Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 92369 |
|---|---|
| ensemblid | ENSG00000175093.5 |
| hgncid | 30630 |
| symbol | SPSB4 |
| name | splA/ryanodine receptor domain and SOCS box containing 4 |
| refseq_nuc | NM_080862.3 |
| refseq_prot | NP_543138.1 |
| ensembl_nuc | ENST00000310546.3 |
| ensembl_prot | ENSP00000311609.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 141051347 |
| end | 141148611 |
| strand | + |
| ver | v1.2 |
| region | chr3:141051347-141148611 |
| region5000 | chr3:141046347-141153611 |
| regionname0 | SPSB4_chr3_141051347_141148611 |
| regionname5000 | SPSB4_chr3_141046347_141153611 |
| 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 | 273 | 252 | 90 | 46 | 90 | 4 | 20 | 70 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0002 | 0/0 | 273 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| 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 | 0/1 | 822 | 130 | 56 | 22 | 40 | 2 | 9 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| c0002 | 1/0 | 822 | 115 | 33 | 24 | 44 | 2 | 11 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| c0003 | 0/0 | 822 | 6 | 0 | 0 | 6 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| c0004 | 0/0 | 822 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| c0005 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| 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 | 0/0 | 2142 | 52 | 2 | 13 | 27 | 1 | 9 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0002 | 0/0 | 2142 | 44 | 2 | 11 | 24 | 1 | 6 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0003 | 0/0 | 2142 | 12 | 6 | 0 | 4 | 0 | 2 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0004 | 0/0 | 2142 | 9 | 3 | 0 | 5 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0005 | 0/0 | 2142 | 8 | 1 | 1 | 6 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0006 | 0/0 | 2142 | 7 | 2 | 0 | 5 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0007 | 0/0 | 2142 | 7 | 4 | 1 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0008 | 0/0 | 2142 | 6 | 4 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0009 | 0/0 | 2142 | 6 | 4 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0010 | 0/0 | 2142 | 6 | 1 | 1 | 4 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0011 | 0/0 | 2142 | 6 | 3 | 0 | 2 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0012 | 0/0 | 2142 | 6 | 6 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0013 | 0/0 | 2142 | 5 | 3 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0014 | 0/0 | 2142 | 5 | 2 | 3 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0015 | 0/0 | 2142 | 4 | 4 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0016 | 0/0 | 2142 | 4 | 0 | 2 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0017 | 0/0 | 2142 | 3 | 2 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0018 | 0/0 | 2142 | 3 | 2 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0019 | 0/0 | 2142 | 3 | 1 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0020 | 0/0 | 2142 | 3 | 3 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0021 | 0/0 | 2142 | 3 | 0 | 0 | 3 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0022 | 0/0 | 2142 | 3 | 0 | 3 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0023 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0024 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0025 | 0/0 | 2142 | 2 | 1 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0026 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0027 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0028 | 0/0 | 2142 | 2 | 0 | 1 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0029 | 0/0 | 2142 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0030 | 0/0 | 2142 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0031 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0032 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0033 | 1/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0034 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0035 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0036 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0037 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0038 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0039 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0040 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0041 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0042 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0043 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0044 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0045 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0046 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0047 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0048 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0049 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0050 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0051 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0052 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0053 | 0/1 | 2142 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0054 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0055 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0056 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0057 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0058 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0059 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0060 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0061 | 0/0 | 2142 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0062 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| t0063 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| 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 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| 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 | 0/1 | 822 | 130 | 56 | 22 | 40 | 2 | 9 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002 | 1/0 | 822 | 115 | 33 | 24 | 44 | 2 | 11 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0003 | 0/0 | 822 | 6 | 0 | 0 | 6 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0005 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0002c0004 | 0/0 | 822 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2963 | 43 | 2 | 11 | 23 | 1 | 6 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0004 | 0/0 | 2963 | 8 | 3 | 0 | 4 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0006 | 0/0 | 2963 | 7 | 2 | 0 | 5 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0009 | 0/0 | 2963 | 6 | 4 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0010 | 0/0 | 2963 | 6 | 1 | 1 | 4 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0011 | 0/0 | 2963 | 6 | 3 | 0 | 2 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0013 | 0/0 | 2963 | 5 | 3 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0015 | 0/0 | 2963 | 4 | 4 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0016 | 0/0 | 2963 | 2 | 0 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0017 | 0/0 | 2963 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0018 | 0/0 | 2963 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0019 | 0/0 | 2963 | 3 | 1 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0020 | 0/0 | 2963 | 3 | 3 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0023 | 0/0 | 2963 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0024 | 0/0 | 2963 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0025 | 0/0 | 2963 | 2 | 1 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0026 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0027 | 0/0 | 2963 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0028 | 0/0 | 2963 | 2 | 0 | 1 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0031 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0034 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0035 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0037 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0038 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0039 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0040 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0041 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0043 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0044 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0047 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0048 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0049 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0050 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0051 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0053 | 0/1 | 2963 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0054 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0055 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0056 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0057 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0062 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0001t0063 | 0/0 | 2963 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0001 | 0/0 | 2963 | 52 | 2 | 13 | 27 | 1 | 9 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0003 | 0/0 | 2963 | 12 | 6 | 0 | 4 | 0 | 2 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0005 | 0/0 | 2963 | 8 | 1 | 1 | 6 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0007 | 0/0 | 2963 | 7 | 4 | 1 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0008 | 0/0 | 2963 | 6 | 4 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0012 | 0/0 | 2963 | 6 | 6 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0014 | 0/0 | 2963 | 5 | 2 | 3 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0021 | 0/0 | 2963 | 3 | 0 | 0 | 3 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0022 | 0/0 | 2963 | 3 | 0 | 3 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0026 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0029 | 0/0 | 2963 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0030 | 0/0 | 2963 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0032 | 0/0 | 2963 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0033 | 1/0 | 2963 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0036 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0052 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0058 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0059 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0060 | 0/0 | 2963 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0002t0061 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0003t0002 | 0/0 | 2963 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0003t0004 | 0/0 | 2963 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0003t0016 | 0/0 | 2963 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0003t0017 | 0/0 | 2963 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0003t0018 | 0/0 | 2963 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0001c0005t0042 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0002c0004t0045 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| a0002c0004t0046 | 0/0 | 2963 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | copy fasta | chr3 | 141046347 | 141153611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0006g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0009g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0010g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0010g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0011g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0013g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0013g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0013g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0015g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0016g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0016g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0017g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0017g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0018g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0019g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0019g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0019g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0020g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0020g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0023g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0024g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0025g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0025g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0026g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0027g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0027g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0028g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0028g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0031g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0034g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0035g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0037g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0038g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0039g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0040g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0041g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0043g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0044g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0047g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0048g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0049g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0050g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0051g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0053g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0054g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0055g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0056g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0057g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0062g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0001t0063g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0008g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0012g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0012g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0012g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0014g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0014g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0014g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0021g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0021g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0022g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0022g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0022g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0026g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0029g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0030g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0030g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0032g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0033g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0036g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0052g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0058g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0059g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0060g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0002t0061g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0003t0016g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0003t0016g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0003t0017g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0003t0018g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0001c0005t0042g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0002c0004t0045g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| a0002c0004t0046g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0095 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CHS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00735 | hp2 | a0001 | c0001 | t0025 | g0144 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00738 | hp2 | a0001 | c0002 | t0008 | g0229 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG00741 | hp2 | a0001 | c0002 | t0060 | g0019 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01074 | hp2 | a0001 | c0002 | t0005 | g0092 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01081 | hp2 | a0001 | c0002 | t0022 | g0127 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0148 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01167 | hp1 | a0001 | c0001 | t0013 | g0150 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0006 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01169 | hp2 | a0001 | c0002 | t0014 | g0101 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01175 | hp1 | a0001 | c0002 | t0014 | g0031 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01243 | hp1 | a0001 | c0001 | t0056 | g0176 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01243 | hp2 | a0001 | c0002 | t0008 | g0224 | AMR | PUR | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01255 | hp1 | a0001 | c0001 | t0016 | g0183 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01255 | hp2 | a0001 | c0002 | t0014 | g0059 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01257 | hp1 | a0001 | c0002 | t0022 | g0129 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01258 | hp2 | a0001 | c0001 | t0028 | g0018 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01433 | hp1 | a0001 | c0001 | t0009 | g0147 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0172 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01496 | hp1 | a0001 | c0002 | t0007 | g0105 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01496 | hp2 | a0001 | c0001 | t0062 | g0243 | AMR | CLM | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01515 | hp2 | a0001 | c0002 | t0032 | g0010 | EUR | IBS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0016 | EUR | IBS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0050 | EUR | IBS | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01884 | hp2 | a0001 | c0001 | t0043 | g0234 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01891 | hp1 | a0001 | c0001 | t0013 | g0140 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02040 | hp1 | a0001 | c0002 | t0007 | g0106 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02040 | hp2 | a0001 | c0001 | t0010 | g0166 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02055 | hp1 | a0001 | c0002 | t0012 | g0077 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02055 | hp2 | a0001 | c0001 | t0020 | g0145 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02145 | hp1 | a0001 | c0002 | t0003 | g0110 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0169 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02155 | hp1 | a0001 | c0002 | t0021 | g0011 | EAS | CDX | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02155 | hp2 | a0001 | c0002 | t0021 | g0100 | EAS | CDX | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0045 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02257 | hp2 | a0001 | c0001 | t0034 | g0217 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02258 | hp1 | a0001 | c0002 | t0058 | g0054 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02258 | hp2 | a0001 | c0001 | t0050 | g0232 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02273 | hp1 | a0001 | c0002 | t0022 | g0094 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0242 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02280 | hp2 | a0002 | c0004 | t0045 | g0240 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02293 | hp1 | a0001 | c0001 | t0016 | g0207 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02451 | hp1 | a0001 | c0001 | t0024 | g0026 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0056 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0048 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02615 | hp1 | a0001 | c0002 | t0012 | g0080 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02630 | hp1 | a0001 | c0001 | t0018 | g0001 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02630 | hp2 | a0001 | c0001 | t0011 | g0117 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02647 | hp1 | a0001 | c0001 | t0038 | g0025 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02647 | hp2 | a0001 | c0002 | t0007 | g0057 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0088 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0001 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02717 | hp2 | a0001 | c0001 | t0031 | g0244 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0136 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02809 | hp2 | a0001 | c0002 | t0014 | g0102 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02818 | hp1 | a0001 | c0002 | t0012 | g0079 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0200 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02886 | hp2 | a0001 | c0002 | t0007 | g0030 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02895 | hp1 | a0001 | c0002 | t0003 | g0137 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02895 | hp2 | a0001 | c0001 | t0023 | g0009 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02896 | hp2 | a0001 | c0002 | t0029 | g0042 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02897 | hp1 | a0001 | c0002 | t0029 | g0043 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02897 | hp2 | a0001 | c0001 | t0023 | g0009 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02922 | hp2 | a0001 | c0001 | t0041 | g0028 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02965 | hp1 | a0001 | c0002 | t0061 | g0112 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02965 | hp2 | a0001 | c0001 | t0044 | g0231 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02970 | hp1 | a0001 | c0002 | t0052 | g0225 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0155 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02976 | hp1 | a0002 | c0004 | t0046 | g0239 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02976 | hp2 | a0001 | c0002 | t0026 | g0142 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03041 | hp1 | a0001 | c0001 | t0015 | g0167 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03098 | hp1 | a0001 | c0002 | t0012 | g0073 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03098 | hp2 | a0001 | c0005 | t0042 | g0245 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0216 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03130 | hp2 | a0001 | c0002 | t0008 | g0223 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03139 | hp1 | a0001 | c0001 | t0020 | g0156 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0061 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03195 | hp1 | a0001 | c0002 | t0005 | g0121 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03195 | hp2 | a0001 | c0001 | t0057 | g0177 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0027 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03209 | hp2 | a0001 | c0001 | t0025 | g0146 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03225 | hp1 | a0001 | c0001 | t0037 | g0153 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0006 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03516 | hp1 | a0001 | c0001 | t0040 | g0170 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03516 | hp2 | a0001 | c0001 | t0054 | g0173 | AFR | ESN | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03540 | hp1 | a0001 | c0002 | t0014 | g0058 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03540 | hp2 | a0001 | c0001 | t0048 | g0238 | AFR | GWD | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03704 | hp2 | a0001 | c0001 | t0063 | g0067 | SAS | PJL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | BEB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | STU | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0053 | SAS | STU | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | STU | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | STU | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0066 | SAS | STU | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0081 | SAS | STU | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0116 | AFR | YRI | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18522 | hp2 | a0001 | c0001 | t0027 | g0235 | AFR | YRI | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | CHB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18906 | hp1 | a0001 | c0002 | t0007 | g0062 | AFR | YRI | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0228 | AFR | YRI | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18939 | hp1 | a0001 | c0002 | t0007 | g0206 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18943 | hp2 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18946 | hp1 | a0001 | c0002 | t0005 | g0087 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18946 | hp2 | a0001 | c0001 | t0006 | g0191 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18950 | hp2 | a0001 | c0001 | t0019 | g0012 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18957 | hp1 | a0001 | c0002 | t0030 | g0082 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18959 | hp2 | a0001 | c0003 | t0016 | g0204 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18968 | hp2 | a0001 | c0003 | t0016 | g0021 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18972 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18972 | hp2 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18977 | hp1 | a0001 | c0003 | t0004 | g0022 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18986 | hp2 | a0001 | c0001 | t0011 | g0198 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18991 | hp1 | a0001 | c0002 | t0030 | g0074 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18992 | hp2 | a0001 | c0003 | t0018 | g0220 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18995 | hp1 | a0001 | c0001 | t0010 | g0209 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19000 | hp2 | a0001 | c0003 | t0017 | g0219 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19005 | hp1 | a0001 | c0001 | t0019 | g0174 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19012 | hp2 | a0001 | c0002 | t0021 | g0089 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19030 | hp1 | a0001 | c0002 | t0008 | g0227 | AFR | LWK | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0178 | AFR | LWK | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19043 | hp1 | a0001 | c0001 | t0047 | g0236 | AFR | LWK | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19043 | hp2 | a0001 | c0001 | t0049 | g0230 | AFR | LWK | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19058 | hp2 | a0001 | c0002 | t0005 | g0107 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19060 | hp2 | a0001 | c0001 | t0011 | g0197 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19065 | hp1 | a0001 | c0001 | t0010 | g0171 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19065 | hp2 | a0001 | c0002 | t0005 | g0114 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19070 | hp2 | a0001 | c0002 | t0005 | g0205 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19090 | hp2 | a0001 | c0002 | t0005 | g0098 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0157 | AFR | YRI | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA19240 | hp2 | a0001 | c0001 | t0055 | g0203 | AFR | YRI | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ASW | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0201 | AFR | ASW | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | GIH | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | GIH | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02109 | hp1 | a0001 | c0002 | t0012 | g0078 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02109 | hp2 | a0001 | c0001 | t0039 | g0221 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0188 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0115 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0226 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03471 | hp1 | a0001 | c0001 | t0027 | g0237 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0222 | AFR | MSL | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG06807 | hp1 | a0001 | c0002 | t0059 | g0126 | AFR | USA | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0149 | AFR | USA | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA20300 | hp1 | a0001 | c0002 | t0036 | g0143 | AFR | USA | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | USA | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0189 | AFR | LWK | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| NA21309 | hp2 | a0001 | c0001 | t0051 | g0233 | AFR | LWK | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0053 | g0020 | REF | REF | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0033 | g0241 | REF | REF | SPSB4_chr3_141046347_141153611 | SPSB4 | chr3 | 141046347 | 141153611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141066631
|
C | T | 1 | a0002 | 2 | HG02280.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.527C>T | p.Ser176Leu | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/3 | 1326/2963 | 527/822 | 176/273 | chr3 | 141066631 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141066122
|
G | C | 1 | a0001c0003 | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
synonymous_variant | LOW | c.18G>C | p.Ser6Ser | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/3 | 817/2963 | 18/822 | 6/273 | chr3 | 141066122 | ||
| chr3:141066333
|
C | A | 3 | a0001c0001a0001c0005a0002c0004 | 133 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(130): Show |
synonymous_variant | LOW | c.229C>A | p.Arg77Arg | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/3 | 1028/2963 | 229/822 | 77/273 | chr3 | 141066333 | ||
| chr3:141066557
|
C | T | 1 | a0001c0005 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.453C>T | p.His151His | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/3 | 1252/2963 | 453/822 | 151/273 | chr3 | 141066557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141051373
|
G | C | 1 | a0001c0001t0031 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-773G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14732 | chr3 | 141051373 | |||||
| chr3:141051415
|
G | A | 1 | a0001c0002t0032 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-731G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14690 | chr3 | 141051415 | |||||
| chr3:141051481
|
A | G | 68 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(65): Show | 253 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(250): Show |
5_prime_UTR_variant | MODIFIER | c.-665A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14624 | chr3 | 141051481 | |||||
| chr3:141051579
|
G | T | 1 | a0001c0001t0063 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-567G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14526 | chr3 | 141051579 | |||||
| chr3:141051615
|
C | G | 1 | a0001c0001t0062 | 1 | HG01496.hp2 | 5_prime_UTR_variant | MODIFIER | c.-531C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14490 | chr3 | 141051615 | |||||
| chr3:141051620
|
C | T | 1 | a0001c0001t0062 | 1 | HG01496.hp2 | 5_prime_UTR_variant | MODIFIER | c.-526C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14485 | chr3 | 141051620 | |||||
| chr3:141051742
|
C | T | 36 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(33): Show | 210 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(207): Show |
