||||
| chr7:35838828 | C | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+5928C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838828 | |||||||
| chr7:35838986 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169+6086A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838986 | |||||||
| chr7:35838988 | A | G | 1 | a0001c0002t0001g0017 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.169+6088A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35838988 | |||||||
| chr7:35839301 | A | G | 1 | a0001c0002t0001g0302 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.169+6401A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839301 | |||||||
| chr7:35839321 | T | C | 208 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(205): Show |
219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.169+6421T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839321 | |||||||
| chr7:35839340 | G | T | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.169+6440G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839340 | |||||||
| chr7:35839460 | G | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+6560G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839460 | |||||||
| chr7:35839523 | T | TTTATG | 193 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(190): Show |
201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.169+6663_169+6667d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839523 | T | TTTATGTT others(3): Show |
66 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0256 others(63): Show |
69 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.169+6658_169+6667d others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839523 | T | TTTATGTT others(8): Show |
11 | a0001c0001t0001g0230 a0001c0001t0001g0239 a0001c0001t0001g0276 others(8): Show |
11 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.169+6653_169+6667d others(17): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839523 | T | TTTATGTT others(13): Show |
1 | a0001c0001t0003g0092 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.169+6648_169+6667d others(22): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839523 | T | TTTATGTT others(18): Show |
1 | a0001c0001t0002g0118 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.169+6643_169+6667d others(27): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839523 | TTTATG | T | 6 | a0001c0001t0001g0286 a0001c0001t0002g0160 a0001c0001t0002g0162 others(3): Show |
6 | HG01123.hp2 HG01175.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+6663_169+6667d others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839523 | TTTATGTT others(3): Show |
T | 22 | a0001c0001t0004g0175 a0001c0001t0005g0013 a0001c0001t0005g0191 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+6658_169+6667d others(12): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839523 | ||||||
| chr7:35839566 | A | ATGTTATG others(6): Show |
1 | a0001c0003t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.169+6667_169+6668i others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35839566 | ||||||
| chr7:35839568 | T | A | 1 | a0001c0003t0002g0085 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.169+6668T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839568 | |||||||
| chr7:35839575 | A | G | 8 | a0001c0001t0001g0270 a0001c0001t0010g0238 a0001c0001t0010g0240 others(5): Show |
8 | HG01934.hp2 NA18948.hp1 NA18997.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+6675A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839575 | |||||||
| chr7:35839677 | C | G | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.169+6777C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839677 | |||||||
| chr7:35839803 | T | C | 1 | a0001c0001t0036g0200 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.169+6903T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839803 | |||||||
| chr7:35839805 | G | A | 1 | a0001c0001t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169+6905G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839805 | |||||||
| chr7:35839989 | T | A | 199 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.169+7089T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35839989 | |||||||
| chr7:35840070 | G | A | 5 | a0001c0001t0005g0201 a0001c0001t0005g0202 a0001c0001t0005g0207 others(2): Show |
6 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+7170G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840070 | |||||||
| chr7:35840136 | C | A | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+7236C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840136 | |||||||
| chr7:35840188 | T | TCCCCCTT others(7): Show |
3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169+7296_169+7309d others(16): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35840188 | ||||||
| chr7:35840200 | C | CTCCCCCC others(15): Show |
1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169+7320_169+7341d others(24): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35840200 | ||||||
| chr7:35840220 | C | G | 1 | a0001c0001t0036g0200 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.169+7320C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840220 | |||||||
| chr7:35840486 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.169+7586C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840486 | |||||||
| chr7:35840540 | A | G | 1 | a0001c0001t0037g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.169+7640A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840540 | |||||||
| chr7:35840570 | G | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+7670G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840570 | |||||||
| chr7:35840605 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.169+7705C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35840605 | |||||||
| chr7:35841059 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.169+8159A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841059 | |||||||
| chr7:35841086 | C | T | 199 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.169+8186C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841086 | |||||||
| chr7:35841093 | C | T | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG00642.hp1 HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.169+8193C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841093 | |||||||
| chr7:35841105 | T | A | 1 | a0001c0001t0004g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169+8205T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841105 | |||||||
| chr7:35841222 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.169+8322C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841222 | |||||||
| chr7:35841404 | A | T | 1 | a0001c0001t0005g0013 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.169+8504A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841404 | |||||||
| chr7:35841424 | T | C | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+8524T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841424 | |||||||
| chr7:35841657 | A | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0101 |
2 | HG00099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.169+8757A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841657 | |||||||
| chr7:35841724 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.169+8824G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35841724 | |||||||
| chr7:35842032 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.169+9132G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842032 | |||||||
| chr7:35842064 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+9164A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842064 | |||||||
| chr7:35842348 | G | GA | 144 | a0001c0001t0001g0258 a0001c0001t0001g0279 a0001c0001t0001g0307 others(141): Show |
152 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.169+9460dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35842348 | ||||||
| chr7:35842348 | G | GAA | 15 | a0001c0001t0002g0080 a0001c0001t0002g0084 a0001c0001t0002g0128 others(12): Show |
15 | HG00597.hp1 HG00609.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.169+9459_169+9460d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35842348 | ||||||
| chr7:35842360 | A | C | 1 | a0001c0001t0016g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.169+9460A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842360 | |||||||
| chr7:35842486 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169+9586A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842486 | |||||||
| chr7:35842556 | A | T | 1 | a0001c0001t0011g0067 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.169+9656A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842556 | |||||||
| chr7:35842577 | T | G | 2 | a0001c0001t0004g0003 a0001c0001t0004g0031 |
3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.169+9677T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842577 | |||||||
| chr7:35842640 | T | C | 1 | a0001c0001t0012g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.169+9740T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842640 | |||||||
| chr7:35842671 | G | A | 5 | a0001c0001t0003g0002 a0001c0001t0003g0185 a0001c0001t0003g0186 others(2): Show |
7 | NA18954.hp2 NA18956.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.169+9771G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842671 | |||||||
| chr7:35842819 | A | G | 4 | a0001c0001t0002g0084 a0001c0001t0002g0122 a0001c0001t0015g0274 others(1): Show |
4 | NA18612.hp1 NA18940.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+9919A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842819 | |||||||
| chr7:35842837 | C | T | 24 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(21): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+9937C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35842837 | |||||||
| chr7:35843049 | C | T | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0306 others(1): Show |
4 | NA18966.hp2 NA18968.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+10149C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843049 | |||||||
| chr7:35843369 | C | T | 133 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(130): Show |
137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+10469C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843369 | |||||||
| chr7:35843434 | T | C | 133 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(130): Show |
137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+10534T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843434 | |||||||
| chr7:35843452 | G | A | 1 | a0001c0001t0006g0055 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.169+10552G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843452 | |||||||
| chr7:35843583 | C | T | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+10683C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843583 | |||||||
| chr7:35843687 | A | G | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+10787A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843687 | |||||||
| chr7:35843791 | C | T | 153 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(150): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.169+10891C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35843791 | |||||||
| chr7:35844030 | C | G | 1 | a0001c0001t0009g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.169+11130C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844030 | |||||||
| chr7:35844233 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+11333G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844233 | |||||||
| chr7:35844524 | A | G | 1 | a0001c0001t0007g0147 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.169+11624A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844524 | |||||||
| chr7:35844607 | CT | C | 208 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(205): Show |
219 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.169+11717delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35844607 | ||||||
| chr7:35844623 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.169+11723G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844623 | |||||||
| chr7:35844686 | G | A | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.169+11786G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844686 | |||||||
| chr7:35844747 | C | T | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.169+11847C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844747 | |||||||
| chr7:35844852 | C | T | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.169+11952C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844852 | |||||||
| chr7:35844931 | C | A | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.169+12031C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35844931 | |||||||
| chr7:35845149 | C | A | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+12249C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845149 | |||||||
| chr7:35845172 | G | A | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+12272G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845172 | |||||||
| chr7:35845387 | G | A | 152 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(149): Show |
159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.169+12487G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845387 | |||||||
| chr7:35845544 | G | A | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+12644G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845544 | |||||||
| chr7:35845567 | C | T | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+12667C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845567 | |||||||
| chr7:35845580 | T | C | 19 | a0001c0001t0001g0270 a0001c0001t0001g0288 a0001c0001t0001g0289 others(16): Show |
19 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.169+12680T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845580 | |||||||
