Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79595 |
|---|---|
| ensemblid | ENSG00000136715.19 |
| hgncid | 29813 |
| symbol | SAP130 |
| name | Sin3A associated protein 130 |
| refseq_nuc | NM_001330301.2 |
| refseq_prot | NP_001317230.1 |
| ensembl_nuc | ENST00000643581.2 |
| ensembl_prot | ENSP00000494423.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 127941222 |
| end | 128028059 |
| strand | - |
| ver | v1.2 |
| region | chr2:127941222-128028059 |
| region5000 | chr2:127936222-128033059 |
| regionname0 | SAP130_chr2_127941222_128028059 |
| regionname5000 | SAP130_chr2_127936222_128033059 |
| 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 | 1057 | 349 | 92 | 60 | 149 | 8 | 38 | 115 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0002 | 0/0 | 1057 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3174 | 248 | 73 | 43 | 101 | 6 | 23 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0002 | 0/0 | 3174 | 44 | 0 | 9 | 21 | 1 | 13 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0003 | 0/0 | 3174 | 31 | 5 | 1 | 24 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0004 | 0/0 | 3174 | 10 | 9 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0005 | 0/0 | 3174 | 5 | 0 | 5 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0006 | 0/0 | 3174 | 2 | 2 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0007 | 0/0 | 3174 | 2 | 1 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0008 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0009 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0010 | 0/0 | 3174 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0011 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0012 | 0/0 | 3174 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0013 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0014 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| c0015 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 911 | 328 | 82 | 57 | 143 | 8 | 36 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0002 | 0/0 | 911 | 4 | 4 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0003 | 0/0 | 911 | 4 | 0 | 0 | 4 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0004 | 0/0 | 911 | 3 | 2 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0005 | 0/0 | 911 | 2 | 1 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0006 | 0/0 | 911 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0007 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0008 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0009 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0010 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0011 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0012 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0013 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| t0014 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| 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 | 0 | 2 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3174 | 248 | 73 | 43 | 101 | 6 | 23 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0002 | 0/0 | 3174 | 44 | 0 | 9 | 21 | 1 | 13 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0003 | 0/0 | 3174 | 31 | 5 | 1 | 24 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0004 | 0/0 | 3174 | 10 | 9 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0005 | 0/0 | 3174 | 5 | 0 | 5 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0006 | 0/0 | 3174 | 2 | 2 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0007 | 0/0 | 3174 | 2 | 1 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0008 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0009 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0010 | 0/0 | 3174 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0011 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0012 | 0/0 | 3174 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0013 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0015 | 0/0 | 3174 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0002c0014 | 0/0 | 3174 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4084 | 234 | 66 | 42 | 96 | 6 | 22 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0001t0002 | 0/0 | 4084 | 4 | 4 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0001t0003 | 0/0 | 4084 | 4 | 0 | 0 | 4 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0001t0004 | 0/0 | 4084 | 3 | 2 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0001t0009 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0001t0010 | 0/0 | 4084 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0001t0014 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0002t0001 | 0/0 | 4084 | 43 | 0 | 9 | 21 | 1 | 12 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0002t0012 | 0/0 | 4084 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0003t0001 | 0/0 | 4084 | 28 | 3 | 1 | 23 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0003t0007 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0003t0008 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0003t0011 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0004t0001 | 0/0 | 4084 | 10 | 9 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0005t0001 | 0/0 | 4084 | 4 | 0 | 4 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0005t0006 | 0/0 | 4084 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0006t0001 | 0/0 | 4084 | 2 | 2 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0007t0005 | 0/0 | 4084 | 2 | 1 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0008t0001 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0009t0001 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0010t0001 | 0/0 | 4084 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0011t0013 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0012t0001 | 0/0 | 4084 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0013t0001 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0001c0015t0001 | 0/0 | 4084 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| a0002c0014t0001 | 0/0 | 4084 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | copy fasta | chr2 | 127936222 | 128033059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0253 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0002t0012g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0003t0011g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0004t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0005t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0005t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0005t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0006t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0007t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0007t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0008t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0009t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0010t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0011t0013g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0012t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0013t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0001c0015t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| a0002c0014t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0022 | EUR | GBR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | FIN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00323 | hp1 | a0001 | c0010 | t0001 | g0327 | EUR | FIN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00408 | hp1 | a0001 | c0011 | t0013 | g0328 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00423 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00735 | hp2 | a0001 | c0005 | t0001 | g0272 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01175 | hp1 | a0001 | c0007 | t0005 | g0313 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01496 | hp1 | a0001 | c0005 | t0001 | g0252 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0088 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0307 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01978 | hp2 | a0001 | c0005 | t0001 | g0301 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02074 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02148 | hp2 | a0001 | c0005 | t0006 | g0005 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0108 | EAS | CDX | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CDX | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02165 | hp1 | a0001 | c0013 | t0001 | g0273 | EAS | CDX | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | CDX | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0093 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02280 | hp1 | a0001 | c0008 | t0001 | g0219 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0131 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02451 | hp1 | a0001 | c0003 | t0008 | g0101 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0092 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0090 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02965 | hp1 | a0001 | c0003 | t0007 | g0111 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0070 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0316 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0087 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0091 | AFR | GWD | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | STU | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03710 | hp2 | a0001 | c0002 | t0012 | g0044 | SAS | PJL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | BEB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03834 | hp2 | a0001 | c0012 | t0001 | g0024 | SAS | BEB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03927 | hp1 | a0001 | c0001 | t0010 | g0083 | SAS | BEB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | STU | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0110 | SAS | STU | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18940 | hp1 | a0002 | c0014 | t0001 | g0120 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18943 | hp2 | a0001 | c0001 | t0009 | g0200 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18947 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18949 | hp2 | a0001 | c0009 | t0001 | g0216 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0102 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18967 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18973 | hp1 | a0001 | c0003 | t0011 | g0133 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18987 | hp2 | a0001 | c0003 | t0001 | g0132 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19030 | hp1 | a0001 | c0007 | t0005 | g0314 | AFR | LWK | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | YRI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | GIH | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0086 | AMR | CLM | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02109 | hp2 | a0001 | c0015 | t0001 | g0060 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0094 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | USA | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| HG06807 | hp2 | a0001 | c0006 | t0001 | g0076 | AFR | USA | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | USA | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0089 | AFR | LWK | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0253 | REF | REF | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0264 | REF | REF | SAP130_chr2_127936222_128033059 | SAP130 | chr2 | 127936222 | 128033059 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127955105
|
G | C | 1 | a0002 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.2303C>G | p.Ala768Gly | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/21 | 2429/4084 | 2303/3174 | 768/1057 | chr2 | 127955105 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127949969
|
T | C | 1 | a0001c0011 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.2697A>G | p.Pro899Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/21 | 2823/4084 | 2697/3174 | 899/1057 | chr2 | 127949969 | ||
| chr2:127950281
|
A | G | 1 | a0001c0013 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.2550T>C | p.His850His | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 17/21 | 2676/4084 | 2550/3174 | 850/1057 | chr2 | 127950281 | ||
| chr2:127955134
|
G | C | 1 | a0001c0007 | 2 | HG01175.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.2274C>G | p.Pro758Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/21 | 2400/4084 | 2274/3174 | 758/1057 | chr2 | 127955134 | ||
| chr2:127986883
|
G | A | 2 | a0001c0003a0002c0014 | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
synonymous_variant | LOW | c.1860C>T | p.Thr620Thr | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/21 | 1986/4084 | 1860/3174 | 620/1057 | chr2 | 127986883 | ||
| chr2:128000084
|
G | C | 1 | a0001c0005 | 5 | HG00735.hp2 HG01496.hp1 HG01928.hp2 others(2): Show |
synonymous_variant | LOW | c.1080C>G | p.Thr360Thr | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 9/21 | 1206/4084 | 1080/3174 | 360/1057 | chr2 | 128000084 | ||
| chr2:128000418
|
T | G | 1 | a0001c0012 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.906A>C | p.Ala302Ala | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 8/21 | 1032/4084 | 906/3174 | 302/1057 | chr2 | 128000418 | ||
| chr2:128000421
|
A | C | 3 | a0001c0002a0001c0010a0001c0012 | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
synonymous_variant | LOW | c.903T>G | p.Ser301Ser | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 8/21 | 1029/4084 | 903/3174 | 301/1057 | chr2 | 128000421 | ||
| chr2:128010292
|
C | T | 1 | a0001c0011 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.846G>A | p.Ala282Ala | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/21 | 972/4084 | 846/3174 | 282/1057 | chr2 | 128010292 | ||
| chr2:128010355
|
A | G | 1 | a0001c0004 | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
synonymous_variant | LOW | c.783T>C | p.Pro261Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/21 | 909/4084 | 783/3174 | 261/1057 | chr2 | 128010355 | ||
| chr2:128016539
|
C | T | 1 | a0001c0010 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.357G>A | p.Pro119Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/21 | 483/4084 | 357/3174 | 119/1057 | chr2 | 128016539 | ||
| chr2:128016542
|
G | A | 1 | a0001c0015 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.354C>T | p.Pro118Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/21 | 480/4084 | 354/3174 | 118/1057 | chr2 | 128016542 | ||
| chr2:128016545
|
C | T | 1 | a0001c0006 | 2 | HG03225.hp2 HG06807.hp2 |
splice_region_variant&synonymous_variant | LOW | c.351G>A | p.Pro117Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/21 | 477/4084 | 351/3174 | 117/1057 | chr2 | 128016545 | ||
| chr2:128017734
|
C | T | 1 | a0001c0009 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.294G>A | p.Pro98Pro | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/21 | 420/4084 | 294/3174 | 98/1057 | chr2 | 128017734 | ||
| chr2:128017890
|
A | G | 2 | a0001c0004a0001c0008 | 11 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
synonymous_variant | LOW | c.138T>C | p.Ser46Ser | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/21 | 264/4084 | 138/3174 | 46/1057 | chr2 | 128017890 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127941251
|
C | T | 1 | a0001c0001t0002 | 4 | HG02451.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*755G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 755 | chr2 | 127941251 | |||||
| chr2:127941252
|
G | A | 1 | a0001c0002t0012 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 754 | chr2 | 127941252 | |||||
| chr2:127941353
|
T | C | 1 | a0001c0001t0004 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*653A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 653 | chr2 | 127941353 | |||||
| chr2:127941416
|
A | T | 1 | a0001c0003t0011 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 590 | chr2 | 127941416 | |||||
| chr2:127941436
|
G | T | 1 | a0001c0007t0005 | 2 | HG01175.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*570C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 570 | chr2 | 127941436 | |||||
| chr2:127941444
|
T | A | 1 | a0001c0003t0008 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 562 | chr2 | 127941444 | |||||
| chr2:127941445
|
A | T | 1 | a0001c0001t0010 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 561 | chr2 | 127941445 | |||||
| chr2:127941505
|
G | A | 1 | a0001c0011t0013 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 501 | chr2 | 127941505 | |||||
| chr2:127941627
|
A | C | 1 | a0001c0001t0009 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 379 | chr2 | 127941627 | |||||
| chr2:127941806
|
C | A | 1 | a0001c0001t0014 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 200 | chr2 | 127941806 | |||||
| chr2:127941812
|
A | G | 2 | a0001c0003t0007a0001c0003t0008 | 2 | HG02451.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*194T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 194 | chr2 | 127941812 | |||||
| chr2:127941813
|
A | C | 2 | a0001c0003t0007a0001c0003t0008 | 2 | HG02451.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 21/21 | 193 | chr2 | 127941813 | |||||
| chr2:128027999
|
T | G | 1 | a0001c0005t0006 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/21 | 1707 | chr2 | 128027999 | |||||
| chr2:128028000
|
C | T | 1 | a0001c0005t0006 | 1 | HG02148.hp2 | 5_prime_UTR_variant | MODIFIER | c.-67G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/21 | 1708 | chr2 | 128028000 | |||||
| chr2:128028022
|
C | A | 1 | a0001c0001t0003 | 4 | NA18947.hp1 NA18950.hp2 NA18952.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-89G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/21 | 1730 | chr2 | 128028022 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:127942176
|
G | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0130others(50): Show | 54 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.3016-12C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 20/20 | chr2 | 127942176 | ||||||
| chr2:127942195
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.3016-31C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 20/20 | chr2 | 127942195 | ||||||
| chr2:127942202
|
T | G | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.3016-38A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 20/20 | chr2 | 127942202 | ||||||
| chr2:127942259
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.3016-95G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 20/20 | chr2 | 127942259 | ||||||
| chr2:127942661
|
C | T | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2902-124G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942661 | ||||||
| chr2:127942700
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0001g0215 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2902-163C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942700 | ||||||
| chr2:127942716
|
C | T | 2 | a0001c0003t0001g0104a0001c0003t0001g0125 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2902-179G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942716 | ||||||
| chr2:127942743
|
C | A | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2902-206G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942743 | ||||||
| chr2:127942759
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2902-222G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942759 | ||||||
| chr2:127942975
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2902-438G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942975 | ||||||
| chr2:127942990
|
AAAATAAA others(5): Show |
A | 2 | a0001c0002t0001g0020a0001c0002t0001g0022 | 2 | HG00140.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2902-465_2902-454d others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127942990 | ||||||
| chr2:127943277
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2902-740G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127943277 | ||||||
| chr2:127943336
|
T | C | 1 | a0001c0001t0001g0251 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2902-799A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127943336 | ||||||
| chr2:127943538
|
T | C | 2 | a0001c0002t0001g0021a0001c0002t0001g0063 | 2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2902-1001A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127943538 | ||||||
| chr2:127943692
|
A | T | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2902-1155T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127943692 | ||||||
| chr2:127943877
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2902-1340A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127943877 | ||||||
| chr2:127944077
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2901+1379C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944077 | ||||||
| chr2:127944094
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2901+1362G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944094 | ||||||
| chr2:127944124
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2901+1332G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944124 | ||||||
| chr2:127944134
|
A | G | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2901+1322T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944134 | ||||||
| chr2:127944165
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2901+1291C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944165 | ||||||
| chr2:127944173
|
G | C | 1 | a0001c0001t0014g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2901+1283C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944173 | ||||||
| chr2:127944193
|
C | T | 61 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0164others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2901+1263G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944193 | ||||||
| chr2:127944231
|
C | T | 31 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.2901+1225G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944231 | ||||||
| chr2:127944270
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2901+1186T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944270 | ||||||
| chr2:127944351
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2901+1105T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944351 | ||||||
| chr2:127944433
|
A | AT | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.2901+1022dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944433 | ||||||
| chr2:127944434
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2901+1022A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944434 | ||||||
| chr2:127944570
|
C | T | 11 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2901+886G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944570 | ||||||
| chr2:127944574
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2901+882G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944574 | ||||||
| chr2:127944730
|
C | A | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2901+726G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944730 | ||||||
| chr2:127944763
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2901+693C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944763 | ||||||
| chr2:127944870
|
C | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2901+586G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944870 | ||||||
| chr2:127944901
|
C | CA | 19 | a0001c0001t0001g0097a0001c0001t0001g0215a0001c0001t0001g0233others(16): Show | 19 | HG00408.hp1 HG01123.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.2901+554dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944901 | ||||||
| chr2:127944901
|
CA | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(118): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2901+554delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944901 | ||||||
| chr2:127944901
|
CAA | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0145a0001c0001t0001g0171others(4): Show | 7 | HG01175.hp1 HG02897.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.2901+553_2901+554d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944901 | ||||||
| chr2:127944951
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2901+505G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944951 | ||||||
| chr2:127944997
|
T | C | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2901+459A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127944997 | ||||||
| chr2:127945115
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2901+341C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127945115 | ||||||
| chr2:127945154
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2901+302C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127945154 | ||||||
| chr2:127945185
|
A | AT | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0084 | 3 | HG01070.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2901+270dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127945185 | ||||||
| chr2:127945215
|
G | A | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2901+241C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127945215 | ||||||
| chr2:127945238
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2901+218T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127945238 | ||||||
| chr2:127945310
|
T | A | 3 | a0001c0001t0001g0231a0001c0001t0001g0238a0001c0001t0001g0241 | 3 | NA18940.hp2 NA18950.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2901+146A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 19/20 | chr2 | 127945310 | ||||||
| chr2:127945628
|
A | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0269a0001c0001t0001g0278 | 3 | HG02155.hp2 NA18941.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2798-69T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945628 | ||||||
| chr2:127945665
|
T | A | 1 | a0001c0003t0001g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2798-106A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945665 | ||||||
| chr2:127945710
|
T | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2798-151A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945710 | ||||||
| chr2:127945850
|
G | C | 1 | a0001c0001t0001g0318 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2798-291C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945850 | ||||||
| chr2:127945903
|
A | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2798-344T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945903 | ||||||
| chr2:127945927
|
A | G | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-368T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945927 | ||||||
| chr2:127945942
|
