Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6683 |
| ensemblid | ENSG00000021574.14 |
| hgncid | 11233 |
| symbol | SPAST |
| name | spastin |
| refseq_nuc | NM_014946.4 |
| refseq_prot | NP_055761.2 |
| ensembl_nuc | ENST00000315285.9 |
| ensembl_prot | ENSP00000320885.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 32063556 |
| end | 32157637 |
| strand | + |
| ver | v1.2 |
| region | chr2:32063556-32157637 |
| region5000 | chr2:32058556-32162637 |
| regionname0 | SPAST_chr2_32063556_32157637 |
| regionname5000 | SPAST_chr2_32058556_32162637 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 616 | 341 | 85 | 70 | 142 | 12 | 30 | 112 | SPAST_chr2_32058556_32162637 | SPAST | MNSPG others(611): Show |
chr2 | 32058556 | 32162637 |
| a0002 | 0/0 | 616 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | MNSPG others(611): Show |
chr2 | 32058556 | 32162637 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1848 | 339 | 85 | 70 | 140 | 12 | 30 | SPAST_chr2_32058556_32162637 | SPAST | ATGAA others(1843): Show |
chr2 | 32058556 | 32162637 | ||
| a0001c0002 | 0/0 | 1848 | 2 | 0 | 0 | 2 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | ATGAA others(1843): Show |
chr2 | 32058556 | 32162637 | ||
| a0002c0003 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | ATGAA others(1843): Show |
chr2 | 32058556 | 32162637 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5271 | 107 | 16 | 15 | 63 | 4 | 9 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0002 | 0/0 | 5271 | 88 | 18 | 20 | 39 | 4 | 7 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0003 | 0/1 | 5271 | 53 | 12 | 5 | 25 | 1 | 9 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0004 | 0/0 | 5271 | 36 | 12 | 17 | 1 | 3 | 3 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0005 | 1/0 | 5268 | 7 | 6 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5263): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0006 | 0/0 | 5271 | 7 | 7 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0007 | 0/0 | 5272 | 6 | 0 | 3 | 3 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5267): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0008 | 0/0 | 5268 | 4 | 4 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5263): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0009 | 0/0 | 5267 | 3 | 3 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5262): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0010 | 0/0 | 5272 | 3 | 1 | 0 | 2 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5267): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0011 | 0/0 | 5271 | 3 | 2 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0012 | 0/0 | 5271 | 3 | 0 | 3 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0013 | 0/0 | 5271 | 3 | 3 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0014 | 0/0 | 5271 | 2 | 1 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0015 | 0/0 | 5271 | 2 | 0 | 2 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0016 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0017 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0018 | 0/0 | 5271 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0019 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0020 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0021 | 0/0 | 5271 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0022 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0023 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0024 | 0/0 | 5271 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0025 | 0/0 | 5271 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0026 | 0/0 | 5271 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0001t0027 | 0/0 | 5271 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0001c0002t0002 | 0/0 | 5271 | 2 | 0 | 0 | 2 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| a0002c0003t0002 | 0/0 | 5271 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | GCGGC others(5266): Show |
chr2 | 32058556 | 32162637 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0005g0316 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0008g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0010g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0012g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0012g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0012g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0013g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0014g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0015g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0015g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0016g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0017g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0018g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0019g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0020g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0021g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0022g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0023g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0024g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0025g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0026g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0001t0027g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| a0002c0003t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | GBR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | GBR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0275 | EUR | GBR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00609 | hp1 | a0001 | c0001 | t0022 | g0018 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00609 | hp2 | a0001 | c0001 | t0017 | g0169 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0335 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0208 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0209 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01081 | hp2 | a0001 | c0001 | t0014 | g0204 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0261 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0201 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0298 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01168 | hp1 | a0001 | c0001 | t0025 | g0320 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01169 | hp1 | a0001 | c0001 | t0015 | g0329 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01175 | hp1 | a0001 | c0001 | t0012 | g0219 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01175 | hp2 | a0001 | c0001 | t0018 | g0114 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0210 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0293 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01361 | hp2 | a0001 | c0001 | t0021 | g0065 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0267 | EUR | IBS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0277 | EUR | IBS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | IBS | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0068 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0299 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0099 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0295 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0294 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01952 | hp2 | a0001 | c0001 | t0012 | g0274 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0297 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0091 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02040 | hp1 | a0001 | c0001 | t0023 | g0242 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0071 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0256 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0165 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CDX | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CDX | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PEL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0336 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0249 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0252 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0311 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02886 | hp1 | a0001 | c0001 | t0014 | g0200 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0106 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0251 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02897 | hp2 | a0001 | c0001 | t0013 | g0341 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0069 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02970 | hp1 | a0002 | c0003 | t0002 | g0284 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0005 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03490 | hp2 | a0001 | c0001 | t0024 | g0245 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0064 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ESN | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0216 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | BEB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0303 | SAS | BEB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG04204 | hp2 | a0001 | c0001 | t0027 | g0144 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | STU | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | YRI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | YRI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18612 | hp2 | a0001 | c0001 | t0026 | g0240 | EAS | CHB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | YRI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18949 | hp1 | a0001 | c0001 | t0010 | g0314 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18995 | hp2 | a0001 | c0001 | t0019 | g0156 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19012 | hp2 | a0001 | c0001 | t0010 | g0255 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0072 | AFR | LWK | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | LWK | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | LWK | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | LWK | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19075 | hp2 | a0001 | c0001 | t0020 | g0183 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19078 | hp2 | a0001 | c0001 | t0016 | g0334 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | YRI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | YRI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ASW | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | ASW | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0205 | EUR | TSI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0022 | EUR | TSI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0211 | EUR | TSI | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | GIH | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | GIH | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01123 | hp1 | a0001 | c0001 | t0012 | g0246 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0321 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0070 | AFR | MSL | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | USA | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | USA | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | USA | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | LWK | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | LWK | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0032 | REF | REF | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0316 | REF | REF | SPAST_chr2_32058556_32162637 | SPAST | chr2 | 32058556 | 32162637 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:32114820 | C | T | 1 | a0002 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.865C>T | p.His289Tyr | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/17 | 1141/5268 | 865/1851 | 289/616 | chr2 | 32114820 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:32114783 | T | C | 1 | a0001c0002 | 2 | NA18982.hp2 NA19064.hp2 |
synonymous_variant | LOW | c.828T>C | p.Ser276Ser | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/17 | 1104/5268 | 828/1851 | 276/616 | chr2 | 32114783 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:32063802 | T | C | 1 | a0001c0001t0016 | 1 | NA19078.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/17 | 30 | chr2 | 32063802 | ||||||
| chr2:32154547 | A | G | 1 | a0001c0001t0013 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*51A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 51 | chr2 | 32154547 | ||||||
| chr2:32154594 | A | G | 2 | a0001c0001t0012 a0001c0001t0015 |
5 | HG01099.hp1 HG01123.hp1 HG01169.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*98A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 98 | chr2 | 32154594 | ||||||
| chr2:32154737 | AAGTT | A | 1 | a0001c0001t0009 | 3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*244_*247delTTAG | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 244 | INFO_REALIGN_3_PRIME | chr2 | 32154737 | |||||
| chr2:32154752 | A | G | 2 | a0001c0001t0008 a0001c0001t0011 |
7 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*256A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 256 | chr2 | 32154752 | ||||||
| chr2:32154760 | A | C | 1 | a0001c0001t0027 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*264A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 264 | chr2 | 32154760 | ||||||
| chr2:32154995 | T | C | 1 | a0001c0001t0017 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*499T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 499 | chr2 | 32154995 | ||||||
| chr2:32155087 | A | T | 1 | a0001c0001t0006 | 7 | HG02257.hp1 HG02622.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*591A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 591 | chr2 | 32155087 | ||||||
| chr2:32155724 | TATC | T | 1 | a0001c0001t0008 | 4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1231_*1233delCAT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1231 | INFO_REALIGN_3_PRIME | chr2 | 32155724 | |||||
| chr2:32155906 | T | G | 1 | a0001c0001t0013 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1410T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1410 | chr2 | 32155906 | ||||||
| chr2:32156037 | T | TG | 1 | a0001c0001t0007 | 6 | HG01934.hp1 HG01978.hp1 HG02071.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1544dupG | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1545 | INFO_REALIGN_3_PRIME | chr2 | 32156037 | |||||
| chr2:32156039 | G | GT | 1 | a0001c0001t0010 | 3 | HG02886.hp2 NA18949.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1543_*1544insT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1544 | chr2 | 32156039 | ||||||
| chr2:32156040 | G | T | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(8): Show |
104 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1544G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1544 | chr2 | 32156040 | ||||||
| chr2:32156041 | T | G | 6 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0018 others(3): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1545T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1545 | chr2 | 32156041 | ||||||
| chr2:32156100 | G | A | 1 | a0001c0001t0013 | 3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1604G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1604 | chr2 | 32156100 | ||||||
| chr2:32156331 | C | G | 1 | a0001c0001t0026 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1835C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1835 | chr2 | 32156331 | ||||||
| chr2:32156458 | A | G | 1 | a0001c0001t0014 | 2 | HG01081.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1962A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1962 | chr2 | 32156458 | ||||||
| chr2:32156459 | A | G | 1 | a0001c0001t0014 | 2 | HG01081.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1963A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 1963 | chr2 | 32156459 | ||||||
| chr2:32156610 | A | T | 1 | a0001c0001t0020 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2114A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2114 | chr2 | 32156610 | ||||||
| chr2:32156612 | T | A | 1 | a0001c0001t0020 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2116 | chr2 | 32156612 | ||||||
| chr2:32156614 | A | G | 1 | a0001c0001t0020 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2118A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2118 | chr2 | 32156614 | ||||||
| chr2:32156646 | G | C | 1 | a0001c0001t0021 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2150G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2150 | chr2 | 32156646 | ||||||
| chr2:32156658 | A | AAGG | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*2164_*2165insGAG | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr2 | 32156658 | |||||
| chr2:32156760 | G | A | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(11): Show |
185 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*2264G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2264 | chr2 | 32156760 | ||||||
| chr2:32156814 | G | A | 1 | a0001c0001t0021 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2318G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2318 | chr2 | 32156814 | ||||||
| chr2:32156895 | C | T | 1 | a0001c0001t0012 | 3 | HG01123.hp1 HG01175.hp1 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2399C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2399 | chr2 | 32156895 | ||||||
| chr2:32157035 | T | C | 1 | a0001c0001t0020 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2539T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2539 | chr2 | 32157035 | ||||||
| chr2:32157036 | C | A | 1 | a0001c0001t0020 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2540C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2540 | chr2 | 32157036 | ||||||
| chr2:32157079 | C | T | 2 | a0001c0001t0022 a0001c0001t0023 |
2 | HG00609.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2583C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2583 | chr2 | 32157079 | ||||||
| chr2:32157085 | T | G | 1 | a0001c0001t0024 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2589T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2589 | chr2 | 32157085 | ||||||
| chr2:32157399 | A | G | 1 | a0001c0001t0018 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2903A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 2903 | chr2 | 32157399 | ||||||
| chr2:32157509 | T | C | 1 | a0001c0001t0025 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3013T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 17/17 | 3013 | chr2 | 32157509 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:32064288 | A | G | 1 | a0001c0001t0001g0342 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.415+42A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064288 | |||||||
| chr2:32064289 | A | G | 1 | a0001c0001t0001g0342 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.415+43A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064289 | |||||||
| chr2:32064426 | C | T | 1 | a0001c0001t0013g0341 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.415+180C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064426 | |||||||
| chr2:32064445 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | NA18971.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.415+199T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064445 | |||||||
| chr2:32064493 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.415+247C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064493 | |||||||
| chr2:32064528 | T | C | 1 | a0001c0001t0002g0003 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.415+282T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064528 | |||||||
| chr2:32064677 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.415+431T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064677 | |||||||
| chr2:32064710 | A | G | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415+464A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064710 | |||||||
| chr2:32064834 | T | G | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+588T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064834 | |||||||
| chr2:32064971 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+725G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32064971 | |||||||
| chr2:32065037 | T | A | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.415+791T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065037 | |||||||
| chr2:32065039 | A | G | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.415+793A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065039 | |||||||
| chr2:32065078 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.415+832G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065078 | |||||||
| chr2:32065101 | C | T | 1 | a0001c0001t0002g0339 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.415+855C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065101 | |||||||
| chr2:32065173 | C | T | 1 | a0001c0001t0007g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.415+927C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065173 | |||||||
| chr2:32065188 | T | G | 1 | a0001c0001t0002g0189 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.415+942T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065188 | |||||||
| chr2:32065209 | G | A | 1 | a0001c0001t0003g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.415+963G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065209 | |||||||
| chr2:32065262 | G | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(210): Show |
213 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.415+1016G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065262 | |||||||
| chr2:32065270 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.415+1024G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065270 | |||||||
| chr2:32065280 | A | G | 4 | a0001c0001t0002g0335 a0001c0001t0002g0336 a0001c0001t0002g0337 others(1): Show |
4 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+1034A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065280 | |||||||
| chr2:32065307 | C | A | 2 | a0001c0001t0005g0190 a0001c0001t0005g0191 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.415+1061C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065307 | |||||||
| chr2:32065310 | G | T | 13 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(10): Show |
13 | NA18949.hp2 NA18950.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.415+1064G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065310 | |||||||
| chr2:32065392 | A | T | 2 | a0001c0001t0002g0336 a0001c0001t0008g0005 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.415+1146A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065392 | |||||||
| chr2:32065411 | C | T | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415+1165C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065411 | |||||||
| chr2:32065442 | C | A | 1 | a0001c0001t0004g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.415+1196C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065442 | |||||||
| chr2:32065628 | G | T | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415+1382G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065628 | |||||||
| chr2:32065700 | A | G | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+1454A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065700 | |||||||
| chr2:32065727 | T | C | 1 | a0001c0001t0011g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415+1481T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065727 | |||||||
| chr2:32065973 | C | CT | 24 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0002g0322 others(21): Show |
24 | HG00438.hp1 HG00673.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+1745dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32065973 | ||||||
| chr2:32065973 | C | T | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415+1727C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32065973 | |||||||
| chr2:32065973 | CT | C | 12 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
12 | HG00741.hp1 HG01975.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+1745delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32065973 | ||||||
| chr2:32066077 | G | T | 1 | a0001c0001t0016g0334 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.415+1831G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066077 | |||||||
| chr2:32066139 | A | C | 1 | a0001c0001t0013g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.415+1893A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066139 | |||||||
| chr2:32066184 | A | G | 1 | a0001c0001t0002g0321 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415+1938A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066184 | |||||||
| chr2:32066197 | A | C | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415+1951A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066197 | |||||||
| chr2:32066248 | A | G | 3 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0025g0320 |
3 | HG01070.hp2 HG01071.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.415+2002A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066248 | |||||||
| chr2:32066265 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.415+2019T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066265 | |||||||
| chr2:32066331 | A | G | 1 | a0001c0001t0004g0317 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.415+2085A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066331 | |||||||
| chr2:32066429 | G | T | 1 | a0001c0001t0016g0334 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.415+2183G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066429 | |||||||
| chr2:32066663 | G | A | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0067 |
3 | HG03491.hp2 HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.415+2417G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066663 | |||||||
| chr2:32066770 | T | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.415+2524T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066770 | |||||||
| chr2:32066834 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(73): Show |
76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.415+2588C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066834 | |||||||
| chr2:32066916 | A | G | 9 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.415+2670A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066916 | |||||||
| chr2:32066972 | C | CA | 126 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(123): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.415+2746dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066972 | ||||||
| chr2:32066972 | C | CAA | 24 | a0001c0001t0001g0223 a0001c0001t0002g0217 a0001c0001t0002g0218 others(21): Show |
24 | HG00673.hp1 HG00735.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.415+2745_415+2746d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066972 | ||||||
| chr2:32066980 | AAAAAAAA others(7): Show |
A | 83 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0001g0078 others(80): Show |
83 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.415+2747_415+2760d others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066980 | ||||||
| chr2:32066981 | AAAAAAAA others(6): Show |
A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.415+2747_415+2759d others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066981 | ||||||
| chr2:32066982 | AAAAAAAA others(5): Show |
A | 16 | a0001c0001t0001g0107 a0001c0001t0001g0122 a0001c0001t0001g0125 others(13): Show |
16 | HG00423.hp2 HG01175.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+2747_415+2758d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066982 | ||||||
| chr2:32066993 | C | A | 9 | a0001c0001t0003g0067 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.415+2747C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066993 | |||||||
| chr2:32066994 | C | A | 2 | a0001c0001t0005g0197 a0001c0001t0010g0314 |
2 | HG03516.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.415+2748C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066994 | |||||||
| chr2:32066994 | CA | C | 6 | a0001c0001t0008g0005 a0001c0001t0013g0068 a0001c0001t0013g0069 others(3): Show |
6 | HG01361.hp2 HG01891.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+2761delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066994 | ||||||
| chr2:32066995 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0003g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.415+2761_415+2762i others(24): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066995 | ||||||
| chr2:32066995 | A | C | 10 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0008g0007 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+2749A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066995 | |||||||
| chr2:32066997 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.415+2751A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32066997 | |||||||
| chr2:32066998 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0003g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.415+2761_415+2762i others(21): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32066998 | ||||||
| chr2:32067054 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415+2808G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32067054 | |||||||
| chr2:32067061 | T | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+2815T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32067061 | |||||||
| chr2:32067126 | A | G | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+2880A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32067126 | |||||||
| chr2:32067304 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.415+3058C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32067304 | |||||||
| chr2:32067758 | C | CT | 16 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0003g0055 others(13): Show |
16 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.415+3526dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32067758 | ||||||
| chr2:32067758 | CT | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(165): Show |
168 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.415+3526delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32067758 | ||||||
| chr2:32067835 | TA | T | 5 | a0001c0001t0002g0310 a0001c0001t0004g0311 a0001c0001t0013g0068 others(2): Show |
5 | HG01891.hp1 HG02735.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+3599delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32067835 | ||||||
| chr2:32068042 | G | A | 21 | a0001c0001t0002g0189 a0001c0001t0002g0217 a0001c0001t0002g0218 others(18): Show |
21 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.415+3796G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068042 | |||||||
| chr2:32068125 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415+3879C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068125 | |||||||
| chr2:32068199 | C | T | 5 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0307 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+3953C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068199 | |||||||
| chr2:32068268 | G | A | 1 | a0001c0001t0005g0191 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.415+4022G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068268 | |||||||
| chr2:32068271 | C | T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.415+4025C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068271 | |||||||
| chr2:32068273 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.415+4027C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068273 | |||||||
| chr2:32068325 | CT | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.415+4093delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32068325 | ||||||
| chr2:32068353 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.415+4107G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068353 | |||||||
| chr2:32068385 | G | A | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415+4139G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068385 | |||||||
| chr2:32068485 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.415+4239A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068485 | |||||||
| chr2:32068515 | C | G | 11 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0202 others(8): Show |
11 | HG00741.hp1 HG02055.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+4269C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068515 | |||||||
| chr2:32068543 | C | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.415+4297C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068543 | |||||||
| chr2:32068590 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.415+4344C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068590 | |||||||
| chr2:32068758 | G | A | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.415+4512G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068758 | |||||||
| chr2:32068893 | C | CA | 38 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(35): Show |
38 | HG00408.hp2 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.415+4662dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32068893 | ||||||
| chr2:32068934 | G | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.415+4688G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32068934 | |||||||
| chr2:32069007 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | NA18972.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.415+4761C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069007 | |||||||
| chr2:32069017 | C | G | 1 | a0001c0001t0002g0306 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.415+4771C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069017 | |||||||
| chr2:32069180 | G | A | 1 | a0001c0001t0002g0321 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415+4934G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069180 | |||||||
| chr2:32069185 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.415+4939C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069185 | |||||||
| chr2:32069214 | C | CA | 11 | a0001c0001t0001g0077 a0001c0001t0002g0322 a0001c0001t0003g0011 others(8): Show |
11 | HG01123.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.415+4984dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32069214 | ||||||
| chr2:32069214 | CA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.415+4984delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32069214 | ||||||
| chr2:32069246 | A | C | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.415+5000A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069246 | |||||||
| chr2:32069301 | G | C | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+5055G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069301 | |||||||
| chr2:32069366 | T | A | 10 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+5120T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069366 | |||||||
| chr2:32069417 | G | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.415+5171G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069417 | |||||||
| chr2:32069509 | G | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.415+5263G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069509 | |||||||
| chr2:32069551 | C | CT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.415+5321dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32069551 | ||||||
| chr2:32069649 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.415+5403C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069649 | |||||||
| chr2:32069775 | G | A | 1 | a0001c0001t0014g0204 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.415+5529G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069775 | |||||||
| chr2:32069840 | T | C | 2 | a0001c0001t0014g0200 a0001c0001t0014g0204 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.415+5594T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32069840 | |||||||
| chr2:32070003 | G | T | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.415+5757G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070003 | |||||||
| chr2:32070012 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.415+5766A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070012 | |||||||