| chr7:35845775 | A | G | 2 | a0001c0001t0004g0007 a0001c0001t0004g0192 |
3 | HG02109.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.169+12875A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845775 | |||||||
| chr7:35845847 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.169+12947G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845847 | |||||||
| chr7:35845962 | G | GT | 24 | a0001c0001t0004g0007 a0001c0001t0004g0192 a0001c0001t0005g0013 others(21): Show |
26 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+13072dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35845962 | ||||||
| chr7:35845964 | T | C | 133 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(130): Show |
137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.169+13064T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845964 | |||||||
| chr7:35845986 | T | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0119 |
3 | HG02976.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.169+13086T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35845986 | |||||||
| chr7:35846008 | T | C | 1 | a0001c0001t0003g0190 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.169+13108T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846008 | |||||||
| chr7:35846145 | T | C | 2 | a0001c0001t0002g0106 a0002c0005t0002g0104 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.169+13245T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846145 | |||||||
| chr7:35846173 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.169+13273T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846173 | |||||||
| chr7:35846359 | T | C | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+13459T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846359 | |||||||
| chr7:35846647 | C | T | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.169+13747C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846647 | |||||||
| chr7:35846718 | T | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+13818T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846718 | |||||||
| chr7:35846806 | C | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.169+13906C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846806 | |||||||
| chr7:35846936 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.169+14036A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846936 | |||||||
| chr7:35846993 | A | G | 24 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(21): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+14093A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35846993 | |||||||
| chr7:35847081 | GTC | G | 18 | a0001c0001t0002g0028 a0001c0001t0002g0078 a0001c0001t0002g0079 others(15): Show |
18 | HG02300.hp1 HG03239.hp1 HG03704.hp2 others(15): Show |
intron_variant | MODIFIER | c.169+14185_169+1418 others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35847081 | ||||||
| chr7:35847120 | A | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+14220A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847120 | |||||||
| chr7:35847122 | A | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.169+14222A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847122 | |||||||
| chr7:35847173 | C | CA | 24 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(21): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+14274dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35847173 | ||||||
| chr7:35847178 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+14278G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847178 | |||||||
| chr7:35847239 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169+14339C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847239 | |||||||
| chr7:35847252 | G | A | 1 | a0001c0001t0009g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.169+14352G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847252 | |||||||
| chr7:35847532 | ATTAT | A | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.169+14639_169+1464 others(8): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35847532 | ||||||
| chr7:35847974 | G | T | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.169+15074G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35847974 | |||||||
| chr7:35848099 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.169+15199C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848099 | |||||||
| chr7:35848138 | G | A | 24 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0012 others(21): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.169+15238G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848138 | |||||||
| chr7:35848146 | C | T | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+15246C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848146 | |||||||
| chr7:35848159 | A | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+15259A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848159 | |||||||
| chr7:35848287 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.170-15265A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848287 | |||||||
| chr7:35848337 | G | A | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 |
3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-15215G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848337 | |||||||
| chr7:35848424 | T | C | 153 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(150): Show |
160 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.170-15128T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848424 | |||||||
| chr7:35848481 | A | G | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-15071A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848481 | |||||||
| chr7:35848505 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.170-15047C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848505 | |||||||
| chr7:35848505 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-15047C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848505 | |||||||
| chr7:35848514 | C | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-15038C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848514 | |||||||
| chr7:35848612 | T | G | 1 | a0001c0001t0010g0269 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.170-14940T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848612 | |||||||
| chr7:35848905 | G | T | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.170-14647G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848905 | |||||||
| chr7:35848925 | T | C | 1 | a0001c0001t0004g0031 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.170-14627T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35848925 | |||||||
| chr7:35849098 | T | C | 3 | a0001c0001t0002g0160 a0001c0001t0002g0162 a0001c0001t0002g0166 |
3 | HG00140.hp2 HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.170-14454T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849098 | |||||||
| chr7:35849278 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0315 |
2 | NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.170-14274G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849278 | |||||||
| chr7:35849286 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0272 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.170-14266C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849286 | |||||||
| chr7:35849460 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.170-14092G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849460 | |||||||
| chr7:35849488 | C | T | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-14064C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849488 | |||||||
| chr7:35849531 | A | G | 133 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(130): Show |
137 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.170-14021A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849531 | |||||||
| chr7:35849791 | A | C | 7 | a0001c0001t0011g0005 a0001c0001t0011g0065 a0001c0001t0011g0067 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.170-13761A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849791 | |||||||
| chr7:35849910 | C | G | 2 | a0001c0001t0002g0042 a0001c0001t0002g0043 |
2 | HG03195.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.170-13642C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35849910 | |||||||
| chr7:35850076 | A | G | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-13476A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850076 | |||||||
| chr7:35850181 | A | G | 2 | a0001c0001t0004g0171 a0001c0001t0004g0179 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.170-13371A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850181 | |||||||
| chr7:35850434 | C | T | 4 | a0001c0001t0012g0062 a0001c0001t0012g0063 a0001c0001t0012g0064 others(1): Show |
4 | NA18970.hp2 NA18975.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-13118C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850434 | |||||||
| chr7:35850438 | T | C | 1 | a0001c0001t0003g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.170-13114T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850438 | |||||||
| chr7:35850804 | C | A | 1 | a0001c0001t0002g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.170-12748C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35850804 | |||||||
| chr7:35851066 | A | C | 1 | a0001c0001t0003g0098 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.170-12486A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851066 | |||||||
| chr7:35851107 | G | A | 3 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 |
3 | HG01243.hp2 HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.170-12445G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851107 | |||||||
| chr7:35851158 | A | G | 5 | a0001c0001t0001g0230 a0001c0001t0001g0237 a0001c0001t0001g0267 others(2): Show |
5 | HG01123.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-12394A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851158 | |||||||
| chr7:35851264 | A | C | 2 | a0001c0001t0003g0099 a0001c0003t0002g0085 |
2 | HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.170-12288A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851264 | |||||||
| chr7:35851299 | T | C | 7 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.170-12253T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851299 | |||||||
| chr7:35851339 | C | A | 1 | a0001c0001t0002g0079 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.170-12213C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851339 | |||||||
| chr7:35851413 | G | A | 209 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(206): Show |
220 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.170-12139G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851413 | |||||||
| chr7:35851429 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.170-12123G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851429 | |||||||
| chr7:35851501 | A | G | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-12051A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851501 | |||||||
| chr7:35851788 | T | G | 1 | a0001c0001t0003g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.170-11764T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851788 | |||||||
| chr7:35851791 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.170-11761A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851791 | |||||||
| chr7:35851975 | C | A | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.170-11577C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35851975 | |||||||
| chr7:35852017 | G | A | 3 | a0001c0001t0004g0171 a0001c0001t0004g0178 a0001c0001t0004g0179 |
3 | HG02055.hp2 HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.170-11535G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852017 | |||||||
| chr7:35852283 | G | A | 199 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.170-11269G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852283 | |||||||
| chr7:35852339 | T | G | 1 | a0001c0002t0001g0301 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.170-11213T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852339 | |||||||
| chr7:35852340 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.170-11212A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852340 | |||||||
| chr7:35852522 | A | G | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.170-11030A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852522 | |||||||
| chr7:35852587 | C | T | 1 | a0001c0001t0005g0204 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.170-10965C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852587 | |||||||
| chr7:35852808 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-10744A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35852808 | |||||||
| chr7:35853129 | A | G | 5 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0040 others(2): Show |
5 | HG01109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-10423A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853129 | |||||||
| chr7:35853198 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.170-10354G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853198 | |||||||
| chr7:35853298 | C | T | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-10254C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853298 | |||||||
| chr7:35853696 | T | G | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.170-9856T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853696 | |||||||
| chr7:35853898 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.170-9654C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35853898 | |||||||
| chr7:35854006 | T | C | 12 | a0001c0001t0001g0228 a0001c0001t0001g0234 a0001c0001t0001g0235 others(9): Show |
12 | HG00558.hp2 HG00673.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.170-9546T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854006 | |||||||