C | G | 1 | a0001c0002t0012g0044 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2798-383G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127945942 | ||||||
| chr2:127946073
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2798-514T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946073 | ||||||
| chr2:127946280
|
G | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2798-721C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946280 | ||||||
| chr2:127946539
|
C | T | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2798-980G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946539 | ||||||
| chr2:127946550
|
T | A | 33 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.2798-991A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946550 | ||||||
| chr2:127946552
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0075 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2798-993A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946552 | ||||||
| chr2:127946681
|
G | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2798-1122C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946681 | ||||||
| chr2:127946776
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2798-1217G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946776 | ||||||
| chr2:127946852
|
G | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2798-1293C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946852 | ||||||
| chr2:127946857
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2798-1298G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946857 | ||||||
| chr2:127946983
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2798-1424C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946983 | ||||||
| chr2:127946993
|
T | TAG | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2798-1436_2798-143 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127946993 | ||||||
| chr2:127947080
|
C | T | 1 | a0001c0003t0001g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2798-1521G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947080 | ||||||
| chr2:127947119
|
G | A | 1 | a0001c0002t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2798-1560C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947119 | ||||||
| chr2:127947330
|
G | A | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2798-1771C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947330 | ||||||
| chr2:127947697
|
T | C | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.2798-2138A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947697 | ||||||
| chr2:127947754
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2797+2115A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947754 | ||||||
| chr2:127947754
|
T | TTGTGTGT others(13): Show |
1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2797+2114_2797+211 others(24): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947754 | ||||||
| chr2:127947754
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2797+2114_2797+211 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947754 | ||||||
| chr2:127947760
|
GTGTC | G | 4 | a0001c0004t0001g0090a0001c0004t0001g0091a0001c0004t0001g0092others(1): Show | 4 | HG02559.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+2105_2797+210 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947760 | ||||||
| chr2:127947762
|
GTC | G | 5 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(2): Show | 5 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2797+2105_2797+210 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947762 | ||||||
| chr2:127947764
|
C | CTG | 17 | a0001c0001t0001g0057a0001c0001t0001g0061a0001c0001t0001g0062others(14): Show | 17 | HG01884.hp1 HG01975.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.2797+2103_2797+210 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTG | 7 | a0001c0001t0001g0069a0001c0001t0004g0006a0001c0001t0004g0059others(4): Show | 7 | HG00140.hp1 HG01243.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.2797+2101_2797+210 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTG | 29 | a0001c0002t0001g0007a0001c0002t0001g0017a0001c0002t0001g0018others(26): Show | 29 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2797+2099_2797+210 others(10): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGA others(1): Show |
4 | a0001c0003t0001g0106a0001c0003t0001g0107a0001c0003t0007g0111others(1): Show | 4 | HG02083.hp2 HG02451.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGA others(3): Show |
23 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(20): Show | 23 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGA others(5): Show |
2 | a0001c0003t0001g0105a0001c0003t0001g0129 | 2 | HG02080.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGA others(7): Show |
2 | a0001c0003t0001g0125a0001c0003t0001g0126 | 2 | HG06807.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(18): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGA others(9): Show |
1 | a0001c0003t0001g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2797+2104_2797+210 others(20): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(1): Show |
8 | a0001c0002t0001g0021a0001c0002t0001g0032a0001c0002t0001g0035others(5): Show | 8 | HG00544.hp2 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2797+2097_2797+210 others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(7): Show |
1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2797+2104_2797+210 others(18): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(17): Show |
2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(28): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0329a0001c0002t0001g0040 | 3 | HG02109.hp1 HG02165.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2797+2095_2797+210 others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(5): Show |
6 | a0001c0001t0001g0237a0001c0001t0001g0261a0001c0001t0001g0287others(3): Show | 6 | HG01123.hp1 HG01175.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(7): Show |
34 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0150others(31): Show | 34 | HG00423.hp2 HG01106.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(18): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(9): Show |
78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(20): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(11): Show |
25 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0095others(22): Show | 25 | HG00323.hp2 HG00741.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(22): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(13): Show |
21 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0149others(18): Show | 22 | HG00438.hp2 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(24): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(15): Show |
41 | a0001c0001t0001g0128a0001c0001t0001g0134a0001c0001t0001g0135others(38): Show | 41 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.2797+2104_2797+210 others(26): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | CTGTGTGT others(5): Show |
1 | a0001c0001t0004g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2797+2093_2797+210 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
C | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0004t0001g0089 | 3 | HG03579.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2797+2105G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947764
|
CTGTG | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+2101_2797+210 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947764 | ||||||
| chr2:127947765
|
T | TGTGTGTG others(3): Show |
3 | a0001c0001t0001g0255a0001c0001t0001g0324a0001c0001t0001g0332 | 3 | HG00735.hp1 HG02717.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2797+2103_2797+210 others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947765 | ||||||
| chr2:127947767
|
T | TGTGTGTG others(1): Show |
14 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0164others(11): Show | 14 | HG02055.hp1 HG02572.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.2797+2101_2797+210 others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947767 | ||||||
| chr2:127947775
|
T | A | 3 | a0001c0001t0001g0170a0001c0001t0001g0215a0001c0001t0001g0224 | 3 | HG03098.hp1 HG03927.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2797+2094A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947775 | ||||||
| chr2:127947801
|
T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2797+2067_2797+206 others(23): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947801 | ||||||
| chr2:127947801
|
T | TGTGTGTG others(14): Show |
1 | a0001c0001t0001g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2797+2067_2797+206 others(25): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947801 | ||||||
| chr2:127947801
|
T | TGTGTGTG others(16): Show |
1 | a0001c0001t0001g0170 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2797+2067_2797+206 others(27): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947801 | ||||||
| chr2:127947823
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2797+2046C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947823 | ||||||
| chr2:127947860
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2797+2009A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947860 | ||||||
| chr2:127947880
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2797+1989G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947880 | ||||||
| chr2:127947921
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2797+1948A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947921 | ||||||
| chr2:127947980
|
AG | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2797+1888delC | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127947980 | ||||||
| chr2:127948009
|
T | C | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.2797+1860A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948009 | ||||||
| chr2:127948159
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2797+1710G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948159 | ||||||
| chr2:127948161
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2797+1708G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948161 | ||||||
| chr2:127948312
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2797+1557G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948312 | ||||||
| chr2:127948328
|
G | GT | 42 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0071others(39): Show | 43 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2797+1540dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948328 | ||||||
| chr2:127948328
|
GT | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0011others(5): Show | 8 | HG00639.hp2 HG02165.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2797+1540delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948328 | ||||||
| chr2:127948369
|
G | T | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2797+1500C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948369 | ||||||
| chr2:127948432
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2797+1437G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948432 | ||||||
| chr2:127948441
|
G | A | 1 | a0001c0004t0001g0088 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2797+1428C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948441 | ||||||
| chr2:127948523
|
G | A | 5 | a0001c0001t0001g0141a0001c0001t0001g0151a0001c0001t0001g0155others(2): Show | 5 | NA18612.hp2 NA18955.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2797+1346C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948523 | ||||||
| chr2:127948585
|
G | A | 1 | a0001c0002t0001g0045 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2797+1284C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948585 | ||||||
| chr2:127948588
|
C | A | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2797+1281G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948588 | ||||||
| chr2:127948621
|
C | T | 1 | a0001c0009t0001g0216 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2797+1248G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948621 | ||||||
| chr2:127948806
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2797+1063G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127948806 | ||||||
| chr2:127949063
|
G | A | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2797+806C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949063 | ||||||
| chr2:127949116
|
C | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2797+753G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949116 | ||||||
| chr2:127949251
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2797+618T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949251 | ||||||
| chr2:127949459
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2797+410C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949459 | ||||||
| chr2:127949546
|
T | C | 1 | a0001c0003t0001g0125 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2797+323A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949546 | ||||||
| chr2:127949779
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2797+90C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949779 | ||||||
| chr2:127949826
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2797+43G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 18/20 | chr2 | 127949826 | ||||||
| chr2:127950060
|
TAAGTGAG others(4): Show |
T | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2672-77_2672-67del others(11): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 17/20 | chr2 | 127950060 | ||||||
| chr2:127950072
|
G | A | 1 | a0001c0001t0010g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2672-78C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 17/20 | chr2 | 127950072 | ||||||
| chr2:127950120
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2671+40A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 17/20 | chr2 | 127950120 | ||||||
| chr2:127950489
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2423-81A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127950489 | ||||||
| chr2:127950721
|
A | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2423-313T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127950721 | ||||||
| chr2:127950762
|
T | C | 1 | a0001c0002t0001g0038 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2423-354A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127950762 | ||||||
| chr2:127950783
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2423-375G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127950783 | ||||||
| chr2:127951085
|
C | T | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2423-677G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951085 | ||||||
| chr2:127951444
|
C | T | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2423-1036G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951444 | ||||||
| chr2:127951469
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2423-1061G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951469 | ||||||
| chr2:127951550
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2423-1142A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951550 | ||||||
| chr2:127951573
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2423-1165A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951573 | ||||||
| chr2:127951732
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2423-1324G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951732 | ||||||
| chr2:127951883
|
T | C | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2423-1475A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951883 | ||||||
| chr2:127951931
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2423-1523A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951931 | ||||||
| chr2:127951946
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2423-1538T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127951946 | ||||||
| chr2:127952078
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2423-1670T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952078 | ||||||
| chr2:127952231
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2423-1823A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952231 | ||||||
| chr2:127952251
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 80 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.2423-1843C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952251 | ||||||
| chr2:127952277
|
C | T | 2 | a0001c0001t0001g0319a0001c0001t0001g0321 | 2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2423-1869G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952277 | ||||||
| chr2:127952435
|
A | G | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.2423-2027T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952435 | ||||||
| chr2:127952450
|
TA | T | 85 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0066others(82): Show | 85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2423-2043delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952450 | ||||||
| chr2:127952450
|
TAA | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(230): Show | 237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.2423-2044_2423-204 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952450 | ||||||
| chr2:127952468
|
AAAT | A | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2423-2063_2423-206 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952468 | ||||||
| chr2:127952521
|
C | T | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2423-2113G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952521 | ||||||
| chr2:127952565
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2423-2157G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952565 | ||||||
| chr2:127952607
|
C | G | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2423-2199G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952607 | ||||||
| chr2:127952893
|
C | T | 1 | a0001c0003t0001g0117 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2422+2093G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127952893 | ||||||
| chr2:127953175
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2422+1811G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953175 | ||||||
| chr2:127953605
|
T | A | 1 | a0001c0001t0001g0239 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2422+1381A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953605 | ||||||
| chr2:127953741
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2422+1245T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953741 | ||||||
| chr2:127953819
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2422+1167C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953819 | ||||||
| chr2:127953838
|
C | T | 11 | a0001c0001t0001g0222a0001c0001t0001g0231a0001c0001t0001g0238others(8): Show | 11 | HG00438.hp2 HG00673.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.2422+1148G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953838 | ||||||
| chr2:127953875
|
T | G | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2422+1111A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953875 | ||||||
| chr2:127953879
|
T | TATACATA others(5): Show |
2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2422+1095_2422+110 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127953879 | ||||||
| chr2:127954031
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2422+955A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127954031 | ||||||
| chr2:127954128
|
C | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2422+858G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127954128 | ||||||
| chr2:127954230
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2422+756C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127954230 | ||||||
| chr2:127954341
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2422+645C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127954341 | ||||||
| chr2:127954558
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2422+428G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127954558 | ||||||
| chr2:127954847
|
A | G | 1 | a0001c0002t0012g0044 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2422+139T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 16/20 | chr2 | 127954847 | ||||||
| chr2:127955358
|
G | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-14C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955358 | ||||||
| chr2:127955523
|
G | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-179C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955523 | ||||||
| chr2:127955547
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2064-203G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955547 | ||||||
| chr2:127955595
|
T | C | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2064-251A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955595 | ||||||
| chr2:127955618
|
C | G | 1 | a0001c0002t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2064-274G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955618 | ||||||
| chr2:127955624
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-280G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955624 | ||||||
| chr2:127955629
|
G | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-285C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955629 | ||||||
| chr2:127955659
|
G | T | 1 | a0001c0001t0001g0306 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2064-315C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955659 | ||||||
| chr2:127955675
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2064-331T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955675 | ||||||
| chr2:127955680
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.2064-336C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955680 | ||||||
| chr2:127955730
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2064-386G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955730 | ||||||
| chr2:127955739
|
C | T | 3 | a0001c0004t0001g0090a0001c0004t0001g0091a0001c0004t0001g0094 | 3 | HG02559.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2064-395G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955739 | ||||||
| chr2:127955763
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-419G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955763 | ||||||
| chr2:127955889
|
CAGT | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2064-548_2064-546d others(5): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955889 | ||||||
| chr2:127955893
|
A | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(7): Show | 10 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.2064-549T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127955893 | ||||||
| chr2:127956081
|
A | G | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2064-737T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956081 | ||||||
| chr2:127956088
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2064-744A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956088 | ||||||
| chr2:127956130
|
G | C | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG02451.hp2 HG02622.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2064-786C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956130 | ||||||
| chr2:127956159
|
A | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-815T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956159 | ||||||
| chr2:127956317
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2064-973A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956317 | ||||||
| chr2:127956559
|
T | TG | 10 | a0001c0001t0001g0141a0001c0001t0001g0149a0001c0001t0001g0160others(7): Show | 10 | HG00408.hp2 HG01978.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2064-1216dupC | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956559 | ||||||
| chr2:127956560
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2064-1216C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956560 | ||||||
| chr2:127956630
|
C | A | 1 | a0001c0001t0001g0336 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2064-1286G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956630 | ||||||
| chr2:127956630
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012 | 3 | HG03041.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2064-1286G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956630 | ||||||
| chr2:127956635
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2064-1291A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956635 | ||||||
| chr2:127956647
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2064-1303T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956647 | ||||||
| chr2:127956702
|
TA | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2064-1359delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956702 | ||||||
| chr2:127956702
|
TAA | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 21 | HG00323.hp1 HG00438.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.2064-1360_2064-135 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956702 | ||||||
| chr2:127956702
|
TAAA | T | 6 | a0001c0001t0001g0008a0001c0004t0001g0086a0001c0004t0001g0089others(3): Show | 6 | HG01123.hp2 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064-1361_2064-135 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956702 | ||||||
| chr2:127956704
|
A | T | 2 | a0001c0001t0001g0208a0001c0008t0001g0219 | 2 | HG02280.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.2064-1360T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956704 | ||||||
| chr2:127956720
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0218 | 2 | HG01069.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2064-1376T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956720 | ||||||
| chr2:127956783
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0084 | 3 | HG01070.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2064-1439G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956783 | ||||||
| chr2:127956864
|
T | G | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2064-1520A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956864 | ||||||
| chr2:127956892
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2064-1548T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956892 | ||||||
| chr2:127956940
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2064-1596A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956940 | ||||||
| chr2:127956955
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2064-1611A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127956955 | ||||||
| chr2:127957143