5_prime_UTR_variant | MODIFIER | c.-404C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14363 | chr3 | 141051742 | |||||
| chr3:141051857
|
C | A | 3 | a0001c0001t0023a0001c0001t0034a0001c0001t0035 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-289C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14248 | chr3 | 141051857 | |||||
| chr3:141051877
|
G | T | 5 | a0001c0001t0049a0001c0001t0050a0001c0001t0051others(2): Show | 10 | HG00738.hp2 HG01243.hp2 HG02258.hp2 others(7): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-269G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | chr3 | 141051877 | ||||||
| chr3:141051920
|
C | T | 7 | a0001c0001t0027a0001c0001t0031a0001c0001t0047others(4): Show | 8 | HG01496.hp2 HG02280.hp2 HG02717.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-226C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/3 | 14185 | chr3 | 141051920 | |||||
| chr3:141066087
|
T | C | 54 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(51): Show | 149 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(146): Show |
5_prime_UTR_variant | MODIFIER | c.-18T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/3 | 18 | chr3 | 141066087 | |||||
| chr3:141147316
|
C | T | 1 | a0001c0002t0030 | 2 | NA18957.hp1 NA18991.hp1 |
3_prime_UTR_variant | MODIFIER | c.*47C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 47 | chr3 | 141147316 | |||||
| chr3:141147506
|
C | G | 2 | a0001c0001t0044a0001c0002t0058 | 2 | HG02258.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*237C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 237 | chr3 | 141147506 | |||||
| chr3:141147582
|
G | C | 1 | a0001c0002t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 313 | chr3 | 141147582 | |||||
| chr3:141147747
|
C | T | 1 | a0001c0001t0057 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 478 | chr3 | 141147747 | |||||
| chr3:141147789
|
C | T | 31 | a0001c0001t0006a0001c0001t0011a0001c0001t0016others(28): Show | 64 | HG00544.hp1 HG00735.hp2 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*520C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 520 | chr3 | 141147789 | |||||
| chr3:141147827
|
C | T | 1 | a0001c0001t0048 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 558 | chr3 | 141147827 | |||||
| chr3:141147886
|
C | A | 16 | a0001c0001t0009a0001c0001t0011a0001c0001t0013others(13): Show | 37 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*617C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 617 | chr3 | 141147886 | |||||
| chr3:141148006
|
C | T | 37 | a0001c0001t0004a0001c0001t0009a0001c0001t0011others(34): Show | 96 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*737C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 737 | chr3 | 141148006 | |||||
| chr3:141148007
|
A | G | 68 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(65): Show | 253 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*738A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 738 | chr3 | 141148007 | |||||
| chr3:141148056
|
C | T | 1 | a0001c0002t0060 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 787 | chr3 | 141148056 | |||||
| chr3:141148214
|
T | C | 4 | a0001c0001t0025a0001c0001t0038a0001c0002t0029others(1): Show | 6 | HG00735.hp2 HG02280.hp2 HG02647.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*945T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 945 | chr3 | 141148214 | |||||
| chr3:141148252
|
A | G | 22 | a0001c0001t0009a0001c0001t0010a0001c0001t0015others(19): Show | 58 | HG00558.hp1 HG00738.hp2 HG01074.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*983A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 983 | chr3 | 141148252 | |||||
| chr3:141148409
|
G | A | 12 | a0001c0001t0015a0001c0001t0020a0001c0001t0031others(9): Show | 22 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 1140 | chr3 | 141148409 | |||||
| chr3:141148446
|
C | T | 3 | a0001c0001t0026a0001c0001t0056a0001c0002t0026 | 3 | HG01243.hp1 HG02976.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1177C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 1177 | chr3 | 141148446 | |||||
| chr3:141148535
|
C | G | 1 | a0001c0001t0024 | 2 | HG02451.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1266C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 3/3 | 1266 | chr3 | 141148535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:141052099
|
C | T | 1 | a0001c0005t0042g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-154+107C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052099 | ||||||
| chr3:141052136
|
G | A | 1 | a0001c0002t0032g0010 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-154+144G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052136 | ||||||
| chr3:141052230
|
C | T | 2 | a0001c0001t0031g0244a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-154+238C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052230 | ||||||
| chr3:141052487
|
A | G | 1 | a0001c0002t0012g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-154+495A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052487 | ||||||
| chr3:141052558
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-154+566G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052558 | ||||||
| chr3:141052577
|
T | A | 219 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(216): Show | 226 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(223): Show |
intron_variant | MODIFIER | c.-154+585T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052577 | ||||||
| chr3:141052587
|
G | A | 1 | a0001c0002t0021g0011 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-154+595G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052587 | ||||||
| chr3:141052733
|
C | T | 1 | a0001c0001t0002g0218 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-154+741C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052733 | ||||||
| chr3:141052799
|
T | C | 219 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(216): Show | 225 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(222): Show |
intron_variant | MODIFIER | c.-154+807T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052799 | ||||||
| chr3:141052911
|
G | A | 1 | a0001c0001t0019g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-154+919G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141052911 | ||||||
| chr3:141053007
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-154+1015G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053007 | ||||||
| chr3:141053032
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(1): Show | 5 | HG01081.hp1 HG01099.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+1040G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053032 | ||||||
| chr3:141053037
|
G | T | 3 | a0001c0001t0023g0009a0001c0001t0034g0217a0001c0001t0035g0216 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+1045G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053037 | ||||||
| chr3:141053041
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-154+1049C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053041 | ||||||
| chr3:141053101
|
C | G | 3 | a0001c0001t0023g0009a0001c0001t0034g0217a0001c0001t0035g0216 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+1109C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053101 | ||||||
| chr3:141053102
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-154+1110G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053102 | ||||||
| chr3:141053168
|
T | C | 4 | a0001c0001t0026g0222a0001c0001t0039g0221a0001c0003t0017g0219others(1): Show | 4 | HG02109.hp2 HG03471.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+1176T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053168 | ||||||
| chr3:141053204
|
C | A | 1 | a0001c0001t0028g0018 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-154+1212C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053204 | ||||||
| chr3:141053212
|
G | C | 2 | a0001c0003t0017g0219a0001c0003t0018g0220 | 2 | NA18992.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-154+1220G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053212 | ||||||
| chr3:141053220
|
C | T | 1 | a0001c0001t0031g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-154+1228C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053220 | ||||||
| chr3:141053296
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-154+1304A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053296 | ||||||
| chr3:141053721
|
G | A | 18 | a0001c0001t0023g0009a0001c0001t0026g0222a0001c0001t0034g0217others(15): Show | 19 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+1729G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053721 | ||||||
| chr3:141053735
|
AT | A | 18 | a0001c0001t0023g0009a0001c0001t0026g0222a0001c0001t0034g0217others(15): Show | 19 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+1752delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141053735 | |||||
| chr3:141053855
|
A | C | 4 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0002t0001g0211others(1): Show | 4 | HG00738.hp1 HG01361.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+1863A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141053855 | ||||||
| chr3:141054261
|
G | A | 2 | a0001c0001t0053g0020a0001c0002t0060g0019 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-154+2269G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054261 | ||||||
| chr3:141054266
|
T | C | 245 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(242): Show | 253 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(250): Show |
intron_variant | MODIFIER | c.-154+2274T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054266 | ||||||
| chr3:141054309
|
A | C | 213 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(210): Show | 219 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.-154+2317A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054309 | ||||||
| chr3:141054353
|
T | A | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-154+2361T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054353 | ||||||
| chr3:141054430
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-154+2438C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054430 | ||||||
| chr3:141054722
|
T | C | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-154+2730T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054722 | ||||||
| chr3:141054822
|
C | T | 209 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(206): Show | 215 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.-154+2830C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141054822 | ||||||
| chr3:141054964
|
CA | C | 230 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(227): Show | 238 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(235): Show |
intron_variant | MODIFIER | c.-154+2988delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141054964 | |||||
| chr3:141054964
|
CAA | C | 9 | a0001c0001t0010g0209a0001c0001t0027g0235a0001c0001t0027g0237others(6): Show | 9 | HG02280.hp2 HG02717.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+2987_-154+298 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141054964 | |||||
| chr3:141055312
|
G | A | 1 | a0001c0002t0001g0035 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-154+3320G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141055312 | ||||||
| chr3:141055368
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-154+3376G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141055368 | ||||||
| chr3:141055551
|
C | T | 1 | a0001c0001t0016g0207 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-154+3559C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141055551 | ||||||
| chr3:141055660
|
G | A | 6 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(3): Show | 6 | HG02280.hp2 HG02976.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+3668G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141055660 | ||||||
| chr3:141055676
|
C | T | 2 | a0001c0001t0026g0222a0001c0001t0039g0221 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-154+3684C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141055676 | ||||||
| chr3:141055912
|
G | A | 5 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(2): Show | 5 | NA18968.hp2 NA18972.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+3920G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141055912 | ||||||
| chr3:141056011
|
A | T | 209 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(206): Show | 215 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(212): Show |
intron_variant | MODIFIER | c.-154+4019A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056011 | ||||||
| chr3:141056095
|
CCAGGAGG others(3): Show |
C | 5 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(2): Show | 5 | NA18968.hp2 NA18972.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-154+4109_-154+411 others(14): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141056095 | |||||
| chr3:141056195
|
C | T | 1 | a0001c0001t0043g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-154+4203C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056195 | ||||||
| chr3:141056243
|
C | T | 2 | a0001c0002t0005g0205a0001c0002t0007g0206 | 2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-154+4251C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056243 | ||||||
| chr3:141056268
|
C | T | 19 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0026g0222others(16): Show | 19 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-154+4276C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056268 | ||||||
| chr3:141056837
|
C | T | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+4845C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056837 | ||||||
| chr3:141056883
|
T | C | 1 | a0001c0002t0001g0003 | 2 | NA18991.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-154+4891T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056883 | ||||||
| chr3:141056886
|
C | T | 6 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(3): Show | 6 | HG02280.hp2 HG02976.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+4894C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141056886 | ||||||
| chr3:141057313
|
G | C | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-154+5321G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141057313 | ||||||
| chr3:141057456
|
T | C | 144 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(141): Show | 149 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.-154+5464T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141057456 | ||||||
| chr3:141057573
|
C | G | 143 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(140): Show | 148 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.-154+5581C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141057573 | ||||||
| chr3:141057693
|
G | C | 1 | a0001c0002t0005g0205 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-154+5701G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141057693 | ||||||
| chr3:141057752
|
T | C | 1 | a0001c0001t0013g0140 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-154+5760T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141057752 | ||||||
| chr3:141058119
|
GCAGTCAT others(1709): Show |
G | 1 | a0001c0002t0003g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-154+6131_-153-611 others(4): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141058119 | |||||
| chr3:141058149
|
T | C | 202 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(199): Show | 209 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(206): Show |
intron_variant | MODIFIER | c.-154+6157T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058149 | ||||||
| chr3:141058289
|
G | A | 7 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0026g0222others(4): Show | 8 | HG02109.hp2 HG02257.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-154+6297G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058289 | ||||||
| chr3:141058339
|
T | A | 1 | a0001c0002t0003g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-154+6347T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058339 | ||||||
| chr3:141058408
|
C | T | 4 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(1): Show | 4 | HG03471.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+6416C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058408 | ||||||
| chr3:141058467
|
T | C | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-154+6475T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058467 | ||||||
| chr3:141058625
|
C | T | 1 | a0002c0004t0045g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-154+6633C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058625 | ||||||
| chr3:141058733
|
C | T | 7 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0038g0025others(4): Show | 7 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-154+6741C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058733 | ||||||
| chr3:141058961
|
C | T | 1 | a0001c0002t0036g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-154+6969C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141058961 | ||||||
| chr3:141059165
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(1): Show | 5 | HG00735.hp1 HG01081.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-6787G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059165 | ||||||
| chr3:141059193
|
G | A | 2 | a0001c0001t0038g0025a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-153-6759G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059193 | ||||||
| chr3:141059284
|
T | C | 1 | a0001c0001t0019g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-153-6668T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059284 | ||||||
| chr3:141059344
|
AAGAAGTT others(4): Show |
A | 1 | a0001c0001t0002g0202 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-153-6607_-153-659 others(15): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059344 | ||||||
| chr3:141059364
|
G | A | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-6588G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059364 | ||||||
| chr3:141059389
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-153-6563C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059389 | ||||||
| chr3:141059453
|
AAGG | A | 9 | a0001c0002t0001g0060a0001c0002t0007g0030a0001c0002t0007g0057others(6): Show | 9 | HG00741.hp2 HG01099.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.-153-6493_-153-649 others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141059453 | |||||
| chr3:141059809
|
G | A | 9 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0026g0222others(6): Show | 10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-6143G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059809 | ||||||
| chr3:141059921
|
T | C | 128 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(125): Show | 132 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.-153-6031T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059921 | ||||||
| chr3:141059967
|
C | T | 1 | a0001c0002t0001g0135 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-153-5985C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141059967 | ||||||
| chr3:141060045
|
G | A | 9 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0026g0222others(6): Show | 10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-5907G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141060045 | ||||||
| chr3:141060569
|
T | A | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-5383T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141060569 | ||||||
| chr3:141060602
|
A | G | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-5350A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141060602 | ||||||
| chr3:141060606
|
T | C | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-5346T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141060606 | ||||||
| chr3:141060813
|
G | A | 4 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(1): Show | 4 | HG03471.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-5139G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141060813 | ||||||
| chr3:141060855
|
T | C | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-5097T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141060855 | ||||||
| chr3:141061183
|
T | C | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-4769T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061183 | ||||||
| chr3:141061450
|
A | G | 1 | a0002c0004t0046g0239 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-153-4502A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061450 | ||||||
| chr3:141061548
|
A | G | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-153-4404A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061548 | ||||||
| chr3:141061628
|
A | G | 1 | a0001c0001t0002g0139 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-153-4324A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061628 | ||||||
| chr3:141061715
|
TTTTTCTT others(3): Show |
T | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-4227_-153-421 others(14): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141061715 | |||||
| chr3:141061738
|
CT | C | 205 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(202): Show | 212 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.-153-4199delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141061738 | |||||
| chr3:141061738
|
CTT | C | 5 | a0001c0001t0002g0064a0001c0001t0002g0202a0001c0002t0026g0142others(2): Show | 5 | HG02258.hp1 HG02976.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-153-4200_-153-419 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141061738 | |||||
| chr3:141061740
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-153-4212T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061740 | ||||||
| chr3:141061859
|
C | T | 27 | a0001c0001t0004g0141a0001c0001t0006g0017a0001c0001t0023g0009others(24): Show | 28 | HG01496.hp2 HG01884.hp2 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-153-4093C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061859 | ||||||
| chr3:141061987
|
G | A | 19 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0024g0026others(16): Show | 20 | HG01496.hp2 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-153-3965G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141061987 | ||||||
| chr3:141062144
|
C | T | 9 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054others(6): Show | 9 | HG02258.hp1 HG02976.hp2 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.-153-3808C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062144 | ||||||
| chr3:141062150
|
C | A | 94 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(91): Show | 98 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.-153-3802C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062150 | ||||||
| chr3:141062166
|
A | G | 1 | a0001c0001t0062g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-153-3786A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062166 | ||||||
| chr3:141062391
|
G | A | 4 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(1): Show | 4 | HG03471.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-153-3561G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062391 | ||||||
| chr3:141062450
|
A | G | 2 | a0001c0001t0010g0209a0001c0001t0019g0174 | 2 | NA18995.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-153-3502A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062450 | ||||||
| chr3:141062466
|
T | G | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-3486T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062466 | ||||||
| chr3:141062552
|
C | T | 23 | a0001c0001t0004g0141a0001c0001t0006g0017a0001c0001t0023g0009others(20): Show | 24 | HG01496.hp2 HG01884.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-153-3400C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062552 | ||||||
| chr3:141062555
|
C | T | 2 | a0001c0001t0031g0244a0001c0001t0054g0173 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-153-3397C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062555 | ||||||
| chr3:141062556
|
G | A | 9 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0026g0222others(6): Show | 10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-153-3396G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062556 | ||||||
| chr3:141062684
|
T | C | 1 | a0001c0002t0014g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-153-3268T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062684 | ||||||
| chr3:141062815
|
A | G | 129 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(126): Show | 134 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.-153-3137A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062815 | ||||||
| chr3:141062834
|
AGAACATG others(151): Show |
A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-153-3115_-153-295 others(4): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 141062834 | |||||
| chr3:141062988
|
C | G | 2 | a0001c0002t0001g0134a0001c0002t0001g0175 | 2 | HG00609.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-153-2964C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141062988 | ||||||
| chr3:141063106
|
A | C | 1 | a0001c0001t0043g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-153-2846A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063106 | ||||||
| chr3:141063159
|
T | C | 1 | a0001c0002t0008g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-153-2793T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063159 | ||||||
| chr3:141063446
|
T | C | 23 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0009g0147others(20): Show | 25 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-153-2506T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063446 | ||||||
| chr3:141063475
|
A | G | 1 | a0001c0001t0010g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-153-2477A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063475 | ||||||
| chr3:141063494
|
T | C | 2 | a0001c0001t0028g0018a0001c0001t0028g0048 | 2 | HG01258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-153-2458T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063494 | ||||||
| chr3:141063626
|
C | T | 1 | a0001c0002t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-153-2326C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063626 | ||||||
| chr3:141063681
|
A | G | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-2271A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063681 | ||||||
| chr3:141063745
|
G | C | 1 | a0001c0001t0017g0157 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-153-2207G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063745 | ||||||
| chr3:141063797
|
A | G | 131 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 136 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.-153-2155A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063797 | ||||||
| chr3:141063869
|
T | C | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-2083T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063869 | ||||||
| chr3:141063896
|
C | T | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-2056C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141063896 | ||||||
| chr3:141064249
|
C | A | 1 | a0001c0002t0003g0037 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-153-1703C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141064249 | ||||||
| chr3:141064286
|
G | A | 1 | a0001c0001t0002g0039 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-153-1666G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141064286 | ||||||
| chr3:141064433
|
A | G | 1 | a0001c0001t0026g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-153-1519A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141064433 | ||||||
| chr3:141064456
|
G | A | 1 | a0001c0001t0049g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-153-1496G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141064456 | ||||||
| chr3:141064588
|
C | T | 1 | a0001c0001t0020g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-153-1364C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141064588 | ||||||
| chr3:141064791
|
C | T | 3 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015 | 4 | HG01081.hp1 HG01099.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-153-1161C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141064791 | ||||||
| chr3:141065245
|
C | A | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-153-707C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065245 | ||||||
| chr3:141065550
|
G | A | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-402G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065550 | ||||||
| chr3:141065593
|
G | A | 118 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(115): Show | 123 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.-153-359G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065593 | ||||||
| chr3:141065640
|
A | T | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-312A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065640 | ||||||
| chr3:141065682
|
C | A | 2 | a0001c0002t0005g0205a0001c0002t0007g0206 | 2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-153-270C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065682 | ||||||
| chr3:141065806
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-153-146G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065806 | ||||||
| chr3:141065833
|
C | T | 1 | a0001c0002t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-153-119C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 1/2 | chr3 | 141065833 | ||||||
| chr3:141066882
|
C | G | 10 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+84C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141066882 | ||||||
| chr3:141066894
|
C | G | 1 | a0001c0001t0031g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.694+96C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141066894 | ||||||
| chr3:141066992
|
C | T | 78 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(75): Show | 80 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.694+194C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141066992 | ||||||
| chr3:141067121
|
G | A | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+323G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067121 | ||||||
| chr3:141067136
|
G | T | 1 | a0001c0001t0010g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.694+338G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067136 | ||||||
| chr3:141067147
|
A | G | 3 | a0001c0001t0017g0157a0001c0001t0017g0169a0001c0001t0040g0170 | 3 | HG02145.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.694+349A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067147 | ||||||
| chr3:141067264
|
A | G | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+466A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067264 | ||||||
| chr3:141067269
|
T | G | 4 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(1): Show | 4 | HG03471.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+471T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067269 | ||||||
| chr3:141067280
|
G | A | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+482G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067280 | ||||||
| chr3:141067694
|
C | G | 6 | a0001c0001t0023g0009a0001c0001t0026g0222a0001c0001t0034g0217others(3): Show | 7 | HG02109.hp2 HG02257.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.694+896C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067694 | ||||||
| chr3:141067711
|