| chr7:35854061 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.170-9491A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854061 | |||||||
| chr7:35854237 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | NA18979.hp1 NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.170-9315A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854237 | |||||||
| chr7:35854629 | C | A | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.170-8923C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854629 | |||||||
| chr7:35854793 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.170-8759A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35854793 | |||||||
| chr7:35855003 | A | G | 1 | a0001c0001t0037g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170-8549A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855003 | |||||||
| chr7:35855127 | C | T | 198 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.170-8425C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855127 | |||||||
| chr7:35855203 | A | G | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-8349A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855203 | |||||||
| chr7:35855322 | C | T | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-8230C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855322 | |||||||
| chr7:35855323 | G | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0041 |
4 | HG02258.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-8229G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855323 | |||||||
| chr7:35855946 | G | C | 309 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(306): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.170-7606G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35855946 | |||||||
| chr7:35856077 | C | A | 1 | a0001c0001t0036g0200 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.170-7475C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856077 | |||||||
| chr7:35856574 | G | A | 285 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(282): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.170-6978G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856574 | |||||||
| chr7:35856625 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.170-6927A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856625 | |||||||
| chr7:35856686 | G | A | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-6866G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856686 | |||||||
| chr7:35856696 | C | G | 1 | a0001c0001t0014g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.170-6856C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856696 | |||||||
| chr7:35856759 | G | A | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-6793G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856759 | |||||||
| chr7:35856907 | A | G | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-6645A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35856907 | |||||||
| chr7:35857339 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.170-6213G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35857339 | |||||||
| chr7:35857600 | G | A | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.170-5952G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35857600 | |||||||
| chr7:35858017 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.170-5535A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858017 | |||||||
| chr7:35858145 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-5407A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858145 | |||||||
| chr7:35858345 | A | G | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-5207A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858345 | |||||||
| chr7:35858395 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.170-5157C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858395 | |||||||
| chr7:35858419 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-5133G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858419 | |||||||
| chr7:35858441 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-5111C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858441 | |||||||
| chr7:35858509 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.170-5043C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858509 | |||||||
| chr7:35858577 | A | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-4975A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858577 | |||||||
| chr7:35858633 | C | T | 1 | a0001c0001t0034g0259 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.170-4919C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858633 | |||||||
| chr7:35858643 | C | T | 1 | a0001c0001t0002g0150 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.170-4909C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858643 | |||||||
| chr7:35858681 | C | CT | 20 | a0001c0001t0002g0108 a0001c0001t0002g0110 a0001c0001t0005g0013 others(17): Show |
21 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-4855dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35858681 | ||||||
| chr7:35858738 | A | G | 36 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(33): Show |
40 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.170-4814A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858738 | |||||||
| chr7:35858872 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.170-4680G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35858872 | |||||||
| chr7:35859014 | G | A | 1 | a0001c0001t0020g0008 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.170-4538G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859014 | |||||||
| chr7:35859081 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.170-4471C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859081 | |||||||
| chr7:35859125 | A | G | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.170-4427A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859125 | |||||||
| chr7:35859145 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-4407A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859145 | |||||||
| chr7:35859180 | G | A | 133 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(130): Show |
135 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.170-4372G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859180 | |||||||
| chr7:35859217 | T | C | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-4335T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859217 | |||||||
| chr7:35859565 | C | G | 1 | a0001c0001t0010g0238 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.170-3987C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35859565 | |||||||
| chr7:35860074 | T | C | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.170-3478T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860074 | |||||||
| chr7:35860096 | A | G | 5 | a0001c0001t0003g0002 a0001c0001t0003g0185 a0001c0001t0003g0186 others(2): Show |
7 | NA18954.hp2 NA18956.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.170-3456A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860096 | |||||||
| chr7:35860114 | C | CT | 15 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(12): Show |
18 | HG00597.hp2 HG02155.hp2 HG03098.hp2 others(15): Show |
intron_variant | MODIFIER | c.170-3427dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35860114 | ||||||
| chr7:35860200 | T | G | 1 | a0001c0001t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.170-3352T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860200 | |||||||
| chr7:35860494 | C | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-3058C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860494 | |||||||
| chr7:35860534 | G | A | 1 | a0001c0001t0012g0260 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.170-3018G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860534 | |||||||
| chr7:35860778 | G | C | 5 | a0001c0001t0004g0007 a0001c0001t0004g0012 a0001c0001t0004g0172 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-2774G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860778 | |||||||
| chr7:35860944 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.170-2608C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860944 | |||||||
| chr7:35860970 | A | G | 1 | a0001c0001t0029g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.170-2582A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35860970 | |||||||
| chr7:35861096 | T | C | 1 | a0001c0001t0013g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.170-2456T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861096 | |||||||
| chr7:35861264 | C | T | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2288C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861264 | |||||||
| chr7:35861470 | C | T | 1 | a0001c0001t0017g0216 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.170-2082C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861470 | |||||||
| chr7:35861539 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-2013G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861539 | |||||||
| chr7:35861542 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.170-2010C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861542 | |||||||
| chr7:35861627 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.170-1925A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861627 | |||||||
| chr7:35861659 | A | C | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.170-1893A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861659 | |||||||
| chr7:35861666 | A | G | 1 | a0001c0001t0039g0195 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.170-1886A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861666 | |||||||
| chr7:35861773 | T | G | 1 | a0001c0001t0003g0212 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.170-1779T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861773 | |||||||
| chr7:35861806 | G | T | 2 | a0001c0001t0001g0304 a0001c0001t0010g0305 |
2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.170-1746G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861806 | |||||||
| chr7:35861880 | G | A | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-1672G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861880 | |||||||
| chr7:35861914 | C | T | 131 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(128): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-1638C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35861914 | |||||||
| chr7:35862074 | A | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.170-1478A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862074 | |||||||
| chr7:35862239 | C | G | 5 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(2): Show |
5 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-1313C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862239 | |||||||
| chr7:35862427 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-1125A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862427 | |||||||
| chr7:35862545 | T | A | 1 | a0001c0001t0021g0051 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.170-1007T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862545 | |||||||
| chr7:35862717 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-835A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862717 | |||||||
| chr7:35862838 | T | C | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.170-714T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862838 | |||||||
| chr7:35862900 | CAA | C | 10 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(7): Show |
11 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.170-647_170-646del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35862900 | ||||||
| chr7:35862989 | A | C | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.170-563A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35862989 | |||||||
| chr7:35863152 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.170-400A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35863152 | |||||||
| chr7:35863239 | A | AT | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.170-307dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr7 | 35863239 | ||||||
| chr7:35863512 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.170-40G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 3/13 | chr7 | 35863512 | |||||||
| chr7:35863688 | G | A | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+30G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35863688 | |||||||
| chr7:35863808 | A | T | 20 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.276+150A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35863808 | |||||||
| chr7:35864278 | A | G | 1 | a0001c0001t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.276+620A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864278 | |||||||
| chr7:35864424 | T | C | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.276+766T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864424 | |||||||
| chr7:35864664 | G | GCTA | 173 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(170): Show |
181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.276+1007_276+1009d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35864664 | ||||||
| chr7:35864770 | A | G | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(131): Show |
136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.276+1112A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864770 | |||||||
| chr7:35864838 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.276+1180G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864838 | |||||||
| chr7:35864991 | T | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+1333T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35864991 | |||||||
| chr7:35865023 | A | AT | 44 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(41): Show |