|
T | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0145others(4): Show | 7 | HG00673.hp1 HG02040.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.2064-1799A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957143 | ||||||
| chr2:127957322
|
G | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2064-1978C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957322 | ||||||
| chr2:127957366
|
A | G | 8 | a0001c0001t0001g0128a0001c0001t0001g0139a0001c0001t0001g0141others(5): Show | 8 | NA18612.hp2 NA18955.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.2064-2022T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957366 | ||||||
| chr2:127957534
|
C | T | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2064-2190G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957534 | ||||||
| chr2:127957535
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2064-2191C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957535 | ||||||
| chr2:127957666
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2064-2322G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957666 | ||||||
| chr2:127957694
|
G | A | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-2350C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957694 | ||||||
| chr2:127957777
|
G | A | 3 | a0001c0004t0001g0090a0001c0004t0001g0091a0001c0004t0001g0094 | 3 | HG02559.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2064-2433C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957777 | ||||||
| chr2:127957798
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-2454A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957798 | ||||||
| chr2:127957855
|
A | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2064-2511T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957855 | ||||||
| chr2:127957856
|
A | T | 1 | a0001c0001t0001g0235 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2064-2512T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127957856 | ||||||
| chr2:127958061
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2064-2717A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958061 | ||||||
| chr2:127958093
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2064-2749A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958093 | ||||||
| chr2:127958163
|
C | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG00639.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064-2819G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958163 | ||||||
| chr2:127958196
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2064-2852G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958196 | ||||||
| chr2:127958282
|
C | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2064-2938G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958282 | ||||||
| chr2:127958593
|
T | C | 1 | a0001c0001t0001g0253 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2064-3249A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958593 | ||||||
| chr2:127958635
|
T | TGA | 30 | a0001c0001t0001g0010a0001c0001t0001g0057a0001c0001t0001g0069others(27): Show | 30 | HG00408.hp1 HG00639.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.2064-3293_2064-329 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
T | TGAGA | 7 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0329others(4): Show | 7 | HG02109.hp1 HG02572.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.2064-3295_2064-329 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
T | TGAGAGA | 6 | a0001c0001t0001g0183a0001c0001t0004g0006a0001c0001t0004g0058others(3): Show | 6 | HG02165.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064-3297_2064-329 others(10): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
T | TGAGAGAG others(3): Show |
1 | a0001c0001t0001g0204 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2064-3301_2064-329 others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
T | TGAGAGAG others(5): Show |
1 | a0001c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2064-3303_2064-329 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGA | T | 24 | a0001c0001t0001g0062a0001c0001t0001g0095a0001c0001t0001g0098others(21): Show | 24 | HG00558.hp1 HG01069.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2064-3293_2064-329 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGA | T | 30 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(27): Show | 30 | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.2064-3295_2064-329 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGA | T | 34 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0147others(31): Show | 34 | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.2064-3297_2064-329 others(10): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(1): Show |
T | 58 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0065others(55): Show | 59 | HG00280.hp1 HG00673.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.2064-3299_2064-329 others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(3): Show |
T | 18 | a0001c0001t0001g0013a0001c0001t0001g0137a0001c0001t0001g0167others(15): Show | 18 | HG01106.hp1 HG01261.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.2064-3301_2064-329 others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(5): Show |
T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 100 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.2064-3303_2064-329 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(9): Show |
T | 5 | a0001c0001t0001g0259a0001c0001t0001g0305a0001c0007t0005g0313others(2): Show | 5 | HG00323.hp1 HG01175.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-3307_2064-329 others(20): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(11): Show |
T | 2 | a0001c0002t0001g0020a0001c0002t0001g0022 | 2 | HG00140.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2064-3309_2064-329 others(22): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(13): Show |
T | 9 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(6): Show | 9 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2064-3311_2064-329 others(24): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958635
|
TGAGAGAG others(17): Show |
T | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2064-3315_2064-329 others(28): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958635 | ||||||
| chr2:127958794
|
G | A | 2 | a0001c0001t0001g0320a0001c0001t0001g0325 | 2 | NA18980.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2064-3450C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958794 | ||||||
| chr2:127958816
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-3472G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958816 | ||||||
| chr2:127958946
|
G | A | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2064-3602C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127958946 | ||||||
| chr2:127959019
|
G | A | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2064-3675C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959019 | ||||||
| chr2:127959125
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2064-3781T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959125 | ||||||
| chr2:127959196
|
T | C | 1 | a0001c0004t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2064-3852A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959196 | ||||||
| chr2:127959243
|
T | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0130others(50): Show | 54 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.2064-3899A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959243 | ||||||
| chr2:127959355
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-4011T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959355 | ||||||
| chr2:127959399
|
G | A | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2064-4055C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959399 | ||||||
| chr2:127959412
|
G | T | 3 | a0001c0002t0001g0042a0001c0002t0001g0045a0001c0002t0001g0055 | 3 | NA18981.hp1 NA19058.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2064-4068C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959412 | ||||||
| chr2:127959435
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-4091G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959435 | ||||||
| chr2:127959507
|
C | T | 2 | a0001c0001t0001g0225a0001c0001t0001g0229 | 2 | NA19010.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2064-4163G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959507 | ||||||
| chr2:127959553
|
C | A | 2 | a0001c0003t0001g0104a0001c0003t0001g0125 | 2 | HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2064-4209G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959553 | ||||||
| chr2:127959752
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0134others(48): Show | 52 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2064-4408A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959752 | ||||||
| chr2:127959769
|
A | G | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2064-4425T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959769 | ||||||
| chr2:127959817
|
A | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2064-4473T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127959817 | ||||||
| chr2:127960079
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2064-4735A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960079 | ||||||
| chr2:127960301
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-4957C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960301 | ||||||
| chr2:127960329
|
T | TGGGCACC others(10): Show |
1 | a0001c0001t0001g0275 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2064-5002_2064-498 others(21): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960329 | ||||||
| chr2:127960485
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2064-5141C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960485 | ||||||
| chr2:127960680
|
A | G | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.2064-5336T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960680 | ||||||
| chr2:127960790
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.2064-5446T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960790 | ||||||
| chr2:127960977
|
TTTTC | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0287a0001c0002t0001g0047others(1): Show | 4 | HG01358.hp2 HG02615.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.2064-5637_2064-563 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960977 | ||||||
| chr2:127960993
|
CT | C | 7 | a0001c0001t0001g0148a0001c0001t0001g0177a0001c0001t0001g0185others(4): Show | 7 | HG00140.hp1 HG01069.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2064-5650delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960993 | ||||||
| chr2:127960997
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-5653A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127960997 | ||||||
| chr2:127961009
|
T | G | 1 | a0001c0002t0001g0068 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2064-5665A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961009 | ||||||
| chr2:127961305
|
A | AT | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.2064-5962dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961305 | ||||||
| chr2:127961305
|
AT | A | 9 | a0001c0001t0001g0074a0001c0002t0001g0030a0001c0002t0001g0031others(6): Show | 9 | HG01175.hp1 HG01975.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2064-5962delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961305 | ||||||
| chr2:127961402
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-6058G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961402 | ||||||
| chr2:127961436
|
C | T | 33 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.2064-6092G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961436 | ||||||
| chr2:127961473
|
C | T | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2064-6129G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961473 | ||||||
| chr2:127961517
|
CT | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2064-6174delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961517 | ||||||
| chr2:127961517
|
CTT | C | 11 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0176others(8): Show | 11 | HG01069.hp2 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2064-6175_2064-617 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961517 | ||||||
| chr2:127961540
|
A | T | 1 | a0001c0001t0001g0156 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2064-6196T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961540 | ||||||
| chr2:127961575
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2064-6231A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961575 | ||||||
| chr2:127961677
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2064-6333G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961677 | ||||||
| chr2:127961688
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-6344G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961688 | ||||||
| chr2:127961698
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-6354C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961698 | ||||||
| chr2:127961734
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-6390T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127961734 | ||||||
| chr2:127962427
|
A | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-7083T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127962427 | ||||||
| chr2:127962513
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0158 | 3 | HG00738.hp1 HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.2064-7169A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127962513 | ||||||
| chr2:127962518
|
C | T | 9 | a0001c0001t0001g0232a0001c0001t0001g0253a0001c0001t0001g0254others(6): Show | 9 | HG01106.hp2 HG01175.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2064-7174G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127962518 | ||||||
| chr2:127962556
|
T | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-7212A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127962556 | ||||||
| chr2:127962890
|
TA | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0081others(86): Show | 90 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2064-7547delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127962890 | ||||||
| chr2:127963007
|
G | GA | 174 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(171): Show | 175 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.2064-7664dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963007 | ||||||
| chr2:127963108
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2064-7764C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963108 | ||||||
| chr2:127963287
|
C | T | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2064-7943G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963287 | ||||||
| chr2:127963314
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0257 | 2 | NA18942.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2064-7970G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963314 | ||||||
| chr2:127963376
|
C | T | 11 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2064-8032G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963376 | ||||||
| chr2:127963427
|
G | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2064-8083C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963427 | ||||||
| chr2:127963536
|
T | A | 1 | a0001c0001t0001g0320 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2064-8192A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963536 | ||||||
| chr2:127963665
|
C | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-8321G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963665 | ||||||
| chr2:127963715
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2064-8371G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963715 | ||||||
| chr2:127963716
|
G | T | 3 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088 | 3 | HG01123.hp2 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2064-8372C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963716 | ||||||
| chr2:127963746
|
C | T | 5 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02965.hp2 HG03130.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064-8402G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963746 | ||||||
| chr2:127963747
|
G | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-8403C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963747 | ||||||
| chr2:127963839
|
A | G | 1 | a0001c0012t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2064-8495T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963839 | ||||||
| chr2:127963875
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2064-8531G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963875 | ||||||
| chr2:127963895
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2064-8551A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963895 | ||||||
| chr2:127963910
|
G | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0258 | 2 | NA19066.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2064-8566C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127963910 | ||||||
| chr2:127964130
|
G | C | 2 | a0001c0003t0001g0102a0001c0003t0001g0121 | 2 | NA18964.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2064-8786C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964130 | ||||||
| chr2:127964137
|
G | T | 1 | a0001c0001t0001g0324 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2064-8793C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964137 | ||||||
| chr2:127964178
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-8834G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964178 | ||||||
| chr2:127964481
|
C | T | 2 | a0001c0002t0001g0016a0001c0002t0001g0019 | 2 | HG02040.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2064-9137G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964481 | ||||||
| chr2:127964482
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2064-9138C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964482 | ||||||
| chr2:127964494
|
CA | C | 46 | a0001c0001t0001g0066a0001c0001t0004g0006a0001c0001t0004g0059others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2064-9151delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964494 | ||||||
| chr2:127964494
|
CAA | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(14): Show | 17 | HG00438.hp2 HG00558.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.2064-9152_2064-915 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964494 | ||||||
| chr2:127964494
|
CAAA | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2064-9153_2064-915 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964494 | ||||||
| chr2:127964494
|
CAAAA | C | 13 | a0001c0001t0001g0014a0001c0001t0001g0194a0001c0001t0001g0223others(10): Show | 13 | HG01070.hp2 HG01175.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.2064-9154_2064-915 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964494 | ||||||
| chr2:127964652
|
A | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-9308T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964652 | ||||||
| chr2:127964724
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2064-9380C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964724 | ||||||
| chr2:127964826
|
G | A | 6 | a0001c0001t0001g0245a0001c0001t0001g0271a0001c0001t0001g0274others(3): Show | 6 | HG02165.hp1 NA18747.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.2064-9482C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964826 | ||||||
| chr2:127964841
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2064-9497A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964841 | ||||||
| chr2:127964905
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(171): Show | 178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2064-9561T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964905 | ||||||
| chr2:127964926
|
G | C | 1 | a0001c0003t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2064-9582C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964926 | ||||||
| chr2:127964931
|
G | A | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0164others(12): Show | 15 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2064-9587C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964931 | ||||||
| chr2:127964998
|
C | CA | 25 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.2064-9655dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964998 | ||||||
| chr2:127964998
|
C | CAA | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2064-9656_2064-965 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964998 | ||||||
| chr2:127964998
|
C | CAAA | 50 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0080others(47): Show | 51 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.2064-9657_2064-965 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127964998 | ||||||
| chr2:127965073
|
G | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2064-9729C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965073 | ||||||
| chr2:127965101
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-9757G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965101 | ||||||
| chr2:127965228
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2064-9884G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965228 | ||||||
| chr2:127965311
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2064-9967C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965311 | ||||||
| chr2:127965521
|
G | T | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2064-10177C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965521 | ||||||
| chr2:127965611
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2064-10267T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965611 | ||||||
| chr2:127965762
|
A | C | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10418T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965762 | ||||||
| chr2:127965780
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2064-10436T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965780 | ||||||
| chr2:127965782
|
T | TCC | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10439_2064-10 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965782 | ||||||
| chr2:127965794
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10450C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965794 | ||||||
| chr2:127965795
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10451T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965795 | ||||||
| chr2:127965796
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10452C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965796 | ||||||
| chr2:127965798
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10454C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965798 | ||||||
| chr2:127965800
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10456C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965800 | ||||||
| chr2:127965802
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10458C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965802 | ||||||
| chr2:127965804
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10460C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965804 | ||||||
| chr2:127965810
|
G | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10466C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965810 | ||||||
| chr2:127965815
|
AGTGT | A | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0306 | 3 | HG01123.hp1 HG01261.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2064-10475_2064-10 others(10): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965815 | ||||||
| chr2:127965818
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2064-10474C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965818 | ||||||
| chr2:127965819
|
T | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0262 | 2 | HG01952.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2064-10475A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965819 | ||||||
| chr2:127965821
|
A | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-10477T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965821 | ||||||
| chr2:127965822
|
T | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10478A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965822 | ||||||
| chr2:127965823
|
T | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10479A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965823 | ||||||
| chr2:127965826
|
C | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10482G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965826 | ||||||
| chr2:127965828
|
C | A | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2064-10484G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965828 | ||||||
| chr2:127965829
|
AGGGAATT others(84): Show |
A | 4 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(1): Show | 4 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.2064-10576_2064-10 others(97): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965829 | ||||||
| chr2:127965830
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2064-10486C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965830 | ||||||
| chr2:127965831
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2064-10487C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965831 | ||||||
| chr2:127965832
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2064-10488C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965832 | ||||||
| chr2:127965834
|
ATTTAATA others(79): Show |
A | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2064-10576_2064-10 others(92): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965834 | ||||||
| chr2:127965845
|
T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0329others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2064-10501A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965845 | ||||||
| chr2:127965880
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-10536T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965880 | ||||||
| chr2:127965899
|
T | G | 1 | a0001c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2064-10555A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127965899 | ||||||
| chr2:127966064
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-10720A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966064 | ||||||
| chr2:127966294
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-10950C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966294 | ||||||
| chr2:127966311
|
