Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 65244 |
|---|---|
| ensemblid | ENSG00000123352.18 |
| hgncid | 18650 |
| symbol | SPATS2 |
| name | spermatogenesis associated serine rich 2 |
| refseq_nuc | NM_023071.4 |
| refseq_prot | NP_075559.2 |
| ensembl_nuc | ENST00000552918.6 |
| ensembl_prot | ENSP00000447947.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 49367462 |
| end | 49527425 |
| strand | + |
| ver | v1.2 |
| region | chr12:49367462-49527425 |
| region5000 | chr12:49362462-49532425 |
| regionname0 | SPATS2_chr12_49367462_49527425 |
| regionname5000 | SPATS2_chr12_49362462_49532425 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 545 | 155 | 82 | 28 | 18 | 7 | 18 | 14 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0002 | 0/0 | 545 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0003 | 0/0 | 545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0004 | 0/0 | 545 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1638 | 153 | 80 | 28 | 18 | 7 | 18 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| c0002 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| c0003 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| c0004 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| c0005 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| c0006 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1603 | 101 | 42 | 20 | 17 | 7 | 13 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0002 | 0/0 | 1603 | 18 | 11 | 5 | 0 | 0 | 2 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0003 | 0/0 | 1604 | 14 | 11 | 0 | 1 | 0 | 2 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0004 | 0/0 | 1601 | 7 | 6 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0005 | 0/0 | 1604 | 5 | 4 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0006 | 0/0 | 1604 | 4 | 4 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0007 | 0/0 | 1600 | 2 | 2 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0008 | 0/0 | 1604 | 2 | 2 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0009 | 0/0 | 1603 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0010 | 0/0 | 1603 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0011 | 0/0 | 1604 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0012 | 0/0 | 1603 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| t0013 | 0/0 | 1603 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1638 | 153 | 80 | 28 | 18 | 7 | 18 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0003 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0005 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0002c0006 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0003c0004 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0004c0002 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3240 | 97 | 39 | 20 | 17 | 6 | 13 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0002 | 0/0 | 3240 | 17 | 10 | 5 | 0 | 0 | 2 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0003 | 0/0 | 3241 | 14 | 11 | 0 | 1 | 0 | 2 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0004 | 0/0 | 3238 | 7 | 6 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0005 | 0/0 | 3241 | 5 | 4 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0006 | 0/0 | 3241 | 4 | 4 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0007 | 0/0 | 3237 | 2 | 2 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0008 | 0/0 | 3241 | 2 | 2 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0009 | 0/0 | 3240 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0010 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0011 | 0/0 | 3241 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0012 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0001t0013 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0003t0001 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0001c0005t0001 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0002c0006t0001 | 0/0 | 3240 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0003c0004t0001 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| a0004c0002t0002 | 0/0 | 3240 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | copy fasta | chr12 | 49362462 | 49532425 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0015 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0121 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0011g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0001c0005t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0002c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0003c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| a0004c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00099 | hp2 | a0002 | c0006 | t0001 | g0136 | EUR | GBR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | CLM | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01361 | hp1 | a0001 | c0001 | t0009 | g0104 | AMR | CLM | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02717 | hp2 | a0003 | c0004 | t0001 | g0081 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0068 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03017 | hp1 | a0001 | c0001 | t0011 | g0042 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03225 | hp1 | a0004 | c0002 | t0002 | g0052 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0049 | AFR | ESN | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | STU | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | STU | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | YRI | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | YRI | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | LWK | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA19043 | hp2 | a0001 | c0005 | t0001 | g0064 | AFR | LWK | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ASW | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ASW | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0056 | EUR | TSI | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | GIH | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | USA | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | USA | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | LWK | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0015 | REF | REF | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0121 | REF | REF | SPATS2_chr12_49362462_49532425 | SPATS2 | chr12 | 49362462 | 49532425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49484605
|
T | C | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.41T>C | p.Ile14Thr | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/14 | 473/3240 | 41/1638 | 14/545 | chr12 | 49484605 | ||
| chr12:49490690
|
A | G | 1 | a0002 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.223A>G | p.Ser75Gly | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/14 | 655/3240 | 223/1638 | 75/545 | chr12 | 49490690 | ||
| chr12:49526116
|
T | C | 1 | a0003 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1499T>C | p.Ile500Thr | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 1931/3240 | 1499/1638 | 500/545 | chr12 | 49526116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49494926
|
T | G | 1 | a0001c0003 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.450T>G | p.Gly150Gly | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 7/14 | 882/3240 | 450/1638 | 150/545 | chr12 | 49494926 | ||
| chr12:49526243
|
C | T | 1 | a0001c0005 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1626C>T | p.Ala542Ala | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 2058/3240 | 1626/1638 | 542/545 | chr12 | 49526243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49367510
|
C | G | 1 | a0001c0001t0013 | 1 | NA20805.hp2 | 5_prime_UTR_variant | MODIFIER | c.-384C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/14 | 93503 | chr12 | 49367510 | |||||
| chr12:49367519
|
G | A | 1 | a0001c0001t0009 | 1 | HG01361.hp1 | 5_prime_UTR_variant | MODIFIER | c.-375G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/14 | 93494 | chr12 | 49367519 | |||||
| chr12:49460971
|
G | A | 1 | a0001c0001t0010 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/14 | 42 | chr12 | 49460971 | |||||
| chr12:49526360
|
T | TA | 2 | a0001c0001t0006a0001c0001t0011 | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*106dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 107 | INFO_REALIGN_3_PRIME | chr12 | 49526360 | ||||
| chr12:49526612
|
C | A | 2 | a0001c0001t0004a0001c0001t0007 | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*357C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 357 | chr12 | 49526612 | |||||
| chr12:49526948
|
G | A | 2 | a0001c0001t0004a0001c0001t0007 | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*693G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 693 | chr12 | 49526948 | |||||
| chr12:49526999
|
C | T | 1 | a0001c0001t0011 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*744C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 744 | chr12 | 49526999 | |||||
| chr12:49527077
|
A | G | 4 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(1): Show | 21 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*822A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 822 | chr12 | 49527077 | |||||
| chr12:49527178
|
G | C | 1 | a0001c0001t0012 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 923 | chr12 | 49527178 | |||||
| chr12:49527226
|
C | CA | 3 | a0001c0001t0003a0001c0001t0005a0001c0001t0008 | 21 | HG01346.hp1 HG02055.hp2 HG02145.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*987dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 988 | INFO_REALIGN_3_PRIME | chr12 | 49527226 | ||||
| chr12:49527242
|
A | AG | 1 | a0001c0001t0004 | 7 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*988dupG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 989 | INFO_REALIGN_3_PRIME | chr12 | 49527242 | ||||
| chr12:49527272
|
T | C | 1 | a0001c0001t0005 | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1017T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 1017 | chr12 | 49527272 | |||||
| chr12:49527403
|
AAAC | A | 2 | a0001c0001t0004a0001c0001t0007 | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1152_*1154delAAC | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 14/14 | 1152 | INFO_REALIGN_3_PRIME | chr12 | 49527403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49367596
|
A | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-307+9A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49367596 | ||||||
| chr12:49367743
|
A | G | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-307+156A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49367743 | ||||||
| chr12:49367793
|
G | C | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-307+206G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49367793 | ||||||
| chr12:49367840
|
T | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-307+253T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49367840 | ||||||
| chr12:49368405
|
C | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-307+818C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49368405 | ||||||
| chr12:49368437
|
T | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(37): Show | 40 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.-307+850T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49368437 | ||||||
| chr12:49368582
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-307+995G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49368582 | ||||||
| chr12:49368616
|
A | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-307+1029A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49368616 | ||||||
| chr12:49368623
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02622.hp2 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-307+1036C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49368623 | ||||||
| chr12:49368743
|
T | TTGTACTA others(9): Show |
1 | a0001c0001t0001g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-307+1158_-307+117 others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 49368743 | |||||
| chr12:49368796
|
C | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-307+1209C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49368796 | ||||||
| chr12:49369030
|
C | CT | 15 | a0001c0001t0001g0036a0001c0001t0001g0135a0001c0001t0001g0137others(12): Show | 15 | HG00099.hp2 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-307+1466dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 49369030 | |||||
| chr12:49369030
|
CT | C | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-307+1466delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 49369030 | |||||
| chr12:49369030
|
CTT | C | 32 | a0001c0001t0001g0058a0001c0001t0001g0155a0001c0001t0001g0156others(29): Show | 32 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.-307+1465_-307+146 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 49369030 | |||||
| chr12:49369030
|
CTTT | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0154a0001c0001t0003g0037others(2): Show | 5 | HG02630.hp1 HG03041.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-307+1464_-307+146 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 49369030 | |||||
| chr12:49369184
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-307+1597C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49369184 | ||||||
| chr12:49369341
|
A | G | 43 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0128others(40): Show | 43 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.-307+1754A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49369341 | ||||||
| chr12:49369392
|
T | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-307+1805T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49369392 | ||||||
| chr12:49369667
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-306-1561G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49369667 | ||||||
| chr12:49369827
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-306-1401A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49369827 | ||||||
| chr12:49369960
|
A | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-306-1268A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49369960 | ||||||
| chr12:49370085
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-306-1143G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 1/13 | chr12 | 49370085 | ||||||
| chr12:49371402
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+112C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49371402 | ||||||
| chr12:49371644
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-244+354C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49371644 | ||||||
| chr12:49371917
|
T | G | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-244+627T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49371917 | ||||||
| chr12:49371952
|
GT | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(133): Show | 136 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.-244+678delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49371952 | |||||
| chr12:49372313
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0002g0001 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-244+1023G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49372313 | ||||||
| chr12:49372324
|
C | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244+1034C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49372324 | ||||||
| chr12:49372366
|
G | C | 1 | a0001c0001t0002g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-244+1076G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49372366 | ||||||
| chr12:49372417
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-244+1127A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49372417 | ||||||
| chr12:49372798
|
T | C | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+1508T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49372798 | ||||||
| chr12:49372937
|
GT | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0071 | 3 | NA18988.hp2 NA19012.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-244+1651delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372937 | |||||
| chr12:49372940
|
T | TTG | 9 | a0001c0001t0001g0067a0001c0001t0001g0110a0001c0001t0001g0111others(6): Show | 9 | HG01515.hp2 HG01943.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+1701_-244+170 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTG | T | 19 | a0001c0001t0001g0040a0001c0001t0001g0066a0001c0001t0001g0069others(16): Show | 19 | HG01123.hp1 HG01175.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.-244+1701_-244+170 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTGTG | T | 27 | a0001c0001t0001g0036a0001c0001t0001g0078a0001c0001t0001g0080others(24): Show | 27 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-244+1699_-244+170 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTGTGTG | T | 23 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0075others(20): Show | 23 | HG00099.hp2 HG00280.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-244+1697_-244+170 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTGTGTGT others(1): Show |
T | 21 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0128others(18): Show | 21 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-244+1695_-244+170 others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTGTGTGT others(3): Show |
T | 8 | a0001c0001t0001g0072a0001c0001t0002g0047a0001c0001t0003g0037others(5): Show | 8 | HG01361.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-244+1693_-244+170 others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-244+1687_-244+170 others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372940
|
TTGTGTGT others(29): Show |
T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+1667_-244+170 others(40): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49372940 | |||||
| chr12:49372991
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+1701T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49372991 | ||||||
| chr12:49373012
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+1722G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373012 | ||||||
| chr12:49373033
|
C | T | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-244+1743C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373033 | ||||||
| chr12:49373087
|
G | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-244+1797G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373087 | ||||||
| chr12:49373089
|
C | T | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+1799C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373089 | ||||||
| chr12:49373607
|
C | CAT | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-244+2318_-244+231 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49373607 | |||||
| chr12:49373722
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-244+2432C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373722 | ||||||
| chr12:49373786
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-244+2496G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373786 | ||||||
| chr12:49373808
|
G | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+2518G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373808 | ||||||
| chr12:49373950
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-244+2660G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373950 | ||||||
| chr12:49373973
|
T | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-244+2683T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49373973 | ||||||
| chr12:49374262
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-244+2972A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374262 | ||||||
| chr12:49374338
|
A | G | 1 | a0001c0001t0013g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-244+3048A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374338 | ||||||
| chr12:49374424
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+3134C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374424 | ||||||
| chr12:49374473
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+3183A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374473 | ||||||
| chr12:49374726
|
C | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02809.hp2 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+3436C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374726 | ||||||
| chr12:49374859
|
G | C | 1 | a0001c0001t0002g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-244+3569G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374859 | ||||||
| chr12:49374958
|
C | CA | 40 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.-244+3695dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49374958 | |||||
| chr12:49374958
|
C | CAA | 37 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(34): Show | 37 | HG00639.hp2 HG01071.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.-244+3694_-244+369 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49374958 | |||||
| chr12:49374958
|
C | CAAA | 17 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0128others(14): Show | 17 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+3693_-244+369 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49374958 | |||||
| chr12:49374958
|
C | CAAAA | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+3692_-244+369 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49374958 | |||||
| chr12:49374999
|
T | C | 1 | a0001c0001t0011g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-244+3709T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49374999 | ||||||
| chr12:49375007
|
T | A | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-244+3717T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375007 | ||||||
| chr12:49375141
|
AGT | A | 9 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0077others(6): Show | 9 | HG00099.hp1 HG01069.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+3905_-244+390 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGT | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0095others(12): Show | 15 | HG01071.hp1 HG01346.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.-244+3903_-244+390 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGT | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0019others(20): Show | 23 | HG01978.hp1 HG02055.hp1 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.-244+3901_-244+390 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(1): Show |
A | 15 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0076others(12): Show | 15 | HG01074.hp1 HG01074.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-244+3899_-244+390 others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(3): Show |
A | 21 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0066others(18): Show | 21 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-244+3897_-244+390 others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(5): Show |
A | 12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(9): Show | 12 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-244+3895_-244+390 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-244+3893_-244+390 others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(9): Show |
A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+3891_-244+390 others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+3889_-244+390 others(22): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375141
|
AGTGTGTG others(17): Show |
A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+3883_-244+390 others(28): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375141 | |||||
| chr12:49375178
|
GTGTGTGT others(8): Show |
G | 2 | a0001c0001t0002g0047a0001c0001t0002g0063 | 2 | HG01361.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-244+3889_-244+390 others(19): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375178 | ||||||
| chr12:49375180
|
GTGTGTGT others(6): Show |
G | 8 | a0001c0001t0002g0048a0001c0001t0002g0059a0001c0001t0002g0149others(5): Show | 8 | HG02145.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-244+3891_-244+390 others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375180 | ||||||
| chr12:49375182
|
GTGTGTGT others(4): Show |
G | 13 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0054others(10): Show | 13 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-244+3893_-244+390 others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375182 | ||||||
| chr12:49375184
|
GTGTGTGT others(2): Show |
G | 6 | a0001c0001t0001g0013a0001c0001t0002g0007a0001c0001t0002g0055others(3): Show | 6 | HG01978.hp2 HG03195.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.-244+3895_-244+390 others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375184 | ||||||
| chr12:49375186
|
GTGTGTGT | G | 11 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+3897_-244+390 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375186 | ||||||
| chr12:49375188
|
GTGTGT | G | 6 | a0001c0001t0001g0018a0001c0001t0001g0133a0001c0001t0001g0154others(3): Show | 6 | HG01943.hp2 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-244+3899_-244+390 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375188 | ||||||
| chr12:49375190
|
GTGT | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0020a0001c0001t0011g0042 | 3 | HG00280.hp1 HG01123.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-244+3901_-244+390 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375190 | ||||||
| chr12:49375742
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0110 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-244+4452G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49375742 | ||||||
| chr12:49375817
|
C | CT | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+4536dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49375817 | |||||
| chr12:49376092
|
A | AT | 25 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(22): Show | 25 | HG01071.hp2 HG01123.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-244+4829dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376092 | |||||
| chr12:49376092
|
AT | A | 44 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0097others(41): Show | 44 | HG00639.hp2 HG01069.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.-244+4829delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376092 | |||||
| chr12:49376092
|
ATT | A | 5 | a0001c0001t0001g0154a0001c0001t0003g0037a0001c0001t0003g0038others(2): Show | 5 | HG02486.hp1 HG03041.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+4828_-244+482 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376092 | |||||
| chr12:49376092
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0004g0068a0001c0001t0004g0123 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-244+4818_-244+482 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376092 | |||||
| chr12:49376301
|
C | T | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-244+5011C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376301 | ||||||
| chr12:49376406
|
A | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+5116A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376406 | ||||||
| chr12:49376543
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-244+5253C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376543 | ||||||
| chr12:49376545
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+5255T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376545 | ||||||
| chr12:49376684
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-244+5394A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376684 | ||||||
| chr12:49376709
|
AT | A | 98 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(95): Show | 98 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.-244+5445delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376709 | |||||
| chr12:49376709
|
ATT | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0095a0001c0001t0002g0048others(16): Show | 19 | HG01346.hp1 HG02257.hp1 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.-244+5444_-244+544 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376709 | |||||
| chr12:49376709
|
ATTT | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(15): Show | 18 | HG00280.hp1 HG01071.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-244+5443_-244+544 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49376709 | |||||
| chr12:49376741
|
G | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+5451G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376741 | ||||||
| chr12:49376742
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-244+5452G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376742 | ||||||
| chr12:49376876
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-244+5586G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49376876 | ||||||
| chr12:49377219
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-244+5929G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49377219 | ||||||
| chr12:49377223
|
A | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+5933A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49377223 | ||||||
| chr12:49377998
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+6708A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49377998 | ||||||
| chr12:49378012
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+6722A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49378012 | ||||||
| chr12:49378083
|
C | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+6793C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49378083 | ||||||
| chr12:49378261
|
G | GTTTAT | 17 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(14): Show | 17 | HG01069.hp2 HG01515.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+7013_-244+701 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49378261 | |||||
| chr12:49378261
|
G | GTTTATTT others(3): Show |
15 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(12): Show | 15 | HG00280.hp1 HG01071.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-244+7008_-244+701 others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49378261 | |||||
| chr12:49378261
|
G | GTTTATTT others(8): Show |
7 | a0001c0001t0004g0041a0001c0001t0005g0022a0001c0001t0005g0023others(4): Show | 7 | HG02257.hp1 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244+7003_-244+701 others(19): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49378261 | |||||
| chr12:49378261
|
G | GTTTATTT others(18): Show |
1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-244+6993_-244+701 others(29): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49378261 | |||||
| chr12:49378261
|
GTTTAT | G | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02258.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-244+7013_-244+701 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49378261 | |||||
| chr12:49378261
|
GTTTATTT others(3): Show |
G | 10 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0002g0051others(7): Show | 10 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-244+7008_-244+701 others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49378261 | |||||
| chr12:49378635
|