48 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.276+1379dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35865023 | ||||||
| chr7:35865077 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.276+1419A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865077 | |||||||
| chr7:35865100 | C | G | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.276+1442C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865100 | |||||||
| chr7:35865207 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+1549T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865207 | |||||||
| chr7:35865282 | C | G | 2 | a0001c0001t0003g0183 a0001c0001t0003g0190 |
2 | NA19072.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.276+1624C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865282 | |||||||
| chr7:35865297 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.276+1639G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865297 | |||||||
| chr7:35865322 | C | A | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(131): Show |
136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.276+1664C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865322 | |||||||
| chr7:35865427 | A | C | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1769A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865427 | |||||||
| chr7:35865453 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+1795T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865453 | |||||||
| chr7:35865471 | T | A | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.276+1813T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865471 | |||||||
| chr7:35865498 | G | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG00673.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.276+1840G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865498 | |||||||
| chr7:35865626 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0252 a0001c0001t0001g0279 others(1): Show |
5 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1968T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865626 | |||||||
| chr7:35865850 | C | A | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+2192C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865850 | |||||||
| chr7:35865944 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.276+2286C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35865944 | |||||||
| chr7:35866021 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+2363A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866021 | |||||||
| chr7:35866023 | G | C | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.276+2365G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866023 | |||||||
| chr7:35866155 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.276+2497C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866155 | |||||||
| chr7:35866201 | C | G | 4 | a0001c0001t0003g0002 a0001c0001t0003g0185 a0001c0001t0003g0186 others(1): Show |
6 | NA18954.hp2 NA18956.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+2543C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866201 | |||||||
| chr7:35866379 | C | G | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.276+2721C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866379 | |||||||
| chr7:35866807 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.276+3149C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866807 | |||||||
| chr7:35866874 | C | A | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+3216C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866874 | |||||||
| chr7:35866907 | T | C | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(131): Show |
136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.276+3249T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35866907 | |||||||
| chr7:35867448 | C | G | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+3790C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867448 | |||||||
| chr7:35867560 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.276+3902G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867560 | |||||||
| chr7:35867617 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0010g0305 |
2 | HG01358.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.276+3959C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867617 | |||||||
| chr7:35867673 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+4015T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867673 | |||||||
| chr7:35867851 | A | T | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.276+4193A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867851 | |||||||
| chr7:35867977 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.276+4319A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867977 | |||||||
| chr7:35867984 | T | C | 1 | a0001c0001t0008g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.276+4326T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35867984 | |||||||
| chr7:35868019 | C | T | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.276+4361C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868019 | |||||||
| chr7:35868020 | G | A | 14 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(11): Show |
17 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+4362G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868020 | |||||||
| chr7:35868253 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277-4413A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868253 | |||||||
| chr7:35868331 | G | A | 256 | a0001c0001t0001g0009 a0001c0001t0001g0181 a0001c0001t0001g0182 others(253): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.277-4335G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868331 | |||||||
| chr7:35868331 | G | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0180 a0001c0001t0001g0221 others(48): Show |
52 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.277-4335G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868331 | |||||||
| chr7:35868551 | C | G | 36 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(33): Show |
40 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.277-4115C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868551 | |||||||
| chr7:35868745 | G | C | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.277-3921G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868745 | |||||||
| chr7:35868791 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.277-3875A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35868791 | |||||||
| chr7:35869123 | A | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.277-3543A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869123 | |||||||
| chr7:35869187 | T | C | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.277-3479T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869187 | |||||||
| chr7:35869198 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.277-3468A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869198 | |||||||
| chr7:35869265 | G | A | 124 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(121): Show |
125 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.277-3401G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869265 | |||||||
| chr7:35869293 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.277-3373G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869293 | |||||||
| chr7:35869324 | A | G | 8 | a0001c0001t0001g0182 a0001c0001t0011g0005 a0001c0001t0011g0065 others(5): Show |
9 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-3342A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869324 | |||||||
| chr7:35869796 | A | G | 2 | a0001c0001t0018g0103 a0001c0001t0018g0121 |
2 | HG02300.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.277-2870A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869796 | |||||||
| chr7:35869959 | G | A | 1 | a0001c0001t0021g0051 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.277-2707G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35869959 | |||||||
| chr7:35870037 | A | T | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.277-2629A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870037 | |||||||
| chr7:35870091 | A | G | 174 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(171): Show |
182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.277-2575A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870091 | |||||||
| chr7:35870093 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.277-2573G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870093 | |||||||
| chr7:35870374 | T | C | 1 | a0001c0001t0015g0052 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.277-2292T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870374 | |||||||
| chr7:35870479 | C | G | 40 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(37): Show |
40 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.277-2187C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870479 | |||||||
| chr7:35870618 | A | G | 2 | a0001c0001t0001g0279 a0001c0001t0001g0294 |
2 | HG00733.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.277-2048A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870618 | |||||||
| chr7:35870713 | C | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0012 a0001c0001t0004g0172 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-1953C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870713 | |||||||
| chr7:35870743 | C | A | 1 | a0001c0001t0002g0035 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.277-1923C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870743 | |||||||
| chr7:35870823 | T | TA | 11 | a0001c0001t0001g0050 a0001c0001t0001g0242 a0001c0001t0001g0258 others(8): Show |
11 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.277-1822dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | ||||||
| chr7:35870823 | T | TAA | 18 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(15): Show |
19 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.277-1823_277-1822d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | ||||||
| chr7:35870823 | TA | T | 7 | a0001c0001t0002g0135 a0001c0001t0002g0141 a0001c0001t0003g0217 others(4): Show |
7 | HG02135.hp1 HG02155.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-1822delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | ||||||
| chr7:35870823 | TAA | T | 109 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0032 others(106): Show |
113 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.277-1823_277-1822d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | ||||||
| chr7:35870823 | TAAA | T | 18 | a0001c0001t0002g0028 a0001c0001t0002g0078 a0001c0001t0002g0079 others(15): Show |
18 | HG00741.hp1 HG01943.hp1 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.277-1824_277-1822d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr7 | 35870823 | ||||||
| chr7:35870871 | C | T | 2 | a0001c0001t0003g0091 a0001c0001t0003g0115 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.277-1795C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870871 | |||||||
| chr7:35870912 | T | C | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.277-1754T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870912 | |||||||
| chr7:35870939 | A | G | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.277-1727A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35870939 | |||||||
| chr7:35871086 | T | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.277-1580T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871086 | |||||||
| chr7:35871105 | T | C | 9 | a0001c0001t0008g0018 a0001c0001t0008g0019 a0001c0001t0008g0020 others(6): Show |
9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-1561T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871105 | |||||||
| chr7:35871197 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.277-1469C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871197 | |||||||
| chr7:35871199 | T | C | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-1467T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871199 | |||||||
| chr7:35871218 | C | T | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.277-1448C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871218 | |||||||
| chr7:35871348 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.277-1318G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871348 | |||||||
| chr7:35871485 | A | G | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.277-1181A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871485 | |||||||
| chr7:35871554 | T | G | 1 | a0001c0001t0003g0112 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.277-1112T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871554 | |||||||
| chr7:35871835 | G | A | 1 | a0001c0001t0013g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-831G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871835 | |||||||
| chr7:35871854 | T | C | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-812T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871854 | |||||||
| chr7:35871999 | G | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.277-667G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35871999 | |||||||
| chr7:35872129 | A | G | 11 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.277-537A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35872129 | |||||||
| chr7:35872254 | A | T | 1 | a0001c0001t0003g0097 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.277-412A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35872254 | |||||||
| chr7:35872500 | A | G | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.277-166A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 4/13 | chr7 | 35872500 | |||||||
| chr7:35872991 | A | T | 15 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(12): Show |
16 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.377+225A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35872991 | |||||||