G | T | 1 | a0001c0002t0001g0131 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.694+913G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067711 | ||||||
| chr3:141067728
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+930T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067728 | ||||||
| chr3:141067875
|
T | G | 1 | a0001c0002t0021g0011 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694+1077T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141067875 | ||||||
| chr3:141068003
|
G | T | 129 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(126): Show | 134 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.694+1205G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141068003 | ||||||
| chr3:141068058
|
G | T | 1 | a0001c0002t0008g0229 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.694+1260G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141068058 | ||||||
| chr3:141068480
|
T | C | 2 | a0001c0002t0001g0032a0001c0002t0001g0065 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.694+1682T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141068480 | ||||||
| chr3:141068710
|
G | A | 131 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 136 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.694+1912G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141068710 | ||||||
| chr3:141068798
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.694+2000G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141068798 | ||||||
| chr3:141069056
|
G | A | 1 | a0001c0001t0056g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.694+2258G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069056 | ||||||
| chr3:141069278
|
A | G | 1 | a0001c0001t0004g0168 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.694+2480A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069278 | ||||||
| chr3:141069301
|
G | A | 1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694+2503G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069301 | ||||||
| chr3:141069448
|
A | C | 4 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(1): Show | 4 | HG03471.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+2650A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069448 | ||||||
| chr3:141069570
|
G | A | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694+2772G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069570 | ||||||
| chr3:141069644
|
C | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+2846C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069644 | ||||||
| chr3:141069917
|
T | G | 19 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0009g0147others(16): Show | 21 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.694+3119T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141069917 | ||||||
| chr3:141070102
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+3304G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070102 | ||||||
| chr3:141070103
|
A | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+3305A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070103 | ||||||
| chr3:141070178
|
G | A | 121 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(118): Show | 126 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.694+3380G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070178 | ||||||
| chr3:141070278
|
G | T | 4 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(1): Show | 4 | HG03471.hp1 HG03540.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+3480G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070278 | ||||||
| chr3:141070312
|
G | T | 131 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 136 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.694+3514G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070312 | ||||||
| chr3:141070315
|
G | T | 1 | a0001c0001t0004g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.694+3517G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070315 | ||||||
| chr3:141070343
|
G | GT | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+3549dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141070343 | |||||
| chr3:141070356
|
A | C | 1 | a0001c0002t0003g0047 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.694+3558A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070356 | ||||||
| chr3:141070363
|
C | T | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694+3565C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070363 | ||||||
| chr3:141070551
|
A | T | 131 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 136 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.694+3753A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070551 | ||||||
| chr3:141070552
|
T | A | 1 | a0001c0001t0063g0067 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.694+3754T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070552 | ||||||
| chr3:141070675
|
G | A | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+3877G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070675 | ||||||
| chr3:141070728
|
G | T | 1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694+3930G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070728 | ||||||
| chr3:141070789
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.694+3991T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070789 | ||||||
| chr3:141070798
|
G | A | 9 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0026g0222others(6): Show | 10 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.694+4000G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070798 | ||||||
| chr3:141070811
|
C | T | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694+4013C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070811 | ||||||
| chr3:141070897
|
G | A | 128 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(125): Show | 133 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(130): Show |
intron_variant | MODIFIER | c.694+4099G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070897 | ||||||
| chr3:141070973
|
C | T | 2 | a0001c0001t0002g0052a0001c0001t0002g0218 | 2 | NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.694+4175C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141070973 | ||||||
| chr3:141071035
|
C | G | 2 | a0001c0002t0001g0130a0001c0002t0022g0129 | 2 | HG01257.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.694+4237C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071035 | ||||||
| chr3:141071152
|
A | G | 1 | a0001c0002t0036g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.694+4354A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071152 | ||||||
| chr3:141071270
|
GCAGGCGG others(13): Show |
G | 5 | a0001c0001t0002g0064a0001c0001t0002g0070a0001c0001t0002g0071others(2): Show | 5 | NA18941.hp1 NA18959.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+4473_694+4492d others(22): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071270 | ||||||
| chr3:141071275
|
C | T | 3 | a0001c0002t0001g0034a0001c0002t0001g0128a0001c0002t0003g0005 | 4 | HG00544.hp2 HG00558.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+4477C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071275 | ||||||
| chr3:141071458
|
C | A | 1 | a0001c0001t0002g0029 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.694+4660C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071458 | ||||||
| chr3:141071480
|
A | AT | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+4692dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141071480 | |||||
| chr3:141071480
|
AT | A | 121 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(118): Show | 126 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.694+4692delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141071480 | |||||
| chr3:141071623
|
C | T | 2 | a0001c0002t0001g0068a0001c0002t0022g0127 | 2 | HG01081.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.694+4825C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071623 | ||||||
| chr3:141071693
|
C | T | 74 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(71): Show | 76 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.694+4895C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071693 | ||||||
| chr3:141071737
|
G | A | 121 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(118): Show | 126 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.694+4939G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141071737 | ||||||
| chr3:141072005
|
C | T | 126 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 131 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.694+5207C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072005 | ||||||
| chr3:141072021
|
T | C | 127 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(124): Show | 132 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(129): Show |
intron_variant | MODIFIER | c.694+5223T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072021 | ||||||
| chr3:141072077
|
G | A | 10 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(7): Show | 10 | HG00738.hp2 HG01243.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+5279G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072077 | ||||||
| chr3:141072352
|
A | C | 244 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(241): Show | 252 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(249): Show |
intron_variant | MODIFIER | c.694+5554A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072352 | ||||||
| chr3:141072352
|
A | T | 1 | a0001c0002t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.694+5554A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072352 | ||||||
| chr3:141072382
|
A | T | 122 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(119): Show | 127 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.694+5584A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072382 | ||||||
| chr3:141072402
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.694+5604G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072402 | ||||||
| chr3:141072431
|
C | T | 1 | a0001c0005t0042g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.694+5633C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072431 | ||||||
| chr3:141072511
|
G | C | 33 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(30): Show | 36 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.694+5713G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072511 | ||||||
| chr3:141072513
|
C | G | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG01074.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.694+5715C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072513 | ||||||
| chr3:141072675
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.694+5877C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072675 | ||||||
| chr3:141072695
|
A | G | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+5897A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072695 | ||||||
| chr3:141072809
|
G | A | 37 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0141others(34): Show | 38 | HG00738.hp2 HG01243.hp2 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.694+6011G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072809 | ||||||
| chr3:141072821
|
G | C | 54 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0038others(51): Show | 57 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.694+6023G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141072821 | ||||||
| chr3:141073220
|
G | T | 1 | a0001c0001t0015g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.694+6422G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073220 | ||||||
| chr3:141073263
|
T | C | 49 | a0001c0001t0002g0213a0001c0001t0002g0214a0001c0001t0004g0038others(46): Show | 52 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.694+6465T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073263 | ||||||
| chr3:141073271
|
C | T | 28 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(25): Show | 31 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.694+6473C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073271 | ||||||
| chr3:141073294
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0011g0050 | 2 | HG01516.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.694+6496G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073294 | ||||||
| chr3:141073410
|
A | G | 5 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(2): Show | 5 | HG02145.hp2 HG02896.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+6612A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073410 | ||||||
| chr3:141073523
|
A | G | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+6725A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073523 | ||||||
| chr3:141073574
|
G | C | 56 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(53): Show | 59 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.694+6776G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073574 | ||||||
| chr3:141073799
|
T | C | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+7001T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073799 | ||||||
| chr3:141073830
|
A | G | 9 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(6): Show | 9 | HG02145.hp2 HG02896.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+7032A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073830 | ||||||
| chr3:141073849
|
C | A | 3 | a0001c0002t0003g0136a0001c0002t0003g0137a0001c0002t0012g0073 | 3 | HG02809.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.694+7051C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073849 | ||||||
| chr3:141073961
|
C | T | 19 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0009g0147others(16): Show | 21 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.694+7163C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141073961 | ||||||
| chr3:141074000
|
T | C | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+7202T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074000 | ||||||
| chr3:141074542
|
C | T | 1 | a0001c0001t0054g0173 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.694+7744C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074542 | ||||||
| chr3:141074553
|
C | G | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+7755C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074553 | ||||||
| chr3:141074617
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+7819G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074617 | ||||||
| chr3:141074619
|
C | T | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+7821C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074619 | ||||||
| chr3:141074620
|
T | G | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+7822T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074620 | ||||||
| chr3:141074787
|
C | T | 3 | a0001c0001t0009g0200a0001c0001t0009g0201a0001c0001t0056g0176 | 3 | HG01243.hp1 HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694+7989C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074787 | ||||||
| chr3:141074799
|
C | T | 1 | a0001c0002t0022g0127 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.694+8001C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074799 | ||||||
| chr3:141074829
|
T | C | 9 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(6): Show | 9 | HG02145.hp2 HG02896.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+8031T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074829 | ||||||
| chr3:141074986
|
A | C | 1 | a0001c0001t0062g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.694+8188A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141074986 | ||||||
| chr3:141075092
|
C | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+8294C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075092 | ||||||
| chr3:141075098
|
G | A | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+8300G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075098 | ||||||
| chr3:141075118
|
C | CAATGCAG others(13): Show |
3 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0204 | 3 | NA18959.hp2 NA18972.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.694+8338_694+8339i others(22): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075118 | |||||
| chr3:141075118
|
C | CAATGCAG others(13): Show |
126 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 131 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.694+8322_694+8341d others(22): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075118 | |||||
| chr3:141075376
|
G | A | 9 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(6): Show | 9 | HG02145.hp2 HG02896.hp1 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.694+8578G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075376 | ||||||
| chr3:141075388
|
A | ATACCCAC others(3): Show |
7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+8596_694+8597i others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075388 | |||||
| chr3:141075410
|
T | G | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 53 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.694+8612T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075410 | ||||||
| chr3:141075561
|
G | T | 1 | a0001c0002t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.694+8763G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075561 | ||||||
| chr3:141075567
|
T | G | 4 | a0001c0001t0023g0009a0001c0001t0034g0217a0001c0001t0035g0216others(1): Show | 5 | HG02257.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+8769T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075567 | ||||||
| chr3:141075701
|
C | G | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+8903C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075701 | ||||||
| chr3:141075768
|
C | T | 20 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0009g0147others(17): Show | 22 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.694+8970C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075768 | ||||||
| chr3:141075822
|
G | A | 1 | a0001c0001t0055g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.694+9024G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075822 | ||||||
| chr3:141075867
|
C | T | 73 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(70): Show | 75 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.694+9069C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075867 | ||||||
| chr3:141075878
|
C | T | 1 | a0001c0001t0020g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.694+9080C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075878 | ||||||
| chr3:141075892
|
C | CA | 11 | a0001c0001t0006g0069a0001c0002t0001g0041a0001c0002t0001g0076others(8): Show | 11 | HG00609.hp1 HG00609.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.694+9116dupA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075892 | |||||
| chr3:141075892
|
CA | C | 70 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(67): Show | 72 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.694+9116delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075892 | |||||
| chr3:141075892
|
CAAAAA | C | 6 | a0001c0001t0004g0141a0001c0001t0023g0009a0001c0001t0026g0222others(3): Show | 7 | HG02257.hp2 HG02280.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.694+9112_694+9116d others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075892 | |||||
| chr3:141075892
|
CAAAAAA | C | 42 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0006g0158others(39): Show | 43 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.694+9111_694+9116d others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075892 | |||||
| chr3:141075892
|
CAAAAAAA | C | 5 | a0001c0001t0006g0017a0001c0001t0009g0154a0001c0001t0018g0001others(2): Show | 6 | HG02630.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+9110_694+9116d others(9): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141075892 | |||||
| chr3:141075923
|
T | C | 5 | a0001c0002t0012g0077a0001c0002t0012g0078a0001c0002t0012g0079others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+9125T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075923 | ||||||
| chr3:141075988
|
G | A | 18 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0009g0147others(15): Show | 20 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.694+9190G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141075988 | ||||||
| chr3:141076014
|
G | A | 59 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(56): Show | 62 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.694+9216G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076014 | ||||||
| chr3:141076080
|
GATAAA | G | 53 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(50): Show | 56 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.694+9290_694+9294d others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141076080 | |||||
| chr3:141076175
|
A | G | 133 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(130): Show | 138 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.694+9377A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076175 | ||||||
| chr3:141076216
|
G | T | 53 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(50): Show | 56 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.694+9418G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076216 | ||||||
| chr3:141076296
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+9498G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076296 | ||||||
| chr3:141076314
|
A | G | 1 | a0001c0002t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.694+9516A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076314 | ||||||
| chr3:141076560
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+9762T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076560 | ||||||
| chr3:141076607
|
C | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+9809C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076607 | ||||||
| chr3:141076636
|
C | G | 59 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(56): Show | 62 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.694+9838C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076636 | ||||||
| chr3:141076673
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.694+9875C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076673 | ||||||
| chr3:141076821
|
G | C | 59 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(56): Show | 62 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.694+10023G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076821 | ||||||
| chr3:141076854
|
T | C | 2 | a0001c0002t0026g0142a0001c0002t0036g0143 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694+10056T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076854 | ||||||
| chr3:141076931
|
T | C | 74 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(71): Show | 76 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.694+10133T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076931 | ||||||
| chr3:141076959
|
C | T | 6 | a0001c0001t0004g0141a0001c0001t0026g0222a0001c0001t0034g0217others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+10161C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076959 | ||||||
| chr3:141076980
|
G | A | 6 | a0001c0003t0002g0023a0001c0003t0004g0022a0001c0003t0016g0021others(3): Show | 6 | NA18959.hp2 NA18968.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+10182G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141076980 | ||||||
| chr3:141077086
|
C | T | 5 | a0001c0001t0026g0222a0001c0001t0034g0217a0001c0001t0035g0216others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+10288C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077086 | ||||||
| chr3:141077110
|
G | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+10312G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077110 | ||||||
| chr3:141077146
|
G | C | 12 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(9): Show | 12 | HG02145.hp2 HG02809.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.694+10348G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077146 | ||||||
| chr3:141077232
|
C | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+10434C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077232 | ||||||
| chr3:141077321
|
G | A | 52 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(49): Show | 54 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.694+10523G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077321 | ||||||
| chr3:141077325
|
G | A | 8 | a0001c0001t0006g0017a0001c0002t0008g0223a0001c0002t0008g0224others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.694+10527G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077325 | ||||||
| chr3:141077335
|
G | A | 1 | a0001c0002t0001g0081 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.694+10537G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077335 | ||||||
| chr3:141077365
|
G | A | 58 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(55): Show | 60 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.694+10567G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077365 | ||||||
| chr3:141077392
|
C | T | 1 | a0001c0001t0015g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.694+10594C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077392 | ||||||
| chr3:141077723
|
C | T | 1 | a0001c0001t0048g0238 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.694+10925C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077723 | ||||||
| chr3:141077738
|
G | A | 8 | a0001c0001t0009g0200a0001c0001t0009g0201a0001c0001t0010g0159others(5): Show | 8 | HG01243.hp1 HG01891.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.694+10940G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077738 | ||||||
| chr3:141077910
|
G | A | 1 | a0001c0001t0002g0139 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.694+11112G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077910 | ||||||
| chr3:141077959
|
C | T | 6 | a0001c0001t0004g0141a0001c0001t0026g0222a0001c0001t0034g0217others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+11161C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077959 | ||||||
| chr3:141077993
|
T | C | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+11195T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141077993 | ||||||
| chr3:141078453
|
C | T | 1 | a0001c0002t0005g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.694+11655C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078453 | ||||||
| chr3:141078474
|
T | G | 9 | a0001c0002t0001g0131a0001c0002t0030g0074a0001c0002t0030g0082others(6): Show | 9 | NA18943.hp1 NA18957.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+11676T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078474 | ||||||
| chr3:141078686
|
T | C | 1 | a0001c0002t0001g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.694+11888T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078686 | ||||||
| chr3:141078768
|
G | T | 1 | a0001c0001t0002g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.694+11970G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078768 | ||||||
| chr3:141078774
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+11976G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078774 | ||||||
| chr3:141078922
|
G | A | 3 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0002t0059g0126 | 3 | HG01891.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.694+12124G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078922 | ||||||
| chr3:141078956
|
C | T | 1 | a0001c0001t0010g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.694+12158C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078956 | ||||||
| chr3:141078957
|
G | A | 9 | a0001c0002t0001g0131a0001c0002t0030g0074a0001c0002t0030g0082others(6): Show | 9 | NA18943.hp1 NA18957.hp1 NA18959.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+12159G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078957 | ||||||
| chr3:141078990
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+12192G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141078990 | ||||||
| chr3:141079117
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.694+12319C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079117 | ||||||
| chr3:141079162
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0084 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.694+12364G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079162 | ||||||
| chr3:141079178
|
G | A | 1 | a0001c0003t0016g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.694+12380G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079178 | ||||||
| chr3:141079185
|
C | T | 1 | a0001c0001t0044g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.694+12387C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079185 | ||||||
| chr3:141079201
|
T | C | 61 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(58): Show | 63 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(60): Show |
intron_variant | MODIFIER | c.694+12403T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079201 | ||||||
| chr3:141079264
|
C | CA | 41 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(38): Show | 43 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.694+12480dupA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141079264 | |||||
| chr3:141079417
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0218 | 2 | NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.694+12619T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079417 | ||||||
| chr3:141079453
|
G | A | 50 | a0001c0001t0004g0038a0001c0001t0004g0141a0001c0001t0004g0152others(47): Show | 52 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.694+12655G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079453 | ||||||
| chr3:141079540
|
C | T | 5 | a0001c0002t0001g0046a0001c0002t0003g0044a0001c0002t0003g0045others(2): Show | 5 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.694+12742C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079540 | ||||||
| chr3:141079596
|
C | G | 1 | a0001c0002t0001g0120 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.694+12798C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079596 | ||||||
| chr3:141079683
|
T | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+12885T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079683 | ||||||
| chr3:141079724
|
T | C | 3 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0041g0028 | 3 | HG02451.hp1 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.694+12926T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079724 | ||||||
| chr3:141079760
|
A | G | 1 | a0002c0004t0046g0239 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.694+12962A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079760 | ||||||
| chr3:141079987
|
T | A | 1 | a0001c0002t0021g0011 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.694+13189T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141079987 | ||||||
| chr3:141080118
|
T | C | 27 | a0001c0001t0002g0052a0001c0001t0002g0138a0001c0001t0002g0179others(24): Show | 28 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.694+13320T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080118 | ||||||
| chr3:141080157
|
A | G | 46 | a0001c0001t0002g0029a0001c0001t0002g0051a0001c0001t0002g0052others(43): Show | 50 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.694+13359A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080157 | ||||||
| chr3:141080185
|
A | G | 49 | a0001c0001t0002g0052a0001c0001t0002g0138a0001c0001t0002g0179others(46): Show | 51 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.694+13387A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080185 | ||||||