G | A | 9 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(6): Show | 9 | HG01346.hp1 HG02257.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+7345G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49378635 | ||||||
| chr12:49378677
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-244+7387C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49378677 | ||||||
| chr12:49378873
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0015 | 2 | HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-244+7583G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49378873 | ||||||
| chr12:49379089
|
T | A | 1 | a0001c0001t0001g0111 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-244+7799T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49379089 | ||||||
| chr12:49379212
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+7922G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49379212 | ||||||
| chr12:49379550
|
C | CA | 29 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(26): Show | 29 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-244+8278dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49379550 | |||||
| chr12:49379550
|
C | CAA | 8 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-244+8277_-244+827 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49379550 | |||||
| chr12:49379550
|
C | CAAAA | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+8275_-244+827 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49379550 | |||||
| chr12:49379623
|
A | AT | 12 | a0001c0001t0001g0142a0001c0001t0003g0012a0001c0001t0003g0016others(9): Show | 12 | HG01175.hp2 HG01346.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-244+8351dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49379623 | |||||
| chr12:49379705
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-244+8415C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49379705 | ||||||
| chr12:49379707
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-244+8417C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49379707 | ||||||
| chr12:49379821
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+8531C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49379821 | ||||||
| chr12:49379923
|
T | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-244+8633T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49379923 | ||||||
| chr12:49380081
|
A | G | 1 | a0002c0006t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-244+8791A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380081 | ||||||
| chr12:49380135
|
T | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+8845T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380135 | ||||||
| chr12:49380167
|
C | CT | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-244+8894dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49380167 | |||||
| chr12:49380403
|
A | G | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG01167.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-244+9113A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380403 | ||||||
| chr12:49380413
|
A | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+9123A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380413 | ||||||
| chr12:49380433
|
C | T | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-244+9143C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380433 | ||||||
| chr12:49380471
|
C | T | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-244+9181C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380471 | ||||||
| chr12:49380480
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+9190C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380480 | ||||||
| chr12:49380483
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+9193A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380483 | ||||||
| chr12:49380600
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+9310A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380600 | ||||||
| chr12:49380705
|
C | CA | 31 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+9425dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49380705 | |||||
| chr12:49380714
|
A | AT | 6 | a0001c0001t0001g0100a0001c0001t0006g0043a0001c0001t0006g0044others(3): Show | 6 | HG00741.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-244+9424_-244+942 others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380714 | ||||||
| chr12:49380714
|
A | T | 3 | a0001c0001t0006g0046a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-244+9424A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380714 | ||||||
| chr12:49380716
|
T | A | 30 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(27): Show | 30 | HG01346.hp1 HG01891.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-244+9426T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380716 | ||||||
| chr12:49380777
|
A | G | 28 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0071others(25): Show | 28 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-244+9487A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380777 | ||||||
| chr12:49380881
|
CT | C | 10 | a0001c0001t0001g0154a0001c0001t0004g0041a0001c0001t0004g0068others(7): Show | 10 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-244+9606delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49380881 | |||||
| chr12:49380977
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+9687C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49380977 | ||||||
| chr12:49381008
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-244+9718C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381008 | ||||||
| chr12:49381046
|
T | TTTG | 2 | a0001c0001t0001g0070a0001c0001t0001g0113 | 2 | NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-244+9780_-244+978 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49381046 | |||||
| chr12:49381046
|
TTTG | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+9780_-244+978 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49381046 | |||||
| chr12:49381097
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-244+9807T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381097 | ||||||
| chr12:49381183
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+9893G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381183 | ||||||
| chr12:49381385
|
A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+10095A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381385 | ||||||
| chr12:49381429
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+10139A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381429 | ||||||
| chr12:49381703
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+10413A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381703 | ||||||
| chr12:49381834
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+10544C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381834 | ||||||
| chr12:49381892
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-244+10602A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49381892 | ||||||
| chr12:49382118
|
A | G | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02647.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-244+10828A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49382118 | ||||||
| chr12:49382229
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+10939C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49382229 | ||||||
| chr12:49382443
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+11153C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49382443 | ||||||
| chr12:49382444
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-244+11154G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49382444 | ||||||
| chr12:49382854
|
G | A | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-244+11564G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49382854 | ||||||
| chr12:49383154
|
A | T | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+11864A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383154 | ||||||
| chr12:49383333
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-244+12043T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383333 | ||||||
| chr12:49383428
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+12138T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383428 | ||||||
| chr12:49383464
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-244+12174G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383464 | ||||||
| chr12:49383533
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-244+12243C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383533 | ||||||
| chr12:49383689
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-244+12399A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383689 | ||||||
| chr12:49383701
|
C | A | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-244+12411C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49383701 | ||||||
| chr12:49384058
|
T | C | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-244+12768T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384058 | ||||||
| chr12:49384286
|
T | G | 1 | a0001c0001t0007g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-244+12996T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384286 | ||||||
| chr12:49384321
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+13031A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384321 | ||||||
| chr12:49384594
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0099 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-244+13304A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384594 | ||||||
| chr12:49384811
|
T | G | 1 | a0001c0001t0002g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-244+13521T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384811 | ||||||
| chr12:49384813
|
A | AT | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+13536dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49384813 | |||||
| chr12:49384887
|
G | A | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+13597G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384887 | ||||||
| chr12:49384958
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-244+13668C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49384958 | ||||||
| chr12:49385098
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+13808T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385098 | ||||||
| chr12:49385101
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+13811A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385101 | ||||||
| chr12:49385136
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+13846T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385136 | ||||||
| chr12:49385280
|
C | CA | 14 | a0001c0001t0001g0145a0001c0001t0003g0027a0001c0001t0003g0028others(11): Show | 14 | HG01167.hp1 HG02135.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-244+14002dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385280 | |||||
| chr12:49385293
|
C | A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+14003C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385293 | ||||||
| chr12:49385357
|
A | AGT | 34 | a0001c0001t0001g0033a0001c0001t0001g0067a0001c0001t0001g0070others(31): Show | 34 | HG00639.hp1 HG00741.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.-244+14099_-244+14 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
A | AGTGT | 17 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0107others(14): Show | 17 | HG00280.hp2 HG01346.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+14097_-244+14 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
A | AGTGTGT | 13 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0014others(10): Show | 13 | HG00639.hp2 HG01071.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-244+14095_-244+14 others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
A | AGTGTGTG others(1): Show |
21 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG01069.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-244+14093_-244+14 others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(9): Show | 12 | HG01192.hp1 HG01361.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-244+14091_-244+14 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
A | AGTGTGTG others(5): Show |
10 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0002g0051others(7): Show | 10 | HG01167.hp1 HG01175.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-244+14089_-244+14 others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
A | AGTGTGTG others(7): Show |
3 | a0001c0001t0002g0151a0001c0001t0004g0068a0001c0001t0004g0123 | 3 | HG01884.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-244+14087_-244+14 others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385357
|
AGT | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0127 | 2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-244+14099_-244+14 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385357 | |||||
| chr12:49385624
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+14334C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385624 | ||||||
| chr12:49385670
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+14380T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385670 | ||||||
| chr12:49385767
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-244+14477T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385767 | ||||||
| chr12:49385826
|
G | GT | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-244+14536_-244+14 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385826 | ||||||
| chr12:49385827
|
G | GT | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+14545dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385827 | |||||
| chr12:49385827
|
G | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-244+14537G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385827 | ||||||
| chr12:49385836
|
G | GTTTT | 16 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(13): Show | 16 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-244+14549_-244+14 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385836 | |||||
| chr12:49385839
|
TTTTG | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0106others(2): Show | 5 | HG02572.hp1 HG03239.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-244+14577_-244+14 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385839 | |||||
| chr12:49385862
|
TG | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.-244+14573delG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49385862 | ||||||
| chr12:49385863
|
G | GTTT | 43 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(40): Show | 43 | HG01167.hp1 HG01361.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.-244+14574_-244+14 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385863 | |||||
| chr12:49385863
|
G | GTTTGTTT | 5 | a0001c0001t0002g0053a0001c0001t0002g0054a0001c0001t0002g0061others(2): Show | 5 | HG00639.hp2 HG01192.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+14584_-244+14 others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385863 | |||||
| chr12:49385874
|
GT | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(27): Show | 30 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-244+14596delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49385874 | |||||
| chr12:49386057
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+14767C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386057 | ||||||
| chr12:49386197
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-244+14907C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386197 | ||||||
| chr12:49386269
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+14979G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386269 | ||||||
| chr12:49386298
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0127 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-244+15008G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386298 | ||||||
| chr12:49386394
|
C | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-244+15104C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386394 | ||||||
| chr12:49386925
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+15635C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386925 | ||||||
| chr12:49386995
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+15705A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49386995 | ||||||
| chr12:49387313
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+16023G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49387313 | ||||||
| chr12:49387552
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+16262T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49387552 | ||||||
| chr12:49387594
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-244+16304G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49387594 | ||||||
| chr12:49387638
|
C | CA | 5 | a0001c0001t0001g0066a0001c0001t0001g0145a0001c0001t0003g0037others(2): Show | 5 | HG01891.hp1 HG02135.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+16369dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49387638 | |||||
| chr12:49387638
|
CA | C | 35 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0128others(32): Show | 35 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.-244+16369delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49387638 | |||||
| chr12:49387641
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+16351A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49387641 | ||||||
| chr12:49387870
|
G | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+16580G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49387870 | ||||||
| chr12:49388229
|
C | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG01167.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-244+16939C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49388229 | ||||||
| chr12:49388371
|
T | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0075a0001c0001t0001g0080others(1): Show | 4 | HG00280.hp2 HG01123.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244+17081T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49388371 | ||||||
| chr12:49388793
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+17503C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49388793 | ||||||
| chr12:49389003
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0115others(1): Show | 4 | HG01361.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244+17713G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49389003 | ||||||
| chr12:49389379
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-244+18089T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49389379 | ||||||
| chr12:49389823
|
A | G | 1 | a0002c0006t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-244+18533A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49389823 | ||||||
| chr12:49390031
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+18741G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49390031 | ||||||
| chr12:49390170
|
C | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+18880C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49390170 | ||||||
| chr12:49390373
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+19083C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49390373 | ||||||
| chr12:49390582
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+19292G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49390582 | ||||||
| chr12:49391077
|
C | CA | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+19796dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49391077 | |||||
| chr12:49391586
|
TG | T | 27 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0071others(24): Show | 27 | HG00280.hp2 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-244+20297delG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49391586 | ||||||
| chr12:49391621
|
ATGT | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+20335_-244+20 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49391621 | |||||
| chr12:49392574
|
G | A | 2 | a0001c0001t0003g0027a0001c0001t0003g0028 | 2 | HG02809.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-244+21284G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49392574 | ||||||
| chr12:49392773
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-244+21483C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49392773 | ||||||
| chr12:49393223
|
A | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+21933A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393223 | ||||||
| chr12:49393273
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-244+21983T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393273 | ||||||
| chr12:49393280
|
T | C | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+21990T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393280 | ||||||
| chr12:49393334
|
A | AT | 4 | a0001c0001t0002g0150a0001c0001t0002g0151a0001c0001t0002g0152others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+22048dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49393334 | |||||
| chr12:49393528
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-244+22238G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393528 | ||||||
| chr12:49393769
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-244+22479T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393769 | ||||||
| chr12:49393943
|
T | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+22653T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393943 | ||||||
| chr12:49393963
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-244+22673G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49393963 | ||||||
| chr12:49394072
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-244+22782G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49394072 | ||||||
| chr12:49394124
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+22834A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49394124 | ||||||
| chr12:49394339
|
C | CA | 10 | a0001c0001t0001g0066a0001c0001t0001g0103a0001c0001t0001g0105others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.-244+23067dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49394339 | |||||
| chr12:49394339
|
CA | C | 36 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(33): Show | 36 | HG01167.hp1 HG01891.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-244+23067delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49394339 | |||||
| chr12:49394339
|
CAA | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(27): Show | 30 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-244+23066_-244+23 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49394339 | |||||
| chr12:49394483
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+23193C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49394483 | ||||||
| chr12:49394809
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-244+23519C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49394809 | ||||||
| chr12:49394912
|
C | CA | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-244+23632dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49394912 | |||||
| chr12:49394922
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-244+23632A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49394922 | ||||||
| chr12:49395022
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0115others(1): Show | 4 | HG01361.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244+23732G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395022 | ||||||
| chr12:49395051
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+23761C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395051 | ||||||
| chr12:49395238
|
A | AC | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+23950dupC | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49395238 | |||||
| chr12:49395426
|
A | AT | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+24152dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49395426 | |||||
| chr12:49395426
|
AT | A | 47 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(44): Show | 47 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(44): Show |
intron_variant | MODIFIER | c.-244+24152delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49395426 | |||||
| chr12:49395447
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-244+24157C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395447 | ||||||
| chr12:49395705
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+24415C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395705 | ||||||
| chr12:49395712
|
C | T | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-244+24422C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395712 | ||||||
| chr12:49395750
|
G | A | 4 | a0001c0001t0002g0048a0001c0001t0002g0060a0001c0001t0008g0049others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244+24460G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395750 | ||||||
| chr12:49395870
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-244+24580G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395870 | ||||||
| chr12:49395885
|
T | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-244+24595T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395885 | ||||||
| chr12:49395935
|
A | G | 4 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0002g0048others(1): Show | 4 | HG00280.hp2 HG02717.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+24645A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49395935 | ||||||
| chr12:49396046
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+24756G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49396046 | ||||||
| chr12:49396071
|
G | A | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+24781G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49396071 | ||||||
| chr12:49396321
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+25031C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49396321 | ||||||
| chr12:49396756
|
C | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02809.hp2 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+25466C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49396756 | ||||||
| chr12:49396773
|
T | G | 2 | a0001c0001t0001g0040a0001c0003t0001g0057 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-244+25483T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49396773 | ||||||
| chr12:49397113
|
T | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+25823T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49397113 | ||||||
| chr12:49397543
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+26253G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49397543 | ||||||
| chr12:49397833
|
T | TA | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-244+26568dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49397833 | |||||
| chr12:49397833
|
TA | T | 8 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0115others(5): Show | 8 | HG01069.hp1 HG01943.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-244+26568delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49397833 | |||||
| chr12:49398135
|
C | CA | 30 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0087others(27): Show | 30 | HG00099.hp2 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-244+26870dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49398135 | |||||
| chr12:49398135
|
C | CAA | 20 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(17): Show | 20 | HG00639.hp2 HG01192.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-244+26869_-244+26 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49398135 | |||||
| chr12:49398135
|
C | CAAA | 23 | a0001c0001t0001g0130a0001c0001t0001g0144a0001c0001t0001g0158others(20): Show | 23 | HG01175.hp1 HG01361.hp2 HG01978.hp2 others(20): Show |
intron_variant | MODIFIER | c.-244+26868_-244+26 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49398135 | |||||
| chr12:49398135
|
CA | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0084a0001c0001t0001g0111others(2): Show | 5 | HG01069.hp2 HG01515.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+26870delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49398135 | |||||
| chr12:49398156
|
A | AG | 2 | a0001c0001t0005g0021a0001c0001t0005g0023 | 2 | HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-244+26866_-244+26 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49398156 | ||||||
| chr12:49398156
|
A | G | 20 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(17): Show | 20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-244+26866A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49398156 | ||||||
| chr12:49398327
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+27037C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49398327 | ||||||
| chr12:49398768
|
A | G | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-244+27478A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49398768 | ||||||
| chr12:49399155
|
C | CT | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+27875dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49399155 | |||||
| chr12:49399255
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-244+27965G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49399255 | ||||||
| chr12:49399419
|
C | T | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-244+28129C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49399419 | ||||||
| chr12:49399501
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+28211C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49399501 | ||||||
| chr12:49399904
|
G | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-244+28614G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49399904 | ||||||
| chr12:49400188
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+28898G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49400188 | ||||||
| chr12:49400524
|
A | G | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-244+29234A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49400524 | ||||||
| chr12:49400581
|
A | G | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-244+29291A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49400581 | ||||||
| chr12:49400996
|
C | T | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-244+29706C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49400996 | ||||||
| chr12:49401153
|
G | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-244+29863G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401153 | ||||||
| chr12:49401164
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+29874C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401164 | ||||||
| chr12:49401493
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+30203G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401493 | ||||||
| chr12:49401519
|
A | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0113others(1): Show | 4 | HG02293.hp1 NA18961.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-244+30229A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401519 | ||||||
| chr12:49401644
|
T | A | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-244+30354T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401644 | ||||||