| chr7:35873027 | A | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.377+261A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873027 | |||||||
| chr7:35873083 | T | C | 309 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(306): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.377+317T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873083 | |||||||
| chr7:35873116 | A | G | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+350A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873116 | |||||||
| chr7:35873391 | G | A | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-250G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873391 | |||||||
| chr7:35873424 | C | T | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378-217C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873424 | |||||||
| chr7:35873503 | A | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378-138A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873503 | |||||||
| chr7:35873563 | C | T | 1 | a0001c0001t0006g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.378-78C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 5/13 | chr7 | 35873563 | |||||||
| chr7:35873952 | T | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.512+177T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35873952 | |||||||
| chr7:35873954 | A | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.512+179A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35873954 | |||||||
| chr7:35874201 | A | G | 1 | a0001c0001t0009g0265 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.512+426A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874201 | |||||||
| chr7:35874439 | T | C | 151 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(148): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.512+664T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874439 | |||||||
| chr7:35874454 | A | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0237 a0001c0001t0001g0267 others(2): Show |
5 | HG01123.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+679A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874454 | |||||||
| chr7:35874463 | G | A | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.512+688G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874463 | |||||||
| chr7:35874615 | G | T | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.512+840G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874615 | |||||||
| chr7:35874652 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.512+877A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874652 | |||||||
| chr7:35874673 | T | C | 2 | a0001c0001t0002g0082 a0001c0003t0002g0085 |
2 | HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.512+898T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874673 | |||||||
| chr7:35874760 | A | T | 1 | a0001c0001t0001g0254 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.512+985A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35874760 | |||||||
| chr7:35875106 | T | C | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.512+1331T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35875106 | |||||||
| chr7:35875770 | T | TATAC | 6 | a0001c0001t0002g0036 a0001c0001t0002g0039 a0001c0001t0002g0040 others(3): Show |
6 | HG01109.hp1 HG01934.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+2017_512+2020d others(6): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35875770 | ||||||
| chr7:35875955 | C | A | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.512+2180C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35875955 | |||||||
| chr7:35876121 | A | G | 1 | a0001c0004t0013g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.512+2346A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876121 | |||||||
| chr7:35876265 | CTTG | C | 11 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0036 others(8): Show |
12 | HG01109.hp1 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.512+2493_512+2495d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35876265 | ||||||
| chr7:35876411 | ATT | A | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.512+2638_512+2639d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35876411 | ||||||
| chr7:35876483 | A | G | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.512+2708A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876483 | |||||||
| chr7:35876576 | G | A | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.512+2801G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876576 | |||||||
| chr7:35876588 | A | C | 1 | a0001c0001t0009g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.512+2813A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876588 | |||||||
| chr7:35876621 | C | G | 1 | a0001c0001t0002g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.512+2846C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876621 | |||||||
| chr7:35876864 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.513-2959G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876864 | |||||||
| chr7:35876949 | A | G | 1 | a0001c0001t0026g0203 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.513-2874A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876949 | |||||||
| chr7:35876977 | A | C | 1 | a0001c0001t0011g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.513-2846A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876977 | |||||||
| chr7:35876977 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.513-2846A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35876977 | |||||||
| chr7:35877231 | T | C | 1 | a0001c0001t0003g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.513-2592T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877231 | |||||||
| chr7:35877289 | G | A | 7 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0002g0153 others(4): Show |
7 | HG00609.hp2 NA18951.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.513-2534G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877289 | |||||||
| chr7:35877299 | A | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.513-2524A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877299 | |||||||
| chr7:35877540 | T | G | 1 | a0001c0001t0001g0295 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.513-2283T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877540 | |||||||
| chr7:35877814 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.513-2009A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877814 | |||||||
| chr7:35877879 | A | C | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.513-1944A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35877879 | |||||||
| chr7:35878294 | G | A | 1 | a0001c0002t0001g0299 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.513-1529G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878294 | |||||||
| chr7:35878315 | G | GC | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1508_513-1507i others(3): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878315 | |||||||
| chr7:35878316 | T | C | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1507T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878316 | |||||||
| chr7:35878317 | A | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1506A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878317 | |||||||
| chr7:35878320 | A | G | 3 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | HG02559.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.513-1503A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878320 | |||||||
| chr7:35878797 | A | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.513-1026A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878797 | |||||||
| chr7:35878943 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.513-880G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878943 | |||||||
| chr7:35878986 | C | T | 2 | a0001c0001t0005g0197 a0001c0001t0005g0199 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.513-837C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878986 | |||||||
| chr7:35878993 | G | T | 1 | a0001c0001t0002g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.513-830G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35878993 | |||||||
| chr7:35879130 | G | C | 1 | a0001c0001t0005g0218 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513-693G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879130 | |||||||
| chr7:35879150 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.513-673C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879150 | |||||||
| chr7:35879305 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0313 |
3 | HG00735.hp2 HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.513-518G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879305 | |||||||
| chr7:35879333 | A | G | 1 | a0001c0001t0019g0264 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.513-490A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879333 | |||||||
| chr7:35879456 | G | T | 3 | a0001c0001t0010g0303 a0001c0001t0010g0327 a0001c0001t0010g0328 |
3 | NA19072.hp2 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513-367G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879456 | |||||||
| chr7:35879458 | A | T | 3 | a0001c0001t0010g0303 a0001c0001t0010g0327 a0001c0001t0010g0328 |
3 | NA19072.hp2 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.513-365A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879458 | |||||||
| chr7:35879490 | T | TA | 8 | a0001c0001t0005g0197 a0001c0001t0005g0198 a0001c0001t0005g0199 others(5): Show |
8 | HG00738.hp1 HG02257.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.513-320dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35879490 | ||||||
| chr7:35879490 | TA | T | 280 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(277): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.513-320delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr7 | 35879490 | ||||||
| chr7:35879789 | T | G | 19 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(16): Show |
22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.513-34T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 6/13 | chr7 | 35879789 | |||||||
| chr7:35879976 | G | A | 19 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(16): Show |
22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.630+36G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35879976 | |||||||
| chr7:35880131 | G | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+191G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880131 | |||||||
| chr7:35880165 | T | C | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.630+225T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880165 | |||||||
| chr7:35880179 | A | ATTTTCTT | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+249_630+255dup others(7): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880179 | ||||||
| chr7:35880186 | T | C | 1 | a0001c0001t0009g0296 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.630+246T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880186 | |||||||
| chr7:35880198 | CTTTTCTT others(8): Show |
C | 13 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(10): Show |
16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.630+278_630+292del others(15): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880198 | ||||||
| chr7:35880223 | C | CT | 19 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0242 others(16): Show |
19 | HG00735.hp1 HG01884.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+303dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | ||||||
| chr7:35880223 | CT | C | 145 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0248 others(142): Show |
151 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.630+303delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | ||||||
| chr7:35880223 | CTT | C | 7 | a0001c0001t0002g0039 a0001c0001t0002g0071 a0001c0001t0002g0119 others(4): Show |
7 | HG02165.hp1 HG02723.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.630+302_630+303del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | ||||||
| chr7:35880223 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0008g0018 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.630+291_630+303del others(13): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35880223 | ||||||
| chr7:35880227 | T | C | 1 | a0001c0001t0006g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.630+287T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880227 | |||||||
| chr7:35880228 | T | C | 1 | a0001c0001t0020g0008 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.630+288T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880228 | |||||||
| chr7:35880229 | T | C | 1 | a0001c0001t0002g0087 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.630+289T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880229 | |||||||
| chr7:35880352 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.630+412C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880352 | |||||||
| chr7:35880422 | T | C | 4 | a0001c0001t0003g0092 a0001c0001t0003g0101 a0001c0001t0003g0169 others(1): Show |
4 | HG00099.hp1 HG01192.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+482T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880422 | |||||||
| chr7:35880660 | T | A | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.630+720T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880660 | |||||||
| chr7:35880701 | G | A | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+761G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880701 | |||||||
| chr7:35880769 | A | C | 2 | a0001c0001t0004g0173 a0001c0001t0004g0176 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.630+829A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880769 | |||||||