| chr3:141080339
|
C | T | 1 | a0001c0001t0004g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.694+13541C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080339 | ||||||
| chr3:141080371
|
G | A | 70 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(67): Show | 74 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.694+13573G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080371 | ||||||
| chr3:141080407
|
T | C | 244 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(241): Show | 252 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(249): Show |
intron_variant | MODIFIER | c.694+13609T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080407 | ||||||
| chr3:141080465
|
A | G | 5 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0001t0047g0236others(2): Show | 5 | HG01243.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+13667A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080465 | ||||||
| chr3:141080592
|
G | A | 72 | a0001c0001t0002g0029a0001c0001t0002g0051a0001c0001t0002g0052others(69): Show | 76 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.694+13794G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080592 | ||||||
| chr3:141080873
|
A | G | 1 | a0001c0001t0027g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.694+14075A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080873 | ||||||
| chr3:141080887
|
G | A | 24 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(21): Show | 24 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+14089G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080887 | ||||||
| chr3:141080956
|
C | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+14158C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141080956 | ||||||
| chr3:141081036
|
G | A | 2 | a0001c0001t0027g0235a0001c0001t0027g0237 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.694+14238G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081036 | ||||||
| chr3:141081142
|
C | T | 3 | a0001c0001t0034g0217a0001c0001t0035g0216a0002c0004t0045g0240 | 3 | HG02257.hp2 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.694+14344C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081142 | ||||||
| chr3:141081243
|
C | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+14445C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081243 | ||||||
| chr3:141081309
|
C | T | 1 | a0001c0001t0026g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.694+14511C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081309 | ||||||
| chr3:141081669
|
GA | G | 25 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(22): Show | 25 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.694+14873delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141081669 | |||||
| chr3:141081793
|
G | A | 3 | a0001c0001t0034g0217a0001c0001t0035g0216a0002c0004t0045g0240 | 3 | HG02257.hp2 HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.694+14995G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081793 | ||||||
| chr3:141081836
|
G | A | 2 | a0001c0001t0050g0232a0001c0001t0051g0233 | 2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.694+15038G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081836 | ||||||
| chr3:141081849
|
C | T | 77 | a0001c0001t0002g0029a0001c0001t0002g0051a0001c0001t0002g0052others(74): Show | 81 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.694+15051C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141081849 | ||||||
| chr3:141082064
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.694+15266C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082064 | ||||||
| chr3:141082150
|
G | A | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.694+15352G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082150 | ||||||
| chr3:141082278
|
C | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+15480C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082278 | ||||||
| chr3:141082422
|
GGGTGGGT others(10): Show |
G | 11 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(8): Show | 11 | HG00735.hp2 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.694+15628_694+1564 others(21): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082422 | |||||
| chr3:141082438
|
T | C | 234 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(231): Show | 242 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(239): Show |
intron_variant | MODIFIER | c.694+15640T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082438 | ||||||
| chr3:141082493
|
G | C | 14 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0009g0147others(11): Show | 15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.694+15695G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082493 | ||||||
| chr3:141082547
|
T | C | 12 | a0001c0001t0002g0064a0001c0001t0002g0070a0001c0001t0002g0071others(9): Show | 13 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.694+15749T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082547 | ||||||
| chr3:141082613
|
C | T | 79 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(76): Show | 83 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.694+15815C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082613 | ||||||
| chr3:141082615
|
G | A | 2 | a0001c0002t0014g0058a0001c0002t0014g0059 | 2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.694+15817G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082615 | ||||||
| chr3:141082618
|
G | GCTAT | 36 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0052others(33): Show | 38 | HG00544.hp1 HG00738.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.694+15863_694+1586 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082618
|
G | GCTATCTA others(1): Show |
28 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0036others(25): Show | 31 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.694+15859_694+1586 others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082618
|
G | GCTATCTA others(5): Show |
3 | a0001c0001t0002g0160a0001c0001t0010g0209a0001c0002t0036g0143 | 3 | NA18995.hp1 NA19091.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694+15855_694+1586 others(16): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082618
|
G | GCTATGTA others(1): Show |
6 | a0001c0001t0063g0067a0001c0002t0001g0065a0001c0002t0001g0086others(3): Show | 6 | HG00597.hp2 HG01175.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+15824_694+1582 others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082618
|
G | GCTATGTA others(5): Show |
2 | a0001c0002t0001g0083a0001c0002t0003g0088 | 2 | HG02129.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.694+15824_694+1582 others(16): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082618
|
GCTAT | G | 13 | a0001c0001t0002g0063a0001c0001t0002g0187a0001c0001t0006g0017others(10): Show | 13 | HG01433.hp2 HG01952.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.694+15863_694+1586 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082618
|
GCTATCTA others(1): Show |
G | 9 | a0001c0001t0006g0158a0001c0001t0023g0009a0001c0001t0025g0144others(6): Show | 10 | HG00735.hp2 HG02809.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+15859_694+1586 others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082618 | |||||
| chr3:141082619
|
C | CTATG | 25 | a0001c0001t0002g0064a0001c0001t0002g0070a0001c0001t0002g0071others(22): Show | 25 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.694+15824_694+1582 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082619 | |||||
| chr3:141082623
|
C | G | 80 | a0001c0001t0002g0039a0001c0001t0002g0049a0001c0001t0002g0051others(77): Show | 82 | HG00558.hp1 HG00639.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.694+15825C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082623 | ||||||
| chr3:141082627
|
C | G | 3 | a0001c0001t0002g0063a0001c0001t0053g0020a0001c0002t0001g0111 | 3 | HG01952.hp1 HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.694+15829C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082627 | ||||||
| chr3:141082745
|
C | A | 79 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(76): Show | 83 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.694+15947C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082745 | ||||||
| chr3:141082745
|
C | T | 11 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(8): Show | 11 | HG00735.hp2 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.694+15947C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082745 | ||||||
| chr3:141082746
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.694+15948G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082746 | ||||||
| chr3:141082812
|
G | C | 79 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(76): Show | 83 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.694+16014G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082812 | ||||||
| chr3:141082905
|
C | T | 2 | a0001c0001t0043g0234a0001c0001t0044g0231 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.694+16107C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082905 | ||||||
| chr3:141082927
|
CTTTG | C | 79 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(76): Show | 83 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.694+16134_694+1613 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141082927 | |||||
| chr3:141082943
|
C | T | 1 | a0001c0002t0007g0206 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.694+16145C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141082943 | ||||||
| chr3:141083063
|
T | C | 25 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(22): Show | 25 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.694+16265T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083063 | ||||||
| chr3:141083134
|
G | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+16336G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083134 | ||||||
| chr3:141083157
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+16359G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083157 | ||||||
| chr3:141083183
|
T | C | 79 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(76): Show | 83 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.694+16385T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083183 | ||||||
| chr3:141083222
|
A | G | 76 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(73): Show | 79 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.694+16424A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083222 | ||||||
| chr3:141083272
|
C | T | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.694+16474C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083272 | ||||||
| chr3:141083275
|
C | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+16477C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083275 | ||||||
| chr3:141083405
|
G | A | 1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694+16607G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083405 | ||||||
| chr3:141083587
|
G | A | 1 | a0001c0001t0019g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.694+16789G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083587 | ||||||
| chr3:141083688
|
C | T | 1 | a0001c0002t0003g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.694+16890C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083688 | ||||||
| chr3:141083709
|
C | T | 63 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(60): Show | 66 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.694+16911C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083709 | ||||||
| chr3:141083750
|
T | C | 2 | a0001c0001t0009g0200a0001c0001t0009g0201 | 2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694+16952T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083750 | ||||||
| chr3:141083793
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0218 | 2 | NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.694+16995T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083793 | ||||||
| chr3:141083893
|
C | G | 11 | a0001c0001t0006g0158a0001c0001t0017g0157a0001c0001t0017g0169others(8): Show | 11 | HG00735.hp2 HG02145.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.694+17095C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141083893 | ||||||
| chr3:141084056
|
G | T | 60 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(57): Show | 63 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.694+17258G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084056 | ||||||
| chr3:141084246
|
T | C | 1 | a0001c0001t0051g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.694+17448T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084246 | ||||||
| chr3:141084301
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.694+17503G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084301 | ||||||
| chr3:141084310
|
C | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+17512C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084310 | ||||||
| chr3:141084310
|
C | G | 53 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(50): Show | 56 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.694+17512C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084310 | ||||||
| chr3:141084363
|
C | T | 1 | a0001c0005t0042g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.694+17565C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084363 | ||||||
| chr3:141084697
|
G | C | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+17899G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084697 | ||||||
| chr3:141084813
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+18015G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084813 | ||||||
| chr3:141084864
|
T | C | 4 | a0001c0001t0050g0232a0001c0002t0026g0142a0001c0002t0036g0143others(1): Show | 4 | HG02258.hp1 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+18066T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141084864 | ||||||
| chr3:141085129
|
T | C | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+18331T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141085129 | ||||||
| chr3:141085332
|
A | T | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+18534A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141085332 | ||||||
| chr3:141085456
|
T | C | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+18658T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141085456 | ||||||
| chr3:141085513
|
G | C | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.694+18715G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141085513 | ||||||
| chr3:141085884
|
C | T | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+19086C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141085884 | ||||||
| chr3:141086074
|
C | T | 9 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0020g0145others(6): Show | 10 | HG01884.hp2 HG02055.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+19276C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141086074 | ||||||
| chr3:141086105
|
G | A | 131 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 137 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.694+19307G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141086105 | ||||||
| chr3:141086297
|
G | C | 1 | a0001c0002t0026g0142 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694+19499G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141086297 | ||||||
| chr3:141086623
|
C | T | 1 | a0001c0002t0060g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.694+19825C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141086623 | ||||||
| chr3:141086886
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.694+20088C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141086886 | ||||||
| chr3:141087070
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+20272G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087070 | ||||||
| chr3:141087071
|
C | T | 1 | a0001c0002t0007g0206 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.694+20273C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087071 | ||||||
| chr3:141087114
|
A | G | 25 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0006g0158others(22): Show | 26 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.694+20316A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087114 | ||||||
| chr3:141087134
|
C | A | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.694+20336C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087134 | ||||||
| chr3:141087224
|
G | T | 24 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(21): Show | 24 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+20426G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087224 | ||||||
| chr3:141087246
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+20448G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087246 | ||||||
| chr3:141087517
|
T | A | 25 | a0001c0001t0004g0038a0001c0001t0004g0152a0001c0001t0006g0158others(22): Show | 26 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.694+20719T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087517 | ||||||
| chr3:141087527
|
G | A | 131 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(128): Show | 137 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.694+20729G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087527 | ||||||
| chr3:141087550
|
T | C | 1 | a0001c0002t0001g0035 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.694+20752T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087550 | ||||||
| chr3:141087638
|
G | A | 3 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0002t0059g0126 | 3 | HG01891.hp2 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.694+20840G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087638 | ||||||
| chr3:141087769
|
G | A | 1 | a0001c0002t0001g0215 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.694+20971G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087769 | ||||||
| chr3:141087835
|
G | C | 25 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(22): Show | 25 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.694+21037G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141087835 | ||||||
| chr3:141088049
|
C | T | 4 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0056g0176others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+21251C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088049 | ||||||
| chr3:141088125
|
G | T | 166 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(163): Show | 172 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.694+21327G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088125 | ||||||
| chr3:141088138
|
C | G | 1 | a0001c0001t0037g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.694+21340C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088138 | ||||||
| chr3:141088251
|
G | T | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+21453G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088251 | ||||||
| chr3:141088354
|
G | A | 4 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0056g0176others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+21556G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088354 | ||||||
| chr3:141088368
|
G | C | 132 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(129): Show | 138 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.694+21570G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088368 | ||||||
| chr3:141088390
|
C | A | 24 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(21): Show | 24 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+21592C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088390 | ||||||
| chr3:141088503
|
A | C | 1 | a0001c0002t0001g0103 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.694+21705A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088503 | ||||||
| chr3:141088581
|
G | A | 1 | a0001c0002t0007g0061 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.694+21783G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088581 | ||||||
| chr3:141088875
|
A | G | 2 | a0001c0001t0015g0178a0001c0001t0015g0189 | 2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.694+22077A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141088875 | ||||||
| chr3:141089105
|
C | T | 1 | a0001c0001t0051g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.694+22307C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089105 | ||||||
| chr3:141089169
|
G | A | 42 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(39): Show | 45 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.694+22371G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089169 | ||||||
| chr3:141089307
|
A | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+22509A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089307 | ||||||
| chr3:141089309
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.694+22511C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089309 | ||||||
| chr3:141089369
|
C | A | 42 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(39): Show | 45 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.694+22571C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089369 | ||||||
| chr3:141089559
|
GA | G | 24 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(21): Show | 24 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+22762delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089559 | ||||||
| chr3:141089578
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0084 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.694+22780A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089578 | ||||||
| chr3:141089662
|
G | C | 2 | a0001c0002t0001g0093a0001c0002t0001g0123 | 2 | NA18974.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.694+22864G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089662 | ||||||
| chr3:141089668
|
C | A | 42 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(39): Show | 45 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.694+22870C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141089668 | ||||||
| chr3:141090022
|
C | T | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+23224C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090022 | ||||||
| chr3:141090048
|
G | A | 148 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(145): Show | 153 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.694+23250G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090048 | ||||||
| chr3:141090262
|
G | T | 37 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.694+23464G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090262 | ||||||
| chr3:141090324
|
T | C | 1 | a0001c0002t0001g0076 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.694+23526T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090324 | ||||||
| chr3:141090393
|
G | T | 142 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(139): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.694+23595G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090393 | ||||||
| chr3:141090466
|
T | C | 1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694+23668T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090466 | ||||||
| chr3:141090480
|
G | A | 26 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694+23682G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090480 | ||||||
| chr3:141090493
|
T | C | 163 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(160): Show | 169 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.694+23695T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090493 | ||||||
| chr3:141090541
|
G | C | 40 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(37): Show | 43 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.694+23743G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090541 | ||||||
| chr3:141090660
|
G | A | 2 | a0001c0001t0025g0144a0001c0001t0025g0146 | 2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+23862G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090660 | ||||||
| chr3:141090689
|
T | C | 89 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(86): Show | 92 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.694+23891T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090689 | ||||||
| chr3:141090814
|
G | A | 26 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694+24016G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090814 | ||||||
| chr3:141090887
|
C | A | 159 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(156): Show | 165 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.694+24089C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090887 | ||||||
| chr3:141090890
|
G | A | 44 | a0001c0001t0004g0038a0001c0001t0004g0091a0001c0001t0010g0159others(41): Show | 44 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.694+24092G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090890 | ||||||
| chr3:141090896
|
G | A | 39 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 41 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.694+24098G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090896 | ||||||
| chr3:141090901
|
A | C | 2 | a0001c0001t0025g0144a0001c0001t0025g0146 | 2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+24103A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090901 | ||||||
| chr3:141090967
|
G | C | 39 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 41 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.694+24169G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141090967 | ||||||
| chr3:141091001
|
T | C | 158 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(155): Show | 163 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(160): Show |
intron_variant | MODIFIER | c.694+24203T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091001 | ||||||
| chr3:141091061
|
G | A | 2 | a0001c0001t0004g0038a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.694+24263G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091061 | ||||||
| chr3:141091077
|
C | G | 1 | a0001c0002t0030g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.694+24279C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091077 | ||||||
| chr3:141091123
|
G | A | 1 | a0001c0002t0032g0010 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.694+24325G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091123 | ||||||
| chr3:141091185
|
T | C | 24 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(21): Show | 25 | HG01081.hp1 HG01099.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.694+24387T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091185 | ||||||
| chr3:141091213
|
G | A | 2 | a0001c0001t0025g0144a0001c0001t0025g0146 | 2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+24415G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091213 | ||||||
| chr3:141091257
|
G | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+24459G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091257 | ||||||
| chr3:141091304
|
G | A | 156 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(153): Show | 161 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.694+24506G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091304 | ||||||
| chr3:141091353
|
T | C | 40 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(37): Show | 43 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.694+24555T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091353 | ||||||
| chr3:141091503
|
G | A | 26 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(23): Show | 26 | HG00639.hp1 HG00735.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.694+24705G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091503 | ||||||
| chr3:141091512
|
G | C | 1 | a0001c0001t0004g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.694+24714G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091512 | ||||||
| chr3:141091604
|
C | T | 6 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(3): Show | 6 | HG01243.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+24806C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091604 | ||||||
| chr3:141091633
|
A | G | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+24835A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091633 | ||||||
| chr3:141091732
|
G | A | 45 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(42): Show | 47 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.694+24934G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091732 | ||||||
| chr3:141091742
|
C | T | 71 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(68): Show | 73 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.694+24944C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091742 | ||||||
| chr3:141091752
|
G | A | 2 | a0001c0001t0056g0176a0002c0004t0045g0240 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.694+24954G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091752 | ||||||
| chr3:141091760
|
T | C | 66 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(63): Show | 68 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.694+24962T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091760 | ||||||
| chr3:141091798
|
G | A | 1 | a0001c0002t0012g0077 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.694+25000G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091798 | ||||||
| chr3:141091808
|
A | G | 71 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(68): Show | 73 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.694+25010A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141091808 | ||||||
| chr3:141091870
|
C | CTTCCTTT others(11): Show |
1 | a0001c0001t0053g0020 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.694+25082_694+2509 others(22): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141091870 | |||||
| chr3:141092064
|
A | C | 2 | a0001c0001t0056g0176a0002c0004t0045g0240 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.694+25266A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092064 | ||||||
| chr3:141092120
|
C | T | 3 | a0001c0001t0026g0222a0001c0001t0043g0234a0001c0001t0044g0231 | 3 | HG01884.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694+25322C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092120 | ||||||
| chr3:141092155
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+25357G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092155 | ||||||
| chr3:141092421
|
A | G | 66 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(63): Show | 68 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.694+25623A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092421 | ||||||
| chr3:141092459
|
G | A | 38 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(35): Show | 40 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.694+25661G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092459 | ||||||
| chr3:141092618
|
T | C | 65 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(62): Show | 67 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(64): Show |
intron_variant | MODIFIER | c.694+25820T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092618 | ||||||
| chr3:141092676
|
C | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(35): Show | 40 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.694+25878C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092676 | ||||||
| chr3:141092797
|
C | T | 30 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(27): Show | 33 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.694+25999C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092797 | ||||||
| chr3:141092890
|