| chr12:49401751
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+30461G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401751 | ||||||
| chr12:49401801
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+30511G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401801 | ||||||
| chr12:49401924
|
C | G | 1 | a0002c0006t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-244+30634C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401924 | ||||||
| chr12:49401956
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-244+30666T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49401956 | ||||||
| chr12:49402007
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+30717C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402007 | ||||||
| chr12:49402012
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+30722T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402012 | ||||||
| chr12:49402032
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-244+30742A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402032 | ||||||
| chr12:49402249
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-244+30959G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402249 | ||||||
| chr12:49402475
|
A | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+31185A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402475 | ||||||
| chr12:49402734
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+31444G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402734 | ||||||
| chr12:49402938
|
G | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-244+31648G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49402938 | ||||||
| chr12:49403104
|
A | T | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02258.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-244+31814A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403104 | ||||||
| chr12:49403185
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-244+31895G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403185 | ||||||
| chr12:49403289
|
GCCAAAGT others(3): Show |
G | 1 | a0001c0001t0001g0138 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-244+32001_-244+32 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403289 | |||||
| chr12:49403444
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-244+32154A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403444 | ||||||
| chr12:49403463
|
A | C | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-244+32173A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403463 | ||||||
| chr12:49403594
|
T | TAC | 20 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG00280.hp2 HG00639.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-244+32350_-244+32 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
T | TACAC | 3 | a0001c0001t0001g0111a0001c0001t0002g0059a0001c0001t0011g0042 | 3 | HG01515.hp2 HG02723.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-244+32348_-244+32 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
T | TACACAC | 2 | a0001c0001t0001g0076a0001c0001t0001g0138 | 2 | HG04228.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.-244+32346_-244+32 others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-244+32342_-244+32 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TAC | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0073others(14): Show | 17 | HG00639.hp1 HG01074.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+32350_-244+32 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TACAC | T | 9 | a0001c0001t0001g0071a0001c0001t0001g0085a0001c0001t0001g0087others(6): Show | 9 | HG00741.hp2 HG01346.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+32348_-244+32 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TACACAC | T | 4 | a0001c0001t0001g0095a0001c0001t0004g0124a0001c0001t0004g0125others(1): Show | 4 | HG01167.hp1 HG02293.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-244+32346_-244+32 others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-244+32342_-244+32 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TACACACA others(5): Show |
T | 13 | a0001c0001t0001g0036a0001c0001t0001g0098a0001c0001t0001g0117others(10): Show | 13 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.-244+32340_-244+32 others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-244+32330_-244+32 others(28): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403594
|
TACACACA others(17): Show |
T | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-244+32328_-244+32 others(30): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403594 | |||||
| chr12:49403640
|
C | A | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+32350C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403640 | ||||||
| chr12:49403640
|
CAA | C | 8 | a0001c0001t0001g0002a0001c0001t0002g0001a0001c0001t0003g0012others(5): Show | 8 | HG02055.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-244+32352_-244+32 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49403640 | |||||
| chr12:49403642
|
A | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(11): Show | 14 | HG01346.hp1 HG01884.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-244+32352A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403642 | ||||||
| chr12:49403647
|
A | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0145 | 2 | HG02135.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-244+32357A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403647 | ||||||
| chr12:49403685
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0110 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-244+32395C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403685 | ||||||
| chr12:49403776
|
G | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+32486G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49403776 | ||||||
| chr12:49404034
|
C | T | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-244+32744C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49404034 | ||||||
| chr12:49404274
|
C | CT | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+32997dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49404274 | |||||
| chr12:49404289
|
A | AT | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+33013dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49404289 | |||||
| chr12:49404305
|
GAGATA | G | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-244+33020_-244+33 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49404305 | |||||
| chr12:49404399
|
G | A | 1 | a0001c0001t0007g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-244+33109G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49404399 | ||||||
| chr12:49404683
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-244+33393T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49404683 | ||||||
| chr12:49404690
|
C | T | 13 | a0001c0001t0001g0033a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-244+33400C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49404690 | ||||||
| chr12:49404733
|
G | A | 9 | a0001c0001t0002g0048a0001c0001t0002g0060a0001c0001t0002g0149others(6): Show | 9 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+33443G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49404733 | ||||||
| chr12:49404975
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-244+33685C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49404975 | ||||||
| chr12:49404983
|
A | AT | 39 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-244+33706dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49404983 | |||||
| chr12:49404983
|
AT | A | 16 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-244+33706delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49404983 | |||||
| chr12:49405110
|
G | T | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-244+33820G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49405110 | ||||||
| chr12:49405131
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+33841T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49405131 | ||||||
| chr12:49405199
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-244+33909G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49405199 | ||||||
| chr12:49405817
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 68 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.-244+34527G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49405817 | ||||||
| chr12:49405881
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+34591A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49405881 | ||||||
| chr12:49406135
|
A | G | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-244+34845A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49406135 | ||||||
| chr12:49406284
|
C | CT | 20 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(17): Show | 20 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-244+35009dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49406284 | |||||
| chr12:49406376
|
C | G | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-244+35086C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49406376 | ||||||
| chr12:49406379
|
A | AGCTCAAG others(12): Show |
1 | a0001c0001t0001g0090 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-244+35090_-244+35 others(25): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49406379 | |||||
| chr12:49406451
|
A | AT | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+35171dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49406451 | |||||
| chr12:49407373
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+36083T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49407373 | ||||||
| chr12:49407771
|
A | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-244+36481A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49407771 | ||||||
| chr12:49407803
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+36513C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49407803 | ||||||
| chr12:49407821
|
A | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-244+36531A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49407821 | ||||||
| chr12:49407883
|
C | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+36593C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49407883 | ||||||
| chr12:49408007
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-244+36717C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408007 | ||||||
| chr12:49408215
|
C | T | 3 | a0001c0001t0005g0021a0001c0001t0005g0023a0001c0001t0005g0024 | 3 | HG01346.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-244+36925C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408215 | ||||||
| chr12:49408252
|
C | CT | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(9): Show | 12 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-244+36979dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49408252 | |||||
| chr12:49408252
|
C | CTT | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-244+36978_-244+36 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49408252 | |||||
| chr12:49408278
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+36988C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408278 | ||||||
| chr12:49408552
|
C | CT | 25 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0130others(22): Show | 25 | HG00639.hp2 HG01192.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.-244+37283dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49408552 | |||||
| chr12:49408552
|
CT | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-244+37283delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49408552 | |||||
| chr12:49408585
|
TTGCTCTG others(39): Show |
T | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-244+37299_-244+37 others(52): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49408585 | |||||
| chr12:49408595
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+37305G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408595 | ||||||
| chr12:49408615
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0140 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-244+37325G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408615 | ||||||
| chr12:49408636
|
G | T | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244+37346G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408636 | ||||||
| chr12:49408702
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+37412C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408702 | ||||||
| chr12:49408807
|
C | T | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-244+37517C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408807 | ||||||
| chr12:49408836
|
T | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+37546T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408836 | ||||||
| chr12:49408888
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-244+37598C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408888 | ||||||
| chr12:49408890
|
T | C | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-244+37600T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49408890 | ||||||
| chr12:49409021
|
A | AG | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+37732dupG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49409021 | |||||
| chr12:49409113
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+37823T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409113 | ||||||
| chr12:49409337
|
G | T | 2 | a0001c0001t0005g0021a0001c0001t0005g0023 | 2 | HG01346.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-244+38047G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409337 | ||||||
| chr12:49409375
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+38085G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409375 | ||||||
| chr12:49409498
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+38208G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409498 | ||||||
| chr12:49409572
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+38282G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409572 | ||||||
| chr12:49409591
|
AATT | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(7): Show | 10 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-244+38302_-244+38 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409591 | ||||||
| chr12:49409591
|
AATTT | A | 11 | a0001c0001t0001g0003a0001c0001t0003g0012a0001c0001t0003g0016others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-244+38302_-244+38 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409591 | ||||||
| chr12:49409591
|
AATTTT | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244+38302_-244+38 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49409591 | ||||||
| chr12:49409592
|
A | AT | 41 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0070others(38): Show | 41 | HG00639.hp2 HG01175.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.-244+38329dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49409592 | |||||
| chr12:49409592
|
A | ATT | 8 | a0001c0001t0001g0066a0001c0001t0001g0107a0001c0001t0002g0047others(5): Show | 8 | HG01361.hp1 HG01361.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-244+38328_-244+38 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49409592 | |||||
| chr12:49409592
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0002g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-244+38318_-244+38 others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49409592 | |||||
| chr12:49410079
|
G | T | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-244+38789G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410079 | ||||||
| chr12:49410151
|
C | T | 2 | a0001c0001t0001g0074a0001c0001t0001g0099 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-244+38861C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410151 | ||||||
| chr12:49410354
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-244+39064G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410354 | ||||||
| chr12:49410368
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-244+39078G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410368 | ||||||
| chr12:49410523
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-244+39233C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410523 | ||||||
| chr12:49410705
|
C | T | 1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-244+39415C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410705 | ||||||
| chr12:49410879
|
T | C | 1 | a0001c0001t0011g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-244+39589T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49410879 | ||||||
| chr12:49410929
|
CTTTTAG | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+39645_-244+39 others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49410929 | |||||
| chr12:49411089
|
ACT | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+39802_-244+39 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49411089 | |||||
| chr12:49411442
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-244+40152C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49411442 | ||||||
| chr12:49411673
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0001 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-244+40383T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49411673 | ||||||
| chr12:49412444
|
G | A | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-244+41154G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49412444 | ||||||
| chr12:49412482
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-244+41192G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49412482 | ||||||
| chr12:49412509
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-244+41219T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49412509 | ||||||
| chr12:49412751
|
TA | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(89): Show | 92 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-244+41474delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49412751 | |||||
| chr12:49412770
|
A | G | 1 | a0001c0001t0006g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-244+41480A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49412770 | ||||||
| chr12:49413526
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 76 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.-244+42236G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49413526 | ||||||
| chr12:49413529
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-244+42239C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49413529 | ||||||
| chr12:49413599
|
T | C | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-244+42309T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49413599 | ||||||
| chr12:49413781
|
TAAAC | T | 37 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(34): Show | 37 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.-244+42493_-244+42 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49413781 | |||||
| chr12:49413803
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+42513C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49413803 | ||||||
| chr12:49413978
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-244+42688A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49413978 | ||||||
| chr12:49414281
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-244+42991G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49414281 | ||||||
| chr12:49414369
|
T | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+43079T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49414369 | ||||||
| chr12:49414452
|
G | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0054 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-244+43162G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49414452 | ||||||
| chr12:49414670
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+43380T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49414670 | ||||||
| chr12:49414921
|
CT | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+43638delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49414921 | |||||
| chr12:49414935
|
C | CT | 35 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(32): Show | 35 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-244+43649dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49414935 | |||||
| chr12:49414939
|
TC | T | 2 | a0001c0001t0001g0118a0001c0001t0006g0043 | 2 | HG02896.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-244+43650delC | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49414939 | ||||||
| chr12:49414940
|
C | T | 69 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(66): Show | 69 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.-244+43650C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49414940 | ||||||
| chr12:49415000
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-244+43710C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415000 | ||||||
| chr12:49415042
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+43752T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415042 | ||||||
| chr12:49415065
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-244+43775G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415065 | ||||||
| chr12:49415474
|
T | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+44184T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415474 | ||||||
| chr12:49415548
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-244+44258A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415548 | ||||||
| chr12:49415652
|
A | G | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-244+44362A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415652 | ||||||
| chr12:49415673
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-244+44383T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415673 | ||||||
| chr12:49415727
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-244+44437G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415727 | ||||||
| chr12:49415803
|
G | A | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-244+44513G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49415803 | ||||||
| chr12:49416020
|
CT | C | 12 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-243-44734delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49416020 | |||||
| chr12:49416036
|
T | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-44734T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49416036 | ||||||
| chr12:49416357
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-243-44413A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49416357 | ||||||
| chr12:49416471
|
T | TTTTTA | 17 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0075others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-243-44269_-243-44 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49416471 | |||||
| chr12:49416471
|
T | TTTTTATT others(3): Show |
1 | a0001c0001t0001g0115 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-243-44274_-243-44 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49416471 | |||||
| chr12:49416471
|
TTTTTATT others(3): Show |
T | 17 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(14): Show | 17 | HG01167.hp1 HG01346.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-243-44274_-243-44 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49416471 | |||||
| chr12:49416905
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-43865C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49416905 | ||||||
| chr12:49417216
|
T | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-43554T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417216 | ||||||
| chr12:49417390
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-43380G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417390 | ||||||
| chr12:49417391
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-43379C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417391 | ||||||
| chr12:49417471
|
T | C | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-43299T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417471 | ||||||
| chr12:49417493
|
T | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-43277T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417493 | ||||||
| chr12:49417528
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-243-43242G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417528 | ||||||
| chr12:49417862
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-243-42908G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49417862 | ||||||
| chr12:49418024
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-42746C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418024 | ||||||
| chr12:49418039
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-243-42731C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418039 | ||||||
| chr12:49418108
|
G | GT | 10 | a0001c0001t0001g0078a0001c0001t0001g0092a0001c0001t0001g0106others(7): Show | 10 | HG01071.hp1 HG01978.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-243-42638dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49418108 | |||||
| chr12:49418108
|
G | GTTT | 21 | a0001c0001t0001g0040a0001c0001t0001g0058a0001c0001t0001g0155others(18): Show | 21 | HG00639.hp2 HG01192.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.-243-42640_-243-42 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49418108 | |||||
| chr12:49418108
|
G | GTTTT | 21 | a0001c0001t0001g0033a0001c0001t0001g0131a0001c0001t0001g0133others(18): Show | 21 | HG01167.hp1 HG01175.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.-243-42641_-243-42 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49418108 | |||||
| chr12:49418108
|
G | GTTTTT | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-42642_-243-42 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49418108 | |||||
| chr12:49418108
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0037 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-243-42647_-243-42 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49418108 | |||||
| chr12:49418108
|
GT | G | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG01069.hp2 HG01123.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.-243-42638delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49418108 | |||||
| chr12:49418122
|
T | G | 1 | a0001c0001t0001g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-243-42648T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418122 | ||||||
| chr12:49418298
|
A | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-42472A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418298 | ||||||
| chr12:49418303
|
A | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00280.hp1 HG01071.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.-243-42467A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418303 | ||||||
| chr12:49418382
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-243-42388C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418382 | ||||||
| chr12:49418457
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-42313G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418457 | ||||||
| chr12:49418934
|
C | G | 2 | a0001c0001t0002g0061a0001c0001t0002g0063 | 2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-243-41836C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49418934 | ||||||
| chr12:49419738
|
G | A | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-41032G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49419738 | ||||||
| chr12:49419778
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-243-40992C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49419778 | ||||||
| chr12:49419780
|
T | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-40990T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49419780 | ||||||
| chr12:49419886
|
A | ACTGT | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-40883_-243-40 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49419886 | |||||
| chr12:49420044
|
G | T | 1 | a0001c0001t0001g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-243-40726G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420044 | ||||||
| chr12:49420063
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-40707A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420063 | ||||||
| chr12:49420067
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-243-40703A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420067 | ||||||
| chr12:49420237
|
A | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-40533A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420237 | ||||||
| chr12:49420266
|
T | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-243-40504T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420266 | ||||||
| chr12:49420365
|
C | T | 18 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-243-40405C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420365 | ||||||
| chr12:49420366
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-243-40404A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420366 | ||||||
| chr12:49420525
|
T | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-243-40245T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420525 | ||||||
| chr12:49420631
|
T | C | 1 | a0001c0001t0003g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-243-40139T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420631 | ||||||
| chr12:49420700
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-40070A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420700 | ||||||
| chr12:49420740
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-243-40030G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420740 | ||||||
| chr12:49420779
|
G | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-39991G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420779 | ||||||
| chr12:49420793
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-39977A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420793 | ||||||
| chr12:49420857
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.-243-39913G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49420857 | ||||||
| chr12:49421088
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-39682T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421088 | ||||||
| chr12:49421119
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-39651C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421119 | ||||||
| chr12:49421191
|
G | A | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-243-39579G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421191 | ||||||
| chr12:49421237
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-39533G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421237 | ||||||
| chr12:49421244
|
C | T | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-243-39526C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421244 | ||||||
| chr12:49421416
|
C | CA | 18 | a0001c0001t0001g0036a0001c0001t0001g0117a0001c0001t0001g0118others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-243-39327dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49421416 | |||||
| chr12:49421416
|