C | T | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2064-10967G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966311 | ||||||
| chr2:127966380
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2064-11036A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966380 | ||||||
| chr2:127966416
|
C | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2064-11072G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966416 | ||||||
| chr2:127966468
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-11124G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966468 | ||||||
| chr2:127966495
|
G | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2064-11151C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966495 | ||||||
| chr2:127966535
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0173 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2064-11191A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966535 | ||||||
| chr2:127966611
|
G | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01257.hp2 HG01258.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2064-11267C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966611 | ||||||
| chr2:127966888
|
C | A | 1 | a0001c0001t0001g0304 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2063+11097G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966888 | ||||||
| chr2:127966903
|
A | G | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2063+11082T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127966903 | ||||||
| chr2:127967144
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2063+10841T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967144 | ||||||
| chr2:127967248
|
A | T | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.2063+10737T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967248 | ||||||
| chr2:127967316
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2063+10669T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967316 | ||||||
| chr2:127967350
|
T | A | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2063+10635A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967350 | ||||||
| chr2:127967419
|
A | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+10566T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967419 | ||||||
| chr2:127967457
|
T | C | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.2063+10528A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967457 | ||||||
| chr2:127967512
|
C | A | 1 | a0001c0007t0005g0314 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2063+10473G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967512 | ||||||
| chr2:127967523
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2063+10462G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967523 | ||||||
| chr2:127967575
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+10410A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967575 | ||||||
| chr2:127967638
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2063+10347G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967638 | ||||||
| chr2:127967677
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2063+10308A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967677 | ||||||
| chr2:127967691
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2063+10294G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967691 | ||||||
| chr2:127967805
|
T | C | 3 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030 | 3 | NA18941.hp2 NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2063+10180A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127967805 | ||||||
| chr2:127968109
|
A | AT | 59 | a0001c0001t0001g0178a0001c0001t0001g0201a0001c0001t0001g0206others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.2063+9875dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968109 | ||||||
| chr2:127968127
|
A | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+9858T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968127 | ||||||
| chr2:127968175
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2063+9810G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968175 | ||||||
| chr2:127968232
|
C | T | 13 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(10): Show | 13 | HG01123.hp1 HG01123.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2063+9753G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968232 | ||||||
| chr2:127968319
|
C | T | 3 | a0001c0002t0001g0017a0001c0002t0001g0023a0001c0002t0001g0034 | 3 | HG02738.hp2 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2063+9666G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968319 | ||||||
| chr2:127968369
|
C | T | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2063+9616G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968369 | ||||||
| chr2:127968406
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+9579G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968406 | ||||||
| chr2:127968414
|
G | GT | 18 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0004g0058others(15): Show | 18 | HG00408.hp1 HG01109.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2063+9570dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968414 | ||||||
| chr2:127968414
|
GT | G | 9 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(6): Show | 9 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2063+9570delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968414 | ||||||
| chr2:127968418
|
T | G | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2063+9567A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968418 | ||||||
| chr2:127968418
|
T | TG | 15 | a0001c0001t0001g0079a0001c0001t0001g0098a0001c0001t0001g0141others(12): Show | 15 | HG01109.hp2 HG01192.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2063+9566_2063+956 others(5): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968418 | ||||||
| chr2:127968419
|
T | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(214): Show | 221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.2063+9566A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968419 | ||||||
| chr2:127968422
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2063+9563A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968422 | ||||||
| chr2:127968490
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+9495G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968490 | ||||||
| chr2:127968763
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+9222T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968763 | ||||||
| chr2:127968785
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2063+9200C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968785 | ||||||
| chr2:127968808
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+9177T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968808 | ||||||
| chr2:127968903
|
A | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.2063+9082T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127968903 | ||||||
| chr2:127969076
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+8909A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127969076 | ||||||
| chr2:127969726
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2063+8259G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127969726 | ||||||
| chr2:127969809
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2063+8176G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127969809 | ||||||
| chr2:127969967
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2063+8018G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127969967 | ||||||
| chr2:127969991
|
A | G | 1 | a0001c0003t0001g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2063+7994T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127969991 | ||||||
| chr2:127970000
|
T | C | 1 | a0001c0002t0001g0036 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2063+7985A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970000 | ||||||
| chr2:127970107
|
A | G | 9 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG02451.hp2 HG02622.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2063+7878T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970107 | ||||||
| chr2:127970165
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0149a0001c0001t0001g0158others(1): Show | 5 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.2063+7820A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970165 | ||||||
| chr2:127970221
|
C | CA | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0134others(18): Show | 21 | HG01928.hp2 HG01978.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.2063+7763dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970221 | ||||||
| chr2:127970423
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2063+7562G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970423 | ||||||
| chr2:127970459
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+7526A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970459 | ||||||
| chr2:127970496
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2063+7489C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970496 | ||||||
| chr2:127970541
|
T | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+7444A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970541 | ||||||
| chr2:127970541
|
T | TA | 28 | a0001c0001t0001g0010a0001c0001t0001g0066a0001c0001t0001g0075others(25): Show | 28 | HG00423.hp1 HG00735.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.2063+7443dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970541 | ||||||
| chr2:127970541
|
T | TAA | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2063+7442_2063+744 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970541 | ||||||
| chr2:127970541
|
T | TAAA | 63 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0084others(60): Show | 64 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2063+7441_2063+744 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970541 | ||||||
| chr2:127970541
|
T | TAAAA | 9 | a0001c0001t0001g0136a0001c0001t0001g0180a0001c0001t0001g0184others(6): Show | 9 | HG02148.hp1 HG02572.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.2063+7440_2063+744 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970541 | ||||||
| chr2:127970927
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+7058G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970927 | ||||||
| chr2:127970959
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+7026A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127970959 | ||||||
| chr2:127971073
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 80 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.2063+6912G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971073 | ||||||
| chr2:127971124
|
T | A | 1 | a0001c0002t0001g0028 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2063+6861A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971124 | ||||||
| chr2:127971156
|
T | C | 1 | a0001c0001t0001g0336 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2063+6829A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971156 | ||||||
| chr2:127971172
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2063+6813G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971172 | ||||||
| chr2:127971185
|
T | A | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2063+6800A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971185 | ||||||
| chr2:127971249
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+6736C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971249 | ||||||
| chr2:127971286
|
CT | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.2063+6698delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971286 | ||||||
| chr2:127971308
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+6677G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971308 | ||||||
| chr2:127971435
|
G | A | 1 | a0001c0003t0001g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2063+6550C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971435 | ||||||
| chr2:127971477
|
C | T | 1 | a0001c0003t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2063+6508G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971477 | ||||||
| chr2:127971531
|
C | A | 30 | a0001c0002t0001g0007a0001c0002t0001g0027a0001c0002t0001g0028others(27): Show | 30 | HG00544.hp2 HG01099.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.2063+6454G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971531 | ||||||
| chr2:127971538
|
T | C | 1 | a0001c0010t0001g0327 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2063+6447A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971538 | ||||||
| chr2:127971613
|
C | T | 1 | a0001c0001t0003g0346 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2063+6372G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971613 | ||||||
| chr2:127971649
|
T | G | 3 | a0001c0004t0001g0090a0001c0004t0001g0091a0001c0004t0001g0094 | 3 | HG02559.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2063+6336A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971649 | ||||||
| chr2:127971761
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 288 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.2063+6224A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971761 | ||||||
| chr2:127971777
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+6208A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127971777 | ||||||
| chr2:127972126
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.2063+5859C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972126 | ||||||
| chr2:127972135
|
C | T | 1 | a0001c0003t0001g0132 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2063+5850G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972135 | ||||||
| chr2:127972136
|
T | C | 1 | a0001c0003t0001g0132 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2063+5849A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972136 | ||||||
| chr2:127972282
|
C | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.2063+5703G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972282 | ||||||
| chr2:127972291
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+5694A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972291 | ||||||
| chr2:127972497
|
C | A | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2063+5488G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972497 | ||||||
| chr2:127972621
|
G | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+5364C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972621 | ||||||
| chr2:127972656
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2063+5329C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972656 | ||||||
| chr2:127972854
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+5131T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972854 | ||||||
| chr2:127972997
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2063+4988C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127972997 | ||||||
| chr2:127973016
|
C | T | 1 | a0001c0003t0007g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2063+4969G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973016 | ||||||
| chr2:127973083
|
T | C | 1 | a0001c0004t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2063+4902A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973083 | ||||||
| chr2:127973090
|
A | C | 1 | a0001c0002t0001g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2063+4895T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973090 | ||||||
| chr2:127973372
|
ACAGGCAT others(135): Show |
A | 1 | a0001c0001t0001g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2063+4471_2063+461 others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973372 | ||||||
| chr2:127973430
|
C | G | 2 | a0001c0003t0007g0111a0001c0003t0008g0101 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2063+4555G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973430 | ||||||
| chr2:127973535
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+4450G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973535 | ||||||
| chr2:127973582
|
G | C | 30 | a0001c0002t0001g0007a0001c0002t0001g0027a0001c0002t0001g0028others(27): Show | 30 | HG00544.hp2 HG01099.hp2 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.2063+4403C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973582 | ||||||
| chr2:127973587
|
C | A | 1 | a0001c0009t0001g0216 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2063+4398G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973587 | ||||||
| chr2:127973588
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2063+4397G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973588 | ||||||
| chr2:127973633
|
A | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+4352T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973633 | ||||||
| chr2:127973767
|
G | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+4218C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973767 | ||||||
| chr2:127973803
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2063+4182C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973803 | ||||||
| chr2:127973829
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(7): Show | 10 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.2063+4156A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973829 | ||||||
| chr2:127973838
|
C | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+4147G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973838 | ||||||
| chr2:127973843
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2063+4142C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127973843 | ||||||
| chr2:127974109
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.2063+3876C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974109 | ||||||
| chr2:127974111
|
T | G | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2063+3874A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974111 | ||||||
| chr2:127974367
|
A | T | 1 | a0001c0001t0001g0230 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2063+3618T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974367 | ||||||
| chr2:127974426
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2063+3559G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974426 | ||||||
| chr2:127974475
|
T | TG | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+3509_2063+351 others(5): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974475 | ||||||
| chr2:127974535
|
C | T | 11 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2063+3450G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974535 | ||||||
| chr2:127974551
|
C | T | 1 | a0001c0003t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2063+3434G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974551 | ||||||
| chr2:127974728
|
G | A | 21 | a0001c0001t0001g0099a0001c0001t0001g0180a0001c0001t0001g0181others(18): Show | 21 | HG00408.hp2 HG00558.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.2063+3257C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974728 | ||||||
| chr2:127974967
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+3018G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127974967 | ||||||
| chr2:127975047
|
G | T | 1 | a0001c0001t0001g0303 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2063+2938C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975047 | ||||||
| chr2:127975076
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+2909A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975076 | ||||||
| chr2:127975080
|
C | A | 1 | a0001c0002t0001g0025 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2063+2905G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975080 | ||||||
| chr2:127975115
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+2870A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975115 | ||||||
| chr2:127975122
|
TA | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2063+2862delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975122 | ||||||
| chr2:127975240
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2063+2745C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975240 | ||||||
| chr2:127975272
|
A | C | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2063+2713T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975272 | ||||||
| chr2:127975297
|
C | A | 1 | a0001c0003t0001g0104 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2063+2688G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975297 | ||||||
| chr2:127975379
|
C | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+2606G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975379 | ||||||
| chr2:127975464
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2063+2521C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975464 | ||||||
| chr2:127975566
|
C | CA | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2063+2418dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975566 | ||||||
| chr2:127975813
|
G | C | 1 | a0001c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2063+2172C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975813 | ||||||
| chr2:127975871
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2063+2114G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975871 | ||||||
| chr2:127975990
|
A | G | 1 | a0001c0002t0001g0031 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2063+1995T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975990 | ||||||
| chr2:127975993
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2063+1992G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127975993 | ||||||
| chr2:127976291
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2063+1694G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127976291 | ||||||
| chr2:127976452
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(128): Show | 132 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2063+1533G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127976452 | ||||||
| chr2:127976631
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(124): Show | 130 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.2063+1354C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127976631 | ||||||
| chr2:127976824
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+1161A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127976824 | ||||||
| chr2:127976909
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2063+1076C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127976909 | ||||||
| chr2:127976998
|
T | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2063+987A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127976998 | ||||||
| chr2:127977056
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+929G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977056 | ||||||
| chr2:127977095
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2063+890T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977095 | ||||||
| chr2:127977230
|
A | T | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2063+755T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977230 | ||||||
| chr2:127977252
|
G | C | 1 | a0001c0012t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2063+733C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977252 | ||||||
| chr2:127977253
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(128): Show | 132 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2063+732C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977253 | ||||||
| chr2:127977313
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2063+672T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977313 | ||||||
| chr2:127977335
|
C | CA | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(254): Show | 261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.2063+649dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977335 | ||||||
| chr2:127977335
|
C | CAA | 19 | a0001c0001t0001g0128a0001c0001t0001g0148a0001c0001t0001g0160others(16): Show | 19 | HG01175.hp2 HG02055.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.2063+648_2063+649d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977335 | ||||||
| chr2:127977378
|
T | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0080 | 2 | HG00323.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.2063+607A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977378 | ||||||
| chr2:127977432
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+553G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977432 | ||||||
| chr2:127977433
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2063+552C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977433 | ||||||
| chr2:127977594
|
T | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063+391A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977594 | ||||||
| chr2:127977736
|
A | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0073 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2063+249T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977736 | ||||||
| chr2:127977766
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+219C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977766 | ||||||
| chr2:127977799
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2063+186A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 15/20 | chr2 | 127977799 | ||||||
| chr2:127978175
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1959-86A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127978175 | ||||||
| chr2:127978214
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1959-125A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127978214 | ||||||
| chr2:127978251
|
ACATTACC others(55): Show |
A | 1 | a0001c0001t0001g0258 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1959-224_1959-163d others(64): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127978251 | ||||||
| chr2:127978318
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1959-229G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127978318 | ||||||
| chr2:127978769
|
C | T | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1959-680G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127978769 | ||||||
| chr2:127978818
|
T | C | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1959-729A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127978818 | ||||||
| chr2:127979034
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1959-945A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979034 | ||||||
| chr2:127979081
|
T | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1959-992A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979081 | ||||||
| chr2:127979097
|