| chr2:32070067 | AAT | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.415+5822_415+5823d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070067 | |||||||
| chr2:32070069 | T | A | 1 | a0001c0001t0002g0243 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.415+5823T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070069 | |||||||
| chr2:32070154 | C | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.415+5908C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070154 | |||||||
| chr2:32070188 | C | A | 1 | a0001c0001t0003g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.415+5942C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070188 | |||||||
| chr2:32070310 | C | T | 3 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 |
3 | HG02300.hp2 HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.415+6064C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070310 | |||||||
| chr2:32070336 | G | A | 1 | a0001c0001t0002g0327 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.415+6090G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070336 | |||||||
| chr2:32070384 | A | G | 2 | a0001c0001t0002g0332 a0001c0001t0002g0339 |
2 | NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.415+6138A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070384 | |||||||
| chr2:32070458 | T | C | 1 | a0001c0001t0004g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.415+6212T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070458 | |||||||
| chr2:32070461 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.415+6215A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070461 | |||||||
| chr2:32070593 | T | C | 2 | a0001c0001t0002g0323 a0001c0001t0002g0328 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.415+6347T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070593 | |||||||
| chr2:32070625 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+6379G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070625 | |||||||
| chr2:32070721 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.415+6475G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070721 | |||||||
| chr2:32070803 | A | T | 1 | a0001c0001t0016g0334 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.415+6557A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070803 | |||||||
| chr2:32070805 | T | A | 1 | a0001c0001t0016g0334 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.415+6559T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070805 | |||||||
| chr2:32070811 | G | A | 1 | a0001c0001t0002g0323 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.415+6565G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070811 | |||||||
| chr2:32070823 | A | G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.415+6577A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070823 | |||||||
| chr2:32070906 | A | G | 1 | a0001c0001t0002g0338 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+6660A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070906 | |||||||
| chr2:32070940 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.415+6694T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070940 | |||||||
| chr2:32070970 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.415+6724T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32070970 | |||||||
| chr2:32071007 | G | A | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.415+6761G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071007 | |||||||
| chr2:32071030 | A | G | 7 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+6784A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071030 | |||||||
| chr2:32071048 | T | A | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+6802T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071048 | |||||||
| chr2:32071065 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.415+6819G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071065 | |||||||
| chr2:32071102 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.415+6856T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071102 | |||||||
| chr2:32071179 | A | G | 2 | a0001c0001t0002g0323 a0001c0001t0002g0328 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.415+6933A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071179 | |||||||
| chr2:32071199 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.415+6953A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071199 | |||||||
| chr2:32071439 | C | T | 1 | a0001c0001t0002g0326 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.415+7193C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071439 | |||||||
| chr2:32071946 | A | C | 1 | a0001c0001t0004g0302 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.415+7700A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32071946 | |||||||
| chr2:32072147 | G | A | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.415+7901G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072147 | |||||||
| chr2:32072167 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(329): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.415+7921T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072167 | |||||||
| chr2:32072204 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(187): Show |
190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.415+7958A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072204 | |||||||
| chr2:32072208 | AT | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.415+7970delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32072208 | ||||||
| chr2:32072275 | C | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+8029C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072275 | |||||||
| chr2:32072290 | G | A | 1 | a0001c0001t0003g0037 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.415+8044G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072290 | |||||||
| chr2:32072356 | A | G | 4 | a0001c0001t0001g0100 a0001c0001t0013g0068 a0001c0001t0013g0069 others(1): Show |
4 | HG01891.hp1 HG02717.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+8110A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072356 | |||||||
| chr2:32072389 | T | C | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+8143T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072389 | |||||||
| chr2:32072417 | G | A | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.415+8171G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072417 | |||||||
| chr2:32072423 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18612.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.415+8177T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072423 | |||||||
| chr2:32072430 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.415+8184A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072430 | |||||||
| chr2:32072440 | A | C | 2 | a0001c0001t0001g0170 a0001c0001t0017g0169 |
2 | HG00609.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.415+8194A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072440 | |||||||
| chr2:32072501 | A | G | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+8255A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072501 | |||||||
| chr2:32072643 | A | G | 1 | a0001c0001t0005g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.415+8397A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072643 | |||||||
| chr2:32072734 | G | C | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.415+8488G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072734 | |||||||
| chr2:32072869 | A | C | 1 | a0001c0001t0013g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.415+8623A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072869 | |||||||
| chr2:32072881 | C | A | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.415+8635C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072881 | |||||||
| chr2:32072915 | G | A | 10 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.415+8669G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32072915 | |||||||
| chr2:32073003 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+8757A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073003 | |||||||
| chr2:32073022 | A | G | 3 | a0001c0001t0004g0209 a0001c0001t0004g0210 a0001c0001t0004g0211 |
3 | HG01070.hp1 HG01261.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.415+8776A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073022 | |||||||
| chr2:32073081 | T | TTTG | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.415+8843_415+8845d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32073081 | ||||||
| chr2:32073204 | T | A | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+8958T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073204 | |||||||
| chr2:32073385 | C | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.415+9139C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073385 | |||||||
| chr2:32073461 | T | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.415+9215T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073461 | |||||||
| chr2:32073490 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.415+9244T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073490 | |||||||
| chr2:32073502 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.415+9256T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32073502 | |||||||
| chr2:32074189 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.415+9943A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074189 | |||||||
| chr2:32074200 | T | C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+9954T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074200 | |||||||
| chr2:32074330 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.415+10084A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074330 | |||||||
| chr2:32074373 | C | T | 3 | a0001c0001t0002g0318 a0001c0001t0002g0319 a0001c0001t0025g0320 |
3 | HG01070.hp2 HG01071.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.415+10127C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074373 | |||||||
| chr2:32074516 | T | G | 4 | a0001c0001t0011g0006 a0001c0001t0013g0068 a0001c0001t0013g0069 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+10270T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074516 | |||||||
| chr2:32074524 | A | T | 2 | a0001c0001t0001g0168 a0001c0001t0003g0015 |
2 | HG03490.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.415+10278A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074524 | |||||||
| chr2:32074583 | T | G | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.415+10337T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074583 | |||||||
| chr2:32074587 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.415+10341G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074587 | |||||||
| chr2:32074734 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.415+10488G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074734 | |||||||
| chr2:32074849 | G | A | 1 | a0001c0001t0004g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.415+10603G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32074849 | |||||||
| chr2:32075026 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.415+10780G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075026 | |||||||
| chr2:32075144 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.415+10898C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075144 | |||||||
| chr2:32075234 | A | G | 1 | a0001c0001t0004g0031 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.415+10988A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075234 | |||||||
| chr2:32075425 | C | CA | 21 | a0001c0001t0002g0217 a0001c0001t0002g0221 a0001c0001t0002g0226 others(18): Show |
21 | HG00735.hp2 HG01070.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.415+11200dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075425 | ||||||
| chr2:32075425 | CA | C | 76 | a0001c0001t0001g0040 a0001c0001t0001g0078 a0001c0001t0001g0079 others(73): Show |
76 | HG00597.hp2 HG00609.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.415+11200delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075425 | ||||||
| chr2:32075425 | CAA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.415+11199_415+1120 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075425 | ||||||
| chr2:32075435 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0007g0080 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.415+11198_415+1119 others(26): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075435 | ||||||
| chr2:32075480 | C | CA | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.415+11247dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075480 | ||||||
| chr2:32075500 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.415+11254G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075500 | |||||||
| chr2:32075547 | C | CT | 52 | a0001c0001t0002g0241 a0001c0001t0002g0257 a0001c0001t0002g0291 others(49): Show |
52 | HG00673.hp1 HG00741.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.415+11321dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075547 | ||||||
| chr2:32075547 | C | CTTT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0074 others(148): Show |
151 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.415+11319_415+1132 others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075547 | ||||||
| chr2:32075547 | C | CTTTT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0107 others(22): Show |
25 | HG00423.hp2 HG00438.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.415+11318_415+1132 others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075547 | ||||||
| chr2:32075547 | CTTT | C | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+11319_415+1132 others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075547 | ||||||
| chr2:32075859 | C | CT | 92 | a0001c0001t0001g0040 a0001c0001t0001g0074 a0001c0001t0001g0077 others(89): Show |
92 | HG00408.hp2 HG00609.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.416-11617dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075859 | ||||||
| chr2:32075859 | C | CTT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.416-11618_416-1161 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075859 | ||||||
| chr2:32075859 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.415+11620_416-1161 others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075859 | ||||||
| chr2:32075894 | C | CT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.416-11597dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075894 | ||||||
| chr2:32075894 | C | CTT | 31 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(28): Show |
31 | HG00408.hp2 HG00621.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.416-11597_416-1159 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075894 | ||||||
| chr2:32075894 | C | CTTT | 3 | a0001c0001t0003g0064 a0001c0001t0003g0066 a0001c0001t0003g0067 |
3 | HG03491.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.416-11597_416-1159 others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075894 | ||||||
| chr2:32075894 | CTCTTTTT others(5): Show |
C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.416-11596_416-1158 others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075894 | ||||||
| chr2:32075896 | C | CT | 11 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0241 others(8): Show |
11 | HG00597.hp1 HG00738.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.416-11574dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075896 | ||||||
| chr2:32075896 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.416-11596C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075896 | |||||||
| chr2:32075896 | CT | C | 6 | a0001c0001t0002g0272 a0001c0001t0002g0319 a0001c0001t0004g0302 others(3): Show |
6 | HG01070.hp2 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-11574delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32075896 | ||||||
| chr2:32075931 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-11561C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075931 | |||||||
| chr2:32075983 | C | G | 1 | a0001c0001t0004g0028 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.416-11509C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32075983 | |||||||
| chr2:32076390 | A | T | 1 | a0001c0001t0002g0289 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.416-11102A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32076390 | |||||||
| chr2:32076392 | T | G | 1 | a0001c0001t0002g0326 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.416-11100T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32076392 | |||||||
| chr2:32076537 | T | A | 1 | a0001c0001t0017g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.416-10955T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32076537 | |||||||
| chr2:32076561 | T | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-10931T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32076561 | |||||||
| chr2:32076562 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(220): Show |
223 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.416-10930G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32076562 | |||||||
| chr2:32076687 | AT | A | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-10794delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32076687 | ||||||
| chr2:32077010 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.416-10482G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077010 | |||||||
| chr2:32077011 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(210): Show |
213 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.416-10481A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077011 | |||||||
| chr2:32077335 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.416-10157A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077335 | |||||||
| chr2:32077339 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.416-10153A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077339 | |||||||
| chr2:32077390 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416-10102G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077390 | |||||||
| chr2:32077463 | C | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.416-10029C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077463 | |||||||
| chr2:32077624 | T | G | 31 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(28): Show |
31 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.416-9868T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077624 | |||||||
| chr2:32077741 | T | C | 4 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0001g0111 others(1): Show |
4 | HG00408.hp2 NA19009.hp1 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-9751T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077741 | |||||||
| chr2:32077907 | A | G | 1 | a0001c0001t0004g0028 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.416-9585A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077907 | |||||||
| chr2:32077973 | T | G | 27 | a0001c0001t0001g0105 a0001c0001t0002g0226 a0001c0001t0002g0258 others(24): Show |
27 | HG00099.hp1 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-9519T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077973 | |||||||
| chr2:32077973 | T | TG | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.416-9519_416-9518i others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077973 | |||||||
| chr2:32077994 | T | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.416-9498T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32077994 | |||||||
| chr2:32078060 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.416-9432G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078060 | |||||||
| chr2:32078082 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.416-9410C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078082 | |||||||
| chr2:32078135 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.416-9357C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078135 | |||||||
| chr2:32078290 | G | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0023 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.416-9202G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078290 | |||||||
| chr2:32078395 | C | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01243.hp2 HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.416-9097C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078395 | |||||||
| chr2:32078532 | C | T | 1 | a0001c0001t0005g0190 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.416-8960C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078532 | |||||||
| chr2:32078693 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.416-8799T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078693 | |||||||
| chr2:32078839 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.416-8653A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078839 | |||||||
| chr2:32078999 | G | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.416-8493G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32078999 | |||||||
| chr2:32079003 | A | G | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.416-8489A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079003 | |||||||
| chr2:32079047 | CCCAGGCT others(3): Show |
C | 1 | a0001c0001t0002g0326 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.416-8443_416-8434d others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32079047 | ||||||
| chr2:32079075 | A | G | 1 | a0001c0001t0002g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.416-8417A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079075 | |||||||
| chr2:32079100 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.416-8392C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079100 | |||||||
| chr2:32079155 | A | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
5 | HG01496.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-8337A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079155 | |||||||
| chr2:32079174 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | NA18972.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.416-8318T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079174 | |||||||
| chr2:32079259 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.416-8233G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079259 | |||||||
| chr2:32079287 | G | T | 1 | a0001c0001t0003g0066 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.416-8205G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079287 | |||||||
| chr2:32079433 | C | T | 6 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0307 others(3): Show |
6 | HG02257.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-8059C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079433 | |||||||
| chr2:32079504 | T | TA | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-7978dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32079504 | ||||||
| chr2:32079587 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.416-7905G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079587 | |||||||
| chr2:32079625 | A | ATC | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-7866_416-7865d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32079625 | ||||||
| chr2:32079724 | A | T | 2 | a0001c0001t0002g0218 a0001c0001t0026g0240 |
2 | HG02071.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.416-7768A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079724 | |||||||
| chr2:32079890 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.416-7602A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079890 | |||||||
| chr2:32079931 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-7561A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32079931 | |||||||
| chr2:32080177 | T | C | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.416-7315T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32080177 | |||||||
| chr2:32080266 | T | C | 1 | a0001c0001t0002g0241 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.416-7226T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32080266 | |||||||
| chr2:32080428 | A | AGATAATG others(17): Show |
175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.416-7063_416-7040d others(26): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32080428 | ||||||
| chr2:32080466 | A | G | 1 | a0001c0001t0004g0299 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.416-7026A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32080466 | |||||||
| chr2:32080600 | T | TA | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.416-6890dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32080600 | ||||||
| chr2:32080727 | A | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0154 others(3): Show |
6 | HG00558.hp2 HG00621.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-6765A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32080727 | |||||||
| chr2:32080783 | C | CT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.416-6680dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32080783 | ||||||
| chr2:32080783 | C | CTT | 36 | a0001c0001t0001g0079 a0001c0001t0001g0082 a0001c0001t0001g0092 others(33): Show |
36 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.416-6681_416-6680d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32080783 | ||||||
| chr2:32080783 | CT | C | 26 | a0001c0001t0002g0217 a0001c0001t0002g0259 a0001c0001t0002g0300 others(23): Show |
26 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.416-6680delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32080783 | ||||||
| chr2:32080812 | T | G | 9 | a0001c0001t0002g0003 a0001c0001t0002g0214 a0001c0001t0002g0254 others(6): Show |
9 | HG01496.hp1 HG02559.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-6680T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32080812 | |||||||
| chr2:32080812 | T | TG | 4 | a0001c0001t0002g0215 a0001c0001t0002g0279 a0001c0001t0002g0285 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-6679dupG | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32080812 | ||||||
| chr2:32080880 | C | T | 2 | a0001c0001t0002g0310 a0001c0001t0004g0298 |
2 | HG01106.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.416-6612C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32080880 | |||||||
| chr2:32081022 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.416-6470G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081022 | |||||||
| chr2:32081044 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.416-6448C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081044 | |||||||
| chr2:32081081 | C | T | 1 | a0001c0001t0004g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.416-6411C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081081 | |||||||
| chr2:32081289 | C | T | 7 | a0001c0001t0004g0195 a0001c0001t0005g0190 a0001c0001t0005g0191 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-6203C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081289 | |||||||
| chr2:32081326 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.416-6166C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081326 | |||||||
| chr2:32081397 | G | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0118 others(10): Show |
13 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.416-6095G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081397 | |||||||
| chr2:32081433 | G | A | 4 | a0001c0001t0004g0205 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | HG01070.hp1 HG01261.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-6059G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081433 | |||||||
| chr2:32081645 | G | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0230 a0001c0001t0026g0240 |
3 | HG02071.hp1 NA18612.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.416-5847G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081645 | |||||||
| chr2:32081736 | A | G | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.416-5756A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081736 | |||||||
| chr2:32081781 | C | CA | 15 | a0001c0001t0002g0238 a0001c0001t0002g0254 a0001c0001t0002g0260 others(12): Show |
15 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.416-5688dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0101 a0001c0001t0003g0015 a0001c0001t0003g0021 others(8): Show |
11 | HG01891.hp1 HG02055.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-5696_416-5688d others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(3): Show |
19 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(16): Show |
19 | HG01168.hp2 HG01257.hp1 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.416-5697_416-5688d others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(4): Show |
40 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0078 others(37): Show |
40 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.416-5698_416-5688d others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(5): Show |
40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0077 others(37): Show |
40 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.416-5699_416-5688d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(6): Show |
25 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0001g0096 others(22): Show |
25 | HG00408.hp1 HG00609.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.416-5700_416-5688d others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(7): Show |
8 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0001g0130 others(5): Show |
8 | HG01943.hp2 NA18939.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-5701_416-5688d others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0129 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.416-5702_416-5688d others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0132 a0001c0001t0001g0172 |
3 | HG00673.hp2 HG02615.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.416-5703_416-5688d others(18): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.416-5704_416-5688d others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | CA | C | 24 | a0001c0001t0001g0040 a0001c0001t0002g0217 a0001c0001t0002g0278 others(21): Show |
24 | HG00741.hp1 HG01069.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-5688delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081781 | CAA | C | 18 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0003g0038 others(15): Show |
18 | HG02083.hp2 HG02965.hp2 HG02970.hp2 others(15): Show |
intron_variant | MODIFIER | c.416-5689_416-5688d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32081781 | ||||||
| chr2:32081815 | G | A | 1 | a0001c0001t0014g0204 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.416-5677G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081815 | |||||||
| chr2:32081907 | T | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.416-5585T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081907 | |||||||
| chr2:32081984 | A | C | 1 | a0001c0001t0004g0222 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.416-5508A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081984 | |||||||
| chr2:32081985 | C | T | 1 | a0001c0001t0004g0222 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.416-5507C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32081985 | |||||||
| chr2:32082005 | C | CT | 13 | a0001c0001t0001g0176 a0001c0001t0002g0003 a0001c0001t0002g0230 others(10): Show |
13 | HG00140.hp2 HG00597.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.416-5464dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32082005 | ||||||
| chr2:32082005 | CT | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-5464delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32082005 | ||||||
| chr2:32082005 | CTT | C | 9 | a0001c0001t0001g0075 a0001c0001t0001g0112 a0001c0001t0002g0326 others(6): Show |
9 | HG01169.hp2 HG01891.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-5465_416-5464d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32082005 | ||||||
| chr2:32082007 | T | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.416-5485T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082007 | |||||||
| chr2:32082008 | T | C | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.416-5484T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082008 | |||||||
| chr2:32082106 | C | T | 1 | a0001c0001t0014g0204 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.416-5386C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082106 | |||||||
| chr2:32082218 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-5274C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082218 | |||||||
| chr2:32082277 | G | A | 4 | a0001c0001t0002g0335 a0001c0001t0002g0336 a0001c0001t0002g0337 others(1): Show |
4 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-5215G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082277 | |||||||
| chr2:32082317 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-5175A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082317 | |||||||
| chr2:32082526 | G | A | 7 | a0001c0001t0001g0113 a0001c0001t0004g0256 a0001c0001t0004g0292 others(4): Show |
7 | HG00099.hp2 HG01261.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-4966G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082526 | |||||||
| chr2:32082559 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0026g0240 |
2 | HG02071.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.416-4933G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082559 | |||||||
| chr2:32082560 | G | A | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.416-4932G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082560 | |||||||
| chr2:32082593 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.416-4899G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082593 | |||||||
| chr2:32082765 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.416-4727G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082765 | |||||||
| chr2:32082789 | G | A | 1 | a0001c0001t0001g0342 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.416-4703G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082789 | |||||||
| chr2:32082953 | G | C | 1 | a0001c0001t0003g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.416-4539G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082953 | |||||||
| chr2:32082964 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.416-4528T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32082964 | |||||||
| chr2:32083033 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-4459G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083033 | |||||||
| chr2:32083120 | C | T | 2 | a0001c0001t0002g0276 a0001c0001t0002g0277 |
2 | HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.416-4372C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083120 | |||||||
| chr2:32083133 | A | G | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-4359A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083133 | |||||||
| chr2:32083411 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-4081C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083411 | |||||||
| chr2:32083474 | G | A | 2 | a0001c0001t0004g0225 a0001c0001t0004g0290 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.416-4018G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083474 | |||||||
| chr2:32083596 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0018g0114 |
3 | HG00099.hp2 HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.416-3896A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083596 | |||||||
| chr2:32083597 | C | T | 10 | a0001c0001t0003g0024 a0001c0001t0003g0026 a0001c0001t0003g0027 others(7): Show |
10 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.416-3895C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083597 | |||||||
| chr2:32083639 | T | C | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-3853T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083639 | |||||||
| chr2:32083655 | C | CTATA | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.416-3819_416-3816d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083655 | ||||||
| chr2:32083655 | CTA | C | 148 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(145): Show |