C | CAA | 6 | a0001c0001t0001g0116a0001c0001t0001g0137a0001c0001t0001g0141others(3): Show | 6 | HG00099.hp2 HG02080.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-39328_-243-39 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49421416 | |||||
| chr12:49421416
|
CA | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 86 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.-243-39327delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49421416 | |||||
| chr12:49421416
|
CAA | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0094a0001c0001t0001g0111others(9): Show | 12 | HG01167.hp1 HG01515.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-243-39328_-243-39 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49421416 | |||||
| chr12:49421423
|
A | C | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-39347A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421423 | ||||||
| chr12:49421424
|
A | C | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-39346A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421424 | ||||||
| chr12:49421428
|
A | C | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-39342A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421428 | ||||||
| chr12:49421429
|
A | C | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-39341A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421429 | ||||||
| chr12:49421433
|
A | C | 2 | a0001c0001t0004g0041a0001c0001t0007g0034 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-243-39337A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421433 | ||||||
| chr12:49421446
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-243-39324A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421446 | ||||||
| chr12:49421612
|
G | C | 2 | a0001c0001t0002g0047a0001c0001t0002g0059 | 2 | HG01361.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-243-39158G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421612 | ||||||
| chr12:49421617
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-243-39153C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49421617 | ||||||
| chr12:49422032
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-38738C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422032 | ||||||
| chr12:49422202
|
T | C | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-243-38568T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422202 | ||||||
| chr12:49422320
|
G | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-38450G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422320 | ||||||
| chr12:49422358
|
C | T | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-38412C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422358 | ||||||
| chr12:49422638
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-38132C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422638 | ||||||
| chr12:49422681
|
G | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-38089G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422681 | ||||||
| chr12:49422747
|
A | T | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-243-38023A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422747 | ||||||
| chr12:49422925
|
A | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 91 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(88): Show |
intron_variant | MODIFIER | c.-243-37845A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422925 | ||||||
| chr12:49422945
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-37825C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49422945 | ||||||
| chr12:49423077
|
C | G | 1 | a0001c0001t0002g0001 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-243-37693C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423077 | ||||||
| chr12:49423128
|
T | C | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-37642T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423128 | ||||||
| chr12:49423135
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-243-37635T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423135 | ||||||
| chr12:49423147
|
T | A | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG01167.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-243-37623T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423147 | ||||||
| chr12:49423650
|
T | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-37120T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423650 | ||||||
| chr12:49423661
|
A | G | 7 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0054others(4): Show | 7 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-243-37109A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423661 | ||||||
| chr12:49423689
|
CT | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0015 | 2 | HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-243-37080delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423689 | ||||||
| chr12:49423844
|
A | C | 3 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0134 | 3 | HG02486.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-243-36926A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423844 | ||||||
| chr12:49423850
|
C | T | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-243-36920C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49423850 | ||||||
| chr12:49424220
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-36550A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49424220 | ||||||
| chr12:49424326
|
A | G | 1 | a0001c0001t0006g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-243-36444A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49424326 | ||||||
| chr12:49424350
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-243-36420C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49424350 | ||||||
| chr12:49424470
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-36300A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49424470 | ||||||
| chr12:49425084
|
A | C | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-35686A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49425084 | ||||||
| chr12:49425141
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-35629G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49425141 | ||||||
| chr12:49425281
|
G | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-35489G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49425281 | ||||||
| chr12:49425309
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-35461A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49425309 | ||||||
| chr12:49425653
|
C | G | 1 | a0001c0001t0005g0021 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-243-35117C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49425653 | ||||||
| chr12:49426058
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-34712C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426058 | ||||||
| chr12:49426205
|
C | CT | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-243-34553dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49426205 | |||||
| chr12:49426398
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-34372T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426398 | ||||||
| chr12:49426627
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-243-34143T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426627 | ||||||
| chr12:49426683
|
A | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-34087A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426683 | ||||||
| chr12:49426786
|
T | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-33984T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426786 | ||||||
| chr12:49426875
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-33895A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426875 | ||||||
| chr12:49426892
|
T | C | 16 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-243-33878T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49426892 | ||||||
| chr12:49427098
|
A | G | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-243-33672A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49427098 | ||||||
| chr12:49427296
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-33474A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49427296 | ||||||
| chr12:49427518
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-33252A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49427518 | ||||||
| chr12:49427619
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0127 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-243-33151T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49427619 | ||||||
| chr12:49427697
|
A | C | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-243-33073A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49427697 | ||||||
| chr12:49427768
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-243-33002A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49427768 | ||||||
| chr12:49427936
|
A | AT | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-32824dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49427936 | |||||
| chr12:49428026
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-32744T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428026 | ||||||
| chr12:49428133
|
T | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-32637T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428133 | ||||||
| chr12:49428146
|
T | G | 17 | a0001c0001t0001g0036a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 17 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-243-32624T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428146 | ||||||
| chr12:49428187
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-243-32583G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428187 | ||||||
| chr12:49428273
|
C | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-32497C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428273 | ||||||
| chr12:49428273
|
CA | C | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-243-32485delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49428273 | |||||
| chr12:49428276
|
A | AC | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-32494_-243-32 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428276 | ||||||
| chr12:49428445
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-243-32325C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428445 | ||||||
| chr12:49428670
|
C | T | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG01167.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-243-32100C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428670 | ||||||
| chr12:49428750
|
A | G | 1 | a0002c0006t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-243-32020A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428750 | ||||||
| chr12:49428763
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-243-32007C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49428763 | ||||||
| chr12:49429003
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-243-31767C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49429003 | ||||||
| chr12:49429144
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-31626T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49429144 | ||||||
| chr12:49429177
|
T | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0097a0001c0001t0001g0108 | 3 | HG02135.hp2 NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-243-31593T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49429177 | ||||||
| chr12:49429336
|
C | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-31434C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49429336 | ||||||
| chr12:49429622
|
A | ATTTTTAT | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-31142_-243-31 others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49429622 | |||||
| chr12:49429786
|
CT | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(67): Show | 70 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.-243-30968delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49429786 | |||||
| chr12:49429787
|
T | TTTTTTTT others(326): Show |
6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-30969_-243-30 others(339): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49429787 | |||||
| chr12:49429838
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-243-30932T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49429838 | ||||||
| chr12:49430099
|
G | GT | 18 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0101others(15): Show | 18 | HG01175.hp2 HG01361.hp1 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.-243-30652dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49430099 | |||||
| chr12:49430099
|
G | GTT | 32 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0095others(29): Show | 32 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.-243-30653_-243-30 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49430099 | |||||
| chr12:49430099
|
G | GTTT | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 25 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.-243-30654_-243-30 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49430099 | |||||
| chr12:49430099
|
G | GTTTT | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.-243-30655_-243-30 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49430099 | |||||
| chr12:49430144
|
A | C | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-243-30626A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49430144 | ||||||
| chr12:49430354
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-30416G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49430354 | ||||||
| chr12:49430444
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-243-30326G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49430444 | ||||||
| chr12:49430909
|
G | A | 20 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 20 | HG01346.hp1 HG01884.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-243-29861G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49430909 | ||||||
| chr12:49431005
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-243-29765G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49431005 | ||||||
| chr12:49431024
|
G | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00741.hp1 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-243-29746G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49431024 | ||||||
| chr12:49431396
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-243-29374G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49431396 | ||||||
| chr12:49432203
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.-243-28567C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49432203 | ||||||
| chr12:49432426
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-28344A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49432426 | ||||||
| chr12:49433009
|
A | G | 2 | a0001c0001t0004g0068a0001c0001t0004g0123 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-243-27761A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433009 | ||||||
| chr12:49433249
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-243-27521G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433249 | ||||||
| chr12:49433284
|
T | A | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-243-27486T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433284 | ||||||
| chr12:49433386
|
C | G | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-27384C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433386 | ||||||
| chr12:49433411
|
C | T | 1 | a0001c0001t0003g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-243-27359C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433411 | ||||||
| chr12:49433414
|
C | T | 42 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(39): Show | 42 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.-243-27356C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433414 | ||||||
| chr12:49433531
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-243-27239C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433531 | ||||||
| chr12:49433626
|
C | A | 51 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(48): Show | 51 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.-243-27144C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433626 | ||||||
| chr12:49433636
|
TTTG | T | 21 | a0001c0001t0002g0007a0001c0001t0002g0047a0001c0001t0002g0048others(18): Show | 21 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-243-27114_-243-27 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49433636 | |||||
| chr12:49433734
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-243-27036C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433734 | ||||||
| chr12:49433918
|
C | A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-26852C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433918 | ||||||
| chr12:49433960
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-243-26810G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433960 | ||||||
| chr12:49433962
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-243-26808G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433962 | ||||||
| chr12:49433992
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-243-26778C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49433992 | ||||||
| chr12:49434069
|
G | T | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-26701G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434069 | ||||||
| chr12:49434202
|
T | C | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-26568T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434202 | ||||||
| chr12:49434250
|
G | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-26520G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434250 | ||||||
| chr12:49434285
|
T | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-26485T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434285 | ||||||
| chr12:49434362
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-243-26408G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434362 | ||||||
| chr12:49434800
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-25970G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434800 | ||||||
| chr12:49434847
|
A | G | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02647.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-243-25923A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434847 | ||||||
| chr12:49434861
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-243-25909C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49434861 | ||||||
| chr12:49435022
|
C | CT | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 18 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-243-25726dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435022 | |||||
| chr12:49435049
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-25721T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435049 | ||||||
| chr12:49435087
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-243-25683G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435087 | ||||||
| chr12:49435526
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-25244A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435526 | ||||||
| chr12:49435622
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-25148G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435622 | ||||||
| chr12:49435638
|
C | CT | 23 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(20): Show | 23 | HG00280.hp1 HG01069.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.-243-25106dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435638 | |||||
| chr12:49435638
|
CT | C | 9 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0111others(6): Show | 9 | HG00099.hp2 HG01515.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-243-25106delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435638 | |||||
| chr12:49435638
|
CTTTTTTT | C | 5 | a0001c0001t0004g0068a0001c0001t0004g0124a0001c0001t0004g0125others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-25112_-243-25 others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435638 | |||||
| chr12:49435638
|
CTTTTTTT others(5): Show |
C | 44 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(41): Show | 44 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.-243-25117_-243-25 others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435638 | |||||
| chr12:49435638
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0006g0043 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-243-25118_-243-25 others(19): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435638 | |||||
| chr12:49435787
|
C | CG | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-24981dupG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49435787 | |||||
| chr12:49435871
|
T | C | 6 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(3): Show | 6 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-24899T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435871 | ||||||
| chr12:49435871
|
T | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-24899T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435871 | ||||||
| chr12:49435896
|
C | T | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-243-24874C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435896 | ||||||
| chr12:49435897
|
A | G | 51 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(48): Show | 51 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.-243-24873A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435897 | ||||||
| chr12:49435911
|
C | T | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-24859C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435911 | ||||||
| chr12:49435935
|
G | A | 1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-243-24835G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435935 | ||||||
| chr12:49435942
|
A | T | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-24828A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435942 | ||||||
| chr12:49435958
|
G | A | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-24812G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49435958 | ||||||
| chr12:49436057
|
T | C | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 18 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-243-24713T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436057 | ||||||
| chr12:49436095
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-243-24675A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436095 | ||||||
| chr12:49436206
|
CCAGTAGG others(120): Show |
C | 1 | a0001c0001t0001g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-243-24531_-243-24 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49436206 | |||||
| chr12:49436254
|
G | A | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-243-24516G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436254 | ||||||
| chr12:49436266
|
GGGGGGCT others(120): Show |
G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-24492_-243-24 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49436266 | |||||
| chr12:49436302
|
C | T | 16 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-243-24468C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436302 | ||||||
| chr12:49436304
|
G | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-24466G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436304 | ||||||
| chr12:49436399
|
C | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-24371C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436399 | ||||||
| chr12:49436424
|
G | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.-243-24346G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436424 | ||||||
| chr12:49436502
|
C | T | 7 | a0001c0001t0002g0007a0001c0001t0004g0068a0001c0001t0004g0123others(4): Show | 7 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-243-24268C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436502 | ||||||
| chr12:49436507
|
CGGCTGGC others(74): Show |
C | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-243-24250_-243-24 others(87): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49436507 | |||||
| chr12:49436509
|
GCTGGCCG others(25): Show |
G | 14 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0128others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-243-24238_-243-24 others(38): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49436509 | |||||
| chr12:49436583
|
C | T | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-243-24187C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436583 | ||||||
| chr12:49436616
|
C | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.-243-24154C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436616 | ||||||
| chr12:49436646
|
G | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0111 | 2 | HG01515.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-243-24124G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436646 | ||||||
| chr12:49436760
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-24010A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436760 | ||||||
| chr12:49436837
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-23933C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436837 | ||||||
| chr12:49436956
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-243-23814G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436956 | ||||||
| chr12:49436971
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-23799C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49436971 | ||||||
| chr12:49437080
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-23690C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437080 | ||||||
| chr12:49437084
|
C | T | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-23686C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437084 | ||||||
| chr12:49437389
|
C | T | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02809.hp2 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-243-23381C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437389 | ||||||
| chr12:49437434
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-243-23336G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437434 | ||||||
| chr12:49437501
|
G | A | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-23269G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437501 | ||||||
| chr12:49437581
|
CCTCGGGA others(8): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-243-23186_-243-23 others(21): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49437581 | |||||
| chr12:49437584
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-243-23186C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437584 | ||||||
| chr12:49437701
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-23069C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437701 | ||||||
| chr12:49437711
|
C | G | 13 | a0001c0001t0001g0033a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-243-23059C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437711 | ||||||
| chr12:49437903
|
A | G | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-22867A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49437903 | ||||||
| chr12:49438021
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-22749A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438021 | ||||||
| chr12:49438234
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-22536C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438234 | ||||||
| chr12:49438277
|
GCAGTGTT others(8): Show |
G | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-243-22477_-243-22 others(21): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49438277 | |||||
| chr12:49438659
|
C | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-22111C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438659 | ||||||
| chr12:49438711
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-243-22059G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438711 | ||||||
| chr12:49438811
|
T | G | 7 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(4): Show | 7 | HG01167.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-243-21959T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438811 | ||||||
| chr12:49438835
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-21935T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438835 | ||||||
| chr12:49438985
|
A | G | 1 | a0001c0001t0011g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-243-21785A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49438985 | ||||||
| chr12:49439292
|
G | C | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-243-21478G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49439292 | ||||||
| chr12:49439322
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-21448A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49439322 | ||||||
| chr12:49439538
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-243-21232C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49439538 | ||||||
| chr12:49439843
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-20927C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49439843 | ||||||
| chr12:49440130
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-243-20640T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440130 | ||||||
| chr12:49440246
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.-243-20524T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440246 | ||||||
| chr12:49440269
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-243-20501G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440269 | ||||||
| chr12:49440367
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-20403C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440367 | ||||||
| chr12:49440453
|
G | A | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-243-20317G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440453 | ||||||
| chr12:49440472
|
A | AT | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(76): Show | 79 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-243-20282dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49440472 | |||||
| chr12:49440572
|
G | A | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-243-20198G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440572 | ||||||
| chr12:49440606
|
C | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0128others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-243-20164C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440606 | ||||||
| chr12:49440719
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-20051G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49440719 | ||||||
| chr12:49441193
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-19577T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441193 | ||||||
| chr12:49441314
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-19456T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441314 | ||||||
| chr12:49441345
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-243-19425A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441345 | ||||||
| chr12:49441440
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-19330C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441440 | ||||||
| chr12:49441462