T | C | 9 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(6): Show | 9 | HG00735.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1959-1008A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979097 | ||||||
| chr2:127979112
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(76): Show | 80 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1959-1023A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979112 | ||||||
| chr2:127979157
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1959-1068T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979157 | ||||||
| chr2:127979162
|
C | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(266): Show | 273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.1959-1073G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979162 | ||||||
| chr2:127979182
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-1093C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979182 | ||||||
| chr2:127979253
|
C | T | 1 | a0001c0002t0001g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1959-1164G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979253 | ||||||
| chr2:127979354
|
C | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-1265G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979354 | ||||||
| chr2:127979499
|
AAGATAGA others(82): Show |
A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1959-1499_1959-141 others(93): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979499 | ||||||
| chr2:127979546
|
A | G | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1959-1457T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979546 | ||||||
| chr2:127979887
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1959-1798A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127979887 | ||||||
| chr2:127980002
|
C | T | 27 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(24): Show | 27 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.1959-1913G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980002 | ||||||
| chr2:127980018
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0278 | 2 | NA18941.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1959-1929A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980018 | ||||||
| chr2:127980099
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-2010C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980099 | ||||||
| chr2:127980159
|
T | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-2070A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980159 | ||||||
| chr2:127980254
|
T | C | 1 | a0001c0003t0001g0132 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1959-2165A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980254 | ||||||
| chr2:127980304
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1959-2215T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980304 | ||||||
| chr2:127980448
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-2359C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980448 | ||||||
| chr2:127980457
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1959-2368G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980457 | ||||||
| chr2:127980646
|
A | G | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1959-2557T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980646 | ||||||
| chr2:127980681
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-2592G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980681 | ||||||
| chr2:127980896
|
T | TCAACAAC others(2): Show |
250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1959-2816_1959-280 others(13): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980896 | ||||||
| chr2:127980896
|
T | TCAACAAC others(5): Show |
11 | a0001c0001t0001g0210a0001c0004t0001g0086a0001c0004t0001g0087others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1959-2819_1959-280 others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980896 | ||||||
| chr2:127980952
|
G | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1959-2863C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127980952 | ||||||
| chr2:127981059
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1959-2970G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981059 | ||||||
| chr2:127981199
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1959-3110C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981199 | ||||||
| chr2:127981324
|
G | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1959-3235C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981324 | ||||||
| chr2:127981335
|
C | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(7): Show | 10 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.1959-3246G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981335 | ||||||
| chr2:127981352
|
T | TACCCCCG others(115): Show |
302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(299): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1959-3264_1959-326 others(126): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981352 | ||||||
| chr2:127981357
|
T | C | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1959-3268A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981357 | ||||||
| chr2:127981371
|
T | C | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1959-3282A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981371 | ||||||
| chr2:127981394
|
ACCC | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1959-3308_1959-330 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981394 | ||||||
| chr2:127981397
|
C | CCTGACTC others(112): Show |
38 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(35): Show | 38 | HG00438.hp1 HG00558.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1959-3309_1959-330 others(123): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981397 | ||||||
| chr2:127981397
|
C | CCTGACTC others(112): Show |
1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1959-3309_1959-330 others(123): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981397 | ||||||
| chr2:127981397
|
C | CGACTCAG others(110): Show |
2 | a0001c0003t0001g0105a0001c0003t0001g0123 | 2 | HG00423.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1959-3309_1959-330 others(121): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981397 | ||||||
| chr2:127981397
|
C | CGACTCAG others(110): Show |
2 | a0001c0003t0001g0106a0001c0003t0001g0107 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1959-3309_1959-330 others(121): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981397 | ||||||
| chr2:127981463
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1959-3374T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981463 | ||||||
| chr2:127981464
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-3375C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981464 | ||||||
| chr2:127981479
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1959-3390G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981479 | ||||||
| chr2:127981491
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-3402G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981491 | ||||||
| chr2:127981498
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-3409G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981498 | ||||||
| chr2:127981518
|
CCT | C | 53 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(50): Show | 53 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1959-3431_1959-343 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981518 | ||||||
| chr2:127981552
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0267 | 2 | HG01109.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1959-3463G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981552 | ||||||
| chr2:127981559
|
CCT | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0230others(1): Show | 4 | HG00408.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1959-3472_1959-347 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981559 | ||||||
| chr2:127981569
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1959-3480G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981569 | ||||||
| chr2:127981603
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-3514C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981603 | ||||||
| chr2:127981662
|
C | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1959-3573G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981662 | ||||||
| chr2:127981672
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1959-3583G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981672 | ||||||
| chr2:127981834
|
T | C | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1959-3745A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127981834 | ||||||
| chr2:127982146
|
ACAATTTC others(51): Show |
A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1959-4115_1959-405 others(62): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982146 | ||||||
| chr2:127982147
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0220 | 2 | NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1959-4058G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982147 | ||||||
| chr2:127982170
|
CA | C | 12 | a0001c0001t0001g0244a0001c0004t0001g0086a0001c0004t0001g0087others(9): Show | 12 | HG01123.hp2 HG01168.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1959-4082delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982170 | ||||||
| chr2:127982249
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1959-4160C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982249 | ||||||
| chr2:127982259
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1959-4170A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982259 | ||||||
| chr2:127982505
|
A | G | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.1958+4280T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982505 | ||||||
| chr2:127982514
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1958+4271A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982514 | ||||||
| chr2:127982583
|
G | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1958+4202C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982583 | ||||||
| chr2:127982630
|
G | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1958+4155C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982630 | ||||||
| chr2:127982633
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1958+4152G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982633 | ||||||
| chr2:127982634
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1958+4151C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982634 | ||||||
| chr2:127982642
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1958+4143C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982642 | ||||||
| chr2:127982765
|
T | G | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1958+4020A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127982765 | ||||||
| chr2:127983130
|
C | T | 1 | a0001c0003t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1958+3655G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983130 | ||||||
| chr2:127983177
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1958+3608G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983177 | ||||||
| chr2:127983323
|
C | T | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1958+3462G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983323 | ||||||
| chr2:127983470
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1958+3315A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983470 | ||||||
| chr2:127983605
|
T | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG00408.hp1 HG02258.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+3180A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983605 | ||||||
| chr2:127983626
|
G | A | 119 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(116): Show | 119 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1958+3159C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983626 | ||||||
| chr2:127983738
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1958+3047A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983738 | ||||||
| chr2:127983822
|
TG | T | 15 | a0001c0001t0001g0169a0001c0001t0001g0223a0001c0001t0001g0244others(12): Show | 15 | HG01168.hp2 HG02155.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1958+2962delC | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983822 | ||||||
| chr2:127983823
|
G | GT | 10 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0061others(7): Show | 10 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1958+2961dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983823 | ||||||
| chr2:127983823
|
G | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 248 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1958+2962C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983823 | ||||||
| chr2:127983828
|
T | G | 1 | a0001c0003t0001g0114 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1958+2957A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983828 | ||||||
| chr2:127983833
|
T | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1958+2952A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983833 | ||||||
| chr2:127983833
|
T | TG | 3 | a0001c0001t0001g0168a0001c0006t0001g0070a0001c0006t0001g0076 | 3 | HG00639.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1958+2951_1958+295 others(5): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983833 | ||||||
| chr2:127983845
|
T | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1958+2940A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983845 | ||||||
| chr2:127983846
|
T | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 114 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1958+2939A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983846 | ||||||
| chr2:127983846
|
T | TA | 123 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1958+2938dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983846 | ||||||
| chr2:127983846
|
T | TTA | 42 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0067others(39): Show | 42 | HG00735.hp1 HG01192.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.1958+2938_1958+293 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983846 | ||||||
| chr2:127983846
|
T | TTTA | 44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 44 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1958+2938_1958+293 others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983846 | ||||||
| chr2:127983846
|
T | TTTTA | 6 | a0001c0002t0001g0022a0001c0002t0001g0033a0001c0002t0001g0042others(3): Show | 6 | HG00140.hp1 HG01358.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1958+2938_1958+293 others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127983846 | ||||||
| chr2:127984249
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1958+2536A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984249 | ||||||
| chr2:127984364
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1958+2421G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984364 | ||||||
| chr2:127984557
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1958+2228C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984557 | ||||||
| chr2:127984648
|
G | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1958+2137C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984648 | ||||||
| chr2:127984771
|
T | C | 96 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 99 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1958+2014A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984771 | ||||||
| chr2:127984850
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1958+1935G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984850 | ||||||
| chr2:127984900
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(244): Show | 251 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1958+1885A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127984900 | ||||||
| chr2:127985147
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1958+1638T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985147 | ||||||
| chr2:127985332
|
A | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1958+1453T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985332 | ||||||
| chr2:127985805
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1958+980G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985805 | ||||||
| chr2:127985842
|
G | A | 2 | a0001c0001t0001g0319a0001c0001t0001g0321 | 2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1958+943C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985842 | ||||||
| chr2:127985853
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1958+932G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985853 | ||||||
| chr2:127985893
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1958+892G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985893 | ||||||
| chr2:127985894
|
A | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG00735.hp1 HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1958+891T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985894 | ||||||
| chr2:127985978
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1958+807C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127985978 | ||||||
| chr2:127986005
|
G | A | 3 | a0001c0004t0001g0090a0001c0004t0001g0091a0001c0004t0001g0094 | 3 | HG02559.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1958+780C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986005 | ||||||
| chr2:127986038
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1958+747C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986038 | ||||||
| chr2:127986045
|
A | G | 1 | a0001c0001t0002g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1958+740T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986045 | ||||||
| chr2:127986140
|
C | A | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1958+645G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986140 | ||||||
| chr2:127986269
|
A | C | 1 | a0001c0002t0001g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1958+516T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986269 | ||||||
| chr2:127986444
|
T | C | 1 | a0001c0001t0010g0083 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1958+341A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986444 | ||||||
| chr2:127986456
|
TA | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1958+328delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986456 | ||||||
| chr2:127986489
|
A | G | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1958+296T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986489 | ||||||
| chr2:127986740
|
T | C | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1958+45A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 14/20 | chr2 | 127986740 | ||||||
| chr2:127986969
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.1781-7C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127986969 | ||||||
| chr2:127987006
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 230 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.1781-44T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987006 | ||||||
| chr2:127987109
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0258 | 2 | NA19066.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1781-147A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987109 | ||||||
| chr2:127987236
|
A | G | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1781-274T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987236 | ||||||
| chr2:127987386
|
G | A | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1781-424C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987386 | ||||||
| chr2:127987417
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1781-455G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987417 | ||||||
| chr2:127987522
|
T | G | 1 | a0001c0002t0001g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1781-560A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987522 | ||||||
| chr2:127987665
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1781-703T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987665 | ||||||
| chr2:127987909
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1781-947A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987909 | ||||||
| chr2:127987921
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1781-959A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127987921 | ||||||
| chr2:127988015
|
C | T | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1781-1053G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988015 | ||||||
| chr2:127988027
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1781-1065G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988027 | ||||||
| chr2:127988166
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(316): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1781-1204G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988166 | ||||||
| chr2:127988299
|
T | C | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1780+1265A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988299 | ||||||
| chr2:127988302
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1780+1262A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988302 | ||||||
| chr2:127988367
|
T | C | 1 | a0001c0004t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1780+1197A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988367 | ||||||
| chr2:127988429
|
T | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1780+1135A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988429 | ||||||
| chr2:127988429
|
T | TA | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1780+1134dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988429 | ||||||
| chr2:127988429
|
T | TAA | 17 | a0001c0001t0001g0179a0001c0001t0001g0202a0001c0001t0001g0224others(14): Show | 17 | HG01978.hp2 HG02055.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1780+1133_1780+113 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988429 | ||||||
| chr2:127988641
|
G | C | 2 | a0001c0001t0001g0078a0001c0001t0001g0080 | 2 | HG00323.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1780+923C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988641 | ||||||
| chr2:127988761
|
G | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1780+803C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988761 | ||||||
| chr2:127988856
|
A | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1780+708T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988856 | ||||||
| chr2:127988881
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1780+683T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988881 | ||||||
| chr2:127988896
|
A | G | 1 | a0001c0002t0001g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1780+668T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988896 | ||||||
| chr2:127988951
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1780+613C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127988951 | ||||||
| chr2:127989046
|
G | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1780+518C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989046 | ||||||
| chr2:127989101
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1780+463A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989101 | ||||||
| chr2:127989160
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1780+404C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989160 | ||||||
| chr2:127989199
|
C | T | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1780+365G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989199 | ||||||
| chr2:127989283
|
T | TAG | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1780+279_1780+280d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989283 | ||||||
| chr2:127989313
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1780+251T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989313 | ||||||
| chr2:127989385
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0134others(49): Show | 53 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1780+179A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989385 | ||||||
| chr2:127989431
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1780+133G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989431 | ||||||
| chr2:127989449
|
A | G | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1780+115T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989449 | ||||||
| chr2:127989474
|
A | T | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1780+90T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989474 | ||||||
| chr2:127989478
|
C | A | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1780+86G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989478 | ||||||
| chr2:127989547
|
C | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1780+17G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989547 | ||||||
| chr2:127989553
|
T | A | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1780+11A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989553 | ||||||
| chr2:127989556
|
A | T | 1 | a0001c0003t0001g0126 | 1 | NA18985.hp2 | splice_region_variant&intron_variant | LOW | c.1780+8T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 13/20 | chr2 | 127989556 | ||||||
| chr2:127989916
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0084 | 3 | HG01070.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1478-50G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127989916 | ||||||
| chr2:127989970
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1478-104G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127989970 | ||||||
| chr2:127989975
|
T | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG00280.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1478-109A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127989975 | ||||||
| chr2:127989994
|
T | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1478-128A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127989994 | ||||||
| chr2:127990014
|
C | T | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1478-148G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990014 | ||||||
| chr2:127990022
|
T | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1478-156A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990022 | ||||||
| chr2:127990025
|
C | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1478-159G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990025 | ||||||
| chr2:127990157
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 275 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1478-291T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990157 | ||||||