C | T | 2 | a0001c0001t0056g0176a0002c0004t0045g0240 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.694+26092C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141092890 | ||||||
| chr3:141093184
|
G | A | 3 | a0001c0001t0015g0178a0001c0001t0015g0188a0001c0001t0015g0189 | 3 | HG02486.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.694+26386G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093184 | ||||||
| chr3:141093272
|
GACA | G | 24 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(21): Show | 24 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+26482_694+2648 others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141093272 | |||||
| chr3:141093326
|
T | A | 1 | a0001c0001t0010g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.694+26528T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093326 | ||||||
| chr3:141093347
|
G | C | 120 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(117): Show | 126 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.694+26549G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093347 | ||||||
| chr3:141093436
|
A | T | 2 | a0001c0001t0056g0176a0002c0004t0045g0240 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.694+26638A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093436 | ||||||
| chr3:141093497
|
C | T | 3 | a0001c0001t0048g0238a0001c0002t0014g0101a0001c0002t0014g0102 | 3 | HG01169.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.694+26699C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093497 | ||||||
| chr3:141093643
|
C | G | 121 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(118): Show | 127 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.694+26845C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093643 | ||||||
| chr3:141093723
|
C | T | 40 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(37): Show | 43 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.694+26925C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093723 | ||||||
| chr3:141093778
|
C | T | 2 | a0001c0001t0043g0234a0001c0001t0044g0231 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.694+26980C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093778 | ||||||
| chr3:141093783
|
G | T | 2 | a0001c0001t0025g0144a0001c0001t0025g0146 | 2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+26985G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093783 | ||||||
| chr3:141093823
|
C | T | 1 | a0001c0002t0060g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.694+27025C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093823 | ||||||
| chr3:141093900
|
C | T | 2 | a0001c0001t0034g0217a0001c0001t0035g0216 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.694+27102C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093900 | ||||||
| chr3:141093913
|
T | G | 1 | a0001c0002t0005g0205 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.694+27115T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141093913 | ||||||
| chr3:141094101
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.694+27303C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094101 | ||||||
| chr3:141094109
|
A | G | 2 | a0001c0001t0025g0144a0001c0001t0025g0146 | 2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+27311A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094109 | ||||||
| chr3:141094126
|
A | G | 82 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(79): Show | 86 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.694+27328A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094126 | ||||||
| chr3:141094169
|
G | A | 32 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(29): Show | 33 | HG00639.hp1 HG00735.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.694+27371G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094169 | ||||||
| chr3:141094293
|
T | A | 82 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(79): Show | 86 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.694+27495T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094293 | ||||||
| chr3:141094321
|
A | C | 5 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(2): Show | 6 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+27523A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094321 | ||||||
| chr3:141094322
|
T | G | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG00735.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.694+27524T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094322 | ||||||
| chr3:141094424
|
C | T | 2 | a0001c0001t0056g0176a0002c0004t0045g0240 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.694+27626C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094424 | ||||||
| chr3:141094435
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.694+27637G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094435 | ||||||
| chr3:141094538
|
A | G | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.694+27740A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094538 | ||||||
| chr3:141094589
|
A | C | 1 | a0001c0001t0002g0036 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.694+27791A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094589 | ||||||
| chr3:141094658
|
T | C | 1 | a0001c0002t0008g0223 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.694+27860T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094658 | ||||||
| chr3:141094769
|
C | T | 81 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(78): Show | 86 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.694+27971C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094769 | ||||||
| chr3:141094802
|
A | G | 98 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(95): Show | 104 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.694+28004A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094802 | ||||||
| chr3:141094880
|
G | C | 89 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(86): Show | 95 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.694+28082G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094880 | ||||||
| chr3:141094880
|
G | T | 1 | a0001c0001t0002g0029 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.694+28082G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094880 | ||||||
| chr3:141094925
|
T | C | 28 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(25): Show | 28 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.694+28127T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094925 | ||||||
| chr3:141094962
|
T | C | 88 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(85): Show | 93 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.694+28164T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141094962 | ||||||
| chr3:141095087
|
C | T | 1 | a0001c0001t0028g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.694+28289C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095087 | ||||||
| chr3:141095177
|
C | T | 42 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(39): Show | 45 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.694+28379C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095177 | ||||||
| chr3:141095180
|
C | T | 39 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(36): Show | 42 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+28382C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095180 | ||||||
| chr3:141095205
|
C | T | 2 | a0001c0002t0003g0136a0001c0002t0003g0137 | 2 | HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.694+28407C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095205 | ||||||
| chr3:141095243
|
A | C | 40 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(37): Show | 42 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.694+28445A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095243 | ||||||
| chr3:141095254
|
A | G | 87 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(84): Show | 90 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.694+28456A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095254 | ||||||
| chr3:141095284
|
T | G | 47 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(44): Show | 48 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.694+28486T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095284 | ||||||
| chr3:141095724
|
T | A | 3 | a0001c0001t0017g0157a0001c0001t0017g0169a0001c0001t0040g0170 | 3 | HG02145.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.694+28926T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095724 | ||||||
| chr3:141095779
|
G | A | 1 | a0002c0004t0045g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.694+28981G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095779 | ||||||
| chr3:141095793
|
G | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+28995G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095793 | ||||||
| chr3:141095821
|
T | G | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.694+29023T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095821 | ||||||
| chr3:141095940
|
A | C | 1 | a0001c0002t0005g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.694+29142A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141095940 | ||||||
| chr3:141096074
|
T | G | 134 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(131): Show | 139 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.694+29276T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141096074 | ||||||
| chr3:141096078
|
G | A | 1 | a0001c0002t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.694+29280G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141096078 | ||||||
| chr3:141096216
|
C | A | 30 | a0001c0001t0006g0017a0001c0001t0009g0147a0001c0001t0009g0148others(27): Show | 31 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.694+29418C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141096216 | ||||||
| chr3:141096480
|
G | A | 1 | a0001c0001t0017g0169 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.694+29682G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141096480 | ||||||
| chr3:141096813
|
T | G | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.694+30015T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141096813 | ||||||
| chr3:141097055
|
G | A | 1 | a0001c0002t0007g0105 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.694+30257G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097055 | ||||||
| chr3:141097278
|
AC | A | 18 | a0001c0001t0006g0017a0001c0001t0009g0147a0001c0001t0009g0148others(15): Show | 19 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.694+30482delC | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141097278 | |||||
| chr3:141097434
|
T | G | 2 | a0001c0001t0050g0232a0002c0004t0045g0240 | 2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.694+30636T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097434 | ||||||
| chr3:141097503
|
C | G | 24 | a0001c0001t0004g0038a0001c0001t0004g0091a0001c0001t0019g0174others(21): Show | 24 | HG01175.hp1 HG01496.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.694+30705C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097503 | ||||||
| chr3:141097604
|
A | G | 11 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(8): Show | 11 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.694+30806A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097604 | ||||||
| chr3:141097671
|
G | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+30873G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097671 | ||||||
| chr3:141097673
|
G | C | 5 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(2): Show | 6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+30875G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097673 | ||||||
| chr3:141097705
|
A | G | 3 | a0001c0002t0026g0142a0001c0002t0036g0143a0001c0002t0058g0054 | 3 | HG02258.hp1 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694+30907A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097705 | ||||||
| chr3:141097750
|
CCCACAGA others(1): Show |
C | 37 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.694+30954_694+3096 others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141097750 | |||||
| chr3:141097756
|
G | C | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0001c0001t0043g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+30958G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097756 | ||||||
| chr3:141097874
|
C | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+31076C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097874 | ||||||
| chr3:141097894
|
G | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+31096G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097894 | ||||||
| chr3:141097918
|
G | C | 243 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(240): Show | 251 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(248): Show |
intron_variant | MODIFIER | c.694+31120G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097918 | ||||||
| chr3:141097947
|
G | A | 70 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(67): Show | 74 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.694+31149G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141097947 | ||||||
| chr3:141098238
|
G | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+31440G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098238 | ||||||
| chr3:141098507
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+31709C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098507 | ||||||
| chr3:141098708
|
T | A | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+31910T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098708 | ||||||
| chr3:141098830
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.694+32032A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098830 | ||||||
| chr3:141098842
|
A | G | 38 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(35): Show | 41 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.694+32044A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098842 | ||||||
| chr3:141098882
|
G | A | 1 | a0001c0001t0062g0243 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.694+32084G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098882 | ||||||
| chr3:141098923
|
C | T | 2 | a0001c0002t0003g0053a0001c0002t0003g0088 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.694+32125C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141098923 | ||||||
| chr3:141099056
|
T | A | 1 | a0001c0001t0031g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.694+32258T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099056 | ||||||
| chr3:141099107
|
TAATACTG others(4): Show |
T | 34 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(31): Show | 34 | HG00639.hp1 HG00738.hp2 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.694+32313_694+3232 others(15): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141099107 | |||||
| chr3:141099111
|
A | G | 1 | a0001c0001t0002g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.694+32313A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099111 | ||||||
| chr3:141099135
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0001c0001t0043g0234 | 3 | HG00735.hp2 HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+32337C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099135 | ||||||
| chr3:141099185
|
C | CT | 9 | a0001c0001t0002g0052a0001c0001t0002g0214a0001c0001t0002g0218others(6): Show | 9 | HG01175.hp2 HG01243.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+32404dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141099185 | |||||
| chr3:141099185
|
CT | C | 27 | a0001c0001t0006g0191a0001c0001t0009g0147a0001c0001t0009g0148others(24): Show | 28 | HG00735.hp2 HG01109.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.694+32404delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141099185 | |||||
| chr3:141099233
|
G | A | 1 | a0001c0001t0020g0155 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.694+32435G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099233 | ||||||
| chr3:141099254
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.694+32456G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099254 | ||||||
| chr3:141099270
|
T | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+32472T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099270 | ||||||
| chr3:141099271
|
G | A | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+32473G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099271 | ||||||
| chr3:141099285
|
C | T | 1 | a0001c0003t0016g0204 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.694+32487C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099285 | ||||||
| chr3:141099329
|
C | T | 4 | a0001c0001t0004g0038a0001c0001t0025g0144a0001c0001t0025g0146others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+32531C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099329 | ||||||
| chr3:141099345
|
C | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+32547C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099345 | ||||||
| chr3:141099823
|
C | G | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+33025C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099823 | ||||||
| chr3:141099919
|
A | G | 1 | a0001c0001t0055g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.694+33121A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141099919 | ||||||
| chr3:141100087
|
C | G | 1 | a0001c0002t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.694+33289C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100087 | ||||||
| chr3:141100120
|
T | C | 1 | a0001c0001t0002g0163 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.694+33322T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100120 | ||||||
| chr3:141100218
|
A | G | 34 | a0001c0001t0004g0141a0001c0001t0006g0017a0001c0001t0009g0147others(31): Show | 36 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.694+33420A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100218 | ||||||
| chr3:141100243
|
C | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.694+33445C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100243 | ||||||
| chr3:141100263
|
A | G | 1 | a0001c0002t0001g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.694+33465A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100263 | ||||||
| chr3:141100387
|
A | G | 110 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(107): Show | 116 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.694+33589A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100387 | ||||||
| chr3:141100396
|
G | A | 2 | a0001c0001t0026g0222a0001c0001t0056g0176 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.694+33598G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100396 | ||||||
| chr3:141100408
|
T | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+33610T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100408 | ||||||
| chr3:141100462
|
C | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+33664C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100462 | ||||||
| chr3:141100473
|
C | T | 2 | a0001c0001t0020g0145a0001c0003t0016g0204 | 2 | HG02055.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.694+33675C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100473 | ||||||
| chr3:141100474
|
G | A | 2 | a0001c0002t0003g0053a0001c0002t0003g0088 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.694+33676G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100474 | ||||||
| chr3:141100515
|
A | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+33717A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100515 | ||||||
| chr3:141100729
|
G | C | 1 | a0001c0002t0026g0142 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.694+33931G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100729 | ||||||
| chr3:141100819
|
C | G | 5 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(2): Show | 6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+34021C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141100819 | ||||||
| chr3:141101028
|
C | T | 4 | a0001c0002t0007g0030a0001c0002t0007g0057a0001c0002t0007g0061others(1): Show | 4 | HG02647.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+34230C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101028 | ||||||
| chr3:141101155
|
G | GC | 6 | a0001c0001t0027g0235a0001c0001t0027g0237a0001c0002t0005g0121others(3): Show | 6 | HG01175.hp1 HG01255.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+34363dupC | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141101155 | |||||
| chr3:141101195
|
T | C | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.694+34397T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101195 | ||||||
| chr3:141101301
|
C | T | 1 | a0001c0003t0004g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.694+34503C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101301 | ||||||
| chr3:141101336
|
C | A | 2 | a0001c0001t0011g0050a0001c0002t0032g0010 | 2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.694+34538C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101336 | ||||||
| chr3:141101525
|
C | T | 2 | a0001c0001t0025g0144a0001c0001t0025g0146 | 2 | HG00735.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.694+34727C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101525 | ||||||
| chr3:141101728
|
G | A | 1 | a0001c0002t0022g0127 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.694+34930G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101728 | ||||||
| chr3:141101794
|
T | G | 1 | a0001c0002t0059g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.694+34996T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101794 | ||||||
| chr3:141101993
|
G | A | 5 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(2): Show | 6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+35195G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141101993 | ||||||
| chr3:141102382
|
T | C | 1 | a0001c0001t0002g0179 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.694+35584T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141102382 | ||||||
| chr3:141102442
|
G | C | 2 | a0001c0002t0001g0119a0001c0002t0001g0215 | 2 | NA18992.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.694+35644G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141102442 | ||||||
| chr3:141102505
|
A | G | 17 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(14): Show | 18 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.694+35707A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141102505 | ||||||
| chr3:141103035
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+36237G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103035 | ||||||
| chr3:141103252
|
G | T | 2 | a0001c0001t0027g0235a0001c0001t0027g0237 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.694+36454G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103252 | ||||||
| chr3:141103301
|
A | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+36503A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103301 | ||||||
| chr3:141103337
|
T | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+36539T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103337 | ||||||
| chr3:141103485
|
A | G | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+36687A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103485 | ||||||
| chr3:141103500
|
G | A | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+36702G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103500 | ||||||
| chr3:141103555
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+36757T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103555 | ||||||
| chr3:141103640
|
A | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+36842A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103640 | ||||||
| chr3:141103712
|
G | C | 3 | a0001c0001t0006g0158a0001c0002t0003g0136a0001c0002t0003g0137 | 3 | HG02809.hp1 HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.694+36914G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103712 | ||||||
| chr3:141103753
|
C | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+36955C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103753 | ||||||
| chr3:141103780
|
G | C | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.694+36982G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103780 | ||||||
| chr3:141103830
|
CT | C | 7 | a0001c0001t0013g0149a0001c0001t0020g0145a0001c0001t0020g0155others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+37046delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141103830 | |||||
| chr3:141103837
|
T | A | 2 | a0001c0001t0043g0234a0001c0002t0058g0054 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.694+37039T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103837 | ||||||
| chr3:141103867
|
G | A | 29 | a0001c0001t0006g0017a0001c0001t0009g0147a0001c0001t0009g0148others(26): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.694+37069G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103867 | ||||||
| chr3:141103936
|
A | G | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+37138A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141103936 | ||||||
| chr3:141104162
|
T | C | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.694+37364T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104162 | ||||||
| chr3:141104372
|
A | G | 3 | a0001c0001t0026g0222a0001c0001t0056g0176a0001c0002t0026g0142 | 3 | HG01243.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694+37574A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104372 | ||||||
| chr3:141104418
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+37620C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104418 | ||||||
| chr3:141104419
|
G | A | 11 | a0001c0001t0002g0139a0001c0001t0004g0192a0001c0001t0006g0007others(8): Show | 12 | HG00544.hp1 HG02015.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.694+37621G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104419 | ||||||
| chr3:141104426
|
A | T | 1 | a0001c0002t0005g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.694+37628A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104426 | ||||||
| chr3:141104490
|
C | G | 3 | a0001c0001t0026g0222a0001c0001t0056g0176a0001c0002t0026g0142 | 3 | HG01243.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694+37692C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104490 | ||||||
| chr3:141104546
|
T | G | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+37748T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104546 | ||||||
| chr3:141104712
|
C | T | 1 | a0001c0002t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.694+37914C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104712 | ||||||
| chr3:141104747
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.694+37949G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104747 | ||||||
| chr3:141104841
|
C | A | 1 | a0001c0002t0005g0114 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.694+38043C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104841 | ||||||
| chr3:141104851
|
G | A | 1 | a0001c0001t0053g0020 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.694+38053G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104851 | ||||||
| chr3:141104875
|
A | G | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.694+38077A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104875 | ||||||
| chr3:141104959
|
A | C | 2 | a0001c0001t0043g0234a0001c0002t0058g0054 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.694+38161A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141104959 | ||||||
| chr3:141105089
|
T | C | 3 | a0001c0001t0002g0064a0001c0001t0002g0070a0001c0001t0002g0071 | 3 | NA18941.hp1 NA18959.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.694+38291T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105089 | ||||||
| chr3:141105095
|
A | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.694+38297A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105095 | ||||||
| chr3:141105245
|
C | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+38447C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105245 | ||||||
| chr3:141105257
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+38459C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105257 | ||||||
| chr3:141105353
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+38555C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105353 | ||||||
| chr3:141105448
|
G | C | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.694+38650G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105448 | ||||||
| chr3:141105499
|
A | G | 1 | a0001c0002t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.694+38701A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105499 | ||||||
| chr3:141105557
|
G | T | 1 | a0001c0001t0019g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.694+38759G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105557 | ||||||
| chr3:141105603
|
G | C | 24 | a0001c0001t0004g0141a0001c0001t0006g0017a0001c0001t0009g0147others(21): Show | 26 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.694+38805G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105603 | ||||||
| chr3:141105689
|
C | G | 1 | a0001c0002t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.694+38891C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105689 | ||||||
| chr3:141105916
|
C | T | 3 | a0001c0002t0001g0128a0001c0002t0021g0011a0001c0002t0021g0089 | 3 | HG02155.hp1 NA18964.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.694+39118C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141105916 | ||||||
| chr3:141106022
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+39224T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106022 | ||||||
| chr3:141106046
|
T | G | 39 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(36): Show | 42 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.694+39248T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106046 | ||||||
| chr3:141106069
|
C | T | 1 | a0001c0001t0053g0020 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.694+39271C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106069 | ||||||
| chr3:141106340
|
CCT | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+39545_694+3954 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141106340 | |||||
| chr3:141106372
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+39574T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106372 | ||||||
| chr3:141106422
|
C | T | 1 | a0001c0002t0012g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.694+39624C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106422 | ||||||
| chr3:141106528
|
C | G | 2 | a0001c0002t0001g0032a0001c0002t0001g0065 | 2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.694+39730C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106528 | ||||||
| chr3:141106688
|
TA | T | 10 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+39892delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141106688 | |||||
| chr3:141106719
|
C | T | 2 | a0001c0002t0022g0094a0001c0002t0022g0129 | 2 | HG01257.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.694+39921C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106719 | ||||||
| chr3:141106755
|
T | G | 1 | a0001c0001t0006g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.694+39957T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106755 | ||||||
| chr3:141106830
|
G | T | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.694+40032G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106830 | ||||||
| chr3:141106850