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-243-19308G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441462 | ||||||
| chr12:49441569
|
T | A | 1 | a0001c0001t0006g0043 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-243-19201T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441569 | ||||||
| chr12:49441635
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-243-19135C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441635 | ||||||
| chr12:49441719
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-19051G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441719 | ||||||
| chr12:49441934
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-18836A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441934 | ||||||
| chr12:49441948
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-18822A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49441948 | ||||||
| chr12:49442388
|
G | A | 1 | a0001c0001t0011g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-243-18382G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442388 | ||||||
| chr12:49442543
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-243-18227G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442543 | ||||||
| chr12:49442785
|
T | TAA | 5 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-17985_-243-17 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
T | TAAA | 2 | a0001c0001t0004g0125a0001c0001t0004g0126 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-243-17985_-243-17 others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
TTAAAAAA | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-17984_-243-17 others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
TTAAAAAA others(2): Show |
T | 11 | a0001c0001t0001g0033a0001c0001t0001g0128a0001c0001t0001g0129others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-17984_-243-17 others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
TTAAAAAA others(3): Show |
T | 2 | a0001c0001t0001g0058a0001c0001t0001g0158 | 2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-243-17984_-243-17 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
TTAAAAAA others(4): Show |
T | 6 | a0001c0001t0001g0040a0001c0001t0003g0039a0001c0001t0008g0049others(3): Show | 6 | HG02145.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-17984_-243-17 others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
TTAAAAAA others(5): Show |
T | 27 | a0001c0001t0001g0006a0001c0001t0002g0007a0001c0001t0002g0047others(24): Show | 27 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.-243-17984_-243-17 others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442785
|
TTAAAAAA others(6): Show |
T | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-243-17984_-243-17 others(19): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442785 | ||||||
| chr12:49442786
|
T | A | 8 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(5): Show | 8 | HG01167.hp1 HG02486.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-243-17984T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49442786 | ||||||
| chr12:49442786
|
T | TA | 9 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0087others(6): Show | 9 | HG00741.hp2 HG01175.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-243-17948dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
T | TAAAA | 10 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0094others(7): Show | 10 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-243-17951_-243-17 others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
T | TAAAAA | 6 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0080others(3): Show | 6 | HG01123.hp1 HG01192.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-17952_-243-17 others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-243-17957_-243-17 others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
T | TAAAAAAA others(7): Show |
1 | a0001c0001t0001g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-243-17961_-243-17 others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-243-17962_-243-17 others(21): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
TAAAAAAA others(6): Show |
T | 2 | a0001c0001t0001g0095a0001c0001t0001g0102 | 2 | HG00639.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-243-17960_-243-17 others(19): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
TAAAAAAA others(10): Show |
T | 19 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0113others(16): Show | 19 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-243-17964_-243-17 others(23): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49442786
|
TAAAAAAA others(11): Show |
T | 2 | a0001c0001t0001g0086a0001c0001t0001g0116 | 2 | NA18982.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-243-17965_-243-17 others(24): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49442786 | |||||
| chr12:49443204
|
A | G | 1 | a0001c0001t0005g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-243-17566A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49443204 | ||||||
| chr12:49443333
|
A | T | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-17437A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49443333 | ||||||
| chr12:49443938
|
A | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-243-16832A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49443938 | ||||||
| chr12:49444111
|
C | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-16659C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49444111 | ||||||
| chr12:49444210
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-243-16560G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49444210 | ||||||
| chr12:49444215
|
TG | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(50): Show | 53 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.-243-16554delG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49444215 | ||||||
| chr12:49444367
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-243-16403G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49444367 | ||||||
| chr12:49444752
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-243-16018C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49444752 | ||||||
| chr12:49445075
|
T | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0110 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-243-15695T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49445075 | ||||||
| chr12:49445550
|
C | T | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-243-15220C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49445550 | ||||||
| chr12:49446177
|
T | C | 3 | a0001c0001t0005g0021a0001c0001t0005g0023a0001c0001t0005g0024 | 3 | HG01346.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-243-14593T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49446177 | ||||||
| chr12:49446190
|
C | T | 5 | a0001c0001t0002g0149a0001c0001t0002g0150a0001c0001t0002g0151others(2): Show | 5 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-14580C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49446190 | ||||||
| chr12:49446632
|
G | C | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-14138G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49446632 | ||||||
| chr12:49446697
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(20): Show | 23 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-243-14073G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49446697 | ||||||
| chr12:49446917
|
A | G | 22 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0070others(19): Show | 22 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-243-13853A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49446917 | ||||||
| chr12:49446932
|
C | CT | 33 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0070others(30): Show | 33 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-243-13824dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49446932 | |||||
| chr12:49446992
|
G | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0067a0001c0001t0001g0070others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-243-13778G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49446992 | ||||||
| chr12:49447307
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-243-13463C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49447307 | ||||||
| chr12:49447374
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-243-13396G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49447374 | ||||||
| chr12:49447626
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-243-13144T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49447626 | ||||||
| chr12:49447641
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-13129A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49447641 | ||||||
| chr12:49447846
|
A | C | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-12924A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49447846 | ||||||
| chr12:49448123
|
A | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0114 | 2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-243-12647A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49448123 | ||||||
| chr12:49448144
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(7): Show | 10 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-243-12626T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49448144 | ||||||
| chr12:49448337
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-243-12433C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49448337 | ||||||
| chr12:49448385
|
C | T | 1 | a0001c0001t0002g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-243-12385C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49448385 | ||||||
| chr12:49448712
|
C | CA | 18 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0076others(15): Show | 18 | HG01175.hp1 HG01175.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.-243-12036dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49448712 | |||||
| chr12:49448897
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-11873C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49448897 | ||||||
| chr12:49449229
|
T | G | 1 | a0001c0001t0003g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-243-11541T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49449229 | ||||||
| chr12:49449365
|
G | A | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG01167.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-243-11405G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49449365 | ||||||
| chr12:49449693
|
C | A | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-243-11077C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49449693 | ||||||
| chr12:49449822
|
GAC | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-10944_-243-10 others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49449822 | |||||
| chr12:49450245
|
A | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(37): Show | 40 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.-243-10525A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450245 | ||||||
| chr12:49450696
|
A | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-10074A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450696 | ||||||
| chr12:49450716
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-10054G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450716 | ||||||
| chr12:49450793
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-243-9977C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450793 | ||||||
| chr12:49450856
|
G | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-9914G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450856 | ||||||
| chr12:49450866
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(23): Show | 26 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.-243-9904G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450866 | ||||||
| chr12:49450943
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-243-9827G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450943 | ||||||
| chr12:49450947
|
G | T | 6 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-9823G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49450947 | ||||||
| chr12:49451646
|
G | A | 8 | a0001c0001t0001g0072a0001c0001t0001g0092a0001c0001t0001g0094others(5): Show | 8 | HG00741.hp1 HG01074.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-243-9124G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49451646 | ||||||
| chr12:49451762
|
A | G | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-243-9008A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49451762 | ||||||
| chr12:49452103
|
G | C | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-243-8667G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452103 | ||||||
| chr12:49452257
|
C | G | 1 | a0001c0001t0002g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-243-8513C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452257 | ||||||
| chr12:49452282
|
A | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-8488A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452282 | ||||||
| chr12:49452425
|
A | G | 50 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0069others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-243-8345A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452425 | ||||||
| chr12:49452516
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-243-8254C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452516 | ||||||
| chr12:49452827
|
T | G | 1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-243-7943T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452827 | ||||||
| chr12:49452843
|
A | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.-243-7927A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49452843 | ||||||
| chr12:49453020
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-7750G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453020 | ||||||
| chr12:49453023
|
A | G | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-7747A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453023 | ||||||
| chr12:49453027
|
C | T | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-7743C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453027 | ||||||
| chr12:49453108
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.-243-7662A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453108 | ||||||
| chr12:49453115
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-7655C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453115 | ||||||
| chr12:49453148
|
G | C | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-243-7622G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453148 | ||||||
| chr12:49453160
|
C | CA | 52 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(49): Show | 52 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.-243-7593dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453160 | |||||
| chr12:49453160
|
C | CAAA | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-243-7595_-243-759 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453160 | |||||
| chr12:49453787
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-243-6983G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453787 | ||||||
| chr12:49453847
|
A | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-6923A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453847 | ||||||
| chr12:49453856
|
C | CT | 24 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0076others(21): Show | 24 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-243-6890dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453856 | |||||
| chr12:49453856
|
C | CTT | 37 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(34): Show | 37 | HG00639.hp2 HG01175.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.-243-6891_-243-689 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453856 | |||||
| chr12:49453856
|
C | CTTT | 8 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0128others(5): Show | 8 | HG00741.hp2 HG01346.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-243-6892_-243-689 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453856 | |||||
| chr12:49453856
|
CT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(14): Show | 17 | HG00280.hp1 HG01071.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-243-6890delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453856 | |||||
| chr12:49453856
|
CTT | C | 12 | a0001c0001t0001g0011a0001c0001t0003g0012a0001c0001t0003g0016others(9): Show | 12 | HG01069.hp2 HG01346.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-243-6891_-243-689 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49453856 | |||||
| chr12:49453902
|
A | G | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-243-6868A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49453902 | ||||||
| chr12:49454508
|
A | G | 1 | a0001c0001t0002g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-243-6262A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49454508 | ||||||
| chr12:49454880
|
T | TA | 29 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0074others(26): Show | 29 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-243-5872dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49454880 | |||||
| chr12:49454880
|
TA | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0006g0043others(2): Show | 5 | HG02080.hp1 HG02647.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-5872delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49454880 | |||||
| chr12:49454881
|
A | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(2): Show | 5 | HG02615.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-5889A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49454881 | ||||||
| chr12:49454889
|
A | C | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-5881A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49454889 | ||||||
| chr12:49455113
|
A | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-5657A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49455113 | ||||||
| chr12:49455202
|
T | G | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-243-5568T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49455202 | ||||||
| chr12:49455399
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-243-5371C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49455399 | ||||||
| chr12:49455682
|
C | A | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00741.hp1 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-243-5088C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49455682 | ||||||
| chr12:49455844
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-243-4926A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49455844 | ||||||
| chr12:49456082
|
G | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-243-4688G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49456082 | ||||||
| chr12:49456551
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0156 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-243-4219A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49456551 | ||||||
| chr12:49456777
|
A | T | 1 | a0001c0001t0006g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-243-3993A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49456777 | ||||||
| chr12:49457007
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-243-3763T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49457007 | ||||||
| chr12:49457315
|
C | G | 1 | a0001c0001t0007g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-243-3455C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49457315 | ||||||
| chr12:49457438
|
C | CT | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(27): Show | 30 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-243-3320dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49457438 | |||||
| chr12:49457531
|
T | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-3239T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49457531 | ||||||
| chr12:49458020
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-243-2750G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49458020 | ||||||
| chr12:49458080
|
A | G | 1 | a0001c0001t0006g0045 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-243-2690A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49458080 | ||||||
| chr12:49458152
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.-243-2618C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49458152 | ||||||
| chr12:49458483
|
GA | G | 6 | a0001c0001t0001g0144a0001c0001t0006g0043a0001c0001t0006g0044others(3): Show | 6 | HG02080.hp2 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-243-2277delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49458483 | |||||
| chr12:49458673
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-243-2097G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49458673 | ||||||
| chr12:49458732
|
G | GT | 24 | a0001c0001t0001g0102a0001c0001t0001g0130a0001c0001t0001g0155others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.-243-2021dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49458732 | |||||
| chr12:49458732
|
G | GTTT | 5 | a0001c0001t0004g0068a0001c0001t0004g0124a0001c0001t0004g0125others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-243-2023_-243-202 others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49458732 | |||||
| chr12:49458749
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-243-2021T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49458749 | ||||||
| chr12:49458999
|
A | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-243-1771A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49458999 | ||||||
| chr12:49459070
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-243-1700G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459070 | ||||||
| chr12:49459174
|
A | G | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-243-1596A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459174 | ||||||
| chr12:49459285
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-243-1485C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459285 | ||||||
| chr12:49459343
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-243-1427A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459343 | ||||||
| chr12:49459374
|
G | T | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-243-1396G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459374 | ||||||
| chr12:49459411
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-243-1359C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459411 | ||||||
| chr12:49459668
|
C | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0063 | 2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-243-1102C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459668 | ||||||
| chr12:49459685
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-243-1085G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459685 | ||||||
| chr12:49459740
|
T | TC | 41 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(38): Show | 41 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.-243-1016dupC | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49459740 | |||||
| chr12:49459740
|
T | TCC | 23 | a0001c0001t0001g0005a0001c0001t0001g0094a0001c0001t0001g0097others(20): Show | 23 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-243-1017_-243-101 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49459740 | |||||
| chr12:49459740
|
TC | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0073a0001c0001t0001g0076others(16): Show | 19 | HG00099.hp2 HG01074.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-243-1016delC | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49459740 | |||||
| chr12:49459890
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-243-880G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49459890 | ||||||
| chr12:49459940
|
G | GA | 5 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0100others(2): Show | 5 | HG00741.hp1 HG01123.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-243-812dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49459940 | |||||
| chr12:49459940
|
GA | G | 53 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(50): Show | 53 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.-243-812delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49459940 | |||||
| chr12:49460008
|
C | T | 1 | a0001c0001t0012g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-243-762C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460008 | ||||||
| chr12:49460011
|
G | A | 1 | a0004c0002t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-243-759G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460011 | ||||||
| chr12:49460052
|
G | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0128others(11): Show | 14 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-243-718G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460052 | ||||||
| chr12:49460173
|
T | C | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-243-597T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460173 | ||||||
| chr12:49460324
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.-243-446C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460324 | ||||||
| chr12:49460343
|
A | T | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-243-427A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460343 | ||||||
| chr12:49460346
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-243-424C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460346 | ||||||
| chr12:49460455
|
CA | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-243-306delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 49460455 | |||||
| chr12:49460619
|
T | G | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-243-151T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460619 | ||||||
| chr12:49460701
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-243-69T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 2/13 | chr12 | 49460701 | ||||||
| chr12:49461147
|
G | T | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.25+110G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49461147 | ||||||
| chr12:49461345
|
T | G | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02809.hp2 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.25+308T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49461345 | ||||||
| chr12:49461388
|
A | G | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+351A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49461388 | ||||||
| chr12:49461426
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+389C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49461426 | ||||||
| chr12:49461784
|
A | G | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.25+747A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49461784 | ||||||
| chr12:49462184
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.25+1147A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49462184 | ||||||
| chr12:49462190
|
A | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.25+1153A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49462190 | ||||||
| chr12:49462411
|
C | T | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.25+1374C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49462411 | ||||||
| chr12:49462412
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.25+1375G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49462412 | ||||||
| chr12:49462619
|
G | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.25+1582G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49462619 | ||||||
| chr12:49462712
|
C | T | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.25+1675C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49462712 | ||||||
| chr12:49463174
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2137G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49463174 | ||||||
| chr12:49463249
|
C | CA | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2226dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49463249 | |||||
| chr12:49463249
|
CA | C | 6 | a0001c0001t0001g0115a0001c0001t0002g0149a0001c0001t0002g0150others(3): Show | 6 | HG01884.hp2 HG01943.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2226delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49463249 | |||||
| chr12:49463269
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.25+2232C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49463269 | ||||||
| chr12:49463306
|
A | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.25+2269A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49463306 | ||||||
| chr12:49463345
|
G | A | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+2308G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49463345 | ||||||
| chr12:49463412
|
C | CA | 17 | a0001c0001t0001g0078a0001c0001t0001g0094a0001c0001t0001g0110others(14): Show | 17 | HG01175.hp2 HG02135.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.25+2395dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49463412 | |||||
| chr12:49463412
|
CA | C | 10 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0011others(7): Show | 10 | HG01069.hp2 HG01071.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+2395delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49463412 | |||||
| chr12:49463710
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+2673T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49463710 | ||||||
| chr12:49464103
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0093 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.25+3066A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49464103 | ||||||
| chr12:49464225
|
TG | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.25+3191delG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49464225 | |||||
| chr12:49464272
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.25+3235G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49464272 | ||||||
| chr12:49464374
|
C | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.25+3337C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49464374 | ||||||
| chr12:49464446
|
C | T | 1 | a0001c0001t0010g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.25+3409C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49464446 | ||||||
| chr12:49464458
|
T | TA | 25 | a0001c0001t0001g0094a0001c0001t0002g0047a0001c0001t0002g0048others(22): Show | 25 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.25+3440dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49464458 | |||||
| chr12:49464542
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.25+3505G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49464542 | ||||||
| chr12:49464627
|
TA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(79): Show | 82 | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.25+3610delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49464627 | |||||
| chr12:49464627
|
TAA | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0002g0153others(2): Show | 5 | HG01884.hp1 HG01943.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+3609_25+3610del others(2): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49464627 | |||||