| chr2:127990250
|
G | A | 3 | a0001c0001t0001g0266a0001c0001t0001g0277a0001c0001t0001g0288 | 3 | HG01106.hp2 HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1478-384C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990250 | ||||||
| chr2:127990261
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1478-395G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990261 | ||||||
| chr2:127990287
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1478-421C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990287 | ||||||
| chr2:127990362
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1478-496T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990362 | ||||||
| chr2:127990513
|
A | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0238 | 2 | NA18940.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1478-647T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990513 | ||||||
| chr2:127990519
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1478-653A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990519 | ||||||
| chr2:127990583
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1478-717G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990583 | ||||||
| chr2:127990634
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1478-768C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990634 | ||||||
| chr2:127990664
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1478-798C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990664 | ||||||
| chr2:127990682
|
G | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1478-816C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990682 | ||||||
| chr2:127990693
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1478-827G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990693 | ||||||
| chr2:127990846
|
T | C | 1 | a0001c0002t0001g0055 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1478-980A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990846 | ||||||
| chr2:127990938
|
C | CA | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1478-1073dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990938 | ||||||
| chr2:127990938
|
C | CAA | 6 | a0001c0001t0001g0128a0001c0001t0001g0142a0001c0001t0001g0158others(3): Show | 6 | HG01070.hp1 HG03490.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1478-1074_1478-107 others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990938 | ||||||
| chr2:127990988
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1478-1122G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127990988 | ||||||
| chr2:127991158
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1478-1292C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991158 | ||||||
| chr2:127991173
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1478-1307G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991173 | ||||||
| chr2:127991223
|
C | A | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-1357G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991223 | ||||||
| chr2:127991245
|
G | A | 1 | a0001c0001t0001g0306 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1478-1379C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991245 | ||||||
| chr2:127991367
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1478-1501G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991367 | ||||||
| chr2:127991368
|
G | A | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1478-1502C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991368 | ||||||
| chr2:127991386
|
G | T | 21 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(18): Show | 21 | HG01069.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1478-1520C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991386 | ||||||
| chr2:127991415
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.1478-1549G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991415 | ||||||
| chr2:127991438
|
C | CA | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(5): Show | 8 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478-1573dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991438 | ||||||
| chr2:127991460
|
C | T | 1 | a0001c0002t0001g0068 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1478-1594G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991460 | ||||||
| chr2:127991485
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0280others(3): Show | 8 | HG00738.hp2 HG01074.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1478-1619G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991485 | ||||||
| chr2:127991624
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1477+1563T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991624 | ||||||
| chr2:127991782
|
G | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1477+1405C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991782 | ||||||
| chr2:127991900
|
C | T | 1 | a0001c0002t0001g0021 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1477+1287G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991900 | ||||||
| chr2:127991901
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1477+1286C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991901 | ||||||
| chr2:127991908
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1477+1279C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991908 | ||||||
| chr2:127991914
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1477+1273A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127991914 | ||||||
| chr2:127992021
|
G | C | 1 | a0001c0002t0001g0007 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1477+1166C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992021 | ||||||
| chr2:127992032
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1477+1155G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992032 | ||||||
| chr2:127992263
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1477+924G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992263 | ||||||
| chr2:127992346
|
T | C | 9 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(6): Show | 9 | HG00735.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1477+841A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992346 | ||||||
| chr2:127992408
|
G | A | 43 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1477+779C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992408 | ||||||
| chr2:127992673
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1477+514A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992673 | ||||||
| chr2:127992701
|
C | T | 1 | a0001c0003t0001g0116 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1477+486G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992701 | ||||||
| chr2:127992702
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0075 | 2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1477+485C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992702 | ||||||
| chr2:127992705
|
A | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1477+482T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992705 | ||||||
| chr2:127992870
|
T | C | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1477+317A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127992870 | ||||||
| chr2:127993065
|
T | C | 1 | a0001c0001t0001g0257 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1477+122A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 12/20 | chr2 | 127993065 | ||||||
| chr2:127993797
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1356-489G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127993797 | ||||||
| chr2:127993798
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1356-490C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127993798 | ||||||
| chr2:127993939
|
T | A | 1 | a0001c0003t0001g0124 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1356-631A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127993939 | ||||||
| chr2:127994040
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1356-732A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994040 | ||||||
| chr2:127994068
|
A | G | 33 | a0001c0001t0001g0286a0001c0003t0001g0100a0001c0003t0001g0102others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1356-760T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994068 | ||||||
| chr2:127994328
|
C | A | 1 | a0001c0001t0001g0292 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1356-1020G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994328 | ||||||
| chr2:127994329
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1356-1021C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994329 | ||||||
| chr2:127994334
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG02717.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1356-1026G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994334 | ||||||
| chr2:127994487
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1356-1179C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994487 | ||||||
| chr2:127994569
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1356-1261C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994569 | ||||||
| chr2:127994624
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1356-1316A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994624 | ||||||
| chr2:127994651
|
C | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-1343G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994651 | ||||||
| chr2:127994652
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1356-1344C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994652 | ||||||
| chr2:127994675
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1356-1367A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994675 | ||||||
| chr2:127994683
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1356-1375G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994683 | ||||||
| chr2:127994749
|
T | C | 332 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(329): Show | 336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1356-1441A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127994749 | ||||||
| chr2:127995046
|
AT | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.1355+1303delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995046 | ||||||
| chr2:127995293
|
T | TA | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1355+1056dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995293 | ||||||
| chr2:127995322
|
G | A | 1 | a0001c0004t0001g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1355+1028C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995322 | ||||||
| chr2:127995352
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0014g0131 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1355+998C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995352 | ||||||
| chr2:127995365
|
G | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0004g0006others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1355+985C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995365 | ||||||
| chr2:127995497
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1355+853C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995497 | ||||||
| chr2:127995511
|
A | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0149a0001c0001t0001g0158others(1): Show | 5 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1355+839T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995511 | ||||||
| chr2:127995545
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1355+805A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995545 | ||||||
| chr2:127995561
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0081 | 2 | HG01192.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1355+789G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995561 | ||||||
| chr2:127995609
|
A | T | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1355+741T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995609 | ||||||
| chr2:127995637
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1355+713C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995637 | ||||||
| chr2:127995912
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1355+438G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127995912 | ||||||
| chr2:127996003
|
T | G | 21 | a0001c0001t0001g0099a0001c0001t0001g0180a0001c0001t0001g0181others(18): Show | 21 | HG00408.hp2 HG00558.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1355+347A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127996003 | ||||||
| chr2:127996215
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1355+135A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127996215 | ||||||
| chr2:127996280
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1355+70A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 11/20 | chr2 | 127996280 | ||||||
| chr2:127996623
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0134others(48): Show | 52 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1214-132T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127996623 | ||||||
| chr2:127996661
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1214-170A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127996661 | ||||||
| chr2:127996777
|
T | A | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | NA18954.hp1 NA18984.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1214-286A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127996777 | ||||||
| chr2:127996831
|
C | T | 3 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088 | 3 | HG01123.hp2 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1214-340G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127996831 | ||||||
| chr2:127996882
|
A | T | 1 | a0001c0001t0004g0059 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1214-391T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127996882 | ||||||
| chr2:127996955
|
C | T | 2 | a0001c0003t0001g0126a0001c0003t0001g0127 | 2 | NA18974.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1214-464G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127996955 | ||||||
| chr2:127997126
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1214-635C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127997126 | ||||||
| chr2:127997169
|
T | C | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1214-678A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127997169 | ||||||
| chr2:127997713
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1214-1222A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127997713 | ||||||
| chr2:127997746
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1214-1255A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127997746 | ||||||
| chr2:127997827
|
A | G | 2 | a0001c0001t0001g0098a0001c0001t0001g0193 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1214-1336T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127997827 | ||||||
| chr2:127997842
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1214-1351T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127997842 | ||||||
| chr2:127998220
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(92): Show | 98 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1213+1521G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998220 | ||||||
| chr2:127998257
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1213+1484A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998257 | ||||||
| chr2:127998259
|
C | T | 307 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(304): Show | 311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1213+1482G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998259 | ||||||
| chr2:127998361
|
G | A | 1 | a0001c0004t0001g0092 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1213+1380C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998361 | ||||||
| chr2:127998440
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1213+1301A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998440 | ||||||
| chr2:127998657
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1213+1084A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998657 | ||||||
| chr2:127998703
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1213+1038C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998703 | ||||||
| chr2:127998745
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1213+996G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998745 | ||||||
| chr2:127998746
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1213+995T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127998746 | ||||||
| chr2:127999280
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1213+461G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999280 | ||||||
| chr2:127999311
|
A | C | 1 | a0001c0002t0001g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1213+430T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999311 | ||||||
| chr2:127999330
|
A | AGCTGAGT others(3): Show |
1 | a0001c0002t0001g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1213+401_1213+410d others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999330 | ||||||
| chr2:127999333
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1213+408A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999333 | ||||||
| chr2:127999393
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1213+348A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999393 | ||||||
| chr2:127999417
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1213+324G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999417 | ||||||
| chr2:127999473
|
A | G | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1213+268T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999473 | ||||||
| chr2:127999616
|
G | A | 1 | a0001c0002t0012g0044 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1213+125C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999616 | ||||||
| chr2:127999616
|
GA | G | 23 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0267others(20): Show | 23 | HG00408.hp1 HG01099.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1213+124delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999616 | ||||||
| chr2:127999672
|
A | T | 1 | a0001c0001t0001g0268 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1213+69T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 10/20 | chr2 | 127999672 | ||||||
| chr2:128000222
|
G | A | 1 | a0001c0001t0001g0297 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1018-76C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 8/20 | chr2 | 128000222 | ||||||
| chr2:128000230
|
C | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 275 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.1017+77G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 8/20 | chr2 | 128000230 | ||||||
| chr2:128000509
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.870-55G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128000509 | ||||||
| chr2:128000710
|
G | A | 9 | a0001c0002t0001g0007a0001c0002t0001g0031a0001c0002t0001g0033others(6): Show | 9 | HG01358.hp2 HG01975.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.870-256C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128000710 | ||||||
| chr2:128000765
|
G | A | 3 | a0001c0004t0001g0090a0001c0004t0001g0091a0001c0004t0001g0094 | 3 | HG02559.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.870-311C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128000765 | ||||||
| chr2:128000938
|
T | C | 4 | a0001c0001t0001g0317a0001c0001t0004g0006a0001c0001t0004g0058others(1): Show | 4 | HG01243.hp1 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-484A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128000938 | ||||||
| chr2:128001055
|
T | C | 14 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(11): Show | 14 | HG00408.hp1 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.870-601A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001055 | ||||||
| chr2:128001281
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.870-827T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001281 | ||||||
| chr2:128001383
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.870-929A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001383 | ||||||
| chr2:128001395
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.870-941G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001395 | ||||||
| chr2:128001464
|
G | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.870-1010C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001464 | ||||||
| chr2:128001526
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.870-1072C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001526 | ||||||
| chr2:128001772
|
G | A | 344 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(341): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.870-1318C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001772 | ||||||
| chr2:128001932
|
C | CT | 12 | a0001c0001t0001g0098a0001c0001t0001g0303a0001c0004t0001g0086others(9): Show | 12 | HG01123.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.870-1479dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001932 | ||||||
| chr2:128001968
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.870-1514G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128001968 | ||||||
| chr2:128002008
|
C | T | 1 | a0001c0005t0001g0301 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.870-1554G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002008 | ||||||
| chr2:128002072
|
G | A | 1 | a0001c0001t0014g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.870-1618C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002072 | ||||||
| chr2:128002279
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.870-1825G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002279 | ||||||
| chr2:128002328
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.870-1874T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002328 | ||||||
| chr2:128002386
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0329others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-1932C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002386 | ||||||
| chr2:128002386
|
G | C | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.870-1932C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002386 | ||||||
| chr2:128002434
|
G | A | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.870-1980C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002434 | ||||||
| chr2:128002514
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.870-2060C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002514 | ||||||
| chr2:128002778
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0285a0001c0001t0001g0302others(1): Show | 5 | NA18939.hp1 NA18972.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.870-2324G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002778 | ||||||
| chr2:128002832
|
ACTTGGGC others(5): Show |
A | 4 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0010t0001g0327others(1): Show | 4 | HG00323.hp1 HG03239.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-2390_870-2379d others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128002832 | ||||||
| chr2:128003088
|
C | G | 1 | a0002c0014t0001g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.870-2634G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003088 | ||||||
| chr2:128003112
|
C | T | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.870-2658G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003112 | ||||||
| chr2:128003121
|
G | A | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.870-2667C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003121 | ||||||
| chr2:128003174
|
A | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.870-2720T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003174 | ||||||
| chr2:128003311
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.870-2857T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003311 | ||||||
| chr2:128003579
|
G | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.870-3125C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003579 | ||||||
| chr2:128003655
|
C | T | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.870-3201G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003655 | ||||||
| chr2:128003728
|
C | CT | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.870-3275dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003728 | ||||||
| chr2:128003957
|
C | CT | 22 | a0001c0001t0001g0085a0001c0001t0001g0223a0001c0001t0001g0229others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.870-3504dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTT | 13 | a0001c0001t0001g0130a0001c0001t0001g0158a0001c0001t0001g0163others(10): Show | 13 | HG01070.hp1 HG01109.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.870-3505_870-3504d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTT | 35 | a0001c0001t0001g0001a0001c0001t0001g0134a0001c0001t0001g0136others(32): Show | 36 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.870-3506_870-3504d others(5): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTT | 22 | a0001c0001t0001g0128a0001c0001t0001g0135a0001c0001t0001g0140others(19): Show | 22 | HG00639.hp2 HG00673.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.870-3507_870-3504d others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTT | 7 | a0001c0001t0001g0077a0001c0001t0001g0082a0001c0001t0001g0138others(4): Show | 7 | HG00280.hp1 HG02055.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.870-3508_870-3504d others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTT | 8 | a0001c0001t0001g0014a0001c0001t0001g0078a0001c0001t0001g0081others(5): Show | 8 | HG00323.hp2 HG01070.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.870-3509_870-3504d others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0344 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.870-3513_870-3504d others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0139 | 2 | NA18906.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.870-3514_870-3504d others(13): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0065a0001c0006t0001g0076 | 2 | HG01168.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.870-3515_870-3504d others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(8): Show |
4 | a0001c0002t0001g0032a0001c0002t0001g0033a0001c0002t0001g0039others(1): Show | 4 | HG01993.hp1 HG02165.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.870-3518_870-3504d others(17): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(9): Show |