148 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.416-3817_416-3816d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083655 | ||||||
| chr2:32083655 | CTATA | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.416-3819_416-3816d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083655 | ||||||
| chr2:32083655 | CTATATA | C | 3 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 |
3 | HG01255.hp2 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.416-3821_416-3816d others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083655 | ||||||
| chr2:32083675 | A | T | 2 | a0001c0001t0004g0194 a0001c0001t0004g0201 |
2 | HG01106.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.416-3817A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083675 | |||||||
| chr2:32083683 | G | T | 1 | a0001c0001t0011g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-3809G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083683 | |||||||
| chr2:32083693 | G | C | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.416-3799G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083693 | |||||||
| chr2:32083707 | TTATACTA others(12): Show |
T | 27 | a0001c0001t0002g0310 a0001c0001t0002g0318 a0001c0001t0002g0319 others(24): Show |
27 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-3751_416-3733d others(21): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083707 | ||||||
| chr2:32083722 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.416-3770T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083722 | |||||||
| chr2:32083731 | C | CTATATAT others(5): Show |
1 | a0001c0001t0004g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.416-3752_416-3751i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083731 | ||||||
| chr2:32083731 | CTATATAT others(14): Show |
C | 20 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(17): Show |
20 | HG01070.hp1 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-3751_416-3731d others(23): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083731 | ||||||
| chr2:32083731 | CTATATAT others(16): Show |
C | 2 | a0001c0001t0003g0013 a0001c0001t0003g0023 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.416-3751_416-3729d others(25): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083731 | ||||||
| chr2:32083733 | ATATATAT others(10): Show |
A | 6 | a0001c0001t0004g0247 a0001c0001t0004g0295 a0001c0001t0005g0197 others(3): Show |
6 | HG01934.hp2 HG02630.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-3751_416-3735d others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083733 | ||||||
| chr2:32083735 | ATATATTT others(8): Show |
A | 1 | a0001c0001t0004g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.416-3751_416-3737d others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083735 | ||||||
| chr2:32083737 | ATATTTAT others(6): Show |
A | 7 | a0001c0001t0004g0225 a0001c0001t0004g0290 a0001c0001t0009g0070 others(4): Show |
7 | HG01081.hp2 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-3751_416-3739d others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083737 | ||||||
| chr2:32083739 | ATTTATAT others(4): Show |
A | 2 | a0001c0001t0003g0030 a0001c0001t0021g0065 |
2 | HG01361.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.416-3751_416-3741d others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083739 | ||||||
| chr2:32083740 | TTTATATA others(2): Show |
T | 6 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-3751_416-3743d others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083740 | |||||||
| chr2:32083741 | T | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(163): Show |
166 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.416-3751T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083741 | |||||||
| chr2:32083743 | ATATATAC | A | 18 | a0001c0001t0001g0040 a0001c0001t0001g0143 a0001c0001t0003g0021 others(15): Show |
18 | HG02083.hp1 HG02083.hp2 HG02895.hp2 others(15): Show |
intron_variant | MODIFIER | c.416-3742_416-3736d others(9): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083743 | ||||||
| chr2:32083744 | TATATACT others(5): Show |
T | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416-3747_416-3736d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083744 | |||||||
| chr2:32083745 | ATATAC | A | 10 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0033 others(7): Show |
10 | HG01516.hp2 HG02129.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3742_416-3738d others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083745 | ||||||
| chr2:32083745 | ATATACTA others(13): Show |
A | 1 | a0001c0001t0004g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.416-3746_416-3727d others(22): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083745 | |||||||
| chr2:32083746 | TATACTAT others(5): Show |
T | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.416-3745_416-3734d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083746 | |||||||
| chr2:32083747 | ATAC | A | 9 | a0001c0001t0001g0075 a0001c0001t0001g0133 a0001c0001t0003g0012 others(6): Show |
9 | HG01069.hp2 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-3742_416-3740d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083747 | ||||||
| chr2:32083748 | TACTATAT others(13): Show |
T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.416-3743_416-3724d others(22): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083748 | |||||||
| chr2:32083749 | AC | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.416-3742delC | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083749 | |||||||
| chr2:32083749 | ACTATATA others(3): Show |
A | 1 | a0001c0001t0001g0139 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.416-3742_416-3733d others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083749 | |||||||
| chr2:32083750 | C | A | 10 | a0001c0001t0001g0146 a0001c0001t0003g0010 a0001c0001t0003g0016 others(7): Show |
10 | HG01255.hp2 HG01496.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.416-3742C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083750 | |||||||
| chr2:32083750 | C | CTA | 10 | a0001c0001t0002g0221 a0001c0001t0002g0229 a0001c0001t0002g0235 others(7): Show |
10 | HG00597.hp1 HG00639.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3716_416-3715d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083750 | ||||||
| chr2:32083750 | C | G | 1 | a0001c0001t0002g0241 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.416-3742C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083750 | |||||||
| chr2:32083758 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416-3734A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083758 | |||||||
| chr2:32083760 | A | T | 9 | a0001c0001t0001g0115 a0001c0001t0001g0139 a0001c0001t0001g0147 others(6): Show |
9 | HG00408.hp1 HG00738.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-3732A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083760 | |||||||
| chr2:32083761 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.416-3731T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083761 | |||||||
| chr2:32083762 | A | ATTTTT | 3 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0007g0081 |
3 | NA18999.hp1 NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.416-3729_416-3728i others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083762 | ||||||
| chr2:32083762 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0186 |
2 | HG02486.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.416-3729_416-3728i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083762 | ||||||
| chr2:32083762 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.416-3729_416-3728i others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083762 | ||||||
| chr2:32083762 | A | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0098 others(8): Show |
11 | HG00408.hp1 HG02083.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-3730A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083762 | |||||||
| chr2:32083764 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.416-3727_416-3726i others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083764 | ||||||
| chr2:32083764 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0173 a0001c0001t0001g0182 |
3 | HG00639.hp2 NA18953.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.416-3727_416-3726i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083764 | ||||||
| chr2:32083764 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.416-3727_416-3726i others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083764 | ||||||
| chr2:32083764 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0166 a0001c0001t0001g0181 |
3 | HG01928.hp1 NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.416-3727_416-3726i others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083764 | ||||||
| chr2:32083764 | A | T | 25 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0079 others(22): Show |
25 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.416-3728A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083764 | |||||||
| chr2:32083766 | A | ATTTTTT | 4 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0100 others(1): Show |
4 | HG00642.hp2 HG01081.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-3725_416-3724i others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083766 | ||||||
| chr2:32083766 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0017g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.416-3725_416-3724i others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083766 | ||||||
| chr2:32083766 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.416-3725_416-3724i others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083766 | ||||||
| chr2:32083766 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0003g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416-3725_416-3724i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083766 | ||||||
| chr2:32083766 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0157 |
2 | HG03710.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.416-3725_416-3724i others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083766 | ||||||
| chr2:32083766 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0177 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.416-3725_416-3724i others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083766 | ||||||
| chr2:32083766 | A | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0077 others(39): Show |
42 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(39): Show |
intron_variant | MODIFIER | c.416-3726A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083766 | |||||||
| chr2:32083767 | TA | T | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.416-3724delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083767 | |||||||
| chr2:32083768 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.416-3723_416-3722i others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083768 | ||||||
| chr2:32083768 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0175 a0001c0001t0002g0155 |
2 | NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.416-3723_416-3722i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083768 | ||||||
| chr2:32083768 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.416-3723_416-3722i others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083768 | ||||||
| chr2:32083768 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0119 a0001c0001t0007g0165 |
2 | HG00438.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.416-3723_416-3722i others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083768 | ||||||
| chr2:32083768 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.416-3723_416-3722i others(22): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083768 | ||||||
| chr2:32083768 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0077 others(52): Show |
55 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-3724A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083768 | |||||||
| chr2:32083770 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0109 a0001c0001t0003g0057 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0342 a0001c0001t0007g0099 |
3 | HG01934.hp1 HG02165.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0132 |
2 | NA18612.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0076 a0001c0001t0001g0122 a0001c0001t0020g0183 |
3 | NA18960.hp1 NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0118 a0001c0001t0001g0171 a0001c0001t0027g0144 |
3 | HG04199.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0128 |
2 | HG01109.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(18): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0159 |
2 | HG00735.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.416-3721_416-3720i others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0018g0114 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.416-3721_416-3720i others(25): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083770 | ||||||
| chr2:32083770 | A | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0077 others(68): Show |
71 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.416-3722A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083770 | |||||||
| chr2:32083771 | TA | T | 12 | a0001c0001t0003g0030 a0001c0001t0003g0038 a0001c0001t0003g0046 others(9): Show |
12 | HG02083.hp2 HG02723.hp1 HG02970.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-3720delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083771 | |||||||
| chr2:32083772 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0142 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.416-3719_416-3718i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083772 | ||||||
| chr2:32083772 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0136 |
2 | HG02723.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.416-3719_416-3718i others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083772 | ||||||
| chr2:32083772 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0172 |
3 | HG00621.hp2 HG00673.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.416-3719_416-3718i others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083772 | ||||||
| chr2:32083772 | A | ATTTTTTT others(9): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0137 a0001c0001t0001g0163 |
3 | HG00140.hp1 HG00423.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.416-3719_416-3718i others(18): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083772 | ||||||
| chr2:32083772 | A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0148 |
2 | HG02129.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.416-3719_416-3718i others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083772 | ||||||
| chr2:32083772 | A | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0075 others(94): Show |
97 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.416-3720A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083772 | |||||||
| chr2:32083773 | TA | T | 23 | a0001c0001t0001g0040 a0001c0001t0002g0243 a0001c0001t0003g0010 others(20): Show |
23 | HG01106.hp1 HG01169.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3718delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083773 | |||||||
| chr2:32083774 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0174 a0001c0001t0003g0073 |
2 | NA18970.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.416-3717_416-3716i others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083774 | ||||||
| chr2:32083774 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0126 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.416-3717_416-3716i others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083774 | ||||||
| chr2:32083774 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.416-3717_416-3716i others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083774 | ||||||
| chr2:32083774 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0153 others(1): Show |
4 | HG00558.hp1 NA18955.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-3717_416-3716i others(20): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083774 | ||||||
| chr2:32083774 | A | ATTTTTTT others(12): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0223 |
2 | NA18963.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.416-3717_416-3716i others(21): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083774 | ||||||
| chr2:32083774 | A | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0074 a0001c0001t0001g0075 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.416-3718A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083774 | |||||||
| chr2:32083775 | TA | T | 7 | a0001c0001t0002g0215 a0001c0001t0003g0019 a0001c0001t0003g0020 others(4): Show |
7 | HG01071.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-3716delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083775 | |||||||
| chr2:32083776 | A | AT | 8 | a0001c0001t0002g0254 a0001c0001t0002g0279 a0001c0001t0002g0285 others(5): Show |
8 | HG01255.hp2 HG02280.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.416-3701dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATAT others(25): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0180 |
2 | HG03669.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.416-3715_416-3714i others(34): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.416-3715_416-3714i others(26): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.416-3715_416-3714i others(32): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.416-3715_416-3714i others(26): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0185 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.416-3715_416-3714i others(27): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATTT others(15): Show |
1 | a0001c0001t0001g0184 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.416-3715_416-3714i others(24): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATATTT others(17): Show |
1 | a0001c0001t0001g0134 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.416-3715_416-3714i others(26): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATATTTTT others(16): Show |
1 | a0001c0001t0001g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.416-3715_416-3714i others(25): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.416-3714_416-3701d others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0146 a0001c0001t0010g0106 |
2 | HG02040.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.416-3701_416-3700i others(18): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0001g0120 a0001c0001t0001g0127 |
2 | HG00597.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.416-3701_416-3700i others(20): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATTTTTTT others(12): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0170 a0001c0001t0001g0340 |
3 | HG02572.hp1 NA18984.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.416-3701_416-3700i others(21): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATTTTTTT others(15): Show |
2 | a0001c0001t0001g0121 a0001c0001t0001g0178 |
2 | HG03688.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.416-3701_416-3700i others(24): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0002 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.416-3701_416-3700i others(25): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083776 | A | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0074 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.416-3716A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083776 | |||||||
| chr2:32083776 | AT | A | 6 | a0001c0001t0002g0262 a0001c0001t0002g0300 a0001c0001t0003g0014 others(3): Show |
6 | HG01069.hp1 HG01433.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-3701delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32083776 | ||||||
| chr2:32083777 | T | TATA | 3 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0289 |
3 | HG00140.hp2 HG01099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.416-3715_416-3714i others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083777 | |||||||
| chr2:32083778 | T | A | 10 | a0001c0001t0002g0260 a0001c0001t0002g0278 a0001c0001t0002g0283 others(7): Show |
10 | HG03486.hp2 HG03579.hp1 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3714T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083778 | |||||||
| chr2:32083842 | G | C | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG03139.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.416-3650G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083842 | |||||||
| chr2:32083848 | C | T | 3 | a0001c0001t0012g0219 a0001c0001t0012g0246 a0001c0001t0012g0274 |
3 | HG01123.hp1 HG01175.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.416-3644C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083848 | |||||||
| chr2:32083968 | G | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.416-3524G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32083968 | |||||||
| chr2:32084222 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.416-3270C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32084222 | |||||||
| chr2:32084285 | G | A | 1 | a0001c0001t0007g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.416-3207G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32084285 | |||||||
| chr2:32084453 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-3039C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32084453 | |||||||
| chr2:32084742 | G | A | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.416-2750G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32084742 | |||||||
| chr2:32084744 | A | T | 3 | a0001c0001t0002g0307 a0001c0001t0002g0308 a0001c0001t0002g0309 |
3 | HG02559.hp2 HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.416-2748A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32084744 | |||||||
| chr2:32084887 | C | CA | 7 | a0001c0001t0002g0218 a0001c0001t0002g0238 a0001c0001t0002g0289 others(4): Show |
7 | HG00597.hp1 HG01099.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-2582dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32084887 | ||||||
| chr2:32084887 | CA | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(153): Show |
156 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.416-2582delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32084887 | ||||||
| chr2:32084887 | CAA | C | 92 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0001g0078 others(89): Show |
92 | HG00099.hp2 HG00408.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.416-2583_416-2582d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32084887 | ||||||
| chr2:32084969 | A | C | 1 | a0001c0001t0003g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.416-2523A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32084969 | |||||||
| chr2:32085035 | C | G | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.416-2457C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085035 | |||||||
| chr2:32085205 | C | CT | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(158): Show |
161 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.416-2268dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32085205 | ||||||
| chr2:32085205 | C | CTT | 8 | a0001c0001t0001g0122 a0001c0001t0001g0150 a0001c0001t0001g0176 others(5): Show |
8 | HG01891.hp1 HG02897.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.416-2269_416-2268d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32085205 | ||||||
| chr2:32085205 | CT | C | 6 | a0001c0001t0002g0233 a0001c0001t0002g0262 a0001c0001t0002g0263 others(3): Show |
6 | HG01361.hp2 HG03486.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-2268delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32085205 | ||||||
| chr2:32085211 | T | G | 1 | a0001c0001t0002g0336 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.416-2281T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085211 | |||||||
| chr2:32085238 | G | GCT | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG03139.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.416-2251_416-2250d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32085238 | ||||||
| chr2:32085566 | T | A | 12 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0201 others(9): Show |
12 | HG00741.hp1 HG01106.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1926T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085566 | |||||||
| chr2:32085580 | C | T | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.416-1912C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085580 | |||||||
| chr2:32085719 | G | A | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.416-1773G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085719 | |||||||
| chr2:32085760 | G | C | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.416-1732G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085760 | |||||||
| chr2:32085764 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.416-1728C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085764 | |||||||
| chr2:32085798 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.416-1694T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085798 | |||||||
| chr2:32085839 | C | G | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.416-1653C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085839 | |||||||
| chr2:32085956 | C | A | 1 | a0001c0001t0011g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.416-1536C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085956 | |||||||
| chr2:32085997 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.416-1495G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32085997 | |||||||
| chr2:32086033 | C | T | 1 | a0001c0001t0003g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.416-1459C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086033 | |||||||
| chr2:32086039 | C | CTAAA | 3 | a0001c0001t0002g0003 a0001c0001t0002g0262 a0002c0003t0002g0284 |
3 | HG01496.hp1 HG02970.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.416-1426_416-1423d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32086039 | ||||||
| chr2:32086039 | CTAAA | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.416-1426_416-1423d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32086039 | ||||||
| chr2:32086191 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0171 |
2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.416-1301C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086191 | |||||||
| chr2:32086215 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.416-1277C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086215 | |||||||
| chr2:32086427 | C | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.416-1065C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086427 | |||||||
| chr2:32086462 | T | TA | 7 | a0001c0001t0003g0051 a0001c0001t0008g0005 a0001c0001t0008g0007 others(4): Show |
7 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-1015dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32086462 | ||||||
| chr2:32086462 | TA | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(123): Show |
126 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.416-1015delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 32086462 | ||||||
| chr2:32086484 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0223 |
2 | NA18950.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.416-1008C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086484 | |||||||
| chr2:32086539 | GATCACC | G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.416-952_416-947del others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086539 | |||||||
| chr2:32086631 | A | G | 1 | a0001c0001t0004g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.416-861A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086631 | |||||||
| chr2:32086683 | G | A | 2 | a0001c0001t0014g0200 a0001c0001t0014g0204 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.416-809G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086683 | |||||||
| chr2:32086707 | G | A | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.416-785G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086707 | |||||||
| chr2:32086758 | A | G | 1 | a0001c0001t0011g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-734A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086758 | |||||||
| chr2:32086805 | A | G | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.416-687A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086805 | |||||||
| chr2:32086891 | A | G | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-601A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32086891 | |||||||
| chr2:32087054 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.416-438T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087054 | |||||||
| chr2:32087063 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.416-429A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087063 | |||||||
| chr2:32087108 | G | C | 1 | a0001c0001t0002g0262 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.416-384G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087108 | |||||||
| chr2:32087127 | A | G | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.416-365A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087127 | |||||||
| chr2:32087130 | A | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.416-362A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087130 | |||||||
| chr2:32087224 | A | T | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.416-268A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087224 | |||||||
| chr2:32087252 | A | G | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.416-240A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087252 | |||||||
| chr2:32087338 | A | G | 1 | a0001c0001t0008g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.416-154A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087338 | |||||||
| chr2:32087339 | C | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-153C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087339 | |||||||
| chr2:32087426 | C | A | 7 | a0001c0001t0004g0195 a0001c0001t0005g0190 a0001c0001t0005g0191 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-66C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087426 | |||||||
| chr2:32087469 | A | G | 1 | a0001c0001t0004g0293 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.416-23A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 1/16 | chr2 | 32087469 | |||||||
| chr2:32087626 | A | G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(1): Show |
4 | NA18949.hp2 NA18967.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+48A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32087626 | |||||||
| chr2:32087631 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.502+53T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32087631 | |||||||
| chr2:32087647 | C | CTATT | 11 | a0001c0001t0001g0095 a0001c0001t0004g0205 a0001c0001t0004g0206 others(8): Show |
11 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.502+87_502+90dupAT others(2): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087647 | ||||||
| chr2:32087691 | TTTC | T | 8 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0087 others(5): Show |
8 | HG00408.hp2 HG01934.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.502+116_502+118del others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087691 | ||||||
| chr2:32087694 | C | CT | 13 | a0001c0001t0001g0086 a0001c0001t0001g0126 a0001c0001t0002g0214 others(10): Show |
13 | HG00597.hp1 HG01109.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.502+134dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087694 | ||||||
| chr2:32087694 | C | CTT | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(103): Show |
106 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.502+133_502+134dup others(2): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087694 | ||||||
| chr2:32087694 | CT | C | 11 | a0001c0001t0002g0243 a0001c0001t0002g0262 a0001c0001t0002g0267 others(8): Show |
11 | HG01255.hp1 HG01515.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.502+134delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087694 | ||||||
| chr2:32087743 | T | G | 1 | a0001c0001t0002g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.502+165T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32087743 | |||||||
| chr2:32087768 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.502+190T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32087768 | |||||||
| chr2:32087861 | A | AATT | 15 | a0001c0001t0001g0083 a0001c0001t0001g0146 a0001c0001t0002g0243 others(12): Show |
15 | HG01069.hp1 HG01255.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.502+312_502+314dup others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087861 | ||||||
| chr2:32087861 | A | AATTATT | 10 | a0001c0001t0001g0076 a0001c0001t0001g0129 a0001c0001t0001g0134 others(7): Show |
10 | HG00741.hp2 HG01433.hp2 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+309_502+314dup others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087861 | ||||||
| chr2:32087861 | AATT | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.502+312_502+314del others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087861 | ||||||
| chr2:32087861 | AATTATT | A | 3 | a0001c0001t0003g0055 a0001c0001t0003g0057 a0001c0001t0004g0299 |
3 | HG01928.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.502+309_502+314del others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32087861 | ||||||
| chr2:32087953 | G | A | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502+375G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32087953 | |||||||
| chr2:32088107 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0142 |
2 | NA18969.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.502+529C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088107 | |||||||
| chr2:32088183 | C | T | 11 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.502+605C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088183 | |||||||
| chr2:32088207 | T | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+629T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088207 | |||||||
| chr2:32088452 | C | G | 1 | a0001c0001t0023g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.502+874C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088452 | |||||||
| chr2:32088575 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0158 |
3 | HG00140.hp1 HG01109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.503-947C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088575 | |||||||
| chr2:32088608 | C | T | 9 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-914C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088608 | |||||||
| chr2:32088717 | AC | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.503-804delC | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088717 | |||||||
| chr2:32088859 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-663G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088859 | |||||||
| chr2:32088981 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.503-541A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32088981 | |||||||
| chr2:32089057 | T | A | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG03139.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.503-465T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089057 | |||||||
| chr2:32089062 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(187): Show |
190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.503-460G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089062 | |||||||
| chr2:32089122 | T | C | 9 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0202 others(6): Show |
9 | HG00741.hp1 HG02055.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.503-400T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089122 | |||||||
| chr2:32089194 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.503-328G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089194 | |||||||
| chr2:32089199 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-313_503-304dup others(10): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32089199 | ||||||