|
C | T | 1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.694+40052C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106850 | ||||||
| chr3:141106968
|
T | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.694+40170T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141106968 | ||||||
| chr3:141107130
|
G | A | 1 | a0001c0001t0047g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-40012G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107130 | ||||||
| chr3:141107262
|
G | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-39880G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107262 | ||||||
| chr3:141107315
|
T | TA | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-39825dupA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141107315 | |||||
| chr3:141107338
|
C | T | 8 | a0001c0001t0002g0138a0001c0001t0002g0180a0001c0001t0002g0184others(5): Show | 8 | HG00639.hp1 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-39804C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107338 | ||||||
| chr3:141107358
|
T | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-39784T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107358 | ||||||
| chr3:141107390
|
AAAAT | A | 17 | a0001c0001t0006g0017a0001c0001t0009g0147a0001c0001t0009g0148others(14): Show | 18 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.695-39745_695-3974 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141107390 | |||||
| chr3:141107403
|
C | T | 56 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(53): Show | 60 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.695-39739C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107403 | ||||||
| chr3:141107406
|
G | A | 1 | a0001c0001t0056g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.695-39736G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107406 | ||||||
| chr3:141107572
|
T | C | 10 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(7): Show | 10 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-39570T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107572 | ||||||
| chr3:141107594
|
T | C | 1 | a0001c0001t0011g0050 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.695-39548T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107594 | ||||||
| chr3:141107664
|
T | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-39478T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107664 | ||||||
| chr3:141107679
|
A | G | 75 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(72): Show | 80 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.695-39463A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107679 | ||||||
| chr3:141107721
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-39421C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107721 | ||||||
| chr3:141107906
|
G | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-39236G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107906 | ||||||
| chr3:141107961
|
AAAAAT | A | 36 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(33): Show | 39 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.695-39171_695-3916 others(9): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141107961 | |||||
| chr3:141107962
|
A | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-39180A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107962 | ||||||
| chr3:141107966
|
TA | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-39172delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141107966 | |||||
| chr3:141107967
|
A | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-39175A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107967 | ||||||
| chr3:141107992
|
C | T | 33 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(30): Show | 36 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.695-39150C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141107992 | ||||||
| chr3:141108029
|
A | C | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-39113A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108029 | ||||||
| chr3:141108088
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-39054G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108088 | ||||||
| chr3:141108139
|
C | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-39003C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108139 | ||||||
| chr3:141108229
|
C | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-38913C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108229 | ||||||
| chr3:141108644
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-38498C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108644 | ||||||
| chr3:141108695
|
T | C | 8 | a0001c0001t0004g0141a0001c0001t0010g0159a0001c0001t0015g0167others(5): Show | 9 | HG01891.hp2 HG02486.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.695-38447T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108695 | ||||||
| chr3:141108851
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-38291G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108851 | ||||||
| chr3:141108886
|
G | A | 1 | a0001c0002t0012g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695-38256G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108886 | ||||||
| chr3:141108892
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.695-38250C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108892 | ||||||
| chr3:141108915
|
C | T | 1 | a0001c0002t0012g0073 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695-38227C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141108915 | ||||||
| chr3:141109166
|
G | A | 1 | a0001c0002t0012g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.695-37976G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109166 | ||||||
| chr3:141109244
|
T | C | 1 | a0001c0001t0002g0218 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.695-37898T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109244 | ||||||
| chr3:141109318
|
T | C | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-37824T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109318 | ||||||
| chr3:141109378
|
C | T | 1 | a0001c0002t0003g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.695-37764C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109378 | ||||||
| chr3:141109481
|
G | C | 1 | a0001c0001t0010g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.695-37661G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109481 | ||||||
| chr3:141109486
|
A | C | 16 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(13): Show | 17 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-37656A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109486 | ||||||
| chr3:141109513
|
C | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-37629C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109513 | ||||||
| chr3:141109558
|
A | G | 2 | a0001c0001t0043g0234a0001c0002t0058g0054 | 2 | HG01884.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.695-37584A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109558 | ||||||
| chr3:141109595
|
C | T | 1 | a0001c0002t0022g0094 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.695-37547C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109595 | ||||||
| chr3:141109635
|
A | G | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-37507A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109635 | ||||||
| chr3:141109715
|
A | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-37427A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109715 | ||||||
| chr3:141109716
|
G | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-37426G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109716 | ||||||
| chr3:141109718
|
C | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-37424C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109718 | ||||||
| chr3:141109719
|
T | G | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-37423T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109719 | ||||||
| chr3:141109752
|
A | G | 1 | a0001c0001t0010g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.695-37390A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109752 | ||||||
| chr3:141109781
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-37361G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109781 | ||||||
| chr3:141109959
|
G | A | 132 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(129): Show | 137 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.695-37183G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141109959 | ||||||
| chr3:141110212
|
T | A | 1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.695-36930T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141110212 | ||||||
| chr3:141110580
|
T | C | 109 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(106): Show | 114 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.695-36562T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141110580 | ||||||
| chr3:141110917
|
G | A | 22 | a0001c0001t0004g0038a0001c0001t0004g0091a0001c0001t0019g0174others(19): Show | 22 | HG01496.hp1 HG01496.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-36225G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141110917 | ||||||
| chr3:141110926
|
G | A | 4 | a0001c0001t0011g0050a0001c0001t0028g0018a0001c0001t0028g0048others(1): Show | 4 | HG01258.hp2 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-36216G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141110926 | ||||||
| chr3:141111139
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.695-36003G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111139 | ||||||
| chr3:141111242
|
G | A | 3 | a0001c0002t0022g0094a0001c0002t0022g0127a0001c0002t0022g0129 | 3 | HG01081.hp2 HG01257.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.695-35900G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111242 | ||||||
| chr3:141111295
|
G | A | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695-35847G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111295 | ||||||
| chr3:141111303
|
T | C | 108 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(105): Show | 113 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.695-35839T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111303 | ||||||
| chr3:141111354
|
C | CT | 126 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(123): Show | 129 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.695-35762dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141111354 | |||||
| chr3:141111354
|
C | CTT | 60 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0071others(57): Show | 64 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.695-35763_695-3576 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141111354 | |||||
| chr3:141111354
|
C | CTTT | 5 | a0001c0001t0002g0051a0001c0001t0004g0195a0001c0001t0011g0117others(2): Show | 5 | HG02148.hp2 HG02258.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-35764_695-3576 others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141111354 | |||||
| chr3:141111354
|
CT | C | 7 | a0001c0001t0002g0210a0001c0002t0008g0223a0001c0002t0008g0224others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-35762delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141111354 | |||||
| chr3:141111408
|
T | A | 3 | a0001c0001t0020g0145a0001c0001t0020g0156a0001c0002t0061g0112 | 3 | HG02055.hp2 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.695-35734T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111408 | ||||||
| chr3:141111486
|
C | T | 16 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(13): Show | 17 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-35656C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111486 | ||||||
| chr3:141111501
|
G | T | 1 | a0001c0001t0010g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.695-35641G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111501 | ||||||
| chr3:141111528
|
G | A | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-35614G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111528 | ||||||
| chr3:141111751
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.695-35391G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111751 | ||||||
| chr3:141111957
|
C | T | 7 | a0001c0001t0002g0186a0001c0001t0004g0152a0001c0001t0041g0028others(4): Show | 7 | HG00639.hp1 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.695-35185C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111957 | ||||||
| chr3:141111966
|
G | A | 1 | a0001c0001t0047g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-35176G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111966 | ||||||
| chr3:141111997
|
A | G | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-35145A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141111997 | ||||||
| chr3:141112003
|
C | A | 3 | a0001c0001t0015g0178a0001c0001t0015g0188a0001c0001t0015g0189 | 3 | HG02486.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.695-35139C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112003 | ||||||
| chr3:141112032
|
G | A | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-35110G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112032 | ||||||
| chr3:141112537
|
T | C | 2 | a0001c0001t0002g0190a0001c0002t0001g0103 | 2 | NA18993.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.695-34605T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112537 | ||||||
| chr3:141112593
|
C | G | 1 | a0001c0002t0021g0011 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.695-34549C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112593 | ||||||
| chr3:141112632
|
G | A | 37 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.695-34510G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112632 | ||||||
| chr3:141112644
|
C | CA | 12 | a0001c0001t0002g0162a0001c0001t0004g0152a0001c0001t0026g0222others(9): Show | 12 | HG00735.hp1 HG02148.hp1 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.695-34473dupA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAA | 27 | a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0181others(24): Show | 27 | HG01081.hp2 HG01255.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-34476_695-3447 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAA | 6 | a0001c0001t0002g0138a0001c0001t0002g0186a0001c0001t0002g0187others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-34477_695-3447 others(9): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(1): Show |
16 | a0001c0001t0002g0218a0001c0001t0004g0192a0001c0001t0006g0008others(13): Show | 18 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.695-34480_695-3447 others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(8): Show | 11 | HG00597.hp1 HG02257.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.695-34481_695-3447 others(13): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0002g0139a0001c0001t0004g0193a0001c0001t0011g0116others(2): Show | 5 | HG03516.hp1 NA18522.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-34482_695-3447 others(14): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0011g0115a0001c0001t0011g0117a0001c0001t0023g0009 | 4 | HG02486.hp2 HG02630.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-34483_695-3447 others(15): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0013g0150a0001c0002t0005g0205 | 2 | HG01167.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.695-34484_695-3447 others(16): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(6): Show |
13 | a0001c0001t0009g0148a0001c0001t0009g0151a0001c0001t0009g0154others(10): Show | 14 | HG01109.hp2 HG01169.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-34485_695-3447 others(17): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(7): Show |
10 | a0001c0001t0004g0038a0001c0001t0004g0091a0001c0001t0009g0200others(7): Show | 10 | HG01496.hp2 HG02145.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-34486_695-3447 others(18): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(8): Show |
5 | a0001c0001t0009g0147a0001c0001t0063g0067a0001c0002t0001g0208others(2): Show | 5 | HG01433.hp1 HG02040.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-34487_695-3447 others(19): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0053g0020a0001c0001t0057g0177a0001c0002t0003g0037 | 3 | HG03195.hp2 NA18947.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.695-34488_695-3447 others(20): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
C | CAAAAAAA others(10): Show |
1 | a0001c0002t0058g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.695-34489_695-3447 others(21): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
CA | C | 16 | a0001c0001t0002g0049a0001c0001t0002g0125a0001c0001t0002g0163others(13): Show | 16 | HG00558.hp1 HG00639.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.695-34473delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112644
|
CAA | C | 11 | a0001c0002t0007g0030a0001c0002t0007g0057a0001c0002t0007g0061others(8): Show | 11 | HG00738.hp2 HG01243.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.695-34474_695-3447 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141112644 | |||||
| chr3:141112787
|
C | T | 7 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0040g0170others(4): Show | 7 | HG02257.hp2 HG02976.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.695-34355C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112787 | ||||||
| chr3:141112891
|
T | C | 4 | a0001c0001t0002g0063a0001c0002t0001g0003a0001c0002t0001g0024others(1): Show | 5 | HG01952.hp1 HG01952.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-34251T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112891 | ||||||
| chr3:141112983
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695-34159C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141112983 | ||||||
| chr3:141113255
|
C | T | 6 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 7 | HG01081.hp1 HG01099.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.695-33887C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113255 | ||||||
| chr3:141113543
|
G | T | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-33599G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113543 | ||||||
| chr3:141113550
|
T | C | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-33592T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113550 | ||||||
| chr3:141113575
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.695-33567T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113575 | ||||||
| chr3:141113867
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-33275G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113867 | ||||||
| chr3:141113870
|
C | A | 2 | a0001c0002t0014g0058a0001c0002t0014g0059 | 2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.695-33272C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113870 | ||||||
| chr3:141113886
|
A | G | 2 | a0001c0001t0004g0141a0001c0001t0018g0001 | 3 | HG02630.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.695-33256A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113886 | ||||||
| chr3:141113956
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-33186C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141113956 | ||||||
| chr3:141114017
|
A | G | 1 | a0001c0001t0002g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.695-33125A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114017 | ||||||
| chr3:141114119
|
T | C | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-33023T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114119 | ||||||
| chr3:141114213
|
G | A | 2 | a0001c0001t0002g0181a0001c0002t0001g0104 | 2 | NA18999.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.695-32929G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114213 | ||||||
| chr3:141114291
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.695-32851G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114291 | ||||||
| chr3:141114431
|
C | A | 2 | a0001c0002t0001g0099a0001c0002t0001g0130 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.695-32711C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114431 | ||||||
| chr3:141114508
|
A | G | 1 | a0001c0003t0016g0204 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.695-32634A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114508 | ||||||
| chr3:141114681
|
G | A | 1 | a0001c0002t0001g0131 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.695-32461G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114681 | ||||||
| chr3:141114774
|
C | G | 10 | a0001c0001t0025g0144a0001c0001t0025g0146a0001c0001t0034g0217others(7): Show | 10 | HG00735.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-32368C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114774 | ||||||
| chr3:141114914
|
G | A | 10 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(7): Show | 10 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-32228G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114914 | ||||||
| chr3:141114997
|
C | T | 2 | a0001c0001t0024g0026a0001c0001t0024g0027 | 2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.695-32145C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141114997 | ||||||
| chr3:141115133
|
A | C | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-32009A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141115133 | ||||||
| chr3:141115191
|
G | T | 3 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0002t0061g0112 | 3 | HG02055.hp2 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.695-31951G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141115191 | ||||||
| chr3:141115530
|
G | A | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-31612G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141115530 | ||||||
| chr3:141115785
|
C | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-31357C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141115785 | ||||||
| chr3:141116028
|
CT | C | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-31112delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141116028 | |||||
| chr3:141116207
|
T | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-30935T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116207 | ||||||
| chr3:141116211
|
G | T | 1 | a0001c0002t0021g0100 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.695-30931G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116211 | ||||||
| chr3:141116331
|
G | A | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-30811G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116331 | ||||||
| chr3:141116451
|
A | T | 2 | a0001c0001t0004g0038a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.695-30691A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116451 | ||||||
| chr3:141116541
|
G | T | 1 | a0001c0001t0002g0070 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.695-30601G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116541 | ||||||
| chr3:141116607
|
C | T | 1 | a0001c0002t0001g0118 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.695-30535C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116607 | ||||||
| chr3:141116636
|
G | A | 3 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0002t0001g0033 | 3 | HG01074.hp1 HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.695-30506G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116636 | ||||||
| chr3:141116922
|
A | G | 1 | a0001c0002t0012g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.695-30220A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141116922 | ||||||
| chr3:141117121
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.695-30021G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117121 | ||||||
| chr3:141117310
|
G | A | 5 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0040g0170others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-29832G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117310 | ||||||
| chr3:141117347
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-29795C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117347 | ||||||
| chr3:141117369
|
C | T | 2 | a0001c0001t0009g0151a0001c0001t0019g0056 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.695-29773C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117369 | ||||||
| chr3:141117584
|
T | C | 10 | a0001c0001t0025g0144a0001c0001t0025g0146a0001c0001t0034g0217others(7): Show | 10 | HG00735.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-29558T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117584 | ||||||
| chr3:141117663
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-29479C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117663 | ||||||
| chr3:141117728
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-29414C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117728 | ||||||
| chr3:141117773
|
G | A | 5 | a0001c0002t0001g0032a0001c0002t0001g0065a0001c0002t0001g0068others(2): Show | 5 | HG02148.hp1 HG03017.hp2 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-29369G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117773 | ||||||
| chr3:141117879
|
A | G | 1 | a0001c0003t0017g0219 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.695-29263A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117879 | ||||||
| chr3:141117938
|
A | C | 1 | a0001c0002t0060g0019 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.695-29204A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141117938 | ||||||
| chr3:141118124
|
T | C | 2 | a0001c0001t0002g0194a0001c0002t0003g0005 | 3 | HG00544.hp2 HG00558.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.695-29018T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118124 | ||||||
| chr3:141118330
|
T | C | 2 | a0001c0001t0004g0141a0001c0001t0018g0001 | 3 | HG02630.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.695-28812T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118330 | ||||||
| chr3:141118371
|
T | C | 1 | a0001c0001t0020g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.695-28771T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118371 | ||||||
| chr3:141118465
|
C | A | 6 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0040g0170others(3): Show | 6 | HG02257.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-28677C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118465 | ||||||
| chr3:141118475
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0031g0244 | 2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.695-28667G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118475 | ||||||
| chr3:141118614
|
A | G | 2 | a0001c0001t0004g0038a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.695-28528A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118614 | ||||||
| chr3:141118723
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-28419T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118723 | ||||||
| chr3:141118733
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-28409C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118733 | ||||||
| chr3:141118894
|
C | A | 1 | a0001c0002t0001g0111 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.695-28248C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141118894 | ||||||
| chr3:141119012
|
T | C | 2 | a0001c0002t0014g0058a0001c0002t0014g0059 | 2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.695-28130T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119012 | ||||||
| chr3:141119043
|
T | C | 1 | a0001c0002t0001g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.695-28099T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119043 | ||||||
| chr3:141119089
|
T | C | 1 | a0001c0001t0044g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.695-28053T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119089 | ||||||
| chr3:141119182
|
G | A | 1 | a0001c0005t0042g0245 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.695-27960G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119182 | ||||||
| chr3:141119271
|
T | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-27871T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119271 | ||||||
| chr3:141119395
|
A | G | 109 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(106): Show | 114 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.695-27747A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119395 | ||||||
| chr3:141119503
|
C | G | 1 | a0001c0001t0038g0025 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-27639C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119503 | ||||||
| chr3:141119530
|
G | T | 1 | a0001c0001t0002g0210 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.695-27612G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119530 | ||||||
| chr3:141119617
|
A | C | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-27525A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119617 | ||||||
| chr3:141119811
|
T | C | 16 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(13): Show | 17 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-27331T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119811 | ||||||
| chr3:141119821
|
G | T | 1 | a0001c0001t0031g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.695-27321G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119821 | ||||||
| chr3:141119887
|
G | T | 1 | a0001c0001t0016g0207 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.695-27255G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119887 | ||||||
| chr3:141119902
|
G | C | 6 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0040g0170others(3): Show | 6 | HG02257.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-27240G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119902 | ||||||
| chr3:141119987
|
G | A | 1 | a0001c0002t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.695-27155G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141119987 | ||||||
| chr3:141120002
|
A | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-27140A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120002 | ||||||
| chr3:141120176
|
T | C | 64 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(61): Show | 69 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.695-26966T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120176 | ||||||
| chr3:141120299
|
G | A | 57 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(54): Show | 62 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.695-26843G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120299 | ||||||
| chr3:141120367
|
T | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-26775T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120367 | ||||||
| chr3:141120523
|
CCATT | C | 10 | a0001c0001t0025g0144a0001c0001t0025g0146a0001c0001t0034g0217others(7): Show | 10 | HG00735.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-26618_695-2661 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120523 | ||||||
| chr3:141120530
|
T | G | 1 | a0001c0001t0006g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.695-26612T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120530 | ||||||
| chr3:141120588
|
T | C | 1 | a0001c0002t0026g0142 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.695-26554T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120588 | ||||||
| chr3:141120902
|
C | G | 1 | a0001c0002t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.695-26240C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120902 | ||||||
| chr3:141120918
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.695-26224G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120918 | ||||||
| chr3:141120945