3 | a0001c0002t0001g0007a0001c0002t0001g0038a0001c0002t0001g0043 | 3 | HG02074.hp2 HG02135.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.870-3519_870-3504d others(18): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0075a0001c0002t0001g0047a0001c0002t0001g0068 | 3 | HG01358.hp2 HG02559.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.870-3520_870-3504d others(19): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(11): Show |
3 | a0001c0002t0001g0031a0001c0002t0001g0037a0001c0002t0001g0051 | 3 | HG01975.hp2 NA19010.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.870-3521_870-3504d others(20): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(12): Show |
1 | a0001c0006t0001g0070 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.870-3522_870-3504d others(21): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.870-3523_870-3504d others(22): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(14): Show |
1 | a0001c0002t0001g0027 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.870-3524_870-3504d others(23): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(15): Show |
2 | a0001c0002t0001g0036a0001c0002t0001g0054 | 2 | HG01099.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.870-3525_870-3504d others(24): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(16): Show |
1 | a0001c0002t0001g0035 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.870-3526_870-3504d others(25): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(17): Show |
1 | a0001c0002t0001g0034 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.870-3527_870-3504d others(26): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.870-3529_870-3504d others(28): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(20): Show |
3 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0004g0058 | 3 | HG02486.hp1 HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.870-3530_870-3504d others(29): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(22): Show |
2 | a0001c0002t0001g0050a0001c0002t0012g0044 | 2 | HG01934.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.870-3532_870-3504d others(31): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0010 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.870-3535_870-3504d others(34): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(26): Show |
1 | a0001c0002t0001g0049 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.870-3504_870-3503i others(35): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0001g0061 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.870-3504_870-3503i others(37): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
C | CTTTTTTT others(30): Show |
1 | a0001c0001t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.870-3504_870-3503i others(39): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CT | C | 30 | a0001c0001t0001g0069a0001c0001t0001g0073a0001c0001t0001g0074others(27): Show | 30 | HG00423.hp1 HG00558.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.870-3504delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CTTTTTT | C | 11 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0019others(8): Show | 11 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.870-3509_870-3504d others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CTTTTTTT others(3): Show |
C | 13 | a0001c0001t0001g0015a0001c0004t0001g0086a0001c0004t0001g0087others(10): Show | 13 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.870-3513_870-3504d others(12): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0312a0001c0002t0001g0042a0001c0002t0001g0055 | 3 | HG02809.hp1 NA18981.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.870-3514_870-3504d others(13): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0003t0007g0111a0001c0003t0008g0101 | 2 | HG02451.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.870-3516_870-3504d others(15): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CTTTTTTT others(7): Show |
C | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.870-3517_870-3504d others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128003957
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0003t0001g0129 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.870-3522_870-3504d others(21): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128003957 | ||||||
| chr2:128004130
|
T | C | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.870-3676A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004130 | ||||||
| chr2:128004361
|
C | CT | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.870-3908dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004361 | ||||||
| chr2:128004361
|
CT | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.870-3908delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004361 | ||||||
| chr2:128004361
|
CTT | C | 60 | a0001c0001t0001g0130a0001c0001t0001g0136a0001c0001t0001g0137others(57): Show | 60 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.870-3909_870-3908d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004361 | ||||||
| chr2:128004361
|
CTTTTTTT | C | 15 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0061others(12): Show | 15 | HG01884.hp1 HG02109.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.870-3914_870-3908d others(9): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004361 | ||||||
| chr2:128004361
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.870-3918_870-3908d others(13): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004361 | ||||||
| chr2:128004361
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.870-3922_870-3908d others(17): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004361 | ||||||
| chr2:128004394
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.870-3940C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004394 | ||||||
| chr2:128004477
|
G | A | 1 | a0001c0003t0001g0117 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.870-4023C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004477 | ||||||
| chr2:128004511
|
G | A | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.870-4057C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004511 | ||||||
| chr2:128004754
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.870-4300G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128004754 | ||||||
| chr2:128005008
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.870-4554T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005008 | ||||||
| chr2:128005034
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.870-4580G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005034 | ||||||
| chr2:128005054
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.870-4600A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005054 | ||||||
| chr2:128005145
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.870-4691G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005145 | ||||||
| chr2:128005272
|
C | G | 1 | a0001c0001t0001g0008 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.870-4818G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005272 | ||||||
| chr2:128005281
|
G | C | 2 | a0001c0003t0001g0118a0001c0003t0001g0132 | 2 | NA18957.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.870-4827C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005281 | ||||||
| chr2:128005388
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+4881C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005388 | ||||||
| chr2:128005434
|
T | C | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | HG01123.hp1 HG01261.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.869+4835A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005434 | ||||||
| chr2:128005441
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+4828G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005441 | ||||||
| chr2:128005563
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+4706A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005563 | ||||||
| chr2:128005571
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.869+4698G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005571 | ||||||
| chr2:128005650
|
C | CT | 7 | a0001c0001t0001g0099a0001c0001t0001g0139a0001c0001t0001g0205others(4): Show | 7 | HG00280.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.869+4618dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005650 | ||||||
| chr2:128005657
|
T | A | 1 | a0001c0001t0001g0283 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.869+4612A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005657 | ||||||
| chr2:128005699
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+4570G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128005699 | ||||||
| chr2:128006100
|
A | G | 1 | a0001c0012t0001g0024 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.869+4169T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006100 | ||||||
| chr2:128006237
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+4032G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006237 | ||||||
| chr2:128006252
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.869+4017A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006252 | ||||||
| chr2:128006343
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.869+3926C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006343 | ||||||
| chr2:128006347
|
T | C | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0164others(12): Show | 15 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.869+3922A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006347 | ||||||
| chr2:128006368
|
T | C | 250 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(247): Show | 251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.869+3901A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006368 | ||||||
| chr2:128006384
|
T | C | 99 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(96): Show | 99 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.869+3885A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006384 | ||||||
| chr2:128006403
|
A | G | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.869+3866T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006403 | ||||||
| chr2:128006554
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.869+3715G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006554 | ||||||
| chr2:128006648
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.869+3621C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006648 | ||||||
| chr2:128006794
|
T | C | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.869+3475A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006794 | ||||||
| chr2:128006860
|
G | C | 1 | a0001c0003t0001g0123 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.869+3409C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006860 | ||||||
| chr2:128006881
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.869+3388C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006881 | ||||||
| chr2:128006987
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+3282A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128006987 | ||||||
| chr2:128007084
|
G | C | 1 | a0001c0001t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.869+3185C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128007084 | ||||||
| chr2:128007084
|
G | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+3185C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128007084 | ||||||
| chr2:128007307
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.869+2962T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128007307 | ||||||
| chr2:128007678
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0218 | 2 | HG01069.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.869+2591G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128007678 | ||||||
| chr2:128007849
|
T | C | 3 | a0001c0002t0001g0031a0001c0002t0001g0033a0001c0002t0001g0047 | 3 | HG01358.hp2 HG01975.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.869+2420A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128007849 | ||||||
| chr2:128008034
|
C | T | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.869+2235G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008034 | ||||||
| chr2:128008133
|
T | C | 1 | a0001c0003t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.869+2136A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008133 | ||||||
| chr2:128008173
|
T | C | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.869+2096A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008173 | ||||||
| chr2:128008382
|
CAG | C | 31 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.869+1885_869+1886d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008382 | ||||||
| chr2:128008469
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.869+1800C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008469 | ||||||
| chr2:128008502
|
C | CTATA | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.869+1763_869+1766d others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008502 | ||||||
| chr2:128008528
|
C | CT | 28 | a0001c0001t0001g0226a0001c0003t0001g0100a0001c0003t0001g0102others(25): Show | 28 | HG00423.hp1 HG00438.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.869+1740dupA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008528 | ||||||
| chr2:128008528
|
CT | C | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 108 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.869+1740delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008528 | ||||||
| chr2:128008647
|
G | A | 1 | a0002c0014t0001g0120 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.869+1622C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008647 | ||||||
| chr2:128008683
|
CTGTT | C | 4 | a0001c0001t0001g0097a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG02615.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.869+1582_869+1585d others(6): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008683 | ||||||
| chr2:128008892
|
C | T | 1 | a0001c0002t0001g0023 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.869+1377G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008892 | ||||||
| chr2:128008984
|
C | A | 1 | a0001c0001t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.869+1285G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128008984 | ||||||
| chr2:128009142
|
G | A | 1 | a0001c0015t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.869+1127C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009142 | ||||||
| chr2:128009234
|
G | C | 1 | a0001c0001t0003g0343 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.869+1035C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009234 | ||||||
| chr2:128009576
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.869+693A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009576 | ||||||
| chr2:128009688
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.869+581G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009688 | ||||||
| chr2:128009732
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+537C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009732 | ||||||
| chr2:128009828
|
C | A | 1 | a0001c0005t0006g0005 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.869+441G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009828 | ||||||
| chr2:128009866
|
G | A | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.869+403C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009866 | ||||||
| chr2:128009981
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869+288G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009981 | ||||||
| chr2:128009988
|
T | C | 15 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0164others(12): Show | 15 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.869+281A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128009988 | ||||||
| chr2:128010160
|
A | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0190 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.869+109T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128010160 | ||||||
| chr2:128010166
|
A | G | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.869+103T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 7/20 | chr2 | 128010166 | ||||||
| chr2:128010419
|
T | C | 1 | a0001c0002t0012g0044 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.745-26A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128010419 | ||||||
| chr2:128010585
|
A | G | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.745-192T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128010585 | ||||||
| chr2:128010787
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.745-394G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128010787 | ||||||
| chr2:128010909
|
T | TA | 31 | a0001c0003t0001g0100a0001c0003t0001g0103a0001c0003t0001g0104others(28): Show | 31 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.745-517dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128010909 | ||||||
| chr2:128010951
|
G | GA | 117 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(114): Show | 117 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.745-559dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128010951 | ||||||
| chr2:128010951
|
G | GAA | 6 | a0001c0002t0001g0019a0001c0003t0001g0112a0001c0003t0001g0121others(3): Show | 6 | HG00408.hp1 HG01175.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.745-560_745-559dup others(2): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128010951 | ||||||
| chr2:128011049
|
T | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.745-656A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011049 | ||||||
| chr2:128011103
|
T | A | 1 | a0001c0001t0001g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.745-710A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011103 | ||||||
| chr2:128011115
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.745-722C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011115 | ||||||
| chr2:128011296
|
T | C | 1 | a0001c0002t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.745-903A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011296 | ||||||
| chr2:128011440
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0023 | 2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.745-1047G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011440 | ||||||
| chr2:128011472
|
A | G | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.745-1079T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011472 | ||||||
| chr2:128011573
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.745-1180C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011573 | ||||||
| chr2:128011631
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1238C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011631 | ||||||
| chr2:128011666
|
G | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(8): Show | 11 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.745-1273C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128011666 | ||||||
| chr2:128012027
|
C | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.744+1003G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012027 | ||||||
| chr2:128012154
|
G | A | 31 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG01928.hp1 others(28): Show |
intron_variant | MODIFIER | c.744+876C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012154 | ||||||
| chr2:128012295
|
T | C | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.744+735A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012295 | ||||||
| chr2:128012450
|
A | G | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.744+580T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012450 | ||||||
| chr2:128012611
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.744+419A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012611 | ||||||
| chr2:128012671
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.744+359A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012671 | ||||||
| chr2:128012852
|
G | C | 1 | a0001c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.744+178C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 6/20 | chr2 | 128012852 | ||||||
| chr2:128013157
|
G | GA | 26 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(23): Show | 26 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.620-4dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128013157 | ||||||
| chr2:128013520
|
C | G | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.620-366G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128013520 | ||||||
| chr2:128013528
|
C | T | 1 | a0001c0002t0001g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.620-374G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128013528 | ||||||
| chr2:128013800
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.620-646G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128013800 | ||||||
| chr2:128013933
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.620-779T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128013933 | ||||||
| chr2:128013963
|
C | T | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.620-809G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128013963 | ||||||
| chr2:128014094
|
T | C | 2 | a0001c0002t0001g0020a0001c0002t0001g0022 | 2 | HG00140.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.619+709A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014094 | ||||||
| chr2:128014130
|
C | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.619+673G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014130 | ||||||
| chr2:128014224
|
G | A | 2 | a0001c0001t0004g0006a0001c0001t0004g0059 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.619+579C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014224 | ||||||
| chr2:128014232
|
TTC | T | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.619+569_619+570del others(2): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014232 | ||||||
| chr2:128014364
|
CATCTCAG others(21): Show |
C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.619+411_619+438del others(28): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014364 | ||||||
| chr2:128014392
|
TATCTCAG others(21): Show |
T | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.619+383_619+410del others(28): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014392 | ||||||
| chr2:128014420
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0130others(65): Show | 69 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.619+383G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014420 | ||||||
| chr2:128014641
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.619+162A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014641 | ||||||
| chr2:128014642
|
T | C | 1 | a0001c0002t0001g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.619+161A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014642 | ||||||
| chr2:128014736
|
C | T | 130 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.619+67G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014736 | ||||||
| chr2:128014737
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.619+66C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014737 | ||||||
| chr2:128014797
|
C | T | 52 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(49): Show | 52 | HG00408.hp2 HG00558.hp1 HG00735.hp1 others(49): Show |
splice_region_variant&intron_variant | LOW | c.619+6G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014797 | ||||||
| chr2:128014798
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.619+5C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 5/20 | chr2 | 128014798 | ||||||
| chr2:128015100
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.508-186T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015100 | ||||||
| chr2:128015267
|
C | T | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 4 | HG00323.hp2 HG01192.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.508-353G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015267 | ||||||
| chr2:128015288
|
T | C | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.508-374A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015288 | ||||||
| chr2:128015457
|
T | C | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.508-543A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015457 | ||||||
| chr2:128015490
|
G | T | 1 | a0001c0002t0001g0055 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.508-576C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015490 | ||||||
| chr2:128015574
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.508-660A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015574 | ||||||
| chr2:128015589
|
C | T | 3 | a0001c0003t0001g0102a0001c0003t0001g0103a0001c0003t0001g0121 | 3 | NA18964.hp1 NA18977.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.508-675G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015589 | ||||||
| chr2:128015713
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.507+676C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015713 | ||||||
| chr2:128015799
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0134others(48): Show | 52 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.507+590C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015799 | ||||||
| chr2:128015860
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.507+529C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015860 | ||||||
| chr2:128015868
|
G | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.507+521C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015868 | ||||||
| chr2:128015870
|
C | T | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.507+519G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015870 | ||||||
| chr2:128015882
|
T | A | 250 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(247): Show | 251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.507+507A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015882 | ||||||
| chr2:128015940
|
C | CA | 21 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(18): Show | 21 | HG01123.hp2 HG01175.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.507+448dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015940 | ||||||
| chr2:128015940
|
C | CAA | 75 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0061others(72): Show | 75 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.507+447_507+448dup others(2): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015940 | ||||||
| chr2:128015991
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.507+398T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128015991 | ||||||