| chr2:32089199 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0011g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.503-314_503-304dup others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32089199 | ||||||
| chr2:32089199 | AT | A | 14 | a0001c0001t0002g0234 a0001c0001t0002g0241 a0001c0001t0002g0259 others(11): Show |
14 | HG01169.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.503-304delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32089199 | ||||||
| chr2:32089199 | ATT | A | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.503-305_503-304del others(2): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32089199 | ||||||
| chr2:32089218 | T | C | 52 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(49): Show |
52 | HG00609.hp1 HG00609.hp2 HG01168.hp2 others(49): Show |
intron_variant | MODIFIER | c.503-304T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(4): Show |
4 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG02165.hp2 HG02258.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-304_503-303ins others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(5): Show |
82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(79): Show |
82 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.503-304_503-303ins others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(6): Show |
30 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0083 others(27): Show |
30 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.503-304_503-303ins others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(7): Show |
2 | a0001c0001t0001g0137 a0001c0001t0007g0187 |
2 | HG00741.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.503-304_503-303ins others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(11): Show |
1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.503-304_503-303ins others(18): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(13): Show |
3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0067 |
3 | HG03491.hp2 HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.503-304_503-303ins others(20): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(14): Show |
1 | a0001c0001t0003g0066 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.503-304_503-303ins others(21): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089218 | T | TTTTTTTT others(24): Show |
1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.503-304_503-303ins others(31): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089218 | |||||||
| chr2:32089234 | C | G | 1 | a0001c0001t0007g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.503-288C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089234 | |||||||
| chr2:32089336 | C | A | 1 | a0001c0001t0002g0326 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.503-186C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089336 | |||||||
| chr2:32089403 | T | A | 1 | a0001c0001t0002g0328 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.503-119T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089403 | |||||||
| chr2:32089404 | A | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(193): Show |
196 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.503-118A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089404 | |||||||
| chr2:32089405 | A | T | 6 | a0001c0001t0003g0056 a0001c0001t0003g0063 a0001c0001t0003g0064 others(3): Show |
6 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.503-117A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089405 | |||||||
| chr2:32089451 | TG | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-68delG | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 32089451 | ||||||
| chr2:32089466 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.503-56C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 2/16 | chr2 | 32089466 | |||||||
| chr2:32089791 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.586+186G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32089791 | |||||||
| chr2:32090010 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.586+405C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090010 | |||||||
| chr2:32090057 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.586+452C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090057 | |||||||
| chr2:32090159 | C | A | 1 | a0001c0001t0002g0326 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.586+554C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090159 | |||||||
| chr2:32090333 | C | G | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.586+728C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090333 | |||||||
| chr2:32090341 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+736G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090341 | |||||||
| chr2:32090574 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.586+969A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090574 | |||||||
| chr2:32090591 | A | G | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.586+986A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090591 | |||||||
| chr2:32090802 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.586+1197C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090802 | |||||||
| chr2:32090894 | G | C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+1289G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090894 | |||||||
| chr2:32090915 | C | A | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.586+1310C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090915 | |||||||
| chr2:32090924 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.586+1319G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090924 | |||||||
| chr2:32090954 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.586+1349T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32090954 | |||||||
| chr2:32091245 | C | CTAT | 18 | a0001c0001t0002g0264 a0001c0001t0003g0024 a0001c0001t0003g0026 others(15): Show |
18 | HG00642.hp1 HG01109.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.586+1690_586+1692d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091245 | CTAT | C | 37 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0229 others(34): Show |
37 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.586+1690_586+1692d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091245 | CTATTAT | C | 86 | a0001c0001t0001g0076 a0001c0001t0001g0104 a0001c0001t0001g0122 others(83): Show |
86 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.586+1687_586+1692d others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091245 | CTATTATT others(2): Show |
C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(133): Show |
136 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.586+1684_586+1692d others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091245 | CTATTATT others(5): Show |
C | 37 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0082 others(34): Show |
37 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.586+1681_586+1692d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091245 | CTATTATT others(8): Show |
C | 1 | a0001c0001t0004g0293 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.586+1678_586+1692d others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091245 | CTATTATT others(11): Show |
C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0157 a0001c0001t0001g0167 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.586+1675_586+1692d others(20): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091245 | ||||||
| chr2:32091350 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.586+1745G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091350 | |||||||
| chr2:32091363 | C | T | 8 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0003g0063 others(5): Show |
8 | HG00408.hp2 HG01361.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.586+1758C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091363 | |||||||
| chr2:32091371 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.586+1766C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091371 | |||||||
| chr2:32091483 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.586+1878G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091483 | |||||||
| chr2:32091604 | G | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+1999G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091604 | |||||||
| chr2:32091633 | C | T | 2 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.586+2028C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091633 | |||||||
| chr2:32091817 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(81): Show |
84 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.586+2212G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091817 | |||||||
| chr2:32091841 | T | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.586+2236T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091841 | |||||||
| chr2:32091842 | AAAAT | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+2241_586+2244d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32091842 | ||||||
| chr2:32091852 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(84): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.586+2247A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091852 | |||||||
| chr2:32091956 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.586+2351C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091956 | |||||||
| chr2:32091959 | T | C | 5 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+2354T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091959 | |||||||
| chr2:32091962 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.586+2357A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32091962 | |||||||
| chr2:32092085 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+2480C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092085 | |||||||
| chr2:32092128 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.586+2523G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092128 | |||||||
| chr2:32092226 | C | T | 2 | a0001c0001t0002g0323 a0001c0001t0002g0328 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.586+2621C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092226 | |||||||
| chr2:32092238 | G | T | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+2633G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092238 | |||||||
| chr2:32092307 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.586+2702G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092307 | |||||||
| chr2:32092481 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.586+2876T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092481 | |||||||
| chr2:32092639 | G | T | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+3034G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092639 | |||||||
| chr2:32092655 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.586+3050C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092655 | |||||||
| chr2:32092733 | C | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+3128C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092733 | |||||||
| chr2:32092799 | G | C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+3194G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092799 | |||||||
| chr2:32092872 | T | C | 1 | a0001c0001t0011g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.586+3267T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092872 | |||||||
| chr2:32092971 | C | T | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+3366C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092971 | |||||||
| chr2:32092988 | C | T | 1 | a0001c0001t0003g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.586+3383C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32092988 | |||||||
| chr2:32093006 | C | CA | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(167): Show |
170 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.586+3414dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32093006 | ||||||
| chr2:32093006 | C | CAA | 19 | a0001c0001t0001g0079 a0001c0001t0001g0108 a0001c0001t0001g0112 others(16): Show |
19 | HG00621.hp2 HG00741.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.586+3413_586+3414d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32093006 | ||||||
| chr2:32093023 | C | T | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.586+3418C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093023 | |||||||
| chr2:32093033 | G | T | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+3428G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093033 | |||||||
| chr2:32093184 | G | A | 1 | a0001c0001t0014g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.586+3579G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093184 | |||||||
| chr2:32093303 | T | C | 8 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+3698T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093303 | |||||||
| chr2:32093305 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.586+3700C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093305 | |||||||
| chr2:32093310 | C | CA | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(161): Show |
164 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.586+3728dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32093310 | ||||||
| chr2:32093310 | C | CAA | 18 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0082 others(15): Show |
18 | HG00423.hp2 HG01123.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.586+3727_586+3728d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32093310 | ||||||
| chr2:32093310 | CA | C | 17 | a0001c0001t0002g0230 a0001c0001t0002g0277 a0001c0001t0002g0307 others(14): Show |
17 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.586+3728delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32093310 | ||||||
| chr2:32093355 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.586+3750A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093355 | |||||||
| chr2:32093359 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.586+3754C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093359 | |||||||
| chr2:32093422 | C | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.586+3817C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093422 | |||||||
| chr2:32093503 | A | C | 1 | a0001c0001t0007g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.586+3898A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093503 | |||||||
| chr2:32093563 | A | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.586+3958A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093563 | |||||||
| chr2:32093714 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.586+4109G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093714 | |||||||
| chr2:32093737 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(209): Show |
212 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.586+4132G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093737 | |||||||
| chr2:32093787 | ATAAATGA others(4): Show |
A | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586+4191_586+4201d others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32093787 | ||||||
| chr2:32093857 | C | T | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+4252C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093857 | |||||||
| chr2:32093924 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.586+4319A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093924 | |||||||
| chr2:32093971 | A | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.586+4366A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32093971 | |||||||
| chr2:32094068 | C | T | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+4463C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094068 | |||||||
| chr2:32094268 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-4528G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094268 | |||||||
| chr2:32094484 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | NA18971.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.587-4312C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094484 | |||||||
| chr2:32094533 | A | G | 38 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(35): Show |
38 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.587-4263A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094533 | |||||||
| chr2:32094583 | C | T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.587-4213C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094583 | |||||||
| chr2:32094626 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-4170T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094626 | |||||||
| chr2:32094645 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.587-4151C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094645 | |||||||
| chr2:32094821 | T | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0158 |
3 | HG00140.hp1 HG01109.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.587-3975T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094821 | |||||||
| chr2:32094911 | G | A | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-3885G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094911 | |||||||
| chr2:32094956 | G | A | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-3840G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094956 | |||||||
| chr2:32094964 | G | A | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-3832G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32094964 | |||||||
| chr2:32095045 | A | G | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-3751A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095045 | |||||||
| chr2:32095301 | T | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.587-3495T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095301 | |||||||
| chr2:32095396 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0110 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.587-3400G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095396 | |||||||
| chr2:32095409 | T | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.587-3387T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095409 | |||||||
| chr2:32095464 | G | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.587-3332G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095464 | |||||||
| chr2:32095474 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.587-3322G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095474 | |||||||
| chr2:32095481 | T | C | 1 | a0001c0001t0004g0256 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.587-3315T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095481 | |||||||
| chr2:32095507 | G | C | 1 | a0001c0001t0017g0169 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.587-3289G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095507 | |||||||
| chr2:32095572 | TA | T | 51 | a0001c0001t0001g0040 a0001c0001t0001g0102 a0001c0001t0001g0126 others(48): Show |
51 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.587-3210delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32095572 | ||||||
| chr2:32095861 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.587-2935G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095861 | |||||||
| chr2:32095876 | G | T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.587-2920G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095876 | |||||||
| chr2:32095877 | C | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.587-2919C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095877 | |||||||
| chr2:32095947 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.587-2849G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32095947 | |||||||
| chr2:32096153 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.587-2643G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096153 | |||||||
| chr2:32096160 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.587-2636C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096160 | |||||||
| chr2:32096218 | TGAGGTCA | T | 10 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.587-2576_587-2570d others(9): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32096218 | ||||||
| chr2:32096325 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-2471T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096325 | |||||||
| chr2:32096488 | C | T | 8 | a0001c0001t0002g0310 a0001c0001t0004g0216 a0001c0001t0004g0256 others(5): Show |
8 | HG01106.hp2 HG01261.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-2308C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096488 | |||||||
| chr2:32096747 | T | C | 9 | a0001c0001t0002g0310 a0001c0001t0004g0216 a0001c0001t0004g0256 others(6): Show |
9 | HG01106.hp2 HG01261.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.587-2049T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096747 | |||||||
| chr2:32096880 | C | CA | 6 | a0001c0001t0002g0322 a0001c0001t0003g0050 a0001c0001t0003g0059 others(3): Show |
6 | HG02723.hp1 HG02738.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1903dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32096880 | ||||||
| chr2:32096880 | CA | C | 6 | a0001c0001t0001g0119 a0001c0001t0002g0229 a0001c0001t0002g0312 others(3): Show |
6 | HG00438.hp2 HG02040.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1903delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32096880 | ||||||
| chr2:32096894 | C | A | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.587-1902C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096894 | |||||||
| chr2:32096904 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.587-1892A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32096904 | |||||||
| chr2:32097036 | T | C | 2 | a0001c0001t0002g0332 a0001c0001t0002g0339 |
2 | NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.587-1760T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097036 | |||||||
| chr2:32097068 | T | C | 2 | a0001c0001t0003g0061 a0001c0001t0003g0062 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.587-1728T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097068 | |||||||
| chr2:32097387 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.587-1409A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097387 | |||||||
| chr2:32097426 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-1370G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097426 | |||||||
| chr2:32097514 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.587-1282G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097514 | |||||||
| chr2:32097524 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.587-1272T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097524 | |||||||
| chr2:32097681 | CT | C | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1104delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32097681 | ||||||
| chr2:32097698 | C | CT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.587-1085dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 32097698 | ||||||
| chr2:32097838 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0093 others(2): Show |
5 | HG00408.hp2 NA19009.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-958C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097838 | |||||||
| chr2:32097854 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-942C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097854 | |||||||
| chr2:32097991 | C | G | 1 | a0001c0001t0006g0249 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.587-805C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32097991 | |||||||
| chr2:32098050 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.587-746T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32098050 | |||||||
| chr2:32098114 | T | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 |
3 | HG01257.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.587-682T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32098114 | |||||||
| chr2:32098179 | C | A | 9 | a0001c0001t0002g0310 a0001c0001t0004g0216 a0001c0001t0004g0256 others(6): Show |
9 | HG01106.hp2 HG01261.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.587-617C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32098179 | |||||||
| chr2:32098255 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.587-541C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32098255 | |||||||
| chr2:32098338 | T | C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-458T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32098338 | |||||||
| chr2:32098348 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.587-448A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 3/16 | chr2 | 32098348 | |||||||
| chr2:32098994 | T | C | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.682+103T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32098994 | |||||||
| chr2:32099003 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.682+112T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099003 | |||||||
| chr2:32099066 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.682+175G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099066 | |||||||
| chr2:32099155 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.682+264G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099155 | |||||||
| chr2:32099232 | G | A | 9 | a0001c0001t0002g0259 a0001c0001t0002g0262 a0001c0001t0002g0270 others(6): Show |
9 | NA18942.hp2 NA18943.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+341G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099232 | |||||||
| chr2:32099325 | G | T | 1 | a0001c0001t0007g0081 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.682+434G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099325 | |||||||
| chr2:32099619 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0140 |
2 | HG03688.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.682+728G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099619 | |||||||
| chr2:32099687 | C | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+796C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099687 | |||||||
| chr2:32099877 | T | C | 1 | a0001c0001t0003g0013 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.682+986T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32099877 | |||||||
| chr2:32099956 | T | TAGTGCTG others(1): Show |
183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.682+1069_682+1076d others(10): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32099956 | ||||||
| chr2:32100029 | A | G | 11 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(8): Show |
11 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.682+1138A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100029 | |||||||
| chr2:32100079 | A | G | 1 | a0001c0001t0002g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.682+1188A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100079 | |||||||
| chr2:32100131 | G | A | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+1240G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100131 | |||||||
| chr2:32100226 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.682+1335G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100226 | |||||||
| chr2:32100261 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.682+1370C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100261 | |||||||
| chr2:32100297 | G | A | 1 | a0001c0001t0025g0320 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.682+1406G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100297 | |||||||
| chr2:32100320 | C | CT | 12 | a0001c0001t0001g0076 a0001c0001t0001g0121 a0001c0001t0001g0140 others(9): Show |
12 | HG00609.hp2 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+1446dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32100320 | ||||||
| chr2:32100320 | CT | C | 56 | a0001c0001t0001g0040 a0001c0001t0001g0107 a0001c0001t0001g0145 others(53): Show |
56 | HG00558.hp1 HG00609.hp1 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.682+1446delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32100320 | ||||||
| chr2:32100345 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.682+1454G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100345 | |||||||
| chr2:32100467 | A | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.682+1576A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100467 | |||||||
| chr2:32100681 | G | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+1790G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100681 | |||||||
| chr2:32100727 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.682+1836T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100727 | |||||||
| chr2:32100729 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.682+1838C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100729 | |||||||
| chr2:32100765 | C | G | 1 | a0001c0001t0005g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.682+1874C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32100765 | |||||||
| chr2:32101050 | T | G | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.682+2159T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101050 | |||||||
| chr2:32101078 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.682+2187C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101078 | |||||||
| chr2:32101096 | G | A | 20 | a0001c0001t0001g0111 a0001c0001t0002g0226 a0001c0001t0002g0227 others(17): Show |
20 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.682+2205G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101096 | |||||||
| chr2:32101134 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.682+2243G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101134 | |||||||
| chr2:32101144 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.682+2253A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101144 | |||||||
| chr2:32101168 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.682+2277C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101168 | |||||||
| chr2:32101206 | G | T | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2315G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101206 | |||||||
| chr2:32101283 | A | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.682+2392A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101283 | |||||||
| chr2:32101437 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.682+2546C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101437 | |||||||
| chr2:32101456 | CTTTAG | C | 8 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+2570_682+2574d others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32101456 | ||||||
| chr2:32101488 | T | G | 2 | a0001c0001t0002g0285 a0001c0001t0002g0286 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.682+2597T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101488 | |||||||
| chr2:32101616 | T | G | 1 | a0001c0001t0002g0264 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.682+2725T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101616 | |||||||
| chr2:32101678 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.682+2787C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101678 | |||||||
| chr2:32101740 | C | G | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.682+2849C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101740 | |||||||
| chr2:32101952 | A | G | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.682+3061A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32101952 | |||||||
| chr2:32102004 | C | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+3113C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102004 | |||||||
| chr2:32102006 | G | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+3115G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102006 | |||||||
| chr2:32102272 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.682+3381T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102272 | |||||||
| chr2:32102310 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.682+3419C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102310 | |||||||
| chr2:32102357 | T | G | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+3466T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102357 | |||||||
| chr2:32102413 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.682+3522C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102413 | |||||||
| chr2:32102422 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.682+3531G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102422 | |||||||
| chr2:32102518 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.682+3627T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102518 | |||||||
| chr2:32102681 | G | C | 1 | a0001c0001t0003g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.682+3790G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102681 | |||||||
| chr2:32102685 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.682+3794G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102685 | |||||||
| chr2:32102814 | T | A | 1 | a0001c0001t0027g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.682+3923T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32102814 | |||||||
| chr2:32103144 | G | A | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.682+4253G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103144 | |||||||
| chr2:32103152 | T | C | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+4261T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103152 | |||||||
| chr2:32103201 | G | A | 4 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+4310G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103201 | |||||||
| chr2:32103408 | A | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.682+4517A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103408 | |||||||
| chr2:32103542 | C | T | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.682+4651C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103542 | |||||||
| chr2:32103631 | A | G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.682+4740A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103631 | |||||||
| chr2:32103717 | C | G | 1 | a0001c0001t0016g0334 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.682+4826C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103717 | |||||||
| chr2:32103769 | G | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.682+4878G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103769 | |||||||
| chr2:32103898 | A | G | 1 | a0001c0001t0002g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.682+5007A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103898 | |||||||
| chr2:32103976 | A | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.682+5085A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32103976 | |||||||
| chr2:32104240 | T | G | 1 | a0001c0001t0007g0165 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.682+5349T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104240 | |||||||
| chr2:32104330 | T | G | 1 | a0001c0001t0002g0278 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.682+5439T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104330 | |||||||
| chr2:32104411 | C | T | 1 | a0001c0001t0004g0201 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.682+5520C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104411 | |||||||
| chr2:32104434 | G | A | 22 | a0001c0001t0002g0189 a0001c0001t0002g0217 a0001c0001t0002g0218 others(19): Show |
22 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.682+5543G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104434 | |||||||
| chr2:32104519 | G | A | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+5628G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104519 | |||||||
| chr2:32104549 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.682+5658A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104549 | |||||||
| chr2:32104576 | G | C | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+5685G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104576 | |||||||
| chr2:32104590 | C | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.682+5699C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104590 | |||||||