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-26197C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120945 | ||||||
| chr3:141120949
|
T | C | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-26193T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120949 | ||||||
| chr3:141120955
|
T | C | 1 | a0001c0001t0051g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.695-26187T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141120955 | ||||||
| chr3:141121005
|
T | C | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-26137T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121005 | ||||||
| chr3:141121012
|
C | G | 38 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(35): Show | 41 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.695-26130C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121012 | ||||||
| chr3:141121021
|
A | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-26121A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121021 | ||||||
| chr3:141121050
|
A | C | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-26092A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121050 | ||||||
| chr3:141121060
|
C | T | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-26082C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121060 | ||||||
| chr3:141121104
|
C | G | 1 | a0001c0001t0015g0188 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.695-26038C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121104 | ||||||
| chr3:141121200
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-25942G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121200 | ||||||
| chr3:141121243
|
A | T | 1 | a0001c0002t0001g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.695-25899A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121243 | ||||||
| chr3:141121249
|
C | T | 109 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(106): Show | 114 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.695-25893C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121249 | ||||||
| chr3:141121281
|
G | A | 1 | a0001c0002t0012g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.695-25861G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121281 | ||||||
| chr3:141121316
|
C | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-25826C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121316 | ||||||
| chr3:141121367
|
G | T | 1 | a0001c0002t0012g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.695-25775G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121367 | ||||||
| chr3:141121393
|
G | C | 1 | a0001c0001t0010g0209 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.695-25749G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121393 | ||||||
| chr3:141121474
|
G | A | 1 | a0001c0002t0003g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.695-25668G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141121474 | ||||||
| chr3:141122140
|
C | T | 1 | a0001c0003t0017g0219 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.695-25002C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122140 | ||||||
| chr3:141122582
|
A | G | 103 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(100): Show | 107 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.695-24560A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122582 | ||||||
| chr3:141122732
|
C | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-24410C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122732 | ||||||
| chr3:141122756
|
G | A | 2 | a0001c0001t0002g0063a0001c0002t0001g0003 | 3 | HG01952.hp1 NA18991.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.695-24386G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122756 | ||||||
| chr3:141122803
|
G | A | 3 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0002t0007g0062 | 4 | HG02630.hp1 HG02717.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-24339G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122803 | ||||||
| chr3:141122883
|
A | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-24259A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122883 | ||||||
| chr3:141122897
|
T | C | 136 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(133): Show | 141 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.695-24245T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141122897 | ||||||
| chr3:141123252
|
A | G | 1 | a0001c0001t0016g0207 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.695-23890A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141123252 | ||||||
| chr3:141123270
|
C | A | 1 | a0001c0002t0003g0075 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.695-23872C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141123270 | ||||||
| chr3:141123327
|
A | G | 1 | a0001c0001t0006g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.695-23815A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141123327 | ||||||
| chr3:141123480
|
C | T | 3 | a0001c0001t0002g0052a0001c0001t0002g0218a0001c0002t0001g0085 | 3 | NA18947.hp1 NA19012.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.695-23662C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141123480 | ||||||
| chr3:141123817
|
C | T | 2 | a0001c0001t0034g0217a0001c0001t0035g0216 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.695-23325C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141123817 | ||||||
| chr3:141123979
|
G | A | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-23163G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141123979 | ||||||
| chr3:141124066
|
T | C | 1 | a0001c0001t0028g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.695-23076T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124066 | ||||||
| chr3:141124148
|
G | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-22994G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124148 | ||||||
| chr3:141124177
|
C | G | 1 | a0001c0002t0008g0226 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.695-22965C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124177 | ||||||
| chr3:141124211
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-22931G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124211 | ||||||
| chr3:141124324
|
A | G | 1 | a0001c0002t0005g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.695-22818A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124324 | ||||||
| chr3:141124400
|
T | A | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-22742T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124400 | ||||||
| chr3:141124431
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-22711G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124431 | ||||||
| chr3:141124442
|
G | A | 5 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(2): Show | 6 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-22700G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124442 | ||||||
| chr3:141124466
|
C | T | 6 | a0001c0001t0034g0217a0001c0001t0035g0216a0001c0001t0040g0170others(3): Show | 6 | HG02257.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-22676C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124466 | ||||||
| chr3:141124481
|
G | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-22661G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124481 | ||||||
| chr3:141124573
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-22569G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124573 | ||||||
| chr3:141124626
|
C | T | 13 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(10): Show | 14 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.695-22516C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124626 | ||||||
| chr3:141124627
|
G | A | 1 | a0001c0001t0049g0230 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.695-22515G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124627 | ||||||
| chr3:141124790
|
G | A | 74 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(71): Show | 79 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.695-22352G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124790 | ||||||
| chr3:141124866
|
A | G | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-22276A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124866 | ||||||
| chr3:141124996
|
G | A | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-22146G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141124996 | ||||||
| chr3:141125161
|
T | G | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-21981T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141125161 | ||||||
| chr3:141125334
|
C | T | 2 | a0001c0002t0029g0042a0001c0002t0029g0043 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.695-21808C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141125334 | ||||||
| chr3:141125755
|
A | G | 109 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(106): Show | 114 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.695-21387A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141125755 | ||||||
| chr3:141125903
|
G | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-21239G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141125903 | ||||||
| chr3:141126075
|
T | G | 74 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(71): Show | 79 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.695-21067T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126075 | ||||||
| chr3:141126146
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-20996T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126146 | ||||||
| chr3:141126155
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-20987G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126155 | ||||||
| chr3:141126279
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-20863G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126279 | ||||||
| chr3:141126294
|
A | G | 1 | a0001c0002t0001g0111 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.695-20848A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126294 | ||||||
| chr3:141126315
|
A | C | 1 | a0001c0001t0044g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.695-20827A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126315 | ||||||
| chr3:141126333
|
C | T | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-20809C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126333 | ||||||
| chr3:141126432
|
C | T | 3 | a0001c0001t0034g0217a0001c0001t0035g0216a0002c0004t0046g0239 | 3 | HG02257.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.695-20710C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126432 | ||||||
| chr3:141126461
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-20681G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126461 | ||||||
| chr3:141126578
|
A | G | 1 | a0001c0003t0016g0204 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.695-20564A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126578 | ||||||
| chr3:141126683
|
G | A | 17 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(14): Show | 17 | HG00735.hp2 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.695-20459G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126683 | ||||||
| chr3:141126742
|
T | C | 30 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(27): Show | 33 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.695-20400T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126742 | ||||||
| chr3:141126787
|
T | C | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-20355T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126787 | ||||||
| chr3:141126822
|
G | A | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-20320G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126822 | ||||||
| chr3:141126935
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0086 | 3 | HG00597.hp2 NA18612.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.695-20207C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126935 | ||||||
| chr3:141126996
|
C | T | 3 | a0001c0002t0022g0094a0001c0002t0022g0127a0001c0002t0022g0129 | 3 | HG01081.hp2 HG01257.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.695-20146C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126996 | ||||||
| chr3:141126997
|
C | G | 31 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(28): Show | 31 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.695-20145C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141126997 | ||||||
| chr3:141127250
|
A | G | 5 | a0001c0002t0012g0077a0001c0002t0012g0078a0001c0002t0012g0079others(2): Show | 5 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-19892A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141127250 | ||||||
| chr3:141127307
|
C | T | 2 | a0001c0002t0001g0119a0001c0002t0001g0215 | 2 | NA18992.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.695-19835C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141127307 | ||||||
| chr3:141127572
|
A | AT | 18 | a0001c0001t0006g0158a0001c0001t0009g0147a0001c0001t0009g0148others(15): Show | 19 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.695-19560dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141127572 | |||||
| chr3:141127727
|
C | A | 1 | a0001c0002t0012g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.695-19415C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141127727 | ||||||
| chr3:141127791
|
C | G | 1 | a0001c0002t0052g0225 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.695-19351C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141127791 | ||||||
| chr3:141127836
|
A | T | 2 | a0001c0001t0011g0050a0001c0002t0032g0010 | 2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.695-19306A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141127836 | ||||||
| chr3:141127934
|
C | T | 2 | a0001c0002t0003g0053a0001c0002t0003g0088 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.695-19208C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141127934 | ||||||
| chr3:141128035
|
A | G | 2 | a0001c0002t0003g0053a0001c0002t0003g0088 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.695-19107A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128035 | ||||||
| chr3:141128036
|
G | A | 13 | a0001c0001t0006g0158a0001c0001t0010g0159a0001c0001t0015g0167others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-19106G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128036 | ||||||
| chr3:141128089
|
G | C | 2 | a0001c0001t0004g0038a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.695-19053G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128089 | ||||||
| chr3:141128129
|
G | T | 1 | a0001c0002t0001g0040 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.695-19013G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128129 | ||||||
| chr3:141128239
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-18903G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128239 | ||||||
| chr3:141128656
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-18486G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128656 | ||||||
| chr3:141128927
|
C | A | 1 | a0002c0004t0045g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.695-18215C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128927 | ||||||
| chr3:141128956
|
G | A | 1 | a0001c0001t0009g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.695-18186G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141128956 | ||||||
| chr3:141129044
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.695-18098G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129044 | ||||||
| chr3:141129097
|
G | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-18045G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129097 | ||||||
| chr3:141129166
|
T | A | 1 | a0001c0002t0022g0129 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.695-17976T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129166 | ||||||
| chr3:141129283
|
T | C | 1 | a0001c0001t0010g0166 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.695-17859T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129283 | ||||||
| chr3:141129712
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-17430G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129712 | ||||||
| chr3:141129729
|
C | T | 25 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(22): Show | 26 | HG01081.hp1 HG01099.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.695-17413C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129729 | ||||||
| chr3:141129782
|
C | A | 2 | a0001c0001t0004g0038a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.695-17360C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141129782 | ||||||
| chr3:141130018
|
A | C | 8 | a0001c0001t0006g0017a0001c0002t0008g0223a0001c0002t0008g0224others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-17124A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130018 | ||||||
| chr3:141130026
|
T | A | 1 | a0001c0002t0001g0041 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.695-17116T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130026 | ||||||
| chr3:141130162
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-16980C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130162 | ||||||
| chr3:141130171
|
T | C | 2 | a0001c0001t0002g0194a0001c0002t0003g0005 | 3 | HG00544.hp2 HG00558.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.695-16971T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130171 | ||||||
| chr3:141130298
|
A | G | 11 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(8): Show | 11 | HG01433.hp2 HG02015.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.695-16844A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130298 | ||||||
| chr3:141130329
|
G | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-16813G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130329 | ||||||
| chr3:141130558
|
A | G | 2 | a0001c0001t0002g0029a0001c0001t0002g0084 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.695-16584A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130558 | ||||||
| chr3:141130611
|
A | G | 1 | a0001c0002t0021g0089 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.695-16531A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130611 | ||||||
| chr3:141130650
|
A | G | 48 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(45): Show | 52 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.695-16492A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130650 | ||||||
| chr3:141130882
|
C | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-16260C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130882 | ||||||
| chr3:141130894
|
T | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-16248T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130894 | ||||||
| chr3:141130911
|
C | T | 13 | a0001c0001t0006g0158a0001c0001t0010g0159a0001c0001t0015g0167others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-16231C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130911 | ||||||
| chr3:141130912
|
A | G | 103 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(100): Show | 108 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.695-16230A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141130912 | ||||||
| chr3:141131121
|
C | T | 48 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(45): Show | 52 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.695-16021C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131121 | ||||||
| chr3:141131237
|
A | G | 111 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(108): Show | 116 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.695-15905A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131237 | ||||||
| chr3:141131395
|
A | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-15747A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131395 | ||||||
| chr3:141131514
|
C | G | 1 | a0001c0002t0005g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.695-15628C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131514 | ||||||
| chr3:141131545
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-15597T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131545 | ||||||
| chr3:141131626
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-15516C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131626 | ||||||
| chr3:141131876
|
G | C | 103 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(100): Show | 108 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.695-15266G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131876 | ||||||
| chr3:141131947
|
A | G | 1 | a0001c0002t0005g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.695-15195A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141131947 | ||||||
| chr3:141132005
|
C | T | 245 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(242): Show | 253 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(250): Show |
intron_variant | MODIFIER | c.695-15137C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132005 | ||||||
| chr3:141132174
|
G | GT | 7 | a0001c0001t0006g0158a0001c0001t0034g0217a0001c0001t0035g0216others(4): Show | 7 | HG02257.hp2 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-14957dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141132174 | |||||
| chr3:141132231
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-14911G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132231 | ||||||
| chr3:141132237
|
G | A | 7 | a0001c0001t0006g0158a0001c0001t0034g0217a0001c0001t0035g0216others(4): Show | 7 | HG02257.hp2 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-14905G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132237 | ||||||
| chr3:141132261
|
G | A | 4 | a0001c0001t0002g0036a0001c0001t0031g0244a0001c0002t0003g0053others(1): Show | 4 | HG02698.hp1 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-14881G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132261 | ||||||
| chr3:141132359
|
G | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-14783G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132359 | ||||||
| chr3:141132390
|
A | G | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-14752A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132390 | ||||||
| chr3:141132412
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-14730C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132412 | ||||||
| chr3:141132458
|
A | G | 1 | a0001c0002t0001g0132 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.695-14684A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132458 | ||||||
| chr3:141132474
|
G | A | 1 | a0001c0002t0007g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.695-14668G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132474 | ||||||
| chr3:141132530
|
A | T | 1 | a0001c0001t0002g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.695-14612A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132530 | ||||||
| chr3:141132652
|
G | GTA | 10 | a0001c0001t0053g0020a0001c0002t0001g0060a0001c0002t0005g0098others(7): Show | 10 | HG00738.hp2 HG01099.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.695-14472_695-1447 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141132652 | |||||
| chr3:141132652
|
G | GTATA | 4 | a0001c0002t0012g0077a0001c0002t0012g0078a0001c0002t0012g0080others(1): Show | 4 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-14474_695-1447 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141132652 | |||||
| chr3:141132652
|
GTA | G | 49 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(46): Show | 53 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.695-14472_695-1447 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141132652 | |||||
| chr3:141132652
|
GTATA | G | 55 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(52): Show | 56 | HG00639.hp1 HG00735.hp2 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.695-14474_695-1447 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141132652 | |||||
| chr3:141132656
|
A | G | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-14486A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132656 | ||||||
| chr3:141132662
|
A | G | 1 | a0001c0001t0004g0091 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.695-14480A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132662 | ||||||
| chr3:141132975
|
G | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-14167G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141132975 | ||||||
| chr3:141133041
|
A | G | 1 | a0001c0002t0014g0031 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.695-14101A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133041 | ||||||
| chr3:141133098
|
A | G | 2 | a0001c0001t0040g0170a0001c0001t0055g0203 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.695-14044A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133098 | ||||||
| chr3:141133204
|
T | A | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-13938T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133204 | ||||||
| chr3:141133452
|
T | C | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-13690T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133452 | ||||||
| chr3:141133466
|
G | A | 1 | a0001c0002t0003g0075 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.695-13676G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133466 | ||||||
| chr3:141133604
|
A | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-13538A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133604 | ||||||
| chr3:141133659
|
T | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-13483T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133659 | ||||||
| chr3:141133661
|
A | G | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-13481A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133661 | ||||||
| chr3:141133729
|
G | T | 1 | a0001c0002t0001g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.695-13413G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133729 | ||||||
| chr3:141133787
|
T | C | 1 | a0001c0002t0007g0206 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.695-13355T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133787 | ||||||
| chr3:141133844
|
G | A | 1 | a0001c0001t0047g0236 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.695-13298G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141133844 | ||||||
| chr3:141134018
|
CT | C | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-13113delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134018 | |||||
| chr3:141134026
|
T | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-13116T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134026 | ||||||
| chr3:141134030
|
CTTTTCTT others(14): Show |
C | 1 | a0001c0002t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.695-13093_695-1307 others(25): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134030 | |||||
| chr3:141134036
|
T | TTTTC | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-13103_695-1310 others(8): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134036 | |||||
| chr3:141134037
|
T | TTTC | 129 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(126): Show | 135 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.695-13103_695-1310 others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134037 | |||||
| chr3:141134040
|
T | C | 2 | a0001c0001t0002g0138a0001c0001t0050g0232 | 2 | HG02258.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.695-13102T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134040 | ||||||
| chr3:141134056
|
C | CT | 13 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0165others(10): Show | 13 | HG02257.hp1 HG02257.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-13067dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134056 | |||||
| chr3:141134056
|
C | CTT | 8 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0040g0170others(5): Show | 8 | HG01255.hp2 HG01891.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-13068_695-1306 others(6): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134056 | |||||
| chr3:141134056
|
C | CTTT | 6 | a0001c0001t0004g0141a0001c0001t0015g0178a0001c0001t0015g0188others(3): Show | 7 | HG02486.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-13069_695-1306 others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134056 | |||||
| chr3:141134056
|
CT | C | 78 | a0001c0001t0002g0052a0001c0001t0002g0125a0001c0001t0002g0138others(75): Show | 82 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.695-13067delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134056 | |||||
| chr3:141134062
|
T | TC | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-13080_695-1307 others(5): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134062 | ||||||
| chr3:141134064
|
T | C | 1 | a0001c0001t0002g0138 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.695-13078T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134064 | ||||||
| chr3:141134279
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.695-12863C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134279 | ||||||
| chr3:141134345
|
C | T | 14 | a0001c0001t0006g0158a0001c0001t0010g0159a0001c0001t0015g0167others(11): Show | 14 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.695-12797C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134345 | ||||||
| chr3:141134549
|
GT | G | 31 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(28): Show | 31 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.695-12587delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134549 | |||||
| chr3:141134641
|
C | A | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0002t0001g0033others(1): Show | 4 | HG01074.hp1 HG01109.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-12501C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141134641 | ||||||
| chr3:141134882
|
C | CT | 5 | a0001c0001t0011g0050a0001c0001t0028g0018a0001c0001t0028g0048others(2): Show | 5 | HG01258.hp2 HG01515.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-12247dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134882 | |||||
| chr3:141134882
|
CT | C | 29 | a0001c0001t0002g0210a0001c0001t0006g0158a0001c0001t0009g0147others(26): Show | 30 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.695-12247delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141134882 | |||||
| chr3:141135098
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-12044C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135098 | ||||||
| chr3:141135274
|
A | G | 2 | a0001c0001t0002g0049a0001c0002t0001g0060 | 2 | HG01099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.695-11868A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135274 | ||||||
| chr3:141135285
|
G | A | 13 | a0001c0001t0006g0158a0001c0001t0010g0159a0001c0001t0015g0167others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-11857G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135285 | ||||||
| chr3:141135338
|
T | TTTATTA | 50 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(47): Show | 54 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.695-11784_695-1177 others(10): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141135338 | |||||
| chr3:141135338
|
T | TTTATTAT others(2): Show |
31 | a0001c0001t0004g0141a0001c0001t0004g0193a0001c0001t0004g0195others(28): Show | 32 | HG00735.hp2 HG00738.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.695-11787_695-1177 others(13): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141135338 | |||||
| chr3:141135338
|
T | TTTATTAT others(5): Show |