| chr2:128016002
|
T | C | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.507+387A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016002 | ||||||
| chr2:128016068
|
C | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0288 | 2 | HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.507+321G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016068 | ||||||
| chr2:128016070
|
C | T | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.507+319G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016070 | ||||||
| chr2:128016081
|
C | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.507+308G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016081 | ||||||
| chr2:128016113
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.507+276C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016113 | ||||||
| chr2:128016194
|
A | G | 1 | a0001c0003t0008g0101 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.507+195T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016194 | ||||||
| chr2:128016275
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.507+114C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016275 | ||||||
| chr2:128016320
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.507+69T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016320 | ||||||
| chr2:128016358
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.507+31A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 4/20 | chr2 | 128016358 | ||||||
| chr2:128016748
|
C | T | 3 | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0030 | 3 | NA18941.hp2 NA19074.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.349-201G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128016748 | ||||||
| chr2:128016840
|
T | G | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.349-293A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128016840 | ||||||
| chr2:128016854
|
G | A | 10 | a0001c0003t0001g0113a0001c0003t0001g0114a0001c0003t0001g0115others(7): Show | 10 | HG00438.hp1 HG00558.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.349-307C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128016854 | ||||||
| chr2:128017087
|
T | C | 3 | a0001c0001t0001g0266a0001c0001t0001g0277a0001c0001t0001g0288 | 3 | HG01106.hp2 HG01175.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.349-540A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128017087 | ||||||
| chr2:128017347
|
A | G | 130 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.348+333T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128017347 | ||||||
| chr2:128017614
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.348+66T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128017614 | ||||||
| chr2:128017629
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.348+51A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 3/20 | chr2 | 128017629 | ||||||
| chr2:128018122
|
A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0173 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.113-207T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018122 | ||||||
| chr2:128018313
|
C | CA | 33 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0170others(30): Show | 33 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.113-399dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018313 | ||||||
| chr2:128018332
|
C | A | 87 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(84): Show | 87 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.113-417G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018332 | ||||||
| chr2:128018332
|
C | CAAACCAA | 8 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(5): Show | 8 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-424_113-418dup others(7): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018332 | ||||||
| chr2:128018336
|
C | A | 1 | a0001c0002t0001g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.113-421G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018336 | ||||||
| chr2:128018429
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-514C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018429 | ||||||
| chr2:128018483
|
C | CA | 88 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(85): Show | 88 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.113-569dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAA | 45 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0015others(42): Show | 47 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.113-570_113-569dup others(2): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(7): Show |
1 | a0001c0004t0001g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.113-582_113-569dup others(14): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(8): Show |
1 | a0001c0004t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.113-583_113-569dup others(15): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(9): Show |
4 | a0001c0004t0001g0089a0001c0004t0001g0316a0001c0007t0005g0313others(1): Show | 4 | HG01175.hp1 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-584_113-569dup others(16): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(10): Show |
2 | a0001c0004t0001g0092a0001c0004t0001g0094 | 2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.113-585_113-569dup others(17): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(15): Show |
1 | a0001c0004t0001g0086 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.113-590_113-569dup others(22): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(17): Show |
1 | a0001c0004t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113-569_113-568ins others(24): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
C | CAAAAAAA others(19): Show |
2 | a0001c0004t0001g0087a0001c0004t0001g0088 | 2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.113-569_113-568ins others(26): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
CA | C | 17 | a0001c0001t0001g0095a0001c0001t0001g0164a0001c0001t0001g0165others(14): Show | 17 | HG00735.hp1 HG01069.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.113-569delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018483
|
CAA | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0098others(99): Show | 103 | HG00280.hp1 HG00408.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.113-570_113-569del others(2): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018483 | ||||||
| chr2:128018544
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0193 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.113-629G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018544 | ||||||
| chr2:128018584
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0329others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-669C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018584 | ||||||
| chr2:128018637
|
T | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0218 | 2 | HG01069.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.113-722A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018637 | ||||||
| chr2:128018796
|
C | CA | 18 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(15): Show | 18 | HG00408.hp1 HG01070.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.113-882dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018796 | ||||||
| chr2:128018924
|
C | T | 1 | a0001c0004t0001g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.113-1009G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018924 | ||||||
| chr2:128018959
|
G | A | 32 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(29): Show | 32 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.113-1044C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018959 | ||||||
| chr2:128018992
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.113-1077C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128018992 | ||||||
| chr2:128019154
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.113-1239T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019154 | ||||||
| chr2:128019256
|
A | T | 1 | a0001c0001t0001g0224 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.113-1341T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019256 | ||||||
| chr2:128019268
|
TA | T | 46 | a0001c0002t0001g0007a0001c0002t0001g0016a0001c0002t0001g0017others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.113-1354delT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019268 | ||||||
| chr2:128019412
|
C | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.113-1497G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019412 | ||||||
| chr2:128019416
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.113-1501A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019416 | ||||||
| chr2:128019425
|
A | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(247): Show | 251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.113-1510T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019425 | ||||||
| chr2:128019426
|
C | T | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-1511G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019426 | ||||||
| chr2:128019608
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113-1693C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019608 | ||||||
| chr2:128019763
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.113-1848A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019763 | ||||||
| chr2:128019923
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.113-2008T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128019923 | ||||||
| chr2:128020049
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.113-2134G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128020049 | ||||||
| chr2:128020597
|
T | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0211a0001c0001t0001g0212others(2): Show | 5 | HG02273.hp1 NA18747.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2682A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128020597 | ||||||
| chr2:128020828
|
C | G | 4 | a0001c0001t0001g0097a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 4 | HG02615.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2913G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128020828 | ||||||
| chr2:128020940
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.113-3025C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128020940 | ||||||
| chr2:128020947
|
G | A | 1 | a0001c0002t0001g0055 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.113-3032C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128020947 | ||||||
| chr2:128020982
|
T | A | 1 | a0001c0004t0001g0094 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.113-3067A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128020982 | ||||||
| chr2:128021186
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.113-3271T>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021186 | ||||||
| chr2:128021264
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.113-3349A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021264 | ||||||
| chr2:128021272
|
C | A | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.113-3357G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021272 | ||||||
| chr2:128021316
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.113-3401C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021316 | ||||||
| chr2:128021426
|
G | A | 40 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0329others(37): Show | 40 | HG00323.hp1 HG00544.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.113-3511C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021426 | ||||||
| chr2:128021446
|
C | CA | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0065others(18): Show | 21 | HG00323.hp2 HG01070.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.113-3532dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021446 | ||||||
| chr2:128021455
|
A | C | 1 | a0001c0001t0001g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.113-3540T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021455 | ||||||
| chr2:128021462
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0084 | 3 | HG01070.hp2 HG01261.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.113-3547G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021462 | ||||||
| chr2:128021529
|
C | T | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-3614G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021529 | ||||||
| chr2:128021619
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.113-3704T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021619 | ||||||
| chr2:128021668
|
A | C | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113-3753T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021668 | ||||||
| chr2:128021782
|
AT | A | 130 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(127): Show | 130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.113-3868delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128021782 | ||||||
| chr2:128022189
|
C | T | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.112+3992G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022189 | ||||||
| chr2:128022213
|
G | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112+3968C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022213 | ||||||
| chr2:128022251
|
C | T | 4 | a0001c0001t0002g0096a0001c0001t0002g0188a0001c0001t0002g0189others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+3930G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022251 | ||||||
| chr2:128022414
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+3767G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022414 | ||||||
| chr2:128022415
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0215 | 2 | HG03098.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.112+3766C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022415 | ||||||
| chr2:128022516
|
A | G | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.112+3665T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022516 | ||||||
| chr2:128022545
|
T | C | 3 | a0001c0001t0001g0222a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | NA18943.hp1 NA18955.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.112+3636A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022545 | ||||||
| chr2:128022599
|
G | A | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.112+3582C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022599 | ||||||
| chr2:128022730
|
T | C | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112+3451A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022730 | ||||||
| chr2:128022779
|
G | A | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0312others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+3402C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022779 | ||||||
| chr2:128022866
|
G | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.112+3315C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022866 | ||||||
| chr2:128022872
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.112+3309G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022872 | ||||||
| chr2:128022935
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.112+3246A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022935 | ||||||
| chr2:128022996
|
AT | A | 14 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0292others(11): Show | 14 | HG00408.hp1 HG01496.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+3184delA | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128022996 | ||||||
| chr2:128023016
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.112+3165G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023016 | ||||||
| chr2:128023119
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.112+3062G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023119 | ||||||
| chr2:128023120
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.112+3061C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023120 | ||||||
| chr2:128023127
|
C | T | 1 | a0001c0001t0001g0222 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.112+3054G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023127 | ||||||
| chr2:128023128
|
G | T | 1 | a0001c0002t0001g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.112+3053C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023128 | ||||||
| chr2:128023140
|
A | G | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG02572.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+3041T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023140 | ||||||
| chr2:128023319
|
T | C | 1 | a0001c0001t0001g0338 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112+2862A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023319 | ||||||
| chr2:128023452
|
C | G | 1 | a0001c0015t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.112+2729G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023452 | ||||||
| chr2:128023498
|
C | T | 2 | a0001c0001t0001g0221a0001c0011t0013g0328 | 2 | HG00408.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.112+2683G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023498 | ||||||
| chr2:128023550
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.112+2631G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023550 | ||||||
| chr2:128023617
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.112+2564T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023617 | ||||||
| chr2:128023733
|
T | C | 3 | a0001c0007t0005g0313a0001c0007t0005g0314a0001c0011t0013g0328 | 3 | HG00408.hp1 HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.112+2448A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023733 | ||||||
| chr2:128023779
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112+2402T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023779 | ||||||
| chr2:128023847
|
T | C | 1 | a0001c0001t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.112+2334A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023847 | ||||||
| chr2:128023890
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.112+2291C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023890 | ||||||
| chr2:128023907
|
T | TTATTCTA others(23): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG02738.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.112+2244_112+2273d others(32): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023907 | ||||||
| chr2:128023928
|
T | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.112+2253A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023928 | ||||||
| chr2:128023930
|
C | T | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.112+2251G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023930 | ||||||
| chr2:128023931
|
TCTAGAA | T | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.112+2244_112+2249d others(8): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023931 | ||||||
| chr2:128023939
|
A | C | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.112+2242T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128023939 | ||||||
| chr2:128024058
|
CAA | C | 31 | a0001c0003t0001g0100a0001c0003t0001g0102a0001c0003t0001g0103others(28): Show | 31 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.112+2121_112+2122d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024058 | ||||||
| chr2:128024266
|
G | T | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112+1915C>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024266 | ||||||
| chr2:128024366
|
T | C | 3 | a0001c0001t0004g0006a0001c0001t0004g0058a0001c0001t0004g0059 | 3 | HG01243.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.112+1815A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024366 | ||||||
| chr2:128024384
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0014g0131 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.112+1797G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024384 | ||||||
| chr2:128024550
|
C | T | 14 | a0001c0002t0001g0016a0001c0002t0001g0017a0001c0002t0001g0018others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+1631G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024550 | ||||||
| chr2:128024693
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0312others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+1488G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024693 | ||||||
| chr2:128024714
|
G | GA | 115 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0097others(112): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.112+1466dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024714 | ||||||
| chr2:128024714
|
G | GAA | 6 | a0001c0001t0001g0099a0001c0001t0001g0217a0001c0001t0001g0317others(3): Show | 6 | HG02055.hp1 HG02723.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+1465_112+1466d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024714 | ||||||
| chr2:128024806
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112+1375C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128024806 | ||||||
| chr2:128025003
|
C | CA | 169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(166): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.112+1177dupT | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025003 | ||||||
| chr2:128025003
|
C | CAA | 82 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0061others(79): Show | 82 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.112+1176_112+1177d others(4): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025003 | ||||||
| chr2:128025108
|
T | G | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+1073A>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025108 | ||||||
| chr2:128025115
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.112+1066C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025115 | ||||||
| chr2:128025392
|
C | T | 3 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088 | 3 | HG01123.hp2 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.112+789G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025392 | ||||||
| chr2:128025428
|
A | C | 1 | a0001c0001t0003g0343 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.112+753T>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025428 | ||||||
| chr2:128025526
|
A | G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.112+655T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025526 | ||||||
| chr2:128025662
|
T | C | 10 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG01123.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+519A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025662 | ||||||
| chr2:128025752
|
A | G | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.112+429T>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 2/20 | chr2 | 128025752 | ||||||
| chr2:128026548
|
T | C | 1 | a0001c0008t0001g0219 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-6-250A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026548 | ||||||
| chr2:128026560
|
CACCATTG others(8): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-6-277_-6-263delAC others(13): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026560 | ||||||
| chr2:128026577
|
C | G | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-279G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026577 | ||||||
| chr2:128026621
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-6-323G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026621 | ||||||
| chr2:128026750
|
C | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(247): Show | 251 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.-6-452G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026750 | ||||||
| chr2:128026832
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG02258.hp1 HG03041.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-534G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026832 | ||||||
| chr2:128026838
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-6-540A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026838 | ||||||
| chr2:128026944
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-6-646C>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128026944 | ||||||
| chr2:128027017
|
C | A | 2 | a0001c0007t0005g0313a0001c0007t0005g0314 | 2 | HG01175.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-6-719G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027017 | ||||||
| chr2:128027057
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-6-759C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027057 | ||||||
| chr2:128027293
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-7+647G>A | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027293 | ||||||
| chr2:128027389
|
G | A | 1 | a0001c0004t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7+551C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027389 | ||||||
| chr2:128027397
|
C | A | 9 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(6): Show | 9 | HG00735.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+543G>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027397 | ||||||
| chr2:128027409
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-7+531A>G | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027409 | ||||||
| chr2:128027605
|
C | G | 1 | a0001c0002t0001g0007 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-7+335G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027605 | ||||||
| chr2:128027622
|
GCCGCCCG others(5): Show |
G | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-7+306_-7+317delGC others(10): Show |
SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027622 | ||||||
| chr2:128027656
|
G | A | 1 | a0001c0010t0001g0327 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-7+284C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027656 | ||||||
| chr2:128027664
|
G | A | 1 | a0001c0011t0013g0328 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-7+276C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027664 | ||||||
| chr2:128027720
|
T | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-7+220A>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027720 | ||||||
| chr2:128027772
|
C | G | 1 | a0001c0001t0004g0006 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-7+168G>C | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027772 | ||||||
| chr2:128027798
|
G | A | 11 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(8): Show | 11 | HG02055.hp1 HG02572.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7+142C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027798 | ||||||
| chr2:128027846
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-7+94C>T | SAP130 | ENSG00000136715.19 | transcript | ENST00000643581.2 | protein_coding | 1/20 | chr2 | 128027846 |