| chr2:32104610 | C | T | 1 | a0001c0001t0003g0022 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+5719C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104610 | |||||||
| chr2:32104618 | C | A | 1 | a0001c0001t0002g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.682+5727C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104618 | |||||||
| chr2:32104661 | T | G | 1 | a0001c0001t0003g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.682+5770T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104661 | |||||||
| chr2:32104773 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.682+5882A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104773 | |||||||
| chr2:32104824 | G | C | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+5933G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32104824 | |||||||
| chr2:32105018 | C | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(330): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.682+6127C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105018 | |||||||
| chr2:32105072 | G | A | 1 | a0001c0001t0011g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.682+6181G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105072 | |||||||
| chr2:32105177 | C | G | 1 | a0001c0001t0002g0215 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+6286C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105177 | |||||||
| chr2:32105187 | T | A | 6 | a0001c0001t0003g0036 a0001c0001t0003g0041 a0001c0001t0003g0042 others(3): Show |
6 | NA18950.hp2 NA18952.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6296T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105187 | |||||||
| chr2:32105201 | T | A | 1 | a0001c0001t0002g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.682+6310T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105201 | |||||||
| chr2:32105209 | C | T | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG03139.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682+6318C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105209 | |||||||
| chr2:32105211 | A | G | 5 | a0001c0001t0004g0194 a0001c0001t0004g0198 a0001c0001t0013g0068 others(2): Show |
5 | HG01891.hp1 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+6320A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105211 | |||||||
| chr2:32105245 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.682+6354G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105245 | |||||||
| chr2:32105413 | C | T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.682+6522C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105413 | |||||||
| chr2:32105534 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.682+6643G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105534 | |||||||
| chr2:32105678 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 |
3 | HG01257.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.682+6787C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105678 | |||||||
| chr2:32105738 | TTTGCCTG others(17): Show |
T | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.682+6848_682+6871d others(26): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105738 | |||||||
| chr2:32105816 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(163): Show |
166 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.682+6925C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105816 | |||||||
| chr2:32105872 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+6981T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105872 | |||||||
| chr2:32105936 | C | T | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.682+7045C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32105936 | |||||||
| chr2:32106171 | C | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.682+7280C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106171 | |||||||
| chr2:32106190 | G | A | 1 | a0001c0001t0026g0240 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.682+7299G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106190 | |||||||
| chr2:32106238 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0241 |
2 | NA18964.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.682+7347C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106238 | |||||||
| chr2:32106272 | T | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.682+7381T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106272 | |||||||
| chr2:32106362 | C | T | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+7471C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106362 | |||||||
| chr2:32106404 | G | A | 2 | a0001c0001t0014g0200 a0001c0001t0014g0204 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.682+7513G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106404 | |||||||
| chr2:32106431 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.682+7540C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106431 | |||||||
| chr2:32106442 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(75): Show |
78 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.682+7551A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106442 | |||||||
| chr2:32106475 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.682+7584C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106475 | |||||||
| chr2:32106519 | G | C | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+7628G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106519 | |||||||
| chr2:32106556 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.682+7665T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106556 | |||||||
| chr2:32106648 | G | A | 5 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+7757G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106648 | |||||||
| chr2:32106685 | A | T | 1 | a0001c0001t0002g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.682+7794A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106685 | |||||||
| chr2:32106696 | C | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.682+7805C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106696 | |||||||
| chr2:32106889 | GA | G | 10 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-7737delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32106889 | ||||||
| chr2:32106896 | A | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-7742A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106896 | |||||||
| chr2:32106940 | G | C | 28 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(25): Show |
28 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.683-7698G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32106940 | |||||||
| chr2:32107095 | G | A | 1 | a0001c0001t0002g0322 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.683-7543G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107095 | |||||||
| chr2:32107254 | A | T | 1 | a0001c0001t0007g0091 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.683-7384A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107254 | |||||||
| chr2:32107293 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.683-7345C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107293 | |||||||
| chr2:32107294 | G | T | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.683-7344G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107294 | |||||||
| chr2:32107474 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.683-7164G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107474 | |||||||
| chr2:32107516 | G | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01243.hp2 HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.683-7122G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107516 | |||||||
| chr2:32107568 | T | C | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.683-7070T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107568 | |||||||
| chr2:32107665 | T | C | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-6973T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107665 | |||||||
| chr2:32107740 | A | G | 4 | a0001c0001t0004g0205 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | HG01070.hp1 HG01261.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-6898A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107740 | |||||||
| chr2:32107800 | A | C | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.683-6838A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107800 | |||||||
| chr2:32107836 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.683-6802G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107836 | |||||||
| chr2:32107848 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.683-6790C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107848 | |||||||
| chr2:32107901 | C | G | 1 | a0001c0001t0002g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.683-6737C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32107901 | |||||||
| chr2:32108158 | G | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-6480G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108158 | |||||||
| chr2:32108159 | T | C | 1 | a0001c0001t0011g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.683-6479T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108159 | |||||||
| chr2:32108275 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.683-6363C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108275 | |||||||
| chr2:32108364 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.683-6274C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108364 | |||||||
| chr2:32108462 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.683-6176G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108462 | |||||||
| chr2:32108520 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.683-6118A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108520 | |||||||
| chr2:32108522 | T | A | 1 | a0001c0001t0002g0327 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.683-6116T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108522 | |||||||
| chr2:32108524 | A | T | 5 | a0001c0001t0002g0324 a0001c0001t0002g0326 a0001c0001t0002g0327 others(2): Show |
5 | HG00438.hp1 HG00673.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-6114A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108524 | |||||||
| chr2:32108556 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.683-6082C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108556 | |||||||
| chr2:32108640 | G | A | 1 | a0001c0001t0002g0296 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.683-5998G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108640 | |||||||
| chr2:32108697 | C | T | 1 | a0001c0001t0011g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.683-5941C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108697 | |||||||
| chr2:32108758 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(95): Show |
98 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.683-5855dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32108758 | ||||||
| chr2:32108758 | C | CTT | 90 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0001g0079 others(87): Show |
90 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.683-5856_683-5855d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32108758 | ||||||
| chr2:32108758 | C | CTTT | 28 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0100 others(25): Show |
28 | HG00609.hp1 HG01123.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.683-5857_683-5855d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32108758 | ||||||
| chr2:32108797 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.683-5841A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108797 | |||||||
| chr2:32108888 | C | T | 1 | a0001c0001t0002g0288 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.683-5750C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108888 | |||||||
| chr2:32108890 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-5748T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108890 | |||||||
| chr2:32108956 | G | T | 2 | a0001c0001t0002g0285 a0001c0001t0002g0286 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.683-5682G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32108956 | |||||||
| chr2:32109000 | G | A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.683-5638G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109000 | |||||||
| chr2:32109164 | A | C | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.683-5474A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109164 | |||||||
| chr2:32109259 | C | T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.683-5379C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109259 | |||||||
| chr2:32109400 | C | T | 1 | a0001c0001t0004g0201 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.683-5238C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109400 | |||||||
| chr2:32109427 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.683-5211A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109427 | |||||||
| chr2:32109428 | A | T | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.683-5210A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109428 | |||||||
| chr2:32109475 | G | T | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.683-5163G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109475 | |||||||
| chr2:32109736 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.683-4902A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109736 | |||||||
| chr2:32109779 | T | C | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.683-4859T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109779 | |||||||
| chr2:32109780 | GCACATAC others(23): Show |
G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-4829_683-4800d others(32): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32109780 | ||||||
| chr2:32109784 | A | G | 129 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0189 others(126): Show |
129 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.683-4854A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109784 | |||||||
| chr2:32109875 | T | TACATATA others(23): Show |
120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.683-4733_683-4704d others(32): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32109875 | ||||||
| chr2:32109875 | T | TACATATA others(24): Show |
1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.683-4743_683-4742i others(33): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32109875 | ||||||
| chr2:32109905 | C | CACATATA others(23): Show |
2 | a0001c0001t0004g0198 a0001c0001t0004g0199 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.683-4707_683-4678d others(32): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32109905 | ||||||
| chr2:32109926 | A | G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-4712A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109926 | |||||||
| chr2:32109949 | CATATGT | C | 5 | a0001c0001t0003g0047 a0001c0001t0008g0005 a0001c0001t0008g0007 others(2): Show |
5 | HG02083.hp2 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-4672_683-4667d others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32109949 | ||||||
| chr2:32109982 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-4656T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32109982 | |||||||
| chr2:32110030 | A | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.683-4608A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110030 | |||||||
| chr2:32110052 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.683-4586A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110052 | |||||||
| chr2:32110104 | GT | G | 6 | a0001c0001t0003g0017 a0001c0001t0003g0063 a0001c0001t0003g0064 others(3): Show |
6 | HG01361.hp2 HG03486.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-4522delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110104 | ||||||
| chr2:32110104 | GTT | G | 57 | a0001c0001t0001g0040 a0001c0001t0001g0086 a0001c0001t0001g0090 others(54): Show |
57 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(54): Show |
intron_variant | MODIFIER | c.683-4523_683-4522d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110104 | ||||||
| chr2:32110104 | GTTT | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.683-4524_683-4522d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110104 | ||||||
| chr2:32110113 | T | G | 1 | a0001c0001t0003g0073 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.683-4525T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110113 | |||||||
| chr2:32110114 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.683-4524T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110114 | |||||||
| chr2:32110115 | T | G | 1 | a0001c0001t0009g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.683-4523T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110115 | |||||||
| chr2:32110118 | T | G | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | NA18972.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.683-4520T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110118 | |||||||
| chr2:32110227 | TCCTGCTT others(14): Show |
T | 2 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.683-4406_683-4386d others(23): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110227 | ||||||
| chr2:32110275 | C | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-4363C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110275 | |||||||
| chr2:32110407 | C | T | 11 | a0001c0001t0003g0188 a0001c0001t0004g0205 a0001c0001t0004g0206 others(8): Show |
11 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.683-4231C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110407 | |||||||
| chr2:32110499 | A | AGTATATA others(24): Show |
5 | a0001c0001t0002g0218 a0001c0001t0002g0230 a0001c0001t0002g0239 others(2): Show |
5 | HG00741.hp1 HG02071.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-4087_683-4057d others(33): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110499 | ||||||
| chr2:32110499 | A | AGTATATA others(55): Show |
1 | a0001c0001t0002g0241 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.683-4118_683-4057d others(64): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110499 | ||||||
| chr2:32110499 | AGTATATA others(24): Show |
A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.683-4087_683-4057d others(33): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110499 | ||||||
| chr2:32110527 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.683-4111G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110527 | |||||||
| chr2:32110528 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.683-4110T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110528 | |||||||
| chr2:32110529 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.683-4109G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110529 | |||||||
| chr2:32110530 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.683-4108T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110530 | |||||||
| chr2:32110539 | A | AGTATATA others(24): Show |
2 | a0001c0001t0002g0217 a0001c0001t0002g0325 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.683-4069_683-4068i others(33): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110539 | ||||||
| chr2:32110551 | C | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4087C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110551 | |||||||
| chr2:32110553 | A | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4085A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110553 | |||||||
| chr2:32110558 | G | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4080G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110558 | |||||||
| chr2:32110559 | T | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4079T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110559 | |||||||
| chr2:32110560 | G | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4078G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110560 | |||||||
| chr2:32110561 | T | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4077T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110561 | |||||||
| chr2:32110569 | T | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4069T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110569 | |||||||
| chr2:32110571 | G | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4067G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110571 | |||||||
| chr2:32110575 | A | ATATATAG others(27): Show |
2 | a0001c0001t0004g0198 a0001c0001t0004g0212 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.683-4046_683-4013d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110575 | ||||||
| chr2:32110576 | T | G | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-4062T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110576 | |||||||
| chr2:32110592 | C | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4046C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110592 | |||||||
| chr2:32110599 | A | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4039A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110599 | |||||||
| chr2:32110600 | C | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4038C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110600 | |||||||
| chr2:32110602 | C | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4036C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110602 | |||||||
| chr2:32110609 | C | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4029C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110609 | |||||||
| chr2:32110611 | ATATAGTG others(15): Show |
A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-4024_683-4003d others(24): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110611 | ||||||
| chr2:32110626 | A | C | 1 | a0001c0001t0001g0340 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.683-4012A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110626 | |||||||
| chr2:32110633 | G | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4005G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110633 | |||||||
| chr2:32110638 | A | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-4000A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110638 | |||||||
| chr2:32110642 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.683-3996A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110642 | |||||||
| chr2:32110656 | A | G | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-3982A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110656 | |||||||
| chr2:32110658 | A | ATATAGT | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3980_683-3979i others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110658 | |||||||
| chr2:32110666 | T | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-3972T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110666 | |||||||
| chr2:32110667 | A | ACT | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3971_683-3970i others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110667 | |||||||
| chr2:32110667 | A | AGTATATA others(15): Show |
1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-3956_683-3935d others(24): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110667 | ||||||
| chr2:32110667 | A | T | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-3971A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110667 | |||||||
| chr2:32110738 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(186): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.683-3900G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110738 | |||||||
| chr2:32110761 | A | ATATAGTA others(21): Show |
6 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0120 others(3): Show |
6 | HG00597.hp2 HG00741.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3851_683-3824d others(30): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110761 | ||||||
| chr2:32110761 | A | ATATAGTA others(245): Show |
1 | a0001c0001t0013g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.683-3868_683-3867i others(254): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110761 | ||||||
| chr2:32110761 | A | ATATAGTA others(273): Show |
1 | a0001c0001t0013g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.683-3868_683-3867i others(282): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110761 | ||||||
| chr2:32110761 | A | ATATAGTA others(329): Show |
1 | a0001c0001t0013g0341 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.683-3868_683-3867i others(338): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110761 | ||||||
| chr2:32110761 | ATATAGTA others(21): Show |
A | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683-3851_683-3824d others(30): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110761 | ||||||
| chr2:32110787 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0003g0053 |
2 | NA18994.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.683-3851T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110787 | |||||||
| chr2:32110788 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.683-3850A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110788 | |||||||
| chr2:32110789 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.683-3849G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110789 | |||||||
| chr2:32110794 | G | GAGTATAT others(31): Show |
1 | a0001c0001t0001g0124 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.683-3844_683-3843i others(40): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110794 | |||||||
| chr2:32110799 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.683-3839C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110799 | |||||||
| chr2:32110801 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.683-3837T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110801 | |||||||
| chr2:32110810 | A | ATATATAG | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3824_683-3823i others(9): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110810 | ||||||
| chr2:32110815 | G | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3823G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110815 | |||||||
| chr2:32110816 | T | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3822T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110816 | |||||||
| chr2:32110817 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03209.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-3821A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110817 | |||||||
| chr2:32110820 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3818T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110820 | |||||||
| chr2:32110822 | G | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3816G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110822 | |||||||
| chr2:32110822 | GAGTA | G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3815_683-3812d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110822 | |||||||
| chr2:32110826 | A | ATAC | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3810_683-3809i others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110826 | ||||||
| chr2:32110831 | T | C | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3807T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110831 | |||||||
| chr2:32110833 | C | T | 6 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3805C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110833 | |||||||
| chr2:32110840 | C | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3798C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110840 | |||||||
| chr2:32110842 | A | ATACATAG | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3794_683-3793i others(9): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110842 | ||||||
| chr2:32110845 | T | TCG | 3 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0021g0065 |
3 | HG01361.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.683-3793_683-3792i others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110845 | |||||||
| chr2:32110845 | T | TCGTGTGT others(29): Show |
2 | a0001c0001t0003g0063 a0001c0001t0003g0064 |
2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.683-3793_683-3792i others(38): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110845 | |||||||
| chr2:32110846 | A | AGT | 3 | a0001c0001t0001g0085 a0001c0001t0001g0124 a0001c0001t0003g0055 |
3 | HG03139.hp2 NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.683-3791_683-3790d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(29): Show |
30 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0082 others(27): Show |
30 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.683-3790_683-3789i others(38): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(63): Show |
94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(91): Show |
94 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.683-3790_683-3789i others(72): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(97): Show |
34 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0127 others(31): Show |
34 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.683-3790_683-3789i others(106): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(131): Show |
3 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0003g0029 |
3 | NA18953.hp1 NA18971.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.683-3790_683-3789i others(140): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(97): Show |
7 | a0001c0001t0003g0010 a0001c0001t0003g0013 a0001c0001t0003g0023 others(4): Show |
7 | HG02723.hp1 HG02738.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-3790_683-3789i others(106): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(63): Show |
1 | a0001c0001t0003g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.683-3790_683-3789i others(72): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(29): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0173 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.683-3790_683-3789i others(38): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | AGTGTGTA others(63): Show |
1 | a0001c0001t0001g0157 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.683-3790_683-3789i others(72): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110846 | ||||||
| chr2:32110846 | A | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-3792A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110846 | |||||||
| chr2:32110847 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3791G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110847 | |||||||
| chr2:32110847 | G | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3791G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110847 | |||||||
| chr2:32110848 | T | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3790T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110848 | |||||||
| chr2:32110849 | A | ATATAGAG others(27): Show |
2 | a0001c0001t0002g0315 a0001c0001t0005g0192 |
2 | NA18522.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.683-3556_683-3523d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110849 | ||||||
| chr2:32110849 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.683-3789A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110849 | |||||||
| chr2:32110849 | ATATAGAG others(27): Show |
A | 6 | a0001c0001t0002g0228 a0001c0001t0004g0194 a0001c0001t0004g0225 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-3556_683-3523d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110849 | ||||||
| chr2:32110854 | G | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3784G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110854 | |||||||
| chr2:32110854 | GAGTATAT others(31): Show |
G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3783_683-3746d others(40): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110854 | |||||||
| chr2:32110860 | A | AG | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3778_683-3777i others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110860 | |||||||
| chr2:32110865 | C | CAGTATAC others(25): Show |
1 | a0001c0001t0003g0055 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.683-3761_683-3760i others(34): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110865 | ||||||
| chr2:32110865 | C | CAT | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3772_683-3771i others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32110865 | ||||||
| chr2:32110878 | C | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(105): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.683-3760C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110878 | |||||||
| chr2:32110879 | G | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3759G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110879 | |||||||
| chr2:32110880 | T | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3758T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110880 | |||||||
| chr2:32110883 | G | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3755G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110883 | |||||||
| chr2:32110890 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3748G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110890 | |||||||
| chr2:32110897 | T | C | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3741T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110897 | |||||||
| chr2:32110899 | C | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3739C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110899 | |||||||
| chr2:32110911 | TCG | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3726_683-3725d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110911 | |||||||
| chr2:32110912 | C | A | 31 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0082 others(28): Show |
31 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.683-3726C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110912 | |||||||
| chr2:32110914 | T | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3724T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110914 | |||||||
| chr2:32110917 | G | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3721G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110917 | |||||||
| chr2:32110924 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3714G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110924 | |||||||
| chr2:32110945 | TCG | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3692_683-3691d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110945 | |||||||
| chr2:32110946 | C | A | 8 | a0001c0001t0001g0085 a0001c0001t0003g0019 a0001c0001t0003g0020 others(5): Show |
8 | HG01109.hp1 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-3692C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110946 | |||||||
| chr2:32110947 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.683-3691G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110947 | |||||||
| chr2:32110948 | T | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3690T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110948 | |||||||
| chr2:32110951 | G | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3687G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110951 | |||||||
| chr2:32110958 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3680G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110958 | |||||||
| chr2:32110980 | C | A | 20 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0012 others(17): Show |
20 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.683-3658C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110980 | |||||||
| chr2:32110982 | T | C | 3 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0004g0198 |
3 | HG02257.hp2 HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.683-3656T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110982 | |||||||
| chr2:32110992 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3646G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32110992 | |||||||
| chr2:32111014 | C | A | 38 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(35): Show |
38 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(35): Show |
intron_variant | MODIFIER | c.683-3624C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111014 | |||||||
| chr2:32111026 | G | C | 2 | a0001c0001t0013g0069 a0001c0001t0013g0341 |