22 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(19): Show | 22 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-11790_695-1177 others(16): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141135338 | |||||
| chr3:141135338
|
T | TTTATTAT others(8): Show |
4 | a0001c0001t0002g0185a0001c0001t0002g0199a0001c0001t0016g0207others(1): Show | 4 | HG01934.hp2 HG02293.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-11793_695-1177 others(19): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141135338 | |||||
| chr3:141135338
|
T | TTTATTAT others(11): Show |
3 | a0001c0002t0022g0094a0001c0002t0022g0129a0001c0002t0036g0143 | 3 | HG01257.hp1 HG02273.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.695-11796_695-1177 others(22): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141135338 | |||||
| chr3:141135499
|
C | A | 1 | a0001c0001t0026g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.695-11643C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135499 | ||||||
| chr3:141135516
|
C | T | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.695-11626C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135516 | ||||||
| chr3:141135740
|
C | A | 1 | a0001c0003t0004g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.695-11402C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135740 | ||||||
| chr3:141135743
|
T | A | 1 | a0001c0003t0004g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.695-11399T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135743 | ||||||
| chr3:141135757
|
G | C | 1 | a0001c0003t0004g0022 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.695-11385G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135757 | ||||||
| chr3:141135804
|
C | A | 4 | a0001c0001t0025g0144a0001c0001t0025g0146a0001c0002t0036g0143others(1): Show | 4 | HG00735.hp2 HG02280.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-11338C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141135804 | ||||||
| chr3:141136159
|
T | G | 48 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(45): Show | 52 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.695-10983T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136159 | ||||||
| chr3:141136173
|
C | T | 1 | a0001c0002t0036g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.695-10969C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136173 | ||||||
| chr3:141136233
|
T | A | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10909T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136233 | ||||||
| chr3:141136236
|
T | C | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10906T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136236 | ||||||
| chr3:141136239
|
G | A | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10903G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136239 | ||||||
| chr3:141136244
|
A | T | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10898A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136244 | ||||||
| chr3:141136254
|
A | G | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10888A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136254 | ||||||
| chr3:141136258
|
G | T | 1 | a0001c0001t0039g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.695-10884G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136258 | ||||||
| chr3:141136259
|
G | A | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10883G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136259 | ||||||
| chr3:141136262
|
C | G | 2 | a0001c0001t0017g0157a0001c0001t0017g0169 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.695-10880C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136262 | ||||||
| chr3:141136408
|
C | T | 2 | a0001c0002t0014g0058a0001c0002t0014g0059 | 2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.695-10734C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136408 | ||||||
| chr3:141136444
|
G | A | 8 | a0001c0001t0006g0017a0001c0002t0008g0223a0001c0002t0008g0224others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-10698G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136444 | ||||||
| chr3:141136500
|
T | A | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-10642T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136500 | ||||||
| chr3:141136554
|
A | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-10588A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136554 | ||||||
| chr3:141136722
|
G | A | 1 | a0002c0004t0045g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.695-10420G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136722 | ||||||
| chr3:141136804
|
G | T | 14 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(11): Show | 15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-10338G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136804 | ||||||
| chr3:141136881
|
T | G | 1 | a0001c0001t0002g0139 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.695-10261T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141136881 | ||||||
| chr3:141137010
|
C | T | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-10132C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137010 | ||||||
| chr3:141137097
|
A | T | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695-10045A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137097 | ||||||
| chr3:141137100
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695-10042C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137100 | ||||||
| chr3:141137103
|
C | T | 164 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(161): Show | 170 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(167): Show |
intron_variant | MODIFIER | c.695-10039C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137103 | ||||||
| chr3:141137105
|
T | G | 1 | a0001c0002t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.695-10037T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137105 | ||||||
| chr3:141137131
|
G | T | 3 | a0001c0001t0015g0178a0001c0001t0015g0188a0001c0001t0015g0189 | 3 | HG02486.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.695-10011G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137131 | ||||||
| chr3:141137169
|
G | C | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-9973G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137169 | ||||||
| chr3:141137202
|
C | A | 2 | a0001c0001t0009g0151a0001c0001t0019g0056 | 2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.695-9940C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137202 | ||||||
| chr3:141137206
|
C | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-9936C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137206 | ||||||
| chr3:141137315
|
A | G | 2 | a0001c0001t0004g0038a0001c0001t0062g0243 | 2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.695-9827A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137315 | ||||||
| chr3:141137361
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0084 | 2 | HG02602.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.695-9781C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137361 | ||||||
| chr3:141137450
|
G | A | 4 | a0001c0002t0030g0074a0001c0002t0030g0082a0001c0003t0016g0021others(1): Show | 4 | NA18957.hp1 NA18968.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.695-9692G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137450 | ||||||
| chr3:141137663
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-9479C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137663 | ||||||
| chr3:141137755
|
T | C | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-9387T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137755 | ||||||
| chr3:141137881
|
A | G | 1 | a0001c0002t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.695-9261A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141137881 | ||||||
| chr3:141138078
|
G | A | 2 | a0001c0001t0025g0146a0001c0001t0043g0234 | 2 | HG01884.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-9064G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138078 | ||||||
| chr3:141138090
|
C | T | 1 | a0001c0001t0002g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.695-9052C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138090 | ||||||
| chr3:141138248
|
G | A | 27 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(24): Show | 27 | HG00639.hp1 HG01081.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.695-8894G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138248 | ||||||
| chr3:141138328
|
A | C | 2 | a0001c0001t0004g0141a0001c0001t0018g0001 | 3 | HG02630.hp1 HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.695-8814A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138328 | ||||||
| chr3:141138388
|
G | A | 1 | a0001c0001t0006g0158 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.695-8754G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138388 | ||||||
| chr3:141138397
|
T | G | 1 | a0001c0003t0016g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.695-8745T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138397 | ||||||
| chr3:141138409
|
T | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-8733T>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138409 | ||||||
| chr3:141138445
|
C | T | 2 | a0001c0002t0022g0094a0001c0002t0022g0129 | 2 | HG01257.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.695-8697C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138445 | ||||||
| chr3:141138492
|
A | T | 30 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(27): Show | 33 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.695-8650A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138492 | ||||||
| chr3:141138572
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-8570C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138572 | ||||||
| chr3:141138633
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695-8509A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138633 | ||||||
| chr3:141138853
|
G | A | 1 | a0001c0001t0010g0171 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.695-8289G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141138853 | ||||||
| chr3:141139095
|
T | G | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-8047T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139095 | ||||||
| chr3:141139204
|
C | G | 3 | a0001c0001t0019g0174a0001c0002t0005g0205a0001c0002t0007g0206 | 3 | NA18939.hp1 NA19005.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.695-7938C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139204 | ||||||
| chr3:141139234
|
C | A | 4 | a0001c0001t0002g0190a0001c0002t0001g0134a0001c0002t0001g0135others(1): Show | 4 | HG00609.hp2 NA18993.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-7908C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139234 | ||||||
| chr3:141139237
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.695-7905G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139237 | ||||||
| chr3:141139282
|
T | C | 1 | a0002c0004t0045g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.695-7860T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139282 | ||||||
| chr3:141139342
|
A | G | 103 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(100): Show | 108 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.695-7800A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139342 | ||||||
| chr3:141139373
|
C | T | 37 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(34): Show | 38 | HG00639.hp1 HG01081.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.695-7769C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139373 | ||||||
| chr3:141139474
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.695-7668C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139474 | ||||||
| chr3:141139695
|
C | T | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-7447C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139695 | ||||||
| chr3:141139787
|
C | G | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.695-7355C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141139787 | ||||||
| chr3:141140015
|
C | T | 103 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(100): Show | 108 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.695-7127C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140015 | ||||||
| chr3:141140095
|
C | T | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-7047C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140095 | ||||||
| chr3:141140141
|
G | T | 4 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0191others(1): Show | 5 | HG00544.hp1 HG02015.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-7001G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140141 | ||||||
| chr3:141140214
|
T | C | 62 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(59): Show | 65 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.695-6928T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140214 | ||||||
| chr3:141140283
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-6859C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140283 | ||||||
| chr3:141140404
|
G | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-6738G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140404 | ||||||
| chr3:141140628
|
G | A | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-6514G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140628 | ||||||
| chr3:141140640
|
A | G | 1 | a0001c0001t0002g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695-6502A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140640 | ||||||
| chr3:141140708
|
G | A | 3 | a0001c0002t0001g0109a0001c0002t0001g0208a0001c0002t0007g0106 | 3 | HG02040.hp1 NA18977.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.695-6434G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140708 | ||||||
| chr3:141140754
|
C | T | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-6388C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140754 | ||||||
| chr3:141140814
|
A | ATC | 29 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(26): Show | 30 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.695-6325_695-6324d others(4): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141140814 | |||||
| chr3:141140833
|
G | A | 7 | a0001c0001t0006g0158a0001c0001t0034g0217a0001c0001t0035g0216others(4): Show | 7 | HG02257.hp2 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-6309G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140833 | ||||||
| chr3:141140838
|
C | T | 13 | a0001c0001t0006g0158a0001c0001t0010g0159a0001c0001t0015g0167others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-6304C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140838 | ||||||
| chr3:141140867
|
G | A | 31 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(28): Show | 34 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.695-6275G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141140867 | ||||||
| chr3:141141052
|
C | G | 6 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0026g0222others(3): Show | 7 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-6090C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141052 | ||||||
| chr3:141141132
|
G | T | 8 | a0001c0002t0001g0004a0001c0002t0008g0223a0001c0002t0008g0224others(5): Show | 9 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.695-6010G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141132 | ||||||
| chr3:141141160
|
G | A | 8 | a0001c0001t0006g0017a0001c0002t0008g0223a0001c0002t0008g0224others(5): Show | 8 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-5982G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141160 | ||||||
| chr3:141141183
|
C | T | 2 | a0001c0001t0006g0158a0001c0005t0042g0245 | 2 | HG02896.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.695-5959C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141183 | ||||||
| chr3:141141252
|
A | G | 140 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(137): Show | 146 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.695-5890A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141252 | ||||||
| chr3:141141263
|
G | A | 13 | a0001c0001t0006g0158a0001c0001t0010g0159a0001c0001t0015g0167others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.695-5879G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141263 | ||||||
| chr3:141141291
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-5851C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141291 | ||||||
| chr3:141141352
|
C | T | 1 | a0001c0002t0001g0103 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.695-5790C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141352 | ||||||
| chr3:141141353
|
G | A | 29 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(26): Show | 30 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.695-5789G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141353 | ||||||
| chr3:141141593
|
A | C | 1 | a0001c0001t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.695-5549A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141593 | ||||||
| chr3:141141670
|
G | C | 28 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(25): Show | 29 | HG01081.hp1 HG01099.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.695-5472G>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141670 | ||||||
| chr3:141141672
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.695-5470T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141672 | ||||||
| chr3:141141736
|
C | G | 1 | a0001c0001t0050g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.695-5406C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141736 | ||||||
| chr3:141141742
|
G | A | 1 | a0001c0002t0036g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.695-5400G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141742 | ||||||
| chr3:141141942
|
C | A | 1 | a0001c0001t0044g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.695-5200C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141942 | ||||||
| chr3:141141993
|
C | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-5149C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141993 | ||||||
| chr3:141141993
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.695-5149C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141141993 | ||||||
| chr3:141142083
|
G | A | 7 | a0001c0001t0006g0158a0001c0001t0034g0217a0001c0001t0035g0216others(4): Show | 7 | HG02257.hp2 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-5059G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142083 | ||||||
| chr3:141142203
|
T | G | 1 | a0001c0001t0006g0017 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.695-4939T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142203 | ||||||
| chr3:141142242
|
A | G | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.695-4900A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142242 | ||||||
| chr3:141142493
|
C | A | 16 | a0001c0001t0002g0160a0001c0001t0002g0161a0001c0001t0002g0162others(13): Show | 16 | HG01433.hp2 HG02015.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.695-4649C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142493 | ||||||
| chr3:141142630
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-4512C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142630 | ||||||
| chr3:141142688
|
A | C | 4 | a0001c0001t0013g0006a0001c0001t0013g0140a0001c0001t0013g0149others(1): Show | 5 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-4454A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142688 | ||||||
| chr3:141142803
|
C | CT | 30 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0051others(27): Show | 31 | HG00597.hp1 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.695-4308dupT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
C | CTT | 7 | a0001c0001t0002g0015a0001c0001t0002g0064a0001c0001t0004g0091others(4): Show | 7 | HG01934.hp1 HG02698.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-4309_695-4308d others(4): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CT | C | 7 | a0001c0001t0002g0124a0001c0001t0002g0162a0001c0001t0041g0028others(4): Show | 7 | HG01074.hp1 HG02523.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-4308delT | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CTTT | C | 5 | a0001c0001t0004g0141a0001c0001t0018g0001a0001c0001t0044g0231others(2): Show | 6 | HG01243.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-4310_695-4308d others(5): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CTTTTT | C | 21 | a0001c0001t0002g0138a0001c0001t0002g0179a0001c0001t0002g0180others(18): Show | 21 | HG01081.hp2 HG01257.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.695-4312_695-4308d others(7): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CTTTTTTT others(1): Show |
C | 37 | a0001c0001t0002g0029a0001c0001t0002g0052a0001c0001t0002g0084others(34): Show | 40 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.695-4315_695-4308d others(10): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-4317_695-4308d others(12): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0006g0017a0001c0001t0010g0159a0001c0001t0015g0167others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-4320_695-4308d others(15): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142803
|
CTTTTTTT others(12): Show |
C | 21 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(18): Show | 22 | HG00738.hp2 HG01109.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-4326_695-4308d others(21): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141142803 | |||||
| chr3:141142821
|
TTTTTTTT others(8): Show |
T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-4320_695-4306d others(17): Show |
SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142821 | ||||||
| chr3:141142843
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-4299G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142843 | ||||||
| chr3:141142859
|
C | T | 1 | a0001c0001t0027g0235 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.695-4283C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142859 | ||||||
| chr3:141142962
|
A | G | 1 | a0001c0002t0001g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.695-4180A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142962 | ||||||
| chr3:141142966
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.695-4176G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141142966 | ||||||
| chr3:141143012
|
T | G | 19 | a0001c0001t0004g0141a0001c0001t0009g0147a0001c0001t0009g0148others(16): Show | 21 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.695-4130T>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143012 | ||||||
| chr3:141143031
|
T | C | 4 | a0001c0001t0020g0145a0001c0001t0020g0155a0001c0001t0020g0156others(1): Show | 4 | HG02055.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-4111T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143031 | ||||||
| chr3:141143038
|
C | A | 1 | a0001c0001t0044g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.695-4104C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143038 | ||||||
| chr3:141143038
|
C | G | 84 | a0001c0001t0002g0029a0001c0001t0002g0084a0001c0001t0002g0138others(81): Show | 88 | HG00544.hp2 HG00558.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.695-4104C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143038 | ||||||
| chr3:141143072
|
A | T | 7 | a0001c0002t0008g0223a0001c0002t0008g0224a0001c0002t0008g0226others(4): Show | 7 | HG00738.hp2 HG01243.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695-4070A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143072 | ||||||
| chr3:141143154
|
TG | T | 10 | a0001c0001t0006g0158a0001c0001t0020g0145a0001c0001t0020g0155others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-3987delG | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143154 | ||||||
| chr3:141143195
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.695-3947G>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143195 | ||||||
| chr3:141143522
|
C | T | 2 | a0001c0001t0027g0235a0001c0001t0027g0237 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.695-3620C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143522 | ||||||
| chr3:141143776
|
A | G | 1 | a0001c0001t0043g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695-3366A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143776 | ||||||
| chr3:141143927
|
G | A | 148 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(145): Show | 154 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.695-3215G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143927 | ||||||
| chr3:141143936
|
C | A | 1 | a0001c0002t0001g0076 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.695-3206C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143936 | ||||||
| chr3:141143957
|
C | G | 1 | a0001c0002t0001g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.695-3185C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141143957 | ||||||
| chr3:141144261
|
C | A | 1 | a0001c0001t0004g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.695-2881C>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144261 | ||||||
| chr3:141144310
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.695-2832C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144310 | ||||||
| chr3:141144349
|
G | A | 2 | a0001c0001t0063g0067a0001c0002t0036g0143 | 2 | HG03704.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.695-2793G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144349 | ||||||
| chr3:141144352
|
T | C | 1 | a0001c0001t0018g0001 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.695-2790T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144352 | ||||||
| chr3:141144524
|
T | C | 1 | a0001c0001t0044g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.695-2618T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144524 | ||||||
| chr3:141144535
|
C | G | 1 | a0001c0002t0001g0041 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.695-2607C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144535 | ||||||
| chr3:141144537
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.695-2605G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144537 | ||||||
| chr3:141144563
|
C | T | 69 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(66): Show | 71 | HG00544.hp2 HG00558.hp2 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.695-2579C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144563 | ||||||
| chr3:141144627
|
G | A | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-2515G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144627 | ||||||
| chr3:141144696
|
G | A | 1 | a0001c0001t0031g0244 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.695-2446G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144696 | ||||||
| chr3:141144715
|
A | G | 1 | a0001c0002t0005g0107 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.695-2427A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141144715 | ||||||
| chr3:141145054
|
C | T | 2 | a0001c0001t0044g0231a0001c0002t0058g0054 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.695-2088C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145054 | ||||||
| chr3:141145225
|
T | TA | 55 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(52): Show | 59 | HG00544.hp1 HG01081.hp1 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.695-1904dupA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141145225 | |||||
| chr3:141145225
|
TA | T | 6 | a0001c0001t0002g0164a0001c0001t0002g0190a0001c0001t0002g0194others(3): Show | 6 | HG00597.hp1 NA18959.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-1904delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141145225 | |||||
| chr3:141145372
|
C | T | 5 | a0001c0002t0007g0030a0001c0002t0007g0057a0001c0002t0007g0061others(2): Show | 5 | HG01496.hp1 HG02647.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.695-1770C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145372 | ||||||
| chr3:141145448
|
G | A | 1 | a0001c0002t0007g0106 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.695-1694G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145448 | ||||||
| chr3:141145461
|
A | T | 1 | a0001c0002t0036g0143 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.695-1681A>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145461 | ||||||
| chr3:141145525
|
C | T | 2 | a0001c0001t0011g0115a0001c0001t0011g0116 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.695-1617C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145525 | ||||||
| chr3:141145759
|
A | C | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-1383A>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145759 | ||||||
| chr3:141145915
|
C | T | 1 | a0001c0002t0001g0096 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.695-1227C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145915 | ||||||
| chr3:141145929
|
A | G | 21 | a0001c0001t0006g0017a0001c0001t0009g0147a0001c0001t0009g0148others(18): Show | 22 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-1213A>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145929 | ||||||
| chr3:141145959
|
C | T | 14 | a0001c0001t0009g0147a0001c0001t0009g0148a0001c0001t0009g0151others(11): Show | 15 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.695-1183C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145959 | ||||||
| chr3:141145995
|
C | G | 6 | a0001c0001t0010g0159a0001c0001t0015g0167a0001c0001t0015g0178others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.695-1147C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141145995 | ||||||
| chr3:141146498
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-644C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146498 | ||||||
| chr3:141146563
|
C | G | 1 | a0001c0001t0004g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.695-579C>G | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146563 | ||||||
| chr3:141146571
|
C | T | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-571C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146571 | ||||||
| chr3:141146642
|
C | T | 4 | a0001c0001t0026g0222a0001c0001t0056g0176a0001c0001t0057g0177others(1): Show | 4 | HG01243.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-500C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146642 | ||||||
| chr3:141146664
|
C | T | 1 | a0001c0001t0057g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.695-478C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146664 | ||||||
| chr3:141146772
|
T | TA | 11 | a0001c0001t0002g0014a0001c0001t0004g0195a0001c0002t0001g0128others(8): Show | 11 | HG01081.hp2 HG01257.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.695-354dupA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141146772 | |||||
| chr3:141146772
|
TA | T | 26 | a0001c0001t0006g0007a0001c0001t0006g0008a0001c0001t0006g0069others(23): Show | 28 | HG00544.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.695-354delA | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 141146772 | |||||
| chr3:141146867
|
C | T | 1 | a0001c0002t0014g0101 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.695-275C>T | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146867 | ||||||
| chr3:141146879
|
T | C | 1 | a0001c0001t0043g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695-263T>C | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141146879 | ||||||
| chr3:141147066
|
G | A | 3 | a0001c0001t0025g0144a0001c0001t0025g0146a0002c0004t0045g0240 | 3 | HG00735.hp2 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.695-76G>A | SPSB4 | ENSG00000175093.5 | transcript | ENST00000310546.3 | protein_coding | 2/2 | chr3 | 141147066 |