| chr12:49464746
|
T | A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+3709T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49464746 | ||||||
| chr12:49465210
|
T | G | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.25+4173T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49465210 | ||||||
| chr12:49465300
|
A | G | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+4263A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49465300 | ||||||
| chr12:49465322
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.25+4285A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49465322 | ||||||
| chr12:49465366
|
C | CT | 57 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(54): Show | 57 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.25+4339dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49465366 | |||||
| chr12:49465535
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+4498A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49465535 | ||||||
| chr12:49465777
|
C | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+4740C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49465777 | ||||||
| chr12:49465863
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.25+4826G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49465863 | ||||||
| chr12:49466603
|
G | A | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.25+5566G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49466603 | ||||||
| chr12:49466742
|
A | G | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.25+5705A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49466742 | ||||||
| chr12:49466743
|
T | C | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.25+5706T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49466743 | ||||||
| chr12:49466938
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.25+5901A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49466938 | ||||||
| chr12:49467044
|
G | GT | 29 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0066others(26): Show | 29 | HG01069.hp1 HG01071.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.25+6033dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49467044 | |||||
| chr12:49467044
|
GT | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02572.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+6033delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49467044 | |||||
| chr12:49467044
|
GTT | G | 8 | a0001c0001t0001g0033a0001c0001t0001g0130a0001c0001t0002g0054others(5): Show | 8 | HG01192.hp1 HG01978.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+6032_25+6033del others(2): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49467044 | |||||
| chr12:49467044
|
GTTT | G | 28 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0001t0001g0129others(25): Show | 28 | HG00639.hp2 HG01175.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.25+6031_25+6033del others(3): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49467044 | |||||
| chr12:49467054
|
T | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.25+6017T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49467054 | ||||||
| chr12:49467060
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.25+6023T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49467060 | ||||||
| chr12:49467215
|
A | AT | 54 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0065others(51): Show | 54 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.25+6198dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49467215 | |||||
| chr12:49467215
|
AT | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0117a0001c0001t0001g0137others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.25+6198delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49467215 | |||||
| chr12:49467408
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.25+6371A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49467408 | ||||||
| chr12:49467722
|
G | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.25+6685G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49467722 | ||||||
| chr12:49467916
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.25+6879G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49467916 | ||||||
| chr12:49468064
|
CTCTTT | C | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.25+7036_25+7040del others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49468064 | |||||
| chr12:49468129
|
T | C | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.25+7092T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49468129 | ||||||
| chr12:49468136
|
CTCTTT | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+7110_25+7114del others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49468136 | |||||
| chr12:49468198
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.25+7161T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49468198 | ||||||
| chr12:49468459
|
C | CT | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+7431dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49468459 | |||||
| chr12:49468463
|
TTTTTTGT others(5): Show |
T | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+7444_25+7455del others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49468463 | |||||
| chr12:49469070
|
T | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0093 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.25+8033T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469070 | ||||||
| chr12:49469275
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.25+8238A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469275 | ||||||
| chr12:49469322
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+8285G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469322 | ||||||
| chr12:49469338
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.25+8301C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469338 | ||||||
| chr12:49469389
|
C | CA | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(56): Show | 59 | HG00639.hp2 HG00741.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.25+8376dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49469389 | |||||
| chr12:49469389
|
C | CAA | 11 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0131others(8): Show | 11 | HG01192.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.25+8375_25+8376dup others(2): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49469389 | |||||
| chr12:49469542
|
TA | T | 8 | a0001c0001t0001g0122a0001c0001t0002g0053a0001c0001t0004g0068others(5): Show | 8 | HG00639.hp2 HG01167.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+8527delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49469542 | |||||
| chr12:49469542
|
TAAA | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(26): Show | 29 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.25+8525_25+8527del others(3): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49469542 | |||||
| chr12:49469557
|
A | G | 18 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.25+8520A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469557 | ||||||
| chr12:49469558
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.25+8521A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469558 | ||||||
| chr12:49469559
|
A | G | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.25+8522A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469559 | ||||||
| chr12:49469577
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.25+8540T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469577 | ||||||
| chr12:49469696
|
G | C | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.25+8659G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469696 | ||||||
| chr12:49469757
|
G | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0115others(1): Show | 4 | HG01361.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+8720G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469757 | ||||||
| chr12:49469963
|
T | A | 1 | a0001c0001t0008g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.25+8926T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49469963 | ||||||
| chr12:49470568
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+9531A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49470568 | ||||||
| chr12:49470691
|
C | A | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.25+9654C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49470691 | ||||||
| chr12:49470756
|
TGAG | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.25+9723_25+9725del others(3): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49470756 | |||||
| chr12:49471494
|
A | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0115others(1): Show | 4 | HG01361.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+10457A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49471494 | ||||||
| chr12:49471513
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.25+10476A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49471513 | ||||||
| chr12:49471586
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+10549C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49471586 | ||||||
| chr12:49471697
|
A | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+10660A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49471697 | ||||||
| chr12:49472020
|
T | TC | 32 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(29): Show | 32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.25+10985dupC | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49472020 | |||||
| chr12:49472096
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.25+11059C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49472096 | ||||||
| chr12:49472580
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.25+11543G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49472580 | ||||||
| chr12:49472611
|
T | TTA | 59 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(56): Show | 59 | HG00639.hp2 HG01167.hp1 HG01175.hp1 others(56): Show |
intron_variant | MODIFIER | c.25+11591_25+11592d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49472611 | |||||
| chr12:49472611
|
T | TTATA | 16 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(13): Show | 16 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.25+11589_25+11592d others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49472611 | |||||
| chr12:49472655
|
A | T | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.25+11618A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49472655 | ||||||
| chr12:49472840
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.26-11750G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49472840 | ||||||
| chr12:49472936
|
G | C | 1 | a0001c0001t0007g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.26-11654G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49472936 | ||||||
| chr12:49473048
|
CA | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(18): Show | 21 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.26-11526delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49473048 | |||||
| chr12:49473406
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.26-11184G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49473406 | ||||||
| chr12:49474056
|
T | C | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.26-10534T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49474056 | ||||||
| chr12:49474473
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0128a0001c0001t0001g0129others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-10117G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49474473 | ||||||
| chr12:49474654
|
C | G | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-9936C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49474654 | ||||||
| chr12:49475057
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.26-9533C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49475057 | ||||||
| chr12:49475322
|
T | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-9268T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49475322 | ||||||
| chr12:49475339
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.26-9251C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49475339 | ||||||
| chr12:49475427
|
C | CTTG | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 33 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.26-9136_26-9134dup others(3): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49475427 | |||||
| chr12:49475427
|
CTTGTTG | C | 3 | a0001c0001t0004g0124a0001c0001t0004g0125a0001c0001t0004g0126 | 3 | HG01167.hp1 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.26-9139_26-9134del others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49475427 | |||||
| chr12:49475430
|
G | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0084 | 3 | HG01167.hp2 HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.26-9160G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49475430 | ||||||
| chr12:49476496
|
CAG | C | 2 | a0001c0001t0002g0007a0001c0005t0001g0064 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.26-8093_26-8092del others(2): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49476496 | ||||||
| chr12:49476501
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.26-8089G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49476501 | ||||||
| chr12:49476901
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-7689T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49476901 | ||||||
| chr12:49477037
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-7553G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49477037 | ||||||
| chr12:49477102
|
TA | T | 5 | a0001c0001t0001g0143a0001c0001t0002g0151a0001c0001t0003g0030others(2): Show | 5 | HG01167.hp1 HG01884.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-7471delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49477102 | |||||
| chr12:49477181
|
A | G | 24 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0072others(21): Show | 24 | HG00280.hp2 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.26-7409A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49477181 | ||||||
| chr12:49477228
|
G | A | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-7362G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49477228 | ||||||
| chr12:49477330
|
G | A | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.26-7260G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49477330 | ||||||
| chr12:49477388
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.26-7202A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49477388 | ||||||
| chr12:49477953
|
T | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0114 | 2 | HG04184.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.26-6637T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49477953 | ||||||
| chr12:49477962
|
C | CT | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0080others(2): Show | 5 | HG00280.hp2 HG00741.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-6605dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49477962 | |||||
| chr12:49477962
|
CT | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(25): Show | 28 | HG01069.hp1 HG01167.hp2 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.26-6605delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49477962 | |||||
| chr12:49477985
|
T | TA | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.26-6603dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49477985 | |||||
| chr12:49478029
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.26-6561T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49478029 | ||||||
| chr12:49478079
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00741.hp1 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.26-6511A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49478079 | ||||||
| chr12:49478479
|
A | G | 1 | a0001c0001t0001g0006 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.26-6111A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49478479 | ||||||
| chr12:49478660
|
T | C | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.26-5930T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49478660 | ||||||
| chr12:49478741
|
C | A | 4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02809.hp2 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.26-5849C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49478741 | ||||||
| chr12:49479211
|
C | T | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.26-5379C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479211 | ||||||
| chr12:49479358
|
C | A | 1 | a0002c0006t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.26-5232C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479358 | ||||||
| chr12:49479626
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.26-4964A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479626 | ||||||
| chr12:49479787
|
C | G | 2 | a0001c0001t0002g0061a0001c0001t0002g0063 | 2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.26-4803C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479787 | ||||||
| chr12:49479817
|
A | G | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.26-4773A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479817 | ||||||
| chr12:49479925
|
A | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0115others(1): Show | 4 | HG01361.hp1 HG01943.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-4665A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479925 | ||||||
| chr12:49479986
|
A | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0113 | 2 | NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.26-4604A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49479986 | ||||||
| chr12:49480086
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-4504C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49480086 | ||||||
| chr12:49480342
|
G | C | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.26-4248G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49480342 | ||||||
| chr12:49480716
|
G | T | 1 | a0001c0001t0003g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-3874G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49480716 | ||||||
| chr12:49480795
|
GT | G | 20 | a0001c0001t0001g0082a0001c0001t0002g0047a0001c0001t0002g0048others(17): Show | 20 | HG00639.hp2 HG01167.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.26-3783delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49480795 | |||||
| chr12:49481437
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.26-3153C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49481437 | ||||||
| chr12:49481457
|
CA | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-3132delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49481457 | ||||||
| chr12:49481458
|
A | AT | 14 | a0001c0001t0001g0066a0001c0001t0001g0076a0001c0001t0001g0078others(11): Show | 14 | HG01175.hp2 HG01891.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.26-3106dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49481458 | |||||
| chr12:49481458
|
A | ATT | 7 | a0001c0001t0001g0117a0001c0001t0001g0137a0001c0001t0001g0139others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-3107_26-3106dup others(2): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49481458 | |||||
| chr12:49481458
|
AT | A | 63 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(60): Show | 63 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.26-3106delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 49481458 | |||||
| chr12:49481741
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0020 | 2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.26-2849G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49481741 | ||||||
| chr12:49482282
|
C | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.26-2308C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49482282 | ||||||
| chr12:49482419
|
C | T | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.26-2171C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49482419 | ||||||
| chr12:49482582
|
C | T | 3 | a0001c0001t0005g0021a0001c0001t0005g0023a0001c0001t0005g0024 | 3 | HG01346.hp1 HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.26-2008C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49482582 | ||||||
| chr12:49482858
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-1732G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49482858 | ||||||
| chr12:49482900
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.26-1690C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49482900 | ||||||
| chr12:49483153
|
A | AT | 2 | a0001c0001t0001g0066a0001c0001t0001g0142 | 2 | HG01175.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.26-1437_26-1436ins others(1): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49483153 | ||||||
| chr12:49483434
|
A | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-1156A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49483434 | ||||||
| chr12:49483770
|
TG | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-819delG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49483770 | ||||||
| chr12:49483894
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.26-696C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49483894 | ||||||
| chr12:49484361
|
A | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0113 | 2 | NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.26-229A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49484361 | ||||||
| chr12:49484548
|
T | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-42T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 3/13 | chr12 | 49484548 | ||||||
| chr12:49484890
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0110 | 2 | HG01074.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.105+221A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49484890 | ||||||
| chr12:49484966
|
C | T | 1 | a0001c0001t0012g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.105+297C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49484966 | ||||||
| chr12:49485067
|
C | CT | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 21 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.105+415dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 49485067 | |||||
| chr12:49485114
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0111 | 2 | HG01515.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.105+445T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49485114 | ||||||
| chr12:49485333
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.105+664C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49485333 | ||||||
| chr12:49485380
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+711G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49485380 | ||||||
| chr12:49485394
|
C | G | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.105+725C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49485394 | ||||||
| chr12:49485412
|
A | AG | 2 | a0001c0001t0003g0012a0001c0001t0003g0016 | 2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.105+744dupG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 49485412 | |||||
| chr12:49485432
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0001 | 2 | HG02055.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.105+763G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49485432 | ||||||
| chr12:49485476
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.105+807C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49485476 | ||||||
| chr12:49486025
|
C | CT | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.105+1357dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 49486025 | |||||
| chr12:49486073
|
A | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0135 | 2 | HG02080.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.105+1404A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49486073 | ||||||
| chr12:49486153
|
C | T | 2 | a0001c0001t0005g0022a0001c0001t0005g0025 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.105+1484C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49486153 | ||||||
| chr12:49486241
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.105+1572G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49486241 | ||||||
| chr12:49486331
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.105+1662G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49486331 | ||||||
| chr12:49486962
|
A | T | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.105+2293A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49486962 | ||||||
| chr12:49487296
|
T | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.106-2169T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49487296 | ||||||
| chr12:49487493
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.106-1972A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49487493 | ||||||
| chr12:49487560
|
C | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.106-1905C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49487560 | ||||||
| chr12:49487589
|
A | G | 1 | a0002c0006t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.106-1876A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49487589 | ||||||
| chr12:49487754
|
C | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1711C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49487754 | ||||||
| chr12:49488108
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014 | 3 | HG01069.hp2 HG01515.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.106-1357G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488108 | ||||||
| chr12:49488145
|
A | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.106-1320A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488145 | ||||||
| chr12:49488250
|
G | C | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.106-1215G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488250 | ||||||
| chr12:49488365
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.106-1100T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488365 | ||||||
| chr12:49488421
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-1044G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488421 | ||||||
| chr12:49488647
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.106-818G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488647 | ||||||
| chr12:49488708
|
T | C | 1 | a0001c0001t0008g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106-757T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49488708 | ||||||
| chr12:49489194
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-271A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49489194 | ||||||
| chr12:49489284
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.106-181C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49489284 | ||||||
| chr12:49489421
|
G | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.106-44G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 4/13 | chr12 | 49489421 | ||||||
| chr12:49489588
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.214+15A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49489588 | ||||||
| chr12:49489810
|
A | G | 5 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0054others(2): Show | 5 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.214+237A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49489810 | ||||||
| chr12:49489824
|
C | T | 18 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(15): Show | 18 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.214+251C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49489824 | ||||||
| chr12:49489929
|
A | G | 1 | a0001c0001t0010g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214+356A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49489929 | ||||||
| chr12:49490110
|
T | C | 1 | a0001c0001t0001g0015 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.214+537T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49490110 | ||||||
| chr12:49490201
|
G | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.215-481G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49490201 | ||||||
| chr12:49490486
|
A | G | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.215-196A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49490486 | ||||||
| chr12:49490553
|
C | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.215-129C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 5/13 | chr12 | 49490553 | ||||||
| chr12:49490868
|
G | T | 21 | a0001c0001t0001g0036a0001c0001t0001g0070a0001c0001t0001g0086others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.264+137G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49490868 | ||||||
| chr12:49491015
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0113 | 2 | NA18961.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.264+284G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49491015 | ||||||
| chr12:49491143
|
C | CA | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG02080.hp2 HG02135.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.264+428dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49491143 | |||||
| chr12:49491295
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.264+564G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49491295 | ||||||
| chr12:49491374
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.264+643C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49491374 | ||||||
| chr12:49492212
|
CTTTTTTC others(6): Show |
C | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.264+1494_264+1506d others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49492212 | |||||
| chr12:49492383
|
G | GCTAATAT others(304): Show |
4 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(1): Show | 4 | HG02809.hp2 HG03471.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+1670_264+1671i others(313): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49492383 | |||||
| chr12:49492383
|
G | GCTAATAT others(320): Show |
1 | a0001c0001t0003g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.264+1670_264+1671i others(329): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49492383 | |||||
| chr12:49492383
|
G | GCTAATAT others(322): Show |
2 | a0001c0001t0003g0012a0001c0001t0005g0022 | 2 | HG02559.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.264+1670_264+1671i others(331): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49492383 | |||||
| chr12:49492383
|
G | GCTAATAT others(323): Show |
4 | a0001c0001t0005g0021a0001c0001t0005g0023a0001c0001t0005g0024others(1): Show | 4 | HG01346.hp1 HG02257.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+1670_264+1671i others(332): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49492383 | |||||
| chr12:49492607
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264+1876A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49492607 | ||||||
| chr12:49492704
|
G | A | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.264+1973G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49492704 | ||||||
| chr12:49492818
|
G | A | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265-1923G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49492818 | ||||||