2 | HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3612G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111026 | |||||||
| chr2:32111030 | A | ATATACAG others(23): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0110 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.683-3603_683-3574d others(32): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111030 | ||||||
| chr2:32111048 | C | A | 41 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(38): Show |
41 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.683-3590C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111048 | |||||||
| chr2:32111048 | C | CGTGTGTA others(27): Show |
4 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0004g0031 others(1): Show |
4 | HG01516.hp2 HG02300.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-3557_683-3556i others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111048 | ||||||
| chr2:32111082 | C | A | 50 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(47): Show |
50 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-3556C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111082 | |||||||
| chr2:32111082 | C | CGTGTGTA others(27): Show |
4 | a0001c0001t0003g0024 a0001c0001t0003g0064 a0001c0001t0009g0070 others(1): Show |
4 | HG03471.hp2 HG03491.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-3443_683-3410d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111082 | ||||||
| chr2:32111082 | C | CGTGTGTA others(61): Show |
6 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0066 others(3): Show |
6 | HG01255.hp2 HG01496.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3477_683-3410d others(70): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111082 | ||||||
| chr2:32111082 | CGTGTGTA others(27): Show |
C | 12 | a0001c0001t0002g0221 a0001c0001t0002g0257 a0001c0001t0002g0258 others(9): Show |
12 | HG00099.hp1 HG00639.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-3443_683-3410d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111082 | ||||||
| chr2:32111082 | CGTGTGTA others(61): Show |
C | 1 | a0001c0001t0004g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.683-3477_683-3410d others(70): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111082 | ||||||
| chr2:32111116 | A | AGTGTGTA others(27): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | NA18955.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.683-3489_683-3488i others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111116 | ||||||
| chr2:32111116 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(78): Show |
81 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.683-3522A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111116 | |||||||
| chr2:32111127 | AGTATATA others(95): Show |
A | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-3477_683-3376d others(2): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111127 | ||||||
| chr2:32111150 | A | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(101): Show |
104 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.683-3488A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111150 | |||||||
| chr2:32111152 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.683-3486T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111152 | |||||||
| chr2:32111184 | A | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(31): Show |
34 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.683-3454A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111184 | |||||||
| chr2:32111195 | A | C | 6 | a0001c0001t0002g0230 a0001c0001t0004g0202 a0001c0001t0004g0247 others(3): Show |
6 | HG02451.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3443A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111195 | |||||||
| chr2:32111195 | AGTATATA others(27): Show |
A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.683-3356_683-3323d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111195 | ||||||
| chr2:32111214 | A | G | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.683-3424A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111214 | |||||||
| chr2:32111218 | A | C | 4 | a0001c0001t0001g0085 a0001c0001t0013g0068 a0001c0001t0013g0069 others(1): Show |
4 | HG01891.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-3420A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111218 | |||||||
| chr2:32111229 | C | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.683-3409C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111229 | |||||||
| chr2:32111248 | A | G | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-3390A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111248 | |||||||
| chr2:32111252 | A | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3386A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111252 | |||||||
| chr2:32111263 | C | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(171): Show |
174 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.683-3375C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111263 | |||||||
| chr2:32111264 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0003g0030 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.683-3374G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111264 | |||||||
| chr2:32111282 | A | ATATAGTG others(61): Show |
1 | a0001c0001t0009g0071 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.683-3342_683-3341i others(70): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111282 | ||||||
| chr2:32111282 | A | ATATAGTG others(27): Show |
1 | a0001c0001t0005g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.683-3297_683-3264d others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111282 | ||||||
| chr2:32111282 | A | G | 10 | a0001c0001t0004g0198 a0001c0001t0005g0196 a0001c0001t0006g0244 others(7): Show |
10 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-3356A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111282 | |||||||
| chr2:32111285 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.683-3353T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111285 | |||||||
| chr2:32111286 | A | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3352A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111286 | |||||||
| chr2:32111288 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.683-3350T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111288 | |||||||
| chr2:32111297 | C | A | 20 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(17): Show |
20 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.683-3341C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111297 | |||||||
| chr2:32111298 | G | A | 92 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(89): Show |
92 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.683-3340G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111298 | |||||||
| chr2:32111316 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(164): Show |
167 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.683-3322G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111316 | |||||||
| chr2:32111316 | G | GTATAGTG others(27): Show |
1 | a0001c0001t0001g0173 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.683-3307_683-3306i others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111316 | ||||||
| chr2:32111332 | G | A | 17 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(14): Show |
17 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.683-3306G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111332 | |||||||
| chr2:32111350 | G | A | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(13): Show |
16 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3288G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111350 | |||||||
| chr2:32111356 | T | C | 2 | a0001c0001t0004g0201 a0001c0001t0005g0192 |
2 | HG01106.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.683-3282T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111356 | |||||||
| chr2:32111365 | C | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(306): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.683-3273C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111365 | |||||||
| chr2:32111365 | C | CGTATATA others(27): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0267 |
2 | HG01515.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.683-3264_683-3263i others(36): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111365 | ||||||
| chr2:32111366 | GTATA | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-3267_683-3264d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111366 | ||||||
| chr2:32111373 | T | TAC | 25 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0082 others(22): Show |
25 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.683-3264_683-3263i others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111373 | ||||||
| chr2:32111388 | C | T | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(13): Show |
16 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3250C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111388 | |||||||
| chr2:32111391 | A | G | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(13): Show |
16 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3247A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111391 | |||||||
| chr2:32111394 | G | T | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(13): Show |
16 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3244G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111394 | |||||||
| chr2:32111397 | T | A | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(13): Show |
16 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3241T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111397 | |||||||
| chr2:32111398 | A | G | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(13): Show |
16 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3240A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111398 | |||||||
| chr2:32111420 | T | C | 18 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0001g0084 others(15): Show |
18 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.683-3218T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111420 | |||||||
| chr2:32111421 | G | A | 3 | a0001c0001t0003g0066 a0001c0001t0003g0067 a0001c0001t0021g0065 |
3 | HG01361.hp2 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.683-3217G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111421 | |||||||
| chr2:32111423 | A | G | 1 | a0001c0001t0004g0203 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.683-3215A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111423 | |||||||
| chr2:32111435 | T | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0028 |
2 | HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.683-3203T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111435 | |||||||
| chr2:32111453 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.683-3185A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111453 | |||||||
| chr2:32111482 | A | G | 10 | a0001c0001t0004g0205 a0001c0001t0004g0206 a0001c0001t0004g0207 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-3156A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111482 | |||||||
| chr2:32111552 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.683-3086C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111552 | |||||||
| chr2:32111588 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(180): Show |
183 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.683-3050C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111588 | |||||||
| chr2:32111610 | A | G | 129 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(126): Show |
129 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.683-3028A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111610 | |||||||
| chr2:32111624 | T | TTTTTTTT others(32): Show |
1 | a0001c0001t0014g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-3009_683-2971d others(41): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111624 | ||||||
| chr2:32111665 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.683-2973T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111665 | |||||||
| chr2:32111853 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-2785G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111853 | |||||||
| chr2:32111941 | T | A | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(328): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.683-2697T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111941 | |||||||
| chr2:32111970 | T | TTAG | 32 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0100 others(29): Show |
32 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.683-2627_683-2625d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | T | TTAGTAG | 34 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0117 others(31): Show |
34 | HG00140.hp1 HG00438.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.683-2630_683-2625d others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | T | TTAGTAGT others(2): Show |
19 | a0001c0001t0001g0101 a0001c0001t0001g0171 a0001c0001t0003g0011 others(16): Show |
19 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-2633_683-2625d others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | T | TTAGTAGT others(5): Show |
10 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0034 others(7): Show |
10 | HG01516.hp2 HG02723.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-2636_683-2625d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | T | TTAGTAGT others(8): Show |
1 | a0001c0001t0003g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683-2639_683-2625d others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | TTAG | T | 113 | a0001c0001t0001g0093 a0001c0001t0001g0167 a0001c0001t0002g0003 others(110): Show |
113 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.683-2627_683-2625d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | TTAGTAG | T | 3 | a0001c0001t0004g0199 a0001c0001t0004g0207 a0001c0001t0004g0208 |
3 | HG01069.hp2 HG01071.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.683-2630_683-2625d others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111970 | TTAGTAGT others(14): Show |
T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-2645_683-2625d others(23): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32111970 | ||||||
| chr2:32111985 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.683-2653G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32111985 | |||||||
| chr2:32112097 | C | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.683-2541C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112097 | |||||||
| chr2:32112140 | A | G | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-2498A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112140 | |||||||
| chr2:32112155 | G | A | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.683-2483G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112155 | |||||||
| chr2:32112177 | T | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-2461T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112177 | |||||||
| chr2:32112244 | C | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-2394C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112244 | |||||||
| chr2:32112245 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.683-2393G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112245 | |||||||
| chr2:32112322 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.683-2316C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112322 | |||||||
| chr2:32112342 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.683-2296G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112342 | |||||||
| chr2:32112346 | C | CT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.683-2276dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32112346 | ||||||
| chr2:32112346 | C | CTT | 9 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(6): Show |
9 | HG01109.hp2 HG01175.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.683-2277_683-2276d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32112346 | ||||||
| chr2:32112370 | C | T | 4 | a0001c0001t0002g0335 a0001c0001t0002g0336 a0001c0001t0002g0337 others(1): Show |
4 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-2268C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112370 | |||||||
| chr2:32112423 | C | T | 20 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0243 others(17): Show |
20 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.683-2215C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112423 | |||||||
| chr2:32112428 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.683-2210A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112428 | |||||||
| chr2:32112604 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.683-2034C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112604 | |||||||
| chr2:32112659 | G | GT | 48 | a0001c0001t0001g0040 a0001c0001t0003g0011 a0001c0001t0003g0012 others(45): Show |
48 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.683-1968dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32112659 | ||||||
| chr2:32112773 | A | G | 1 | a0001c0001t0014g0200 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-1865A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112773 | |||||||
| chr2:32112780 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0285 a0001c0001t0002g0286 others(1): Show |
4 | HG01496.hp1 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1858A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112780 | |||||||
| chr2:32112803 | G | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.683-1835G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112803 | |||||||
| chr2:32112814 | A | G | 4 | a0001c0001t0002g0335 a0001c0001t0002g0336 a0001c0001t0002g0337 others(1): Show |
4 | HG00738.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1824A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32112814 | |||||||
| chr2:32112837 | C | CT | 50 | a0001c0001t0001g0040 a0001c0001t0001g0153 a0001c0001t0003g0010 others(47): Show |
50 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-1792dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32112837 | ||||||
| chr2:32113132 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.683-1506A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113132 | |||||||
| chr2:32113135 | A | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(119): Show |
122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.683-1503A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113135 | |||||||
| chr2:32113365 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-1273G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113365 | |||||||
| chr2:32113367 | G | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-1271G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113367 | |||||||
| chr2:32113380 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.683-1258C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113380 | |||||||
| chr2:32113560 | C | CT | 10 | a0001c0001t0002g0189 a0001c0001t0002g0232 a0001c0001t0002g0296 others(7): Show |
10 | HG00621.hp1 HG01175.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1055dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32113560 | ||||||
| chr2:32113560 | CT | C | 68 | a0001c0001t0001g0040 a0001c0001t0001g0074 a0001c0001t0001g0079 others(65): Show |
68 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.683-1055delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32113560 | ||||||
| chr2:32113560 | CTT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.683-1056_683-1055d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32113560 | ||||||
| chr2:32113846 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.683-792T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113846 | |||||||
| chr2:32113859 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.683-779G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113859 | |||||||
| chr2:32113895 | G | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0087 others(4): Show |
7 | HG01934.hp1 HG01978.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-743G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113895 | |||||||
| chr2:32113921 | T | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0007g0081 |
3 | HG00408.hp2 NA19009.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.683-717T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113921 | |||||||
| chr2:32113971 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.683-667A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32113971 | |||||||
| chr2:32114056 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.683-582G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32114056 | |||||||
| chr2:32114077 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0018g0114 |
2 | HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.683-561G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32114077 | |||||||
| chr2:32114245 | T | TA | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-385dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | 32114245 | ||||||
| chr2:32114492 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.683-146C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32114492 | |||||||
| chr2:32114629 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.683-9C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 4/16 | chr2 | 32114629 | |||||||
| chr2:32114947 | A | G | 3 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 |
3 | HG02300.hp2 HG03927.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.870+122A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | chr2 | 32114947 | |||||||
| chr2:32114957 | A | AT | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(266): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.870+150dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 32114957 | ||||||
| chr2:32114957 | A | ATT | 19 | a0001c0001t0001g0102 a0001c0001t0001g0162 a0001c0001t0002g0226 others(16): Show |
19 | HG01109.hp1 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.870+149_870+150dup others(2): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 32114957 | ||||||
| chr2:32114957 | A | ATTT | 30 | a0001c0001t0001g0040 a0001c0001t0003g0012 a0001c0001t0003g0013 others(27): Show |
30 | HG00609.hp1 HG01168.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.870+148_870+150dup others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 32114957 | ||||||
| chr2:32115052 | G | A | 1 | a0001c0001t0014g0204 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.870+227G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | chr2 | 32115052 | |||||||
| chr2:32115068 | C | A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.870+243C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | chr2 | 32115068 | |||||||
| chr2:32115108 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.870+283C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | chr2 | 32115108 | |||||||
| chr2:32115413 | C | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(329): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.871-289C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | chr2 | 32115413 | |||||||
| chr2:32115655 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.871-47G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 5/16 | chr2 | 32115655 | |||||||
| chr2:32115888 | A | G | 1 | a0001c0001t0020g0183 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1004+53A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 6/16 | chr2 | 32115888 | |||||||
| chr2:32116038 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1005-81T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 6/16 | chr2 | 32116038 | |||||||
| chr2:32116317 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0142 |
2 | NA18969.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1098+105A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32116317 | |||||||
| chr2:32116330 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(187): Show |
190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1098+118A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32116330 | |||||||
| chr2:32116339 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1098+127A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32116339 | |||||||
| chr2:32116387 | A | G | 1 | a0001c0001t0003g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1098+175A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32116387 | |||||||
| chr2:32116674 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1098+462C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32116674 | |||||||
| chr2:32117158 | C | T | 1 | a0001c0001t0025g0320 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1098+946C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117158 | |||||||
| chr2:32117214 | C | G | 1 | a0001c0001t0004g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1098+1002C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117214 | |||||||
| chr2:32117230 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1098+1018C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117230 | |||||||
| chr2:32117274 | A | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 |
3 | HG01257.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1098+1062A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117274 | |||||||
| chr2:32117278 | A | G | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1098+1066A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117278 | |||||||
| chr2:32117390 | A | AGT | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098+1182_1098+118 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32117390 | ||||||
| chr2:32117439 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1098+1227A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117439 | |||||||
| chr2:32117470 | T | A | 4 | a0001c0001t0001g0001 a0001c0001t0013g0068 a0001c0001t0013g0069 others(1): Show |
4 | HG01891.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+1258T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117470 | |||||||
| chr2:32117531 | C | CT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1098+1336dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32117531 | ||||||
| chr2:32117531 | C | CTT | 13 | a0001c0001t0001g0088 a0001c0001t0001g0153 a0001c0001t0003g0188 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1098+1335_1098+133 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32117531 | ||||||
| chr2:32117819 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1098+1607A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117819 | |||||||
| chr2:32117839 | C | A | 1 | a0001c0001t0002g0306 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1098+1627C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117839 | |||||||
| chr2:32117920 | T | G | 2 | a0001c0001t0015g0261 a0001c0001t0015g0329 |
2 | HG01099.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1098+1708T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32117920 | |||||||
| chr2:32118098 | T | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1098+1886T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118098 | |||||||
| chr2:32118168 | C | T | 1 | a0001c0001t0004g0297 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1098+1956C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118168 | |||||||
| chr2:32118341 | A | G | 5 | a0001c0001t0002g0273 a0001c0001t0002g0335 a0001c0001t0002g0336 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+2129A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118341 | |||||||
| chr2:32118600 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1098+2388G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118600 | |||||||
| chr2:32118604 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1098+2392A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118604 | |||||||
| chr2:32118613 | G | A | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG03139.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1098+2401G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118613 | |||||||
| chr2:32118630 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1098+2418T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118630 | |||||||
| chr2:32118845 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1098+2633T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118845 | |||||||
| chr2:32118868 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1098+2656T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118868 | |||||||
| chr2:32118937 | T | C | 3 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 |
3 | HG00140.hp2 HG01258.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1098+2725T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118937 | |||||||
| chr2:32118950 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0139 others(1): Show |
4 | HG00408.hp1 HG02083.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+2738C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118950 | |||||||
| chr2:32118953 | G | A | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+2741G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32118953 | |||||||
| chr2:32119033 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1098+2821A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32119033 | |||||||
| chr2:32119299 | C | CAGTT | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0223 |
3 | NA18950.hp1 NA18972.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1098+3088_1098+308 others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32119299 | ||||||
| chr2:32119301 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0223 |
3 | NA18950.hp1 NA18972.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1098+3089C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32119301 | |||||||
| chr2:32119360 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1098+3148A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32119360 | |||||||
| chr2:32119619 | T | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0162 |
2 | HG00738.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1098+3407T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32119619 | |||||||
| chr2:32119648 | G | A | 4 | a0001c0001t0004g0205 a0001c0001t0004g0209 a0001c0001t0004g0210 others(1): Show |
4 | HG01070.hp1 HG01261.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+3436G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32119648 | |||||||
| chr2:32119765 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.1098+3553C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32119765 | |||||||
| chr2:32120026 | C | CT | 9 | a0001c0001t0002g0326 a0001c0001t0003g0034 a0001c0001t0008g0005 others(6): Show |
9 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1098+3827dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32120026 | ||||||
| chr2:32120054 | C | T | 49 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(46): Show |
49 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.1098+3842C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120054 | |||||||
| chr2:32120092 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0325 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1098+3880C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120092 | |||||||
| chr2:32120099 | C | G | 6 | a0001c0001t0004g0256 a0001c0001t0004g0292 a0001c0001t0004g0293 others(3): Show |
6 | HG01261.hp2 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1098+3887C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120099 | |||||||
| chr2:32120234 | A | C | 1 | a0001c0001t0002g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1098+4022A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120234 | |||||||
| chr2:32120256 | A | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(187): Show |
190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1098+4044A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120256 | |||||||
| chr2:32120276 | T | G | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1098+4064T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120276 | |||||||
| chr2:32120494 | T | C | 127 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(124): Show |
127 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1098+4282T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120494 | |||||||
| chr2:32120572 | C | CT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1098+4378dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32120572 | ||||||
| chr2:32120621 | T | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0052 |
2 | NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1098+4409T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120621 | |||||||
| chr2:32120734 | A | C | 1 | a0001c0001t0002g0308 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1098+4522A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32120734 | |||||||
| chr2:32121020 | T | C | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1098+4808T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121020 | |||||||
| chr2:32121228 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1098+5016C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121228 | |||||||
| chr2:32121284 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1098+5072C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121284 | |||||||
| chr2:32121424 | A | G | 128 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(125): Show |
128 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1098+5212A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121424 | |||||||
| chr2:32121433 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1098+5221G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121433 | |||||||
| chr2:32121535 | C | CT | 173 | a0001c0001t0001g0040 a0001c0001t0001g0110 a0001c0001t0001g0129 others(170): Show |
173 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1098+5346dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32121535 | ||||||
| chr2:32121558 | T | TA | 5 | a0001c0001t0002g0265 a0001c0001t0002g0281 a0001c0001t0002g0324 others(2): Show |
5 | HG00438.hp1 HG00673.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+5348dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32121558 | ||||||
| chr2:32121587 | C | T | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1099-5361C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121587 | |||||||
| chr2:32121705 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1099-5243G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121705 | |||||||
| chr2:32121833 | C | T | 1 | a0001c0001t0002g0330 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1099-5115C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121833 | |||||||
| chr2:32121859 | A | G | 1 | a0001c0001t0013g0341 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1099-5089A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121859 | |||||||
| chr2:32121895 | C | G | 3 | a0001c0001t0009g0070 a0001c0001t0009g0071 a0001c0001t0009g0072 |
3 | HG02055.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1099-5053C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121895 | |||||||
| chr2:32121981 | T | C | 3 | a0001c0001t0004g0201 a0001c0001t0004g0203 a0001c0001t0004g0212 |
3 | HG01106.hp1 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1099-4967T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32121981 | |||||||
| chr2:32122017 | A | G | 6 | a0001c0001t0001g0040 a0001c0001t0003g0039 a0001c0001t0003g0044 others(3): Show |
6 | NA18974.hp2 NA18986.hp1 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-4931A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122017 | |||||||
| chr2:32122073 | T | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1099-4875T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122073 | |||||||
| chr2:32122107 | A | C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-4841A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122107 | |||||||
| chr2:32122541 | C | T | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-4407C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122541 | |||||||