| chr7:35880932 | C | A | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+992C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35880932 | |||||||
| chr7:35881145 | T | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+1205T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881145 | |||||||
| chr7:35881157 | A | G | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.630+1217A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881157 | |||||||
| chr7:35881512 | T | A | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.631-972T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881512 | |||||||
| chr7:35881525 | G | A | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-959G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881525 | |||||||
| chr7:35881702 | G | A | 1 | a0001c0002t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.631-782G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881702 | |||||||
| chr7:35881768 | G | A | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.631-716G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881768 | |||||||
| chr7:35881939 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.631-545A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881939 | |||||||
| chr7:35881970 | G | A | 2 | a0001c0001t0001g0279 a0001c0001t0001g0294 |
2 | HG00733.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.631-514G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35881970 | |||||||
| chr7:35882030 | A | C | 1 | a0001c0002t0001g0301 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.631-454A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882030 | |||||||
| chr7:35882160 | A | T | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.631-324A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882160 | |||||||
| chr7:35882302 | T | TA | 50 | a0001c0001t0001g0181 a0001c0001t0001g0250 a0001c0001t0002g0004 others(47): Show |
53 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.631-168dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35882302 | ||||||
| chr7:35882302 | TA | T | 8 | a0001c0001t0001g0273 a0001c0001t0005g0202 a0001c0001t0006g0001 others(5): Show |
11 | HG01258.hp2 HG01928.hp1 NA18942.hp2 others(8): Show |
intron_variant | MODIFIER | c.631-168delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr7 | 35882302 | ||||||
| chr7:35882353 | G | C | 1 | a0001c0001t0036g0200 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.631-131G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882353 | |||||||
| chr7:35882448 | A | G | 1 | a0001c0001t0005g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.631-36A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 7/13 | chr7 | 35882448 | |||||||
| chr7:35882598 | C | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.723+22C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882598 | |||||||
| chr7:35882599 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.723+23G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882599 | |||||||
| chr7:35882652 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.723+76A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882652 | |||||||
| chr7:35882876 | G | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0244 a0001c0001t0001g0252 others(2): Show |
6 | HG00733.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+300G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882876 | |||||||
| chr7:35882979 | G | A | 3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0176 |
3 | HG02258.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.723+403G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35882979 | |||||||
| chr7:35883139 | A | G | 15 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(12): Show |
16 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.723+563A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883139 | |||||||
| chr7:35883235 | T | C | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-656T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883235 | |||||||
| chr7:35883283 | G | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.724-608G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883283 | |||||||
| chr7:35883393 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724-498A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883393 | |||||||
| chr7:35883786 | A | AT | 131 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(128): Show |
133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.724-91dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 35883786 | ||||||
| chr7:35883786 | A | ATT | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0313 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-92_724-91dupTT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 35883786 | ||||||
| chr7:35883786 | AT | A | 20 | a0001c0001t0005g0206 a0001c0001t0006g0001 a0001c0001t0006g0027 others(17): Show |
23 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.724-91delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr7 | 35883786 | ||||||
| chr7:35883831 | T | A | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-60T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 8/13 | chr7 | 35883831 | |||||||
| chr7:35884050 | T | G | 3 | a0001c0001t0004g0007 a0001c0001t0004g0012 a0001c0001t0004g0192 |
4 | HG02109.hp1 HG02109.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.820+63T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884050 | |||||||
| chr7:35884066 | G | A | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+79G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884066 | |||||||
| chr7:35884132 | T | C | 7 | a0001c0001t0011g0005 a0001c0001t0011g0065 a0001c0001t0011g0067 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+145T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884132 | |||||||
| chr7:35884191 | A | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.820+204A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884191 | |||||||
| chr7:35884236 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.820+249A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884236 | |||||||
| chr7:35884283 | G | A | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.820+296G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884283 | |||||||
| chr7:35884357 | A | C | 2 | a0001c0001t0002g0156 a0001c0001t0007g0157 |
2 | NA18991.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.820+370A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884357 | |||||||
| chr7:35884370 | G | A | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.820+383G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884370 | |||||||
| chr7:35884546 | A | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.820+559A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884546 | |||||||
| chr7:35884592 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.820+605T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884592 | |||||||
| chr7:35884788 | GT | G | 2 | a0001c0001t0004g0003 a0001c0001t0004g0031 |
3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.820+807delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 35884788 | ||||||
| chr7:35884892 | A | C | 2 | a0001c0001t0006g0057 a0001c0001t0028g0054 |
2 | NA18940.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.820+905A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35884892 | |||||||
| chr7:35885010 | T | C | 1 | a0001c0001t0010g0240 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.821-818T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885010 | |||||||
| chr7:35885020 | GT | G | 19 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(16): Show |
22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.821-797delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr7 | 35885020 | ||||||
| chr7:35885231 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.821-597T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885231 | |||||||
| chr7:35885550 | A | T | 1 | a0001c0001t0003g0215 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.821-278A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885550 | |||||||
| chr7:35885732 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.821-96C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885732 | |||||||
| chr7:35885807 | C | T | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.821-21C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 9/13 | chr7 | 35885807 | |||||||
| chr7:35885890 | G | A | 40 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(37): Show |
40 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.872+11G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35885890 | |||||||
| chr7:35885953 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.872+74G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35885953 | |||||||
| chr7:35886009 | A | G | 41 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(38): Show |
45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.872+130A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886009 | |||||||
| chr7:35886037 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.872+158A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886037 | |||||||
| chr7:35886055 | C | G | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.872+176C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886055 | |||||||
| chr7:35886135 | A | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+256A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886135 | |||||||
| chr7:35886157 | A | C | 3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0176 |
3 | HG02258.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.872+278A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886157 | |||||||
| chr7:35886169 | C | A | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.872+290C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886169 | |||||||
| chr7:35886248 | T | C | 1 | a0001c0001t0005g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.872+369T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886248 | |||||||
| chr7:35886268 | G | A | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+389G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886268 | |||||||
| chr7:35886433 | T | TG | 309 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(306): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.872+555dupG | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35886433 | ||||||
| chr7:35886509 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0146 |
2 | NA18941.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.872+630C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886509 | |||||||
| chr7:35886532 | A | G | 134 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(131): Show |
136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.872+653A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886532 | |||||||
| chr7:35886742 | CTT | C | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | HG02486.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.872+866_872+867del others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35886742 | ||||||
| chr7:35886786 | G | A | 1 | a0001c0001t0031g0167 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.872+907G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886786 | |||||||
| chr7:35886975 | T | A | 71 | a0001c0001t0001g0009 a0001c0001t0001g0230 a0001c0001t0001g0231 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.872+1096T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35886975 | |||||||
| chr7:35887161 | A | G | 1 | a0001c0001t0004g0178 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.872+1282A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887161 | |||||||
| chr7:35887190 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.872+1311A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887190 | |||||||
| chr7:35887315 | C | T | 1 | a0001c0001t0005g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.872+1436C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887315 | |||||||
| chr7:35887413 | G | A | 2 | a0001c0001t0004g0003 a0001c0001t0004g0031 |
3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.872+1534G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887413 | |||||||
| chr7:35887432 | C | T | 7 | a0001c0001t0011g0005 a0001c0001t0011g0065 a0001c0001t0011g0067 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.872+1553C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887432 | |||||||
| chr7:35887509 | A | G | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.872+1630A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887509 | |||||||
| chr7:35887622 | C | A | 3 | a0001c0001t0002g0140 a0001c0001t0002g0150 a0001c0001t0027g0145 |
3 | NA18954.hp1 NA18968.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.872+1743C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887622 | |||||||
| chr7:35887622 | C | G | 2 | a0001c0001t0003g0091 a0001c0001t0003g0115 |
2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.872+1743C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887622 | |||||||
| chr7:35887622 | C | T | 20 | a0001c0001t0002g0006 a0001c0001t0002g0116 a0001c0001t0002g0118 others(17): Show |
24 | HG00597.hp2 HG00733.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.872+1743C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887622 | |||||||
| chr7:35887775 | A | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.872+1896A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887775 | |||||||
| chr7:35887823 | T | A | 1 | a0001c0001t0036g0200 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.872+1944T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887823 | |||||||
| chr7:35887847 | A | G | 3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0176 |
3 | HG02258.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.872+1968A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35887847 | |||||||