| chr12:49493002
|
T | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.265-1739T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493002 | ||||||
| chr12:49493099
|
TA | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 84 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.265-1624delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49493099 | |||||
| chr12:49493117
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.265-1624A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493117 | ||||||
| chr12:49493169
|
A | G | 1 | a0001c0001t0005g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.265-1572A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493169 | ||||||
| chr12:49493183
|
G | A | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.265-1558G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493183 | ||||||
| chr12:49493397
|
C | CT | 34 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(31): Show | 34 | HG00280.hp1 HG00639.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.265-1327dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49493397 | |||||
| chr12:49493420
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-1321G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493420 | ||||||
| chr12:49493602
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.265-1139C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493602 | ||||||
| chr12:49493664
|
A | C | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.265-1077A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493664 | ||||||
| chr12:49493950
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 85 | HG00280.hp1 HG00639.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.265-791C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49493950 | ||||||
| chr12:49494212
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(42): Show | 45 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.265-529C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49494212 | ||||||
| chr12:49494486
|
T | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.265-255T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | chr12 | 49494486 | ||||||
| chr12:49494701
|
CTTTCTTT others(3): Show |
C | 1 | a0001c0001t0007g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.265-31_265-22delCT others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 49494701 | |||||
| chr12:49495078
|
A | G | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.526+76A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 7/13 | chr12 | 49495078 | ||||||
| chr12:49495334
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.526+332C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 7/13 | chr12 | 49495334 | ||||||
| chr12:49495998
|
T | G | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.527-835T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 7/13 | chr12 | 49495998 | ||||||
| chr12:49496319
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.527-514C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 7/13 | chr12 | 49496319 | ||||||
| chr12:49496360
|
G | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.527-473G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 7/13 | chr12 | 49496360 | ||||||
| chr12:49497392
|
CT | C | 7 | a0001c0001t0001g0116a0001c0001t0004g0068a0001c0001t0004g0123others(4): Show | 7 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+398delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49497392 | |||||
| chr12:49497407
|
T | C | 54 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(51): Show | 54 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.703+398T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497407 | ||||||
| chr12:49497555
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.703+546C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497555 | ||||||
| chr12:49497647
|
G | T | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+638G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497647 | ||||||
| chr12:49497648
|
C | T | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+639C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497648 | ||||||
| chr12:49497703
|
A | G | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+694A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497703 | ||||||
| chr12:49497723
|
C | G | 13 | a0001c0001t0001g0036a0001c0001t0001g0117a0001c0001t0001g0137others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+714C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497723 | ||||||
| chr12:49497947
|
A | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+938A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49497947 | ||||||
| chr12:49498056
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+1047T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498056 | ||||||
| chr12:49498137
|
A | AATATATA others(3): Show |
2 | a0001c0001t0004g0125a0001c0001t0004g0134 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.703+1129_703+1130i others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498137 | |||||
| chr12:49498137
|
A | AATATATA others(5): Show |
3 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124 | 3 | HG01167.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703+1129_703+1130i others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498137 | |||||
| chr12:49498137
|
A | AATATATA others(9): Show |
1 | a0001c0001t0004g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.703+1129_703+1130i others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498137 | |||||
| chr12:49498139
|
A | T | 7 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(4): Show | 7 | HG01167.hp1 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+1130A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498139 | ||||||
| chr12:49498141
|
A | AT | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.703+1132_703+1133i others(3): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498141 | ||||||
| chr12:49498141
|
A | T | 8 | a0001c0001t0001g0127a0001c0001t0004g0068a0001c0001t0004g0123others(5): Show | 8 | HG01167.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+1132A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498141 | ||||||
| chr12:49498143
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.703+1135_703+1136i others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498143 | |||||
| chr12:49498143
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.703+1135_703+1136i others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498143 | |||||
| chr12:49498143
|
A | T | 38 | a0001c0001t0001g0065a0001c0001t0001g0071a0001c0001t0001g0072others(35): Show | 38 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.703+1134A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498143 | ||||||
| chr12:49498145
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+1137_703+1138i others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAAAAAT others(6): Show |
1 | a0001c0001t0002g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAAAAAT others(8): Show |
1 | a0001c0001t0001g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.703+1137_703+1138i others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0006g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.703+1137_703+1138i others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAAAATA others(9): Show |
2 | a0001c0001t0002g0051a0001c0001t0002g0055 | 2 | HG01175.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.703+1137_703+1138i others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAAATAT others(6): Show |
1 | a0001c0001t0008g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATAT | 8 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0013others(5): Show | 8 | HG01069.hp2 HG01515.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+1137_703+1138i others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(5): Show |
4 | a0001c0001t0001g0155a0001c0001t0002g0053a0001c0001t0002g0150others(1): Show | 4 | HG00639.hp2 HG02451.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+1137_703+1138i others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0001g0133 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.703+1137_703+1138i others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(9): Show |
3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131 | 3 | HG01891.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.703+1137_703+1138i others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0002g0061 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(22): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(15): Show |
1 | a0001c0001t0002g0063 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.703+1137_703+1138i others(24): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAAATATA others(17): Show |
1 | a0001c0001t0008g0049 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(26): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAATATAT others(2): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0137a0001c0001t0001g0139others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+1137_703+1138i others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAATATAT others(4): Show |
2 | a0001c0001t0001g0147a0004c0002t0002g0052 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.703+1137_703+1138i others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AAATATAT others(6): Show |
1 | a0001c0001t0013g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.703+1137_703+1138i others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AATAT | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG02055.hp1 HG02809.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+1157_703+1160d others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0156 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.703+1151_703+1160d others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AATATATA others(5): Show |
5 | a0001c0001t0002g0054a0001c0001t0002g0060a0001c0001t0002g0149others(2): Show | 5 | HG01192.hp1 HG01884.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+1149_703+1160d others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AATATATA others(7): Show |
1 | a0001c0001t0012g0062 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.703+1147_703+1160d others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.703+1143_703+1160d others(20): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498145
|
A | ATATATAT | 2 | a0001c0001t0001g0009a0001c0001t0001g0015 | 2 | HG01071.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.703+1136_703+1137i others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498145 | ||||||
| chr12:49498145
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0048 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.703+1136_703+1137i others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498145 | ||||||
| chr12:49498145
|
A | T | 50 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0069others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.703+1136A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498145 | ||||||
| chr12:49498145
|
AAT | A | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+1159_703+1160d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498145 | |||||
| chr12:49498146
|
ATAT | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+1138_703+1140d others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498146 | ||||||
| chr12:49498147
|
T | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.703+1138T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498147 | ||||||
| chr12:49498149
|
T | A | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+1140T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498149 | ||||||
| chr12:49498293
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.703+1284A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498293 | ||||||
| chr12:49498368
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00741.hp1 HG01074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.703+1359T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498368 | ||||||
| chr12:49498746
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.704-1324A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498746 | ||||||
| chr12:49498750
|
C | T | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(93): Show |
intron_variant | MODIFIER | c.704-1320C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498750 | ||||||
| chr12:49498790
|
A | AT | 62 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(59): Show | 62 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.704-1260dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498790 | |||||
| chr12:49498790
|
A | ATTT | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-1262_704-1260d others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49498790 | |||||
| chr12:49498850
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.704-1220A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498850 | ||||||
| chr12:49498887
|
A | G | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.704-1183A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49498887 | ||||||
| chr12:49499012
|
C | G | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.704-1058C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499012 | ||||||
| chr12:49499075
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.704-995C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499075 | ||||||
| chr12:49499108
|
C | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.704-962C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499108 | ||||||
| chr12:49499250
|
T | C | 1 | a0001c0001t0004g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.704-820T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499250 | ||||||
| chr12:49499391
|
G | GTTATT | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-677_704-676ins others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
G | GTTATTTT others(3): Show |
2 | a0001c0001t0003g0026a0001c0001t0003g0029 | 2 | HG03471.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.704-677_704-676ins others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
G | GTTGTT | 14 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0077others(11): Show | 14 | HG00099.hp2 HG00741.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.704-631_704-627dup others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
G | GTTGTTTT others(3): Show |
7 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0122others(4): Show | 7 | HG01167.hp1 HG02293.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.704-636_704-627dup others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
GTTGTT | G | 36 | a0001c0001t0001g0036a0001c0001t0001g0089a0001c0001t0001g0110others(33): Show | 36 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-631_704-627del others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
GTTGTTTT others(3): Show |
G | 16 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0002g0048others(13): Show | 16 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.704-636_704-627del others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
GTTGTTTT others(8): Show |
G | 15 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0128others(12): Show | 15 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-641_704-627del others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499391
|
GTTGTTTT others(18): Show |
G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.704-651_704-627del others(25): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49499391 | |||||
| chr12:49499394
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0017others(4): Show | 7 | HG00280.hp1 HG01123.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-676G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499394 | ||||||
| chr12:49499399
|
G | A | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-671G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499399 | ||||||
| chr12:49499476
|
T | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.704-594T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499476 | ||||||
| chr12:49499689
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.704-381C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499689 | ||||||
| chr12:49499849
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.704-221T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49499849 | ||||||
| chr12:49500032
|
C | CT | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 87 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(84): Show |
intron_variant | MODIFIER | c.704-25dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 49500032 | |||||
| chr12:49500062
|
T | C | 3 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032 | 3 | HG02258.hp1 NA18906.hp1 NA19043.hp1 |
splice_region_variant&intron_variant | LOW | c.704-8T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 8/13 | chr12 | 49500062 | ||||||
| chr12:49500474
|
C | G | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.839+269C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49500474 | ||||||
| chr12:49500501
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.839+296G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49500501 | ||||||
| chr12:49500538
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.839+333C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49500538 | ||||||
| chr12:49500689
|
G | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.839+484G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49500689 | ||||||
| chr12:49500695
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.839+490C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49500695 | ||||||
| chr12:49500818
|
A | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+613A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49500818 | ||||||
| chr12:49501642
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.839+1437G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49501642 | ||||||
| chr12:49501713
|
G | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(93): Show |
intron_variant | MODIFIER | c.839+1508G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49501713 | ||||||
| chr12:49501760
|
CAT | C | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.839+1556_839+1557d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49501760 | ||||||
| chr12:49501839
|
G | A | 4 | a0001c0001t0002g0048a0001c0001t0002g0060a0001c0001t0008g0049others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.839+1634G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49501839 | ||||||
| chr12:49502320
|
A | G | 1 | a0001c0001t0004g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.839+2115A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49502320 | ||||||
| chr12:49503173
|
AACCCCAT others(4): Show |
A | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.839+2971_839+2981d others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49503173 | |||||
| chr12:49503202
|
T | C | 1 | a0001c0001t0009g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.839+2997T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503202 | ||||||
| chr12:49503402
|
C | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.839+3197C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503402 | ||||||
| chr12:49503477
|
G | A | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.839+3272G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503477 | ||||||
| chr12:49503603
|
C | T | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.839+3398C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503603 | ||||||
| chr12:49503606
|
G | T | 1 | a0001c0001t0002g0152 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.839+3401G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503606 | ||||||
| chr12:49503620
|
T | G | 16 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0058others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.839+3415T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503620 | ||||||
| chr12:49503648
|
C | CA | 74 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(71): Show | 74 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(71): Show |
intron_variant | MODIFIER | c.839+3455dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49503648 | |||||
| chr12:49503648
|
C | CAA | 12 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(9): Show | 12 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.839+3454_839+3455d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49503648 | |||||
| chr12:49503665
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.839+3460A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503665 | ||||||
| chr12:49503668
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.839+3463G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503668 | ||||||
| chr12:49503909
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.839+3704T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503909 | ||||||
| chr12:49503949
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.839+3744C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49503949 | ||||||
| chr12:49504151
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.839+3946C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504151 | ||||||
| chr12:49504285
|
G | A | 11 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(8): Show | 11 | HG01346.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.839+4080G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504285 | ||||||
| chr12:49504572
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+4367G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504572 | ||||||
| chr12:49504734
|
GT | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.839+4540delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49504734 | |||||
| chr12:49504737
|
T | C | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.839+4532T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504737 | ||||||
| chr12:49504754
|
T | TTTTC | 27 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(24): Show | 27 | HG01071.hp1 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.839+4565_839+4568d others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49504754 | |||||
| chr12:49504770
|
C | CT | 24 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(21): Show | 24 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.839+4585dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49504770 | |||||
| chr12:49504770
|
C | CTTTCT | 19 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0051others(16): Show | 19 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.839+4568_839+4569i others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49504770 | |||||
| chr12:49504770
|
CT | C | 6 | a0001c0001t0001g0065a0001c0001t0001g0084a0001c0001t0001g0098others(3): Show | 6 | HG01943.hp1 HG02451.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.839+4585delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49504770 | |||||
| chr12:49504771
|
T | TTTC | 5 | a0001c0001t0001g0117a0001c0001t0003g0037a0001c0001t0003g0038others(2): Show | 5 | HG01069.hp1 HG02572.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.839+4568_839+4569i others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49504771 | |||||
| chr12:49504773
|
T | TC | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(15): Show | 18 | HG01167.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.839+4568_839+4569i others(3): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504773 | ||||||
| chr12:49504777
|
T | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+4572T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504777 | ||||||
| chr12:49504809
|
A | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+4604A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49504809 | ||||||
| chr12:49505025
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+4820G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505025 | ||||||
| chr12:49505069
|
C | CT | 12 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106others(9): Show | 12 | HG00741.hp1 HG01074.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.839+4874dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49505069 | |||||
| chr12:49505195
|
T | C | 2 | a0001c0001t0001g0040a0001c0003t0001g0057 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.839+4990T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505195 | ||||||
| chr12:49505323
|
C | A | 13 | a0001c0001t0001g0033a0001c0001t0001g0128a0001c0001t0001g0129others(10): Show | 13 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.839+5118C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505323 | ||||||
| chr12:49505377
|
TTAACTC | T | 7 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(4): Show | 7 | HG02258.hp1 HG02809.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.839+5177_839+5182d others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49505377 | |||||
| chr12:49505582
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0099 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.839+5377A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505582 | ||||||
| chr12:49505655
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+5450G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505655 | ||||||
| chr12:49505718
|
T | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+5513T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505718 | ||||||
| chr12:49505762
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0063 | 2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.839+5557G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505762 | ||||||
| chr12:49505852
|
C | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.839+5647C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505852 | ||||||
| chr12:49505934
|
A | C | 1 | a0001c0001t0001g0009 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.839+5729A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49505934 | ||||||
| chr12:49506006
|
C | CAT | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.839+5803_839+5804d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49506006 | |||||
| chr12:49506032
|
T | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+5827T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506032 | ||||||
| chr12:49506249
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+6044C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506249 | ||||||
| chr12:49506323
|
A | AG | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.839+6119dupG | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49506323 | |||||
| chr12:49506343
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.839+6138C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506343 | ||||||
| chr12:49506396
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.839+6191G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506396 | ||||||
| chr12:49506511
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.839+6306A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506511 | ||||||
| chr12:49506549
|
T | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+6344T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506549 | ||||||
| chr12:49506788
|
T | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+6583T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506788 | ||||||
| chr12:49506802
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.839+6597C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506802 | ||||||
| chr12:49506836
|
TA | T | 15 | a0001c0001t0001g0036a0001c0001t0001g0073a0001c0001t0001g0108others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.839+6648delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49506836 | |||||
| chr12:49506842
|
A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.839+6637A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506842 | ||||||
| chr12:49506887
|
C | G | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.839+6682C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49506887 | ||||||
| chr12:49507032
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.839+6827C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49507032 | ||||||
| chr12:49507438
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0099 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.840-7117G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49507438 | ||||||
| chr12:49507589
|
C | A | 1 | a0001c0001t0011g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.840-6966C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49507589 | ||||||
| chr12:49507686
|
G | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-6869G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49507686 | ||||||
| chr12:49507896
|
A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-6659A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49507896 | ||||||
| chr12:49508018
|
G | A | 57 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(54): Show | 57 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.840-6537G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49508018 | ||||||
| chr12:49508269
|
G | A | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.840-6286G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49508269 | ||||||
| chr12:49508521
|
TCA | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-6031_840-6030d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49508521 | |||||
| chr12:49508646
|
TCTGGTCT others(7): Show |
T | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.840-5904_840-5891d others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49508646 | |||||
| chr12:49508654
|
T | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-5901T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49508654 | ||||||
| chr12:49508745
|
CT | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(21): Show | 24 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.840-5796delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49508745 | |||||
| chr12:49508925
|
G | T | 1 | a0001c0001t0007g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.840-5630G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49508925 | ||||||
| chr12:49509273
|
C | CT | 49 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(46): Show | 49 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(46): Show |
intron_variant | MODIFIER | c.840-5257dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49509273 | |||||
| chr12:49509273
|
C | CTT | 11 | a0001c0001t0001g0129a0001c0001t0002g0007a0001c0001t0002g0051others(8): Show | 11 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.840-5258_840-5257d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49509273 | |||||
| chr12:49509273
|
CT | C | 15 | a0001c0001t0001g0067a0001c0001t0001g0082a0001c0001t0001g0114others(12): Show | 15 | HG00099.hp1 HG01167.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.840-5257delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49509273 | |||||
| chr12:49509276