| chr2:32122646 | A | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1099-4302A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122646 | |||||||
| chr2:32122716 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1099-4232G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122716 | |||||||
| chr2:32122742 | C | A | 1 | a0001c0001t0014g0204 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1099-4206C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122742 | |||||||
| chr2:32122778 | TA | T | 84 | a0001c0001t0001g0182 a0001c0001t0002g0189 a0001c0001t0002g0217 others(81): Show |
84 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1099-4158delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32122778 | ||||||
| chr2:32122825 | G | A | 3 | a0001c0001t0003g0024 a0001c0001t0003g0026 a0001c0001t0003g0027 |
3 | HG02129.hp2 HG02155.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1099-4123G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32122825 | |||||||
| chr2:32123037 | A | G | 1 | a0001c0001t0004g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1099-3911A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32123037 | |||||||
| chr2:32123053 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-3895G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32123053 | |||||||
| chr2:32123135 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1099-3813G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32123135 | |||||||
| chr2:32123261 | C | CA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(170): Show |
173 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1099-3676dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32123261 | ||||||
| chr2:32123520 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1099-3428T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32123520 | |||||||
| chr2:32123896 | C | T | 1 | a0001c0001t0005g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1099-3052C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32123896 | |||||||
| chr2:32124003 | G | GA | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(166): Show |
169 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1099-2935dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32124003 | ||||||
| chr2:32124341 | A | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-2607A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32124341 | |||||||
| chr2:32124499 | TAC | T | 10 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1099-2447_1099-244 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32124499 | ||||||
| chr2:32124611 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1099-2337A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32124611 | |||||||
| chr2:32124696 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1099-2252A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32124696 | |||||||
| chr2:32124740 | A | T | 28 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(25): Show |
28 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1099-2208A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32124740 | |||||||
| chr2:32124744 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1099-2204T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32124744 | |||||||
| chr2:32125018 | T | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-1930T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125018 | |||||||
| chr2:32125257 | C | A | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1099-1691C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125257 | |||||||
| chr2:32125267 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1099-1681A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125267 | |||||||
| chr2:32125333 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1099-1615C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125333 | |||||||
| chr2:32125358 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1099-1590A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125358 | |||||||
| chr2:32125380 | C | T | 1 | a0001c0001t0006g0220 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1099-1568C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125380 | |||||||
| chr2:32125477 | C | T | 1 | a0001c0001t0008g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1099-1471C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125477 | |||||||
| chr2:32125502 | C | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-1446C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125502 | |||||||
| chr2:32125837 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1099-1111C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125837 | |||||||
| chr2:32125881 | G | A | 1 | a0001c0001t0004g0201 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1099-1067G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125881 | |||||||
| chr2:32125896 | G | A | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1052G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125896 | |||||||
| chr2:32125940 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1099-1008A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125940 | |||||||
| chr2:32125971 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1099-977A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125971 | |||||||
| chr2:32125995 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1099-953T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32125995 | |||||||
| chr2:32126101 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1099-847G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32126101 | |||||||
| chr2:32126122 | C | T | 1 | a0001c0001t0002g0330 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1099-826C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32126122 | |||||||
| chr2:32126197 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0161 |
3 | HG00558.hp2 HG00621.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1099-751G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32126197 | |||||||
| chr2:32126469 | C | CT | 38 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0129 others(35): Show |
38 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1099-450dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | C | CTT | 8 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0123 others(5): Show |
8 | HG00735.hp1 HG00738.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1099-451_1099-450d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | CT | C | 135 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(132): Show |
135 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1099-450delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | CTT | C | 7 | a0001c0001t0001g0111 a0001c0001t0002g0230 a0001c0001t0002g0276 others(4): Show |
7 | HG01258.hp1 HG02257.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1099-451_1099-450d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | CTTT | C | 6 | a0001c0001t0003g0021 a0001c0001t0003g0056 a0001c0001t0003g0057 others(3): Show |
6 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-452_1099-450d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0140 |
2 | HG03710.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1099-460_1099-450d others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0171 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1099-461_1099-450d others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126469 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-464_1099-450d others(17): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 32126469 | ||||||
| chr2:32126684 | C | G | 1 | a0001c0001t0003g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1099-264C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32126684 | |||||||
| chr2:32126817 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1099-131G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 7/16 | chr2 | 32126817 | |||||||
| chr2:32127117 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1173+95G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32127117 | |||||||
| chr2:32127422 | C | G | 1 | a0001c0001t0002g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1173+400C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32127422 | |||||||
| chr2:32127652 | T | C | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1173+630T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32127652 | |||||||
| chr2:32127655 | C | CT | 48 | a0001c0001t0001g0040 a0001c0001t0002g0289 a0001c0001t0003g0010 others(45): Show |
48 | HG00609.hp1 HG01099.hp2 HG01106.hp1 others(45): Show |
intron_variant | MODIFIER | c.1173+647dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 32127655 | ||||||
| chr2:32127849 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1174-559T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32127849 | |||||||
| chr2:32127944 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1174-464T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32127944 | |||||||
| chr2:32128086 | C | T | 46 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(43): Show |
46 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1174-322C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128086 | |||||||
| chr2:32128088 | G | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 |
3 | HG01257.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1174-320G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128088 | |||||||
| chr2:32128090 | G | A | 1 | a0001c0001t0002g0259 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1174-318G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128090 | |||||||
| chr2:32128094 | A | C | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1174-314A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128094 | |||||||
| chr2:32128103 | T | G | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0067 |
3 | HG03491.hp2 HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1174-305T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128103 | |||||||
| chr2:32128119 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(330): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1174-289T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128119 | |||||||
| chr2:32128143 | C | A | 1 | a0001c0001t0002g0321 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1174-265C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128143 | |||||||
| chr2:32128200 | G | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1174-208G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128200 | |||||||
| chr2:32128247 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1174-161G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128247 | |||||||
| chr2:32128254 | G | A | 28 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(25): Show |
28 | HG00408.hp2 HG00642.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1174-154G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128254 | |||||||
| chr2:32128255 | A | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1174-153A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 8/16 | chr2 | 32128255 | |||||||
| chr2:32128936 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1245+457G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32128936 | |||||||
| chr2:32128961 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1245+482C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32128961 | |||||||
| chr2:32129251 | A | AT | 121 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0145 others(118): Show |
121 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1245+788dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32129251 | ||||||
| chr2:32129377 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1245+898C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129377 | |||||||
| chr2:32129445 | C | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 |
3 | HG01255.hp2 HG01496.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1245+966C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129445 | |||||||
| chr2:32129489 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1245+1010C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129489 | |||||||
| chr2:32129560 | G | T | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1245+1081G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129560 | |||||||
| chr2:32129569 | T | C | 2 | a0001c0001t0004g0207 a0001c0001t0004g0208 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1245+1090T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129569 | |||||||
| chr2:32129704 | A | C | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+1225A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129704 | |||||||
| chr2:32129904 | C | T | 125 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(122): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1245+1425C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129904 | |||||||
| chr2:32129915 | C | G | 1 | a0001c0001t0002g0291 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1245+1436C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32129915 | |||||||
| chr2:32130014 | G | C | 1 | a0001c0001t0004g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1245+1535G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130014 | |||||||
| chr2:32130115 | G | A | 125 | a0001c0001t0002g0003 a0001c0001t0002g0189 a0001c0001t0002g0214 others(122): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1245+1636G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130115 | |||||||
| chr2:32130121 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1245+1642C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130121 | |||||||
| chr2:32130145 | A | G | 12 | a0001c0001t0002g0227 a0001c0001t0004g0025 a0001c0001t0004g0028 others(9): Show |
12 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1245+1666A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130145 | |||||||
| chr2:32130187 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1245+1708C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130187 | |||||||
| chr2:32130343 | ATACT | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1245+1867_1245+187 others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32130343 | ||||||
| chr2:32130421 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1245+1942C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130421 | |||||||
| chr2:32130470 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0075 others(74): Show |
77 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1245+1991G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130470 | |||||||
| chr2:32130548 | G | A | 1 | a0001c0001t0002g0330 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1245+2069G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130548 | |||||||
| chr2:32130553 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245+2074G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130553 | |||||||
| chr2:32130553 | G | T | 1 | a0001c0001t0011g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1245+2074G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130553 | |||||||
| chr2:32130611 | C | T | 2 | a0001c0001t0013g0068 a0001c0001t0013g0069 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1245+2132C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130611 | |||||||
| chr2:32130718 | C | CA | 37 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0102 others(34): Show |
37 | HG00438.hp2 HG00741.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.1245+2260dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32130718 | ||||||
| chr2:32130718 | CA | C | 9 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0241 others(6): Show |
9 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1245+2260delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32130718 | ||||||
| chr2:32130737 | AAATCCAG others(5): Show |
A | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1245+2272_1245+228 others(16): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32130737 | ||||||
| chr2:32130738 | AATCCAGA others(4): Show |
A | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1245+2261_1245+227 others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32130738 | ||||||
| chr2:32130886 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0004g0199 |
2 | HG00639.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1245+2407G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130886 | |||||||
| chr2:32130896 | T | C | 1 | a0001c0001t0003g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1245+2417T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130896 | |||||||
| chr2:32130978 | G | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+2499G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32130978 | |||||||
| chr2:32131379 | G | C | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245+2900G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131379 | |||||||
| chr2:32131539 | G | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(331): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1245+3060G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131539 | |||||||
| chr2:32131565 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1245+3086C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131565 | |||||||
| chr2:32131631 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0004g0222 a0001c0001t0010g0314 |
3 | NA18949.hp1 NA18955.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1245+3152G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131631 | |||||||
| chr2:32131633 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0004g0222 a0001c0001t0010g0314 |
3 | NA18949.hp1 NA18955.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1245+3154G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131633 | |||||||
| chr2:32131671 | C | CT | 118 | a0001c0001t0001g0109 a0001c0001t0001g0174 a0001c0001t0001g0175 others(115): Show |
118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1245+3213dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32131671 | ||||||
| chr2:32131671 | C | CTT | 11 | a0001c0001t0002g0217 a0001c0001t0002g0270 a0001c0001t0002g0278 others(8): Show |
11 | HG00438.hp1 HG00673.hp1 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.1245+3212_1245+321 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32131671 | ||||||
| chr2:32131671 | CT | C | 9 | a0001c0001t0001g0184 a0001c0001t0003g0012 a0001c0001t0003g0062 others(6): Show |
9 | HG01168.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1245+3213delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32131671 | ||||||
| chr2:32131691 | T | C | 1 | a0001c0001t0025g0320 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1245+3212T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131691 | |||||||
| chr2:32131811 | C | T | 1 | a0001c0001t0004g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1245+3332C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131811 | |||||||
| chr2:32131812 | G | A | 2 | a0001c0001t0014g0200 a0001c0001t0014g0204 |
2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1245+3333G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131812 | |||||||
| chr2:32131907 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1245+3428G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131907 | |||||||
| chr2:32131939 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+3460G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32131939 | |||||||
| chr2:32132050 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1245+3571C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132050 | |||||||
| chr2:32132087 | G | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+3608G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132087 | |||||||
| chr2:32132271 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1245+3792G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132271 | |||||||
| chr2:32132430 | C | T | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1245+3951C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132430 | |||||||
| chr2:32132431 | T | A | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1245+3952T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132431 | |||||||
| chr2:32132519 | A | G | 12 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 others(9): Show |
12 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1245+4040A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132519 | |||||||
| chr2:32132529 | CT | C | 56 | a0001c0001t0001g0040 a0001c0001t0003g0010 a0001c0001t0003g0011 others(53): Show |
56 | HG00609.hp1 HG01109.hp1 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.1246-4021delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32132529 | ||||||
| chr2:32132529 | CTT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(119): Show |
122 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1246-4022_1246-402 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32132529 | ||||||
| chr2:32132591 | C | T | 11 | a0001c0001t0004g0247 a0001c0001t0004g0253 a0001c0001t0004g0302 others(8): Show |
11 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1246-3972C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132591 | |||||||
| chr2:32132637 | C | T | 4 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0277 others(1): Show |
4 | HG00140.hp2 HG01099.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-3926C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132637 | |||||||
| chr2:32132909 | T | C | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1246-3654T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132909 | |||||||
| chr2:32132986 | C | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18967.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1246-3577C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32132986 | |||||||
| chr2:32133046 | C | CA | 129 | a0001c0001t0002g0003 a0001c0001t0002g0155 a0001c0001t0002g0189 others(126): Show |
129 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1246-3506dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32133046 | ||||||
| chr2:32133394 | C | G | 1 | a0001c0001t0002g0264 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1246-3169C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32133394 | |||||||
| chr2:32133422 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1246-3141C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32133422 | |||||||
| chr2:32133570 | A | C | 1 | a0001c0001t0003g0063 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1246-2993A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32133570 | |||||||
| chr2:32133655 | T | TA | 10 | a0001c0001t0001g0104 a0001c0001t0001g0150 a0001c0001t0002g0270 others(7): Show |
10 | HG01243.hp2 HG02486.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1246-2895dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32133655 | ||||||
| chr2:32133655 | TA | T | 7 | a0001c0001t0001g0040 a0001c0001t0008g0005 a0001c0001t0008g0007 others(4): Show |
7 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1246-2895delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32133655 | ||||||
| chr2:32133778 | GA | G | 10 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0093 others(7): Show |
10 | HG00408.hp2 HG02071.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.1246-2776delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32133778 | ||||||
| chr2:32133795 | A | C | 14 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 others(11): Show |
14 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1246-2768A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32133795 | |||||||
| chr2:32133938 | A | C | 1 | a0001c0001t0005g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1246-2625A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32133938 | |||||||
| chr2:32134028 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1246-2535C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134028 | |||||||
| chr2:32134073 | T | G | 1 | a0001c0001t0005g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1246-2490T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134073 | |||||||
| chr2:32134273 | C | T | 1 | a0001c0001t0003g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1246-2290C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134273 | |||||||
| chr2:32134298 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1246-2265C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134298 | |||||||
| chr2:32134463 | C | CA | 111 | a0001c0001t0002g0003 a0001c0001t0002g0155 a0001c0001t0002g0189 others(108): Show |
111 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1246-2088dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32134463 | ||||||
| chr2:32134667 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1246-1896G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134667 | |||||||
| chr2:32134683 | A | G | 1 | a0001c0001t0002g0234 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1246-1880A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134683 | |||||||
| chr2:32134708 | T | A | 1 | a0001c0001t0002g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1246-1855T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134708 | |||||||
| chr2:32134783 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1780A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134783 | |||||||
| chr2:32134784 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1779C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134784 | |||||||
| chr2:32134807 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1756C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134807 | |||||||
| chr2:32134820 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1743C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134820 | |||||||
| chr2:32134821 | G | C | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1742G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134821 | |||||||
| chr2:32134829 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1734G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134829 | |||||||
| chr2:32134831 | G | C | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1732G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134831 | |||||||
| chr2:32134832 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1731A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134832 | |||||||
| chr2:32134833 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1730T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134833 | |||||||
| chr2:32134856 | C | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0021 |
3 | HG01257.hp1 HG01258.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1246-1707C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134856 | |||||||
| chr2:32134985 | C | T | 1 | a0001c0001t0003g0015 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1246-1578C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32134985 | |||||||
| chr2:32135100 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1463C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135100 | |||||||
| chr2:32135101 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1462T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135101 | |||||||
| chr2:32135118 | T | TTG | 6 | a0001c0001t0002g0217 a0001c0001t0002g0228 a0001c0001t0002g0325 others(3): Show |
6 | HG01109.hp1 HG02970.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-1416_1246-141 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32135118 | ||||||
| chr2:32135118 | T | TTGTG | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(102): Show |
105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1246-1418_1246-141 others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32135118 | ||||||
| chr2:32135118 | T | TTGTGTG | 63 | a0001c0001t0001g0074 a0001c0001t0001g0084 a0001c0001t0001g0098 others(60): Show |
63 | HG01243.hp2 HG01257.hp1 HG01258.hp2 others(60): Show |
intron_variant | MODIFIER | c.1246-1420_1246-141 others(10): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32135118 | ||||||
| chr2:32135118 | T | TTGTGTGT others(1): Show |
8 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0015 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1246-1422_1246-141 others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 32135118 | ||||||
| chr2:32135164 | C | G | 1 | a0001c0001t0002g0328 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1246-1399C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135164 | |||||||
| chr2:32135199 | G | A | 2 | a0001c0001t0002g0332 a0001c0001t0002g0339 |
2 | NA18960.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1246-1364G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135199 | |||||||
| chr2:32135257 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-1306G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135257 | |||||||
| chr2:32135269 | A | G | 1 | a0001c0001t0004g0209 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1246-1294A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135269 | |||||||
| chr2:32135457 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1246-1106C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135457 | |||||||
| chr2:32135585 | G | T | 1 | a0001c0001t0002g0260 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1246-978G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135585 | |||||||
| chr2:32135654 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-909A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135654 | |||||||
| chr2:32135655 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-908T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135655 | |||||||
| chr2:32135657 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0167 |
2 | HG02258.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1246-906T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135657 | |||||||
| chr2:32135679 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0093 others(2): Show |
5 | HG00408.hp2 NA19009.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246-884G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135679 | |||||||
| chr2:32135757 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-806A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135757 | |||||||
| chr2:32135758 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-805G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135758 | |||||||
| chr2:32135759 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-804C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135759 | |||||||
| chr2:32135783 | A | G | 4 | a0001c0001t0003g0188 a0001c0001t0009g0070 a0001c0001t0009g0071 others(1): Show |
4 | HG02055.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-780A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135783 | |||||||
| chr2:32135795 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-768T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135795 | |||||||
| chr2:32135798 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-765C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135798 | |||||||
| chr2:32135818 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1246-745G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135818 | |||||||
| chr2:32135861 | C | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0214 a0001c0001t0002g0215 others(10): Show |
13 | HG01496.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1246-702C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135861 | |||||||
| chr2:32135869 | A | G | 2 | a0001c0001t0008g0008 a0001c0001t0008g0009 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1246-694A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135869 | |||||||
| chr2:32135989 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1246-574A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32135989 | |||||||
| chr2:32136152 | C | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1246-411C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136152 | |||||||
| chr2:32136162 | G | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1246-401G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136162 | |||||||
| chr2:32136167 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-396G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136167 | |||||||
| chr2:32136208 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1246-355T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136208 | |||||||
| chr2:32136252 | C | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-311C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136252 | |||||||
| chr2:32136270 | C | G | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1246-293C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136270 | |||||||
| chr2:32136288 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1246-275G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136288 | |||||||
| chr2:32136313 | G | A | 1 | a0001c0001t0007g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1246-250G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136313 | |||||||
| chr2:32136413 | T | TC | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1246-150_1246-149i others(3): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136413 | |||||||
| chr2:32136522 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG00438.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.1246-41G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 9/16 | chr2 | 32136522 | |||||||
| chr2:32137010 | G | GTATA | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(183): Show |
186 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1413+44_1413+47dup others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 32137010 | ||||||
| chr2:32137297 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1493+109T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137297 | |||||||
| chr2:32137315 | T | G | 2 | a0001c0001t0004g0198 a0001c0001t0004g0199 |
2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1493+127T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137315 | |||||||
| chr2:32137416 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1493+228G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137416 | |||||||
| chr2:32137604 | G | T | 10 | a0001c0001t0002g0310 a0001c0001t0004g0216 a0001c0001t0004g0256 others(7): Show |
10 | HG01106.hp2 HG01261.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.1493+416G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137604 | |||||||
| chr2:32137714 | T | C | 1 | a0001c0001t0007g0187 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1493+526T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137714 | |||||||
| chr2:32137740 | T | A | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1493+552T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137740 | |||||||
| chr2:32137744 | T | C | 1 | a0001c0001t0019g0156 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1493+556T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137744 | |||||||
| chr2:32137834 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1493+646C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32137834 | |||||||
| chr2:32138009 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1493+821G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32138009 | |||||||
| chr2:32138029 | G | T | 1 | a0001c0001t0003g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1493+841G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32138029 | |||||||
| chr2:32138102 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1493+914A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32138102 | |||||||
| chr2:32138344 | A | G | 1 | a0001c0001t0002g0306 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1493+1156A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32138344 | |||||||
| chr2:32138789 | T | C | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1493+1601T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32138789 | |||||||
| chr2:32139024 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(168): Show |
171 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1493+1836C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139024 | |||||||