| chr7:35888033 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 |
3 | HG00438.hp2 NA18944.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.872+2154G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888033 | |||||||
| chr7:35888091 | G | T | 19 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(16): Show |
22 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.872+2212G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888091 | |||||||
| chr7:35888203 | CTA | C | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.872+2326_872+2327d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888203 | ||||||
| chr7:35888227 | T | G | 1 | a0001c0001t0018g0103 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.872+2348T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888227 | |||||||
| chr7:35888488 | GA | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0035 |
3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2179delA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888488 | |||||||
| chr7:35888491 | T | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0035 |
3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2177T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888491 | |||||||
| chr7:35888492 | T | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0035 |
3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2176T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888492 | |||||||
| chr7:35888494 | T | G | 2 | a0001c0001t0002g0004 a0001c0001t0002g0035 |
3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.873-2174T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888494 | |||||||
| chr7:35888645 | C | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.873-2023C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888645 | |||||||
| chr7:35888649 | G | A | 28 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(25): Show |
31 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.873-2019G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888649 | |||||||
| chr7:35888665 | C | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.873-2003C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888665 | |||||||
| chr7:35888783 | G | A | 2 | a0001c0001t0004g0003 a0001c0001t0004g0031 |
3 | HG02615.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.873-1885G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888783 | |||||||
| chr7:35888823 | C | CA | 222 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(219): Show |
229 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.873-1823dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888823 | ||||||
| chr7:35888823 | C | CAA | 55 | a0001c0001t0001g0182 a0001c0001t0001g0221 a0001c0001t0001g0222 others(52): Show |
56 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.873-1824_873-1823d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888823 | ||||||
| chr7:35888823 | C | CAAA | 8 | a0001c0001t0002g0126 a0001c0001t0002g0135 a0001c0001t0011g0068 others(5): Show |
8 | HG00609.hp1 HG02083.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-1825_873-1823d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr7 | 35888823 | ||||||
| chr7:35888888 | G | A | 1 | a0001c0001t0013g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.873-1780G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888888 | |||||||
| chr7:35888941 | A | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.873-1727A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888941 | |||||||
| chr7:35888960 | G | C | 5 | a0001c0001t0003g0090 a0001c0001t0003g0093 a0001c0001t0003g0098 others(2): Show |
5 | HG00642.hp2 HG01081.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.873-1708G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35888960 | |||||||
| chr7:35889035 | T | G | 41 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(38): Show |
45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.873-1633T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889035 | |||||||
| chr7:35889068 | T | A | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.873-1600T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889068 | |||||||
| chr7:35889170 | G | A | 13 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(10): Show |
16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.873-1498G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889170 | |||||||
| chr7:35889235 | T | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.873-1433T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889235 | |||||||
| chr7:35889315 | C | T | 13 | a0001c0001t0006g0001 a0001c0001t0006g0027 a0001c0001t0006g0053 others(10): Show |
16 | HG00597.hp2 HG02155.hp2 HG06807.hp2 others(13): Show |
intron_variant | MODIFIER | c.873-1353C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889315 | |||||||
| chr7:35889349 | A | T | 3 | a0001c0001t0022g0193 a0001c0001t0022g0194 a0001c0001t0039g0195 |
3 | HG03471.hp1 HG03486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.873-1319A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889349 | |||||||
| chr7:35889378 | A | G | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.873-1290A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889378 | |||||||
| chr7:35889548 | T | A | 6 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0160 others(3): Show |
6 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.873-1120T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889548 | |||||||
| chr7:35889690 | C | T | 3 | a0001c0001t0008g0019 a0001c0001t0008g0023 a0001c0001t0008g0024 |
3 | HG02886.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.873-978C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889690 | |||||||
| chr7:35889700 | C | A | 1 | a0001c0001t0002g0151 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.873-968C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889700 | |||||||
| chr7:35889764 | G | A | 1 | a0001c0001t0010g0327 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.873-904G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35889764 | |||||||
| chr7:35890170 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.873-498A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35890170 | |||||||
| chr7:35890583 | A | C | 1 | a0001c0001t0005g0191 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.873-85A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35890583 | |||||||
| chr7:35890650 | G | T | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.873-18G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 10/13 | chr7 | 35890650 | |||||||
| chr7:35890827 | A | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+34A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890827 | |||||||
| chr7:35890833 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.998+40G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890833 | |||||||
| chr7:35890944 | T | A | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.998+151T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890944 | |||||||
| chr7:35890959 | C | T | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+166C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35890959 | |||||||
| chr7:35891099 | A | C | 2 | a0001c0001t0005g0191 a0001c0001t0005g0204 |
2 | HG03239.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.998+306A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891099 | |||||||
| chr7:35891189 | G | A | 2 | a0001c0001t0022g0193 a0001c0001t0022g0194 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.998+396G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891189 | |||||||
| chr7:35891205 | T | G | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.998+412T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891205 | |||||||
| chr7:35891208 | G | A | 1 | a0001c0001t0005g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.998+415G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891208 | |||||||
| chr7:35891291 | C | T | 1 | a0001c0001t0004g0175 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.998+498C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891291 | |||||||
| chr7:35891367 | C | CAT | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+576_998+577dup others(2): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35891367 | ||||||
| chr7:35891762 | C | G | 1 | a0001c0001t0001g0266 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.998+969C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891762 | |||||||
| chr7:35891884 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0313 |
3 | HG00735.hp2 HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.998+1091T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35891884 | |||||||
| chr7:35892213 | T | C | 41 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(38): Show |
45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.998+1420T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892213 | |||||||
| chr7:35892267 | T | C | 1 | a0001c0001t0038g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.998+1474T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892267 | |||||||
| chr7:35892306 | C | G | 1 | a0001c0001t0002g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.998+1513C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892306 | |||||||
| chr7:35892337 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.998+1544A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892337 | |||||||
| chr7:35892656 | G | T | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.998+1863G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892656 | |||||||
| chr7:35892730 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.998+1937G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892730 | |||||||
| chr7:35892763 | G | GA | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+1974dupA | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35892763 | ||||||
| chr7:35892879 | G | C | 9 | a0001c0001t0008g0018 a0001c0001t0008g0019 a0001c0001t0008g0020 others(6): Show |
9 | HG02622.hp1 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.998+2086G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892879 | |||||||
| chr7:35892931 | G | A | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.998+2138G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35892931 | |||||||
| chr7:35893234 | T | TCC | 308 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(305): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.998+2441_998+2442i others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893234 | |||||||
| chr7:35893539 | C | T | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+2746C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893539 | |||||||
| chr7:35893609 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.998+2816G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893609 | |||||||
| chr7:35893760 | T | C | 5 | a0001c0001t0001g0258 a0001c0001t0001g0261 a0001c0001t0001g0273 others(2): Show |
5 | HG01074.hp1 HG01243.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.998+2967T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893760 | |||||||
| chr7:35893868 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0272 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.998+3075G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35893868 | |||||||
| chr7:35894125 | CT | C | 165 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(162): Show |
170 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.998+3349delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35894125 | ||||||
| chr7:35894125 | CTT | C | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.998+3348_998+3349d others(4): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35894125 | ||||||
| chr7:35894227 | G | T | 1 | a0001c0001t0004g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.998+3434G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894227 | |||||||
| chr7:35894252 | T | C | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.998+3459T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894252 | |||||||
| chr7:35894343 | C | A | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.998+3550C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894343 | |||||||
| chr7:35894389 | A | G | 1 | a0001c0001t0012g0263 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.998+3596A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894389 | |||||||
| chr7:35894664 | T | G | 2 | a0001c0001t0021g0051 a0001c0001t0021g0059 |
2 | HG02155.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.999-3584T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894664 | |||||||
| chr7:35894702 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.999-3546G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894702 | |||||||
| chr7:35894726 | A | G | 1 | a0001c0001t0009g0257 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.999-3522A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894726 | |||||||
| chr7:35894928 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.999-3320A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35894928 | |||||||
| chr7:35895481 | A | T | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-2767A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895481 | |||||||
| chr7:35895792 | T | C | 2 | a0001c0001t0001g0286 a0001c0001t0001g0315 |
2 | NA18973.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.999-2456T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895792 | |||||||
| chr7:35895864 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.999-2384A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895864 | |||||||
| chr7:35895884 | C | T | 1 | a0001c0001t0005g0204 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.999-2364C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895884 | |||||||