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.840-5279T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49509276 | ||||||
| chr12:49509349
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-5206C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49509349 | ||||||
| chr12:49509426
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.840-5129G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49509426 | ||||||
| chr12:49509654
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-4901G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49509654 | ||||||
| chr12:49509810
|
C | CA | 26 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(23): Show | 26 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.840-4729dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49509810 | |||||
| chr12:49509810
|
C | CAAA | 8 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(5): Show | 8 | HG02486.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.840-4731_840-4729d others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49509810 | |||||
| chr12:49510074
|
T | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-4481T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510074 | ||||||
| chr12:49510112
|
A | T | 1 | a0003c0004t0001g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.840-4443A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510112 | ||||||
| chr12:49510242
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.840-4313G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510242 | ||||||
| chr12:49510286
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.840-4269G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510286 | ||||||
| chr12:49510562
|
C | CA | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 78 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.840-3975dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49510562 | |||||
| chr12:49510562
|
C | CAA | 11 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(8): Show | 11 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.840-3976_840-3975d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49510562 | |||||
| chr12:49510562
|
CAA | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-3976_840-3975d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49510562 | |||||
| chr12:49510615
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.840-3940A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510615 | ||||||
| chr12:49510812
|
T | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.840-3743T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510812 | ||||||
| chr12:49510893
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-3662G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510893 | ||||||
| chr12:49510950
|
G | A | 1 | a0001c0001t0003g0037 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.840-3605G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510950 | ||||||
| chr12:49510966
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-3589C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49510966 | ||||||
| chr12:49511044
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.840-3511T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49511044 | ||||||
| chr12:49511376
|
A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-3179A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49511376 | ||||||
| chr12:49511541
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.840-3014T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49511541 | ||||||
| chr12:49511854
|
A | G | 14 | a0001c0001t0003g0012a0001c0001t0003g0016a0001c0001t0003g0026others(11): Show | 14 | HG01346.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.840-2701A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49511854 | ||||||
| chr12:49511930
|
T | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.840-2625T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49511930 | ||||||
| chr12:49511995
|
G | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0048a0001c0001t0002g0060others(7): Show | 10 | HG01884.hp2 HG02145.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.840-2560G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49511995 | ||||||
| chr12:49512152
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.840-2403G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49512152 | ||||||
| chr12:49512381
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.840-2174G>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49512381 | ||||||
| chr12:49512509
|
C | CA | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-2041dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49512509 | |||||
| chr12:49512602
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-1953C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49512602 | ||||||
| chr12:49512789
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.840-1766A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49512789 | ||||||
| chr12:49512905
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.840-1650G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49512905 | ||||||
| chr12:49513041
|
G | A | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.840-1514G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513041 | ||||||
| chr12:49513149
|
A | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.840-1406A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513149 | ||||||
| chr12:49513198
|
C | T | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.840-1357C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513198 | ||||||
| chr12:49513210
|
A | AGT | 28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(25): Show | 28 | HG00099.hp2 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.840-1320_840-1319d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49513210 | |||||
| chr12:49513210
|
A | AGTGT | 9 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0014others(6): Show | 9 | HG01069.hp2 HG01071.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-1322_840-1319d others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49513210 | |||||
| chr12:49513210
|
A | AGTGTGT | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(6): Show | 9 | HG00280.hp1 HG01123.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.840-1324_840-1319d others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49513210 | |||||
| chr12:49513210
|
AGT | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.840-1320_840-1319d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49513210 | |||||
| chr12:49513235
|
GTT | G | 8 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(5): Show | 8 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.840-1318_840-1317d others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49513235 | |||||
| chr12:49513240
|
A | T | 8 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(5): Show | 8 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.840-1315A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513240 | ||||||
| chr12:49513480
|
C | T | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.840-1075C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513480 | ||||||
| chr12:49513646
|
T | A | 1 | a0001c0001t0002g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.840-909T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513646 | ||||||
| chr12:49513732
|
T | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.840-823T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513732 | ||||||
| chr12:49513797
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.840-758T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513797 | ||||||
| chr12:49513879
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.840-676G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513879 | ||||||
| chr12:49513939
|
G | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.840-616G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49513939 | ||||||
| chr12:49514154
|
CA | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.840-385delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49514154 | |||||
| chr12:49514237
|
T | TA | 66 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.840-312dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr12 | 49514237 | |||||
| chr12:49514293
|
G | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.840-262G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49514293 | ||||||
| chr12:49514370
|
G | A | 3 | a0001c0001t0004g0041a0001c0001t0007g0034a0001c0001t0007g0035 | 3 | HG02809.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.840-185G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 9/13 | chr12 | 49514370 | ||||||
| chr12:49514931
|
T | G | 7 | a0001c0001t0002g0001a0001c0001t0002g0149a0001c0001t0002g0150others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.898+318T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49514931 | ||||||
| chr12:49515015
|
A | G | 1 | a0001c0001t0004g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.898+402A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49515015 | ||||||
| chr12:49515374
|
A | G | 66 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.898+761A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49515374 | ||||||
| chr12:49515410
|
A | G | 66 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.898+797A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49515410 | ||||||
| chr12:49515868
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.898+1255G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49515868 | ||||||
| chr12:49515979
|
A | G | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.898+1366A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49515979 | ||||||
| chr12:49516138
|
C | CA | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG00280.hp1 HG01884.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+1554dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516138 | |||||
| chr12:49516138
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0113 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.898+1541_898+1554d others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516138 | |||||
| chr12:49516153
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.898+1540A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516153 | ||||||
| chr12:49516153
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.898+1542_898+1556d others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516153 | |||||
| chr12:49516154
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0006g0043 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.898+1543_898+1556d others(16): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516154 | |||||
| chr12:49516155
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0117a0001c0001t0001g0140a0001c0001t0002g0061others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.898+1544_898+1556d others(15): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516155 | |||||
| chr12:49516155
|
AAAAAAAA others(8): Show |
A | 12 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0141others(9): Show | 12 | HG02055.hp2 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.898+1544_898+1558d others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516155 | |||||
| chr12:49516156
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0058a0001c0001t0002g0001 | 2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.898+1545_898+1560d others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516156 | |||||
| chr12:49516157
|
AAAAAAAA others(8): Show |
A | 22 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0154others(19): Show | 22 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.898+1546_898+1560d others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516157 | |||||
| chr12:49516157
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0003g0038a0001c0001t0003g0039 | 2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.898+1546_898+1562d others(19): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516157 | |||||
| chr12:49516157
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.898+1546_898+1564d others(21): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516157 | |||||
| chr12:49516158
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0005t0001g0064 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.898+1547_898+1558d others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516158 | |||||
| chr12:49516158
|
AAAAAAAA others(9): Show |
A | 5 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(2): Show | 5 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+1547_898+1562d others(18): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516158 | |||||
| chr12:49516159
|
AAAAAAAA others(8): Show |
A | 6 | a0001c0001t0001g0040a0001c0001t0001g0101a0001c0001t0001g0133others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.898+1548_898+1562d others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516159 | |||||
| chr12:49516161
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0001g0130 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.898+1550_898+1564d others(17): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516161 | |||||
| chr12:49516162
|
AAAAAATA others(3): Show |
A | 1 | a0001c0001t0002g0007 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.898+1551_898+1560d others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516162 | |||||
| chr12:49516166
|
A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0144 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.898+1554_898+1555i others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516166 | |||||
| chr12:49516166
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0001g0116 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.898+1554_898+1555i others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516166 | |||||
| chr12:49516166
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0019others(1): Show | 4 | HG01069.hp2 HG02683.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.898+1553A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516166 | ||||||
| chr12:49516166
|
AATAT | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0111a0001c0001t0004g0124others(2): Show | 5 | HG01167.hp1 HG01515.hp2 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.898+1593_898+1596d others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516166 | |||||
| chr12:49516166
|
AATATATA others(1): Show |
A | 9 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0088others(6): Show | 9 | HG00099.hp1 HG00741.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.898+1589_898+1596d others(10): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516166 | |||||
| chr12:49516166
|
AATATATA others(3): Show |
A | 2 | a0001c0001t0003g0030a0002c0006t0001g0136 | 2 | HG00099.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.898+1587_898+1596d others(12): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516166 | |||||
| chr12:49516166
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0003g0031 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.898+1585_898+1596d others(14): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516166 | |||||
| chr12:49516167
|
AT | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0118 | 2 | HG02109.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.898+1555delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516167
|
ATAT | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0098others(1): Show | 4 | HG02886.hp1 HG03041.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.898+1555_898+1557d others(5): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516167
|
ATATAT | A | 9 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0080others(6): Show | 9 | HG00280.hp2 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.898+1555_898+1559d others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516167
|
ATATATAT | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0094others(3): Show | 6 | HG01891.hp1 HG02615.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.898+1555_898+1561d others(9): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516167
|
ATATATAT others(2): Show |
A | 9 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0082others(6): Show | 9 | HG00639.hp1 HG01167.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.898+1555_898+1563d others(11): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516167
|
ATATATAT others(4): Show |
A | 5 | a0001c0001t0003g0026a0001c0001t0003g0027a0001c0001t0003g0028others(2): Show | 5 | HG02258.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+1555_898+1565d others(13): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516167
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898+1555_898+1573d others(21): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516167 | ||||||
| chr12:49516168
|
T | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0067others(4): Show | 7 | HG00741.hp2 HG01346.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.898+1555T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516168 | ||||||
| chr12:49516170
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0090others(3): Show | 6 | HG01361.hp1 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.898+1557T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516170 | ||||||
| chr12:49516172
|
T | A | 11 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0090others(8): Show | 11 | HG01167.hp1 HG01515.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.898+1559T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516172 | ||||||
| chr12:49516174
|
T | A | 14 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0089others(11): Show | 14 | HG00280.hp2 HG01123.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.898+1561T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516174 | ||||||
| chr12:49516176
|
T | A | 13 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0075others(10): Show | 13 | HG00099.hp1 HG00280.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.898+1563T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516176 | ||||||
| chr12:49516178
|
T | A | 15 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0078others(12): Show | 15 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.898+1565T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516178 | ||||||
| chr12:49516180
|
T | A | 13 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(10): Show | 13 | HG00639.hp1 HG01074.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.898+1567T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516180 | ||||||
| chr12:49516182
|
T | A | 5 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(2): Show | 5 | HG00639.hp1 HG01167.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.898+1569T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516182 | ||||||
| chr12:49516188
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898+1575T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516188 | ||||||
| chr12:49516190
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898+1577T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516190 | ||||||
| chr12:49516192
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.898+1579T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516192 | ||||||
| chr12:49516196
|
T | A | 59 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(56): Show | 59 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.898+1583T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516196 | ||||||
| chr12:49516198
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006 | 3 | HG01884.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.898+1585T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516198 | ||||||
| chr12:49516200
|
T | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 82 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.898+1587T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516200 | ||||||
| chr12:49516200
|
T | TAA | 2 | a0001c0001t0001g0019a0001c0001t0001g0095 | 2 | HG02293.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.898+1588_898+1589i others(4): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516200 | |||||
| chr12:49516200
|
T | TAAAA | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.898+1588_898+1589i others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516200 | |||||
| chr12:49516204
|
T | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 91 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.898+1591T>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516204 | ||||||
| chr12:49516204
|
T | TAAATAA | 4 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0003g0012others(1): Show | 4 | HG02559.hp2 HG04228.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.898+1592_898+1593i others(8): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516204 | |||||
| chr12:49516204
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0004 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.898+1596_898+1597i others(24): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516204 | |||||
| chr12:49516292
|
C | T | 6 | a0001c0001t0004g0068a0001c0001t0004g0123a0001c0001t0004g0124others(3): Show | 6 | HG01167.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.898+1679C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516292 | ||||||
| chr12:49516339
|
G | A | 66 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.898+1726G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516339 | ||||||
| chr12:49516365
|
TA | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 97 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(94): Show |
intron_variant | MODIFIER | c.898+1761delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516365 | |||||
| chr12:49516472
|
C | A | 10 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0001g0113others(7): Show | 10 | HG00099.hp2 HG02080.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.898+1859C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516472 | ||||||
| chr12:49516578
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0093 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.898+1965C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49516578 | ||||||
| chr12:49516710
|
T | TA | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.898+2110dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516710 | |||||
| chr12:49516710
|
TA | T | 66 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.898+2110delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 49516710 | |||||
| chr12:49517425
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.899-1648C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49517425 | ||||||
| chr12:49517751
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.899-1322A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49517751 | ||||||
| chr12:49517952
|
C | G | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.899-1121C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49517952 | ||||||
| chr12:49517983
|
A | G | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.899-1090A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49517983 | ||||||
| chr12:49518743
|
T | G | 1 | a0001c0001t0010g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.899-330T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49518743 | ||||||
| chr12:49519000
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.899-73A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 10/13 | chr12 | 49519000 | ||||||
| chr12:49519246
|
A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+64A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49519246 | ||||||
| chr12:49519305
|
C | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG01167.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008+123C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49519305 | ||||||
| chr12:49519427
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008+245A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49519427 | ||||||
| chr12:49519508
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1008+326G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49519508 | ||||||
| chr12:49519814
|
A | AT | 22 | a0001c0001t0001g0132a0001c0001t0002g0001a0001c0001t0002g0007others(19): Show | 22 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1008+648dupT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 49519814 | |||||
| chr12:49519814
|
AT | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0069a0001c0001t0003g0012others(19): Show | 22 | HG01167.hp1 HG01346.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1008+648delT | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 49519814 | |||||
| chr12:49520097
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0087 | 2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1008+915A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49520097 | ||||||
| chr12:49520409
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1008+1227C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49520409 | ||||||
| chr12:49520736
|
T | TTG | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1555_1008+155 others(6): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 49520736 | |||||
| chr12:49520879
|
C | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1697C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49520879 | ||||||
| chr12:49521099
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1009-1652G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49521099 | ||||||
| chr12:49521236
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1009-1515C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49521236 | ||||||
| chr12:49521309
|
A | G | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1009-1442A>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49521309 | ||||||
| chr12:49521344
|
G | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1009-1407G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49521344 | ||||||
| chr12:49521347
|
T | G | 2 | a0001c0001t0001g0014a0001c0001t0009g0104 | 2 | HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1009-1404T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49521347 | ||||||
| chr12:49521502
|
G | A | 4 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | HG01167.hp2 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1249G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49521502 | ||||||
| chr12:49522028
|
G | GA | 36 | a0001c0001t0001g0033a0001c0001t0001g0058a0001c0001t0001g0093others(33): Show | 36 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1009-710dupA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 49522028 | |||||
| chr12:49522028
|
GA | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0003g0037others(16): Show | 19 | HG00639.hp1 HG01069.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1009-710delA | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 49522028 | |||||
| chr12:49522047
|
C | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1009-704C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49522047 | ||||||
| chr12:49522157
|
G | A | 5 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009-594G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49522157 | ||||||
| chr12:49522228
|
G | GTTGAT | 57 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(54): Show | 57 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(54): Show |
intron_variant | MODIFIER | c.1009-519_1009-518i others(7): Show |
SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr12 | 49522228 | |||||
| chr12:49522590
|
A | C | 21 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0047others(18): Show | 21 | HG00639.hp2 HG01175.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1009-161A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49522590 | ||||||
| chr12:49522676
|
A | T | 66 | a0001c0001t0001g0033a0001c0001t0001g0036a0001c0001t0001g0040others(63): Show | 66 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.1009-75A>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 11/13 | chr12 | 49522676 | ||||||
| chr12:49522889
|
T | C | 5 | a0001c0001t0005g0021a0001c0001t0005g0022a0001c0001t0005g0023others(2): Show | 5 | HG01346.hp1 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+36T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49522889 | ||||||
| chr12:49523339
|
G | T | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111+486G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49523339 | ||||||
| chr12:49523438
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1111+585T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49523438 | ||||||
| chr12:49523519
|
T | C | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111+666T>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49523519 | ||||||
| chr12:49523519
|
T | G | 1 | a0001c0001t0001g0138 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1111+666T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49523519 | ||||||
| chr12:49523861
|
A | C | 3 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0039 | 3 | HG04115.hp1 HG04199.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.1112-821A>C | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49523861 | ||||||
| chr12:49523975
|
C | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1112-707C>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49523975 | ||||||
| chr12:49524365
|
G | T | 1 | a0001c0001t0010g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1112-317G>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49524365 | ||||||
| chr12:49524460
|
C | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(28): Show | 31 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1112-222C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 12/13 | chr12 | 49524460 | ||||||
| chr12:49525103
|
C | T | 3 | a0001c0001t0002g0051a0001c0001t0002g0055a0001c0001t0013g0056 | 3 | HG01175.hp1 HG01978.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1326+207C>T | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 13/13 | chr12 | 49525103 | ||||||
| chr12:49525185
|
C | G | 2 | a0001c0001t0007g0034a0001c0001t0007g0035 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1326+289C>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 13/13 | chr12 | 49525185 | ||||||
| chr12:49525298
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1326+402G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 13/13 | chr12 | 49525298 | ||||||
| chr12:49525299
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1326+403T>G | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 13/13 | chr12 | 49525299 | ||||||
| chr12:49525458
|
G | A | 9 | a0001c0001t0004g0041a0001c0001t0004g0068a0001c0001t0004g0123others(6): Show | 9 | HG01167.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327-486G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 13/13 | chr12 | 49525458 | ||||||
| chr12:49525894
|
G | A | 1 | a0001c0001t0003g0016 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1327-50G>A | SPATS2 | ENSG00000123352.18 | transcript | ENST00000552918.6 | protein_coding | 13/13 | chr12 | 49525894 |