| chr2:32139062 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(176): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1493+1874G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139062 | |||||||
| chr2:32139087 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1493+1899G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139087 | |||||||
| chr2:32139132 | A | C | 1 | a0001c0001t0005g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1493+1944A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139132 | |||||||
| chr2:32139144 | T | G | 11 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0012 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1493+1956T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139144 | |||||||
| chr2:32139172 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1493+1984T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139172 | |||||||
| chr2:32139262 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1493+2074C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139262 | |||||||
| chr2:32139579 | G | T | 45 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0012 others(42): Show |
45 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.1494-2325G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139579 | |||||||
| chr2:32139618 | A | C | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1494-2286A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139618 | |||||||
| chr2:32139666 | A | G | 14 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 others(11): Show |
14 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1494-2238A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139666 | |||||||
| chr2:32139673 | C | A | 2 | a0001c0001t0002g0318 a0001c0001t0002g0319 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1494-2231C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139673 | |||||||
| chr2:32139847 | AAAAG | A | 9 | a0001c0001t0002g0155 a0001c0001t0002g0259 a0001c0001t0002g0262 others(6): Show |
9 | NA18942.hp2 NA18943.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494-2053_1494-205 others(8): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 32139847 | ||||||
| chr2:32139953 | G | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(324): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1494-1951G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32139953 | |||||||
| chr2:32140092 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1494-1812G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140092 | |||||||
| chr2:32140094 | C | A | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494-1810C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140094 | |||||||
| chr2:32140357 | C | T | 9 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(6): Show |
9 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1494-1547C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140357 | |||||||
| chr2:32140572 | G | A | 1 | a0001c0001t0021g0065 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1494-1332G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140572 | |||||||
| chr2:32140573 | C | T | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1494-1331C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140573 | |||||||
| chr2:32140616 | C | CA | 7 | a0001c0001t0002g0288 a0001c0001t0002g0291 a0001c0001t0002g0296 others(4): Show |
7 | HG02055.hp2 HG02293.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1494-1277dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 32140616 | ||||||
| chr2:32140697 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1494-1207A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140697 | |||||||
| chr2:32140772 | A | AAAAAAAT others(317): Show |
8 | a0001c0001t0002g0310 a0001c0001t0004g0256 a0001c0001t0004g0292 others(5): Show |
8 | HG01106.hp2 HG01261.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1494-1116_1494-111 others(328): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 32140772 | ||||||
| chr2:32140772 | A | AAAAAAAT others(318): Show |
2 | a0001c0001t0004g0216 a0001c0001t0004g0295 |
2 | HG01934.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1494-1116_1494-111 others(329): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 32140772 | ||||||
| chr2:32140812 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1494-1092G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140812 | |||||||
| chr2:32140943 | GT | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(189): Show |
192 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1494-942delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 32140943 | ||||||
| chr2:32140946 | T | G | 2 | a0001c0001t0002g0279 a0001c0001t0022g0018 |
2 | HG00609.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1494-958T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140946 | |||||||
| chr2:32140947 | T | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1494-957T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140947 | |||||||
| chr2:32140949 | T | G | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1494-955T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140949 | |||||||
| chr2:32140950 | T | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1494-954T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140950 | |||||||
| chr2:32140952 | T | G | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1494-952T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140952 | |||||||
| chr2:32140953 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(166): Show |
169 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1494-951T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140953 | |||||||
| chr2:32140956 | T | G | 11 | a0001c0001t0001g0083 a0001c0001t0001g0089 a0001c0001t0001g0123 others(8): Show |
11 | HG00558.hp2 HG00738.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1494-948T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32140956 | |||||||
| chr2:32141201 | A | C | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1494-703A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32141201 | |||||||
| chr2:32141322 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1494-582A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32141322 | |||||||
| chr2:32141438 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1494-466G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 12/16 | chr2 | 32141438 | |||||||
| chr2:32142109 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1536+163C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142109 | |||||||
| chr2:32142203 | C | A | 1 | a0001c0001t0018g0114 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1536+257C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142203 | |||||||
| chr2:32142212 | A | G | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+266A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142212 | |||||||
| chr2:32142232 | T | C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1536+286T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142232 | |||||||
| chr2:32142283 | C | T | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+337C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142283 | |||||||
| chr2:32142484 | G | A | 1 | a0001c0001t0027g0144 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1536+538G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142484 | |||||||
| chr2:32142702 | C | A | 1 | a0001c0001t0002g0265 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1537-634C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142702 | |||||||
| chr2:32142742 | A | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1537-594A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142742 | |||||||
| chr2:32142827 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1537-509G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142827 | |||||||
| chr2:32142870 | C | T | 41 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0012 others(38): Show |
41 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.1537-466C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142870 | |||||||
| chr2:32142917 | G | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(177): Show |
180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1537-419G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142917 | |||||||
| chr2:32142997 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0325 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1537-339G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 13/16 | chr2 | 32142997 | |||||||
| chr2:32143635 | T | C | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1616+220T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32143635 | |||||||
| chr2:32143807 | T | G | 334 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(331): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1616+392T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32143807 | |||||||
| chr2:32143828 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0094 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1616+413C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32143828 | |||||||
| chr2:32143889 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1616+474A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32143889 | |||||||
| chr2:32144252 | T | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1617-685T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32144252 | |||||||
| chr2:32144394 | G | A | 7 | a0001c0001t0002g0324 a0001c0001t0002g0326 a0001c0001t0002g0327 others(4): Show |
7 | HG00438.hp1 HG00673.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1617-543G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32144394 | |||||||
| chr2:32144547 | T | C | 1 | a0001c0001t0002g0323 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1617-390T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32144547 | |||||||
| chr2:32144684 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0018g0114 |
3 | HG00099.hp2 HG01175.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1617-253G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32144684 | |||||||
| chr2:32144832 | T | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(326): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1617-105T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 14/16 | chr2 | 32144832 | |||||||
| chr2:32145036 | G | C | 1 | a0001c0001t0003g0188 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1687+29G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145036 | |||||||
| chr2:32145090 | G | A | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687+83G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145090 | |||||||
| chr2:32145189 | C | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(167): Show |
170 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1687+182C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145189 | |||||||
| chr2:32145275 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1687+268C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145275 | |||||||
| chr2:32145293 | C | T | 1 | a0001c0001t0004g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1687+286C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145293 | |||||||
| chr2:32145413 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1687+406C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145413 | |||||||
| chr2:32145490 | T | G | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1687+483T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145490 | |||||||
| chr2:32145496 | G | C | 1 | a0001c0001t0004g0216 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1687+489G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145496 | |||||||
| chr2:32145559 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1687+552C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145559 | |||||||
| chr2:32145650 | T | A | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(1): Show |
4 | HG03491.hp2 HG03669.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1687+643T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145650 | |||||||
| chr2:32145655 | A | AT | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1687+649dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32145655 | ||||||
| chr2:32145920 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1687+913T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32145920 | |||||||
| chr2:32146007 | A | G | 1 | a0001c0001t0008g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1687+1000A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146007 | |||||||
| chr2:32146040 | G | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687+1033G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146040 | |||||||
| chr2:32146174 | T | C | 3 | a0001c0001t0008g0007 a0001c0001t0008g0008 a0001c0001t0008g0009 |
3 | HG02258.hp1 HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1688-1044T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146174 | |||||||
| chr2:32146187 | A | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-1031A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146187 | |||||||
| chr2:32146263 | A | G | 1 | a0001c0001t0002g0336 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1688-955A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146263 | |||||||
| chr2:32146277 | G | A | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1688-941G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146277 | |||||||
| chr2:32146282 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1688-936G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146282 | |||||||
| chr2:32146313 | C | T | 1 | a0001c0001t0004g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1688-905C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146313 | |||||||
| chr2:32146419 | G | T | 1 | a0001c0001t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1688-799G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146419 | |||||||
| chr2:32146493 | G | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1688-725G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146493 | |||||||
| chr2:32146570 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1688-648A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146570 | |||||||
| chr2:32146631 | C | T | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1688-587C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146631 | |||||||
| chr2:32146640 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1688-578G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32146640 | |||||||
| chr2:32146801 | TTGCAGTA others(10): Show |
T | 7 | a0001c0001t0002g0189 a0001c0001t0002g0231 a0001c0001t0002g0232 others(4): Show |
7 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(4): Show |
intron_variant | MODIFIER | c.1688-411_1688-395d others(19): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146801 | ||||||
| chr2:32146851 | C | CA | 67 | a0001c0001t0001g0040 a0001c0001t0001g0074 a0001c0001t0001g0077 others(64): Show |
67 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1688-338dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32146851 | CA | C | 30 | a0001c0001t0002g0263 a0001c0001t0002g0285 a0001c0001t0002g0300 others(27): Show |
30 | HG01069.hp1 HG01069.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1688-338delA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32146851 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0003g0036 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1688-347_1688-338d others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32146851 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0166 a0001c0001t0003g0056 |
2 | HG01928.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1688-348_1688-338d others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32146851 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1688-350_1688-338d others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32146851 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0004g0225 a0001c0001t0004g0290 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1688-353_1688-338d others(18): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32146851 | CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0011g0004 a0001c0001t0011g0006 |
2 | HG01109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1688-355_1688-338d others(20): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 32146851 | ||||||
| chr2:32147027 | A | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1688-191A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 15/16 | chr2 | 32147027 | |||||||
| chr2:32147274 | A | G | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1728+16A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147274 | |||||||
| chr2:32147330 | ATG | A | 31 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0013 others(28): Show |
31 | HG01168.hp2 HG01169.hp2 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1728+85_1728+86del others(2): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147330 | ||||||
| chr2:32147342 | GT | G | 13 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(10): Show |
13 | HG01258.hp2 HG01891.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1728+85delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147342 | |||||||
| chr2:32147343 | T | G | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1728+85T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147343 | |||||||
| chr2:32147344 | G | T | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1728+86G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147344 | |||||||
| chr2:32147345 | G | GT | 17 | a0001c0001t0002g0218 a0001c0001t0002g0232 a0001c0001t0002g0234 others(14): Show |
17 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.1728+112dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147345 | ||||||
| chr2:32147345 | G | GTT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0076 others(75): Show |
78 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1728+111_1728+112d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147345 | ||||||
| chr2:32147345 | G | GTTT | 44 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0074 others(41): Show |
44 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1728+110_1728+112d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147345 | ||||||
| chr2:32147345 | G | GTTTT | 8 | a0001c0001t0001g0102 a0001c0001t0001g0108 a0001c0001t0001g0109 others(5): Show |
8 | HG02572.hp1 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1728+109_1728+112d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147345 | ||||||
| chr2:32147345 | G | GTTTTTTT others(3): Show |
3 | a0001c0001t0002g0335 a0001c0001t0002g0337 a0001c0001t0002g0338 |
3 | HG00738.hp1 HG02572.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1728+103_1728+112d others(12): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147345 | ||||||
| chr2:32147345 | G | T | 14 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0017 others(11): Show |
14 | HG00609.hp1 HG01258.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1728+87G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147345 | |||||||
| chr2:32147345 | GT | G | 84 | a0001c0001t0002g0003 a0001c0001t0002g0214 a0001c0001t0002g0221 others(81): Show |
84 | HG00140.hp2 HG00639.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.1728+112delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147345 | ||||||
| chr2:32147618 | TTTTG | T | 13 | a0001c0001t0002g0280 a0001c0001t0002g0308 a0001c0001t0004g0247 others(10): Show |
13 | HG01361.hp1 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1728+389_1728+392d others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147618 | ||||||
| chr2:32147629 | T | TGTTTG | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1728+372_1728+376d others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147629 | ||||||
| chr2:32147646 | G | GTTTGTTT others(5): Show |
7 | a0001c0001t0001g0098 a0001c0001t0001g0108 a0001c0001t0001g0136 others(4): Show |
7 | HG02055.hp2 HG02155.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1728+392_1728+393i others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147646 | ||||||
| chr2:32147646 | G | GTTTGTTT others(1): Show |
157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(154): Show |
157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1728+392_1728+393i others(10): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147646 | ||||||
| chr2:32147646 | G | GTTTT | 14 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0100 others(11): Show |
14 | HG01109.hp1 HG01361.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1728+391_1728+392i others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147646 | ||||||
| chr2:32147646 | G | T | 8 | a0001c0001t0001g0150 a0001c0001t0003g0059 a0001c0001t0003g0060 others(5): Show |
8 | HG01891.hp1 HG02723.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1728+388G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147646 | |||||||
| chr2:32147724 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1728+466C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147724 | |||||||
| chr2:32147724 | CG | C | 4 | a0001c0001t0002g0003 a0001c0001t0002g0285 a0001c0001t0002g0286 others(1): Show |
4 | HG01496.hp1 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728+469delG | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147724 | ||||||
| chr2:32147725 | G | A | 2 | a0001c0001t0003g0016 a0001c0001t0003g0017 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1728+467G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147725 | |||||||
| chr2:32147789 | G | A | 2 | a0001c0001t0003g0063 a0001c0001t0003g0064 |
2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1728+531G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147789 | |||||||
| chr2:32147849 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1728+591T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147849 | |||||||
| chr2:32147906 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0160 |
2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1728+648C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147906 | |||||||
| chr2:32147923 | G | A | 45 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0012 others(42): Show |
45 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.1728+665G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32147923 | |||||||
| chr2:32147930 | C | CT | 15 | a0001c0001t0002g0189 a0001c0001t0002g0254 a0001c0001t0002g0267 others(12): Show |
15 | HG00438.hp1 HG00741.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1728+691dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147930 | ||||||
| chr2:32147930 | C | CTT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(146): Show |
149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1728+690_1728+691d others(4): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147930 | ||||||
| chr2:32147930 | C | CTTT | 29 | a0001c0001t0001g0040 a0001c0001t0001g0108 a0001c0001t0001g0109 others(26): Show |
29 | HG00735.hp1 HG00741.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.1728+689_1728+691d others(5): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32147930 | ||||||
| chr2:32148174 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0023 |
2 | HG03831.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1728+916C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148174 | |||||||
| chr2:32148229 | C | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(169): Show |
172 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1728+971C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148229 | |||||||
| chr2:32148356 | A | G | 1 | a0001c0001t0011g0004 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1728+1098A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148356 | |||||||
| chr2:32148399 | C | T | 1 | a0001c0001t0004g0247 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1728+1141C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148399 | |||||||
| chr2:32148445 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(173): Show |
176 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1728+1187G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148445 | |||||||
| chr2:32148576 | G | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(117): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1728+1318G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148576 | |||||||
| chr2:32148581 | G | A | 4 | a0001c0001t0004g0025 a0001c0001t0004g0028 a0001c0001t0004g0031 others(1): Show |
4 | HG01255.hp2 HG01496.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1728+1323G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148581 | |||||||
| chr2:32148810 | C | CA | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0178 others(5): Show |
8 | HG02738.hp1 HG03486.hp2 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.1728+1567dupA | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32148810 | ||||||
| chr2:32148810 | C | CAA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(171): Show |
174 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.1728+1566_1728+156 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32148810 | ||||||
| chr2:32148810 | C | CAAA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0129 others(4): Show |
7 | HG00140.hp1 HG01978.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1728+1565_1728+156 others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32148810 | ||||||
| chr2:32148847 | G | A | 4 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1728+1589G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148847 | |||||||
| chr2:32148931 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1728+1673C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32148931 | |||||||
| chr2:32149169 | A | C | 1 | a0001c0001t0004g0199 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1728+1911A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149169 | |||||||
| chr2:32149213 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1728+1955C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149213 | |||||||
| chr2:32149256 | A | ATTTTT | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(176): Show |
179 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.1728+2008_1728+201 others(9): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32149256 | ||||||
| chr2:32149256 | A | ATTTTTT | 142 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0121 others(139): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1728+2007_1728+201 others(10): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32149256 | ||||||
| chr2:32149256 | A | ATTTTTTT | 8 | a0001c0001t0002g0238 a0001c0001t0002g0243 a0001c0001t0002g0260 others(5): Show |
8 | HG00597.hp1 HG01255.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.1728+2006_1728+201 others(11): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32149256 | ||||||
| chr2:32149327 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1728+2069G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149327 | |||||||
| chr2:32149508 | C | A | 2 | a0001c0001t0004g0225 a0001c0001t0004g0290 |
2 | HG02486.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1728+2250C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149508 | |||||||
| chr2:32149510 | C | T | 1 | a0001c0001t0002g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1728+2252C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149510 | |||||||
| chr2:32149533 | G | A | 1 | a0001c0001t0002g0260 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1728+2275G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149533 | |||||||
| chr2:32149563 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1728+2305G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149563 | |||||||
| chr2:32149853 | G | A | 2 | a0001c0001t0003g0061 a0001c0001t0003g0062 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1728+2595G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149853 | |||||||
| chr2:32149951 | G | A | 3 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 |
3 | HG03139.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1728+2693G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149951 | |||||||
| chr2:32149958 | C | G | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1728+2700C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32149958 | |||||||
| chr2:32150197 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1728+2939C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150197 | |||||||
| chr2:32150230 | G | A | 3 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0014 |
3 | HG01168.hp2 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1728+2972G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150230 | |||||||
| chr2:32150239 | A | AT | 8 | a0001c0001t0002g0331 a0001c0001t0002g0339 a0001c0001t0003g0012 others(5): Show |
8 | HG00438.hp1 HG01168.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1728+3005dupT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32150239 | ||||||
| chr2:32150239 | AT | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(222): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1728+3005delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32150239 | ||||||
| chr2:32150239 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0003g0055 a0001c0001t0003g0057 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1728+2995_1728+300 others(15): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32150239 | ||||||
| chr2:32150361 | G | C | 3 | a0001c0001t0013g0068 a0001c0001t0013g0069 a0001c0001t0013g0341 |
3 | HG01891.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1728+3103G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150361 | |||||||
| chr2:32150386 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1728+3128C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150386 | |||||||
| chr2:32150439 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1728+3181T>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150439 | |||||||
| chr2:32150542 | ATCC | A | 5 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG01361.hp2 HG03491.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1728+3289_1728+329 others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32150542 | ||||||
| chr2:32150576 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1728+3318T>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150576 | |||||||
| chr2:32150579 | G | A | 29 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0078 others(26): Show |
29 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1728+3321G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32150579 | |||||||
| chr2:32150951 | C | CTTTTTTT others(2): Show |
177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(174): Show |
177 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1729-3421_1729-341 others(13): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32150951 | ||||||
| chr2:32150951 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0127 a0001c0001t0003g0023 a0001c0001t0003g0044 others(1): Show |
4 | HG03831.hp1 NA18943.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1729-3422_1729-341 others(14): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32150951 | ||||||
| chr2:32151132 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(172): Show |
175 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1729-3242G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151132 | |||||||
| chr2:32151205 | A | C | 31 | a0001c0001t0003g0010 a0001c0001t0003g0011 a0001c0001t0003g0012 others(28): Show |
31 | HG00609.hp1 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1729-3169A>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151205 | |||||||
| chr2:32151234 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1729-3140T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151234 | |||||||
| chr2:32151480 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1729-2894A>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151480 | |||||||
| chr2:32151872 | C | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0186 |
3 | NA18953.hp1 NA18977.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1729-2502C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151872 | |||||||
| chr2:32151877 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1729-2497C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151877 | |||||||
| chr2:32151898 | C | A | 1 | a0001c0001t0002g0271 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1729-2476C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151898 | |||||||
| chr2:32151899 | G | A | 1 | a0001c0001t0022g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1729-2475G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32151899 | |||||||
| chr2:32152207 | T | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG01243.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1729-2167T>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32152207 | |||||||
| chr2:32152402 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1729-1972C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32152402 | |||||||
| chr2:32152522 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1729-1852A>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32152522 | |||||||
| chr2:32152615 | C | T | 1 | a0001c0001t0002g0324 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1729-1759C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32152615 | |||||||
| chr2:32152892 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1729-1482C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32152892 | |||||||
| chr2:32152893 | G | A | 6 | a0001c0001t0008g0005 a0001c0001t0008g0007 a0001c0001t0008g0008 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1729-1481G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32152893 | |||||||
| chr2:32153287 | G | A | 2 | a0001c0001t0002g0254 a0001c0001t0002g0279 |
2 | HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1729-1087G>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32153287 | |||||||
| chr2:32153318 | AT | A | 15 | a0001c0001t0001g0167 a0001c0001t0003g0010 a0001c0001t0004g0194 others(12): Show |
15 | HG01106.hp1 HG02055.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.1729-1033delT | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32153318 | ||||||
| chr2:32153318 | ATT | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0040 others(278): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1729-1034_1729-103 others(6): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32153318 | ||||||
| chr2:32153318 | ATTT | A | 28 | a0001c0001t0001g0083 a0001c0001t0001g0133 a0001c0001t0001g0141 others(25): Show |
28 | HG00639.hp1 HG01175.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1729-1035_1729-103 others(7): Show |
SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 32153318 | ||||||
| chr2:32153385 | C | A | 1 | a0001c0001t0004g0028 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1729-989C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32153385 | |||||||
| chr2:32153385 | C | G | 1 | a0001c0001t0003g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1729-989C>G | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32153385 | |||||||
| chr2:32153474 | C | T | 1 | a0001c0001t0003g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1729-900C>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32153474 | |||||||
| chr2:32153505 | G | T | 1 | a0001c0001t0002g0258 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1729-869G>T | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32153505 | |||||||
| chr2:32153535 | C | A | 128 | a0001c0001t0002g0003 a0001c0001t0002g0155 a0001c0001t0002g0189 others(125): Show |
128 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1729-839C>A | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32153535 | |||||||
| chr2:32154007 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1729-367G>C | SPAST | ENSG00000021574.14 | transcript | ENST00000315285.9 | protein_coding | 16/16 | chr2 | 32154007 |