| chr7:35895888 | G | A | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.999-2360G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895888 | |||||||
| chr7:35895998 | A | G | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.999-2250A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35895998 | |||||||
| chr7:35896037 | G | C | 309 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(306): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.999-2211G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896037 | |||||||
| chr7:35896055 | T | C | 286 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(283): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.999-2193T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896055 | |||||||
| chr7:35896058 | C | T | 8 | a0001c0001t0001g0182 a0001c0001t0011g0005 a0001c0001t0011g0065 others(5): Show |
9 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.999-2190C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896058 | |||||||
| chr7:35896075 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.999-2173C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896075 | |||||||
| chr7:35896142 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.999-2106C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896142 | |||||||
| chr7:35896342 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.999-1906G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896342 | |||||||
| chr7:35896388 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.999-1860C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896388 | |||||||
| chr7:35896450 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.999-1798A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896450 | |||||||
| chr7:35896595 | T | C | 2 | a0001c0001t0021g0051 a0001c0001t0021g0059 |
2 | HG02155.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.999-1653T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896595 | |||||||
| chr7:35896970 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.999-1278C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35896970 | |||||||
| chr7:35897088 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.999-1160C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897088 | |||||||
| chr7:35897150 | A | T | 12 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0010g0238 others(9): Show |
12 | HG01934.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.999-1098A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897150 | |||||||
| chr7:35897189 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.999-1059A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897189 | |||||||
| chr7:35897509 | AT | A | 26 | a0001c0001t0002g0073 a0001c0001t0002g0113 a0001c0001t0002g0114 others(23): Show |
29 | HG00597.hp2 HG01255.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.999-728delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35897509 | ||||||
| chr7:35897588 | G | T | 2 | a0001c0001t0006g0057 a0001c0001t0028g0054 |
2 | NA18940.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.999-660G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897588 | |||||||
| chr7:35897640 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0041 |
4 | HG02258.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-608C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897640 | |||||||
| chr7:35897698 | T | C | 1 | a0001c0001t0008g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.999-550T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | chr7 | 35897698 | |||||||
| chr7:35897916 | A | AT | 40 | a0001c0001t0005g0013 a0001c0001t0005g0196 a0001c0001t0005g0197 others(37): Show |
44 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.999-331dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35897916 | ||||||
| chr7:35897983 | A | AT | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.999-258dupT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr7 | 35897983 | ||||||
| chr7:35898515 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1134+132C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898515 | |||||||
| chr7:35898597 | T | G | 4 | a0001c0001t0002g0081 a0001c0001t0002g0106 a0001c0001t0030g0107 others(1): Show |
4 | HG01433.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+214T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898597 | |||||||
| chr7:35898714 | A | T | 1 | a0001c0001t0002g0110 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1134+331A>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898714 | |||||||
| chr7:35898798 | A | G | 2 | a0001c0001t0019g0264 a0001c0001t0019g0308 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1134+415A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898798 | |||||||
| chr7:35898970 | A | G | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1134+587A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898970 | |||||||
| chr7:35898987 | C | T | 286 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(283): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1134+604C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35898987 | |||||||
| chr7:35899210 | G | C | 22 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(19): Show |
23 | HG00738.hp1 HG01081.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1134+827G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899210 | |||||||
| chr7:35899281 | C | T | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1134+898C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899281 | |||||||
| chr7:35899399 | G | A | 6 | a0001c0001t0013g0045 a0001c0001t0013g0046 a0001c0001t0013g0047 others(3): Show |
6 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+1016G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899399 | |||||||
| chr7:35899420 | A | G | 2 | a0001c0001t0002g0108 a0001c0001t0002g0110 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1134+1037A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899420 | |||||||
| chr7:35899536 | A | G | 4 | a0001c0001t0002g0081 a0001c0001t0002g0106 a0001c0001t0030g0107 others(1): Show |
4 | HG01433.hp2 HG02896.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+1153A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899536 | |||||||
| chr7:35899551 | A | G | 1 | a0001c0001t0007g0163 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1134+1168A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899551 | |||||||
| chr7:35899557 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1134+1174A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899557 | |||||||
| chr7:35899711 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1134+1328A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899711 | |||||||
| chr7:35899751 | G | T | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1134+1368G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899751 | |||||||
| chr7:35899808 | T | G | 4 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0016 others(1): Show |
4 | HG00408.hp2 HG01952.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+1425T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899808 | |||||||
| chr7:35899813 | G | T | 1 | a0001c0001t0002g0166 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1134+1430G>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899813 | |||||||
| chr7:35899894 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1134+1511A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35899894 | |||||||
| chr7:35900037 | AT | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0035 |
3 | HG02258.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1134+1656delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 35900037 | ||||||
| chr7:35900042 | T | C | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1134+1659T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900042 | |||||||
| chr7:35900105 | G | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1134+1722G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900105 | |||||||
| chr7:35900588 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1134+2205G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900588 | |||||||
| chr7:35900696 | A | G | 135 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1134+2313A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900696 | |||||||
| chr7:35900752 | C | T | 4 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0162 others(1): Show |
4 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-2324C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900752 | |||||||
| chr7:35900817 | A | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0035 a0001c0001t0002g0041 |
4 | HG02258.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2259A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35900817 | |||||||
| chr7:35901063 | C | A | 1 | a0001c0001t0004g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1135-2013C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901063 | |||||||
| chr7:35901266 | A | G | 1 | a0001c0001t0005g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1135-1810A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901266 | |||||||
| chr7:35901619 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1135-1457C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901619 | |||||||
| chr7:35901670 | G | A | 41 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0196 others(38): Show |
45 | HG00597.hp2 HG00738.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.1135-1406G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901670 | |||||||
| chr7:35901853 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1135-1223C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901853 | |||||||
| chr7:35901856 | T | G | 19 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0090 others(16): Show |
19 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1135-1220T>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35901856 | |||||||
| chr7:35902030 | T | A | 1 | a0001c0001t0009g0241 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1135-1046T>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902030 | |||||||
| chr7:35902368 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1135-708A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902368 | |||||||
| chr7:35902376 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1135-700A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902376 | |||||||
| chr7:35902472 | G | C | 1 | a0001c0001t0004g0003 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1135-604G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902472 | |||||||
| chr7:35902710 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1135-366G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902710 | |||||||
| chr7:35902840 | CT | C | 278 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0050 others(275): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1135-223delT | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr7 | 35902840 | ||||||
| chr7:35902855 | C | A | 13 | a0001c0001t0005g0013 a0001c0001t0005g0191 a0001c0001t0005g0201 others(10): Show |
14 | HG00738.hp1 HG01081.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1135-221C>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902855 | |||||||
| chr7:35902894 | G | C | 1 | a0001c0001t0005g0202 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1135-182G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902894 | |||||||
| chr7:35902895 | G | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0134 |
2 | NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1135-181G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902895 | |||||||
| chr7:35902895 | G | C | 1 | a0001c0001t0005g0202 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1135-181G>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35902895 | |||||||
| chr7:35903018 | A | G | 4 | a0001c0001t0002g0078 a0001c0001t0002g0083 a0001c0001t0002g0087 others(1): Show |
4 | NA18957.hp1 NA18960.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-58A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35903018 | |||||||
| chr7:35903019 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1135-57T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 12/13 | chr7 | 35903019 | |||||||
| chr7:35903374 | A | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0182 a0001c0001t0011g0005 others(6): Show |
10 | HG02257.hp2 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1274+159A>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903374 | |||||||
| chr7:35903395 | TAGC | T | 125 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0180 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1274+183_1274+185d others(5): Show |
SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr7 | 35903395 | ||||||
| chr7:35903443 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1274+228T>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903443 | |||||||
| chr7:35903457 | C | T | 4 | a0001c0001t0005g0196 a0001c0001t0005g0197 a0001c0001t0005g0198 others(1): Show |
4 | HG01255.hp2 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1274+242C>T | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903457 | |||||||
| chr7:35903510 | C | G | 37 | a0001c0001t0003g0002 a0001c0001t0003g0029 a0001c0001t0003g0030 others(34): Show |
39 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1274+295C>G | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903510 | |||||||
| chr7:35903817 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1275-437G>A | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903817 | |||||||
| chr7:35903837 | A | C | 132 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0028 others(129): Show |
136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1275-417A>C | SEPTIN7 | ENSG00000122545.22 | transcript | ENST00000350320.11 | protein_coding | 13/13 | chr7 | 35903837 |