Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6450 |
|---|---|
| ensemblid | ENSG00000185437.16 |
| hgncid | 10822 |
| symbol | SH3BGR |
| name | SH3 domain binding glutamate rich protein |
| refseq_nuc | NM_007341.3 |
| refseq_prot | NP_031367.2 |
| ensembl_nuc | ENST00000333634.10 |
| ensembl_prot | ENSP00000332513.5 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 39451970 |
| end | 39515504 |
| strand | + |
| ver | v1.2 |
| region | chr21:39451970-39515504 |
| region5000 | chr21:39446970-39520504 |
| regionname0 | SH3BGR_chr21_39451970_39515504 |
| regionname5000 | SH3BGR_chr21_39446970_39520504 |
| 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 | 0/0 | 177 | 159 | 46 | 29 | 55 | 9 | 20 | 39 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0002 | 1/1 | 176 | 135 | 30 | 27 | 51 | 6 | 19 | 39 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0003 | 0/0 | 177 | 6 | 3 | 2 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0004 | 0/0 | 176 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0005 | 0/0 | 177 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 534 | 159 | 46 | 29 | 55 | 9 | 20 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| c0002 | 1/1 | 531 | 135 | 30 | 27 | 51 | 6 | 19 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| c0003 | 0/0 | 534 | 6 | 3 | 2 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| c0004 | 0/0 | 531 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| c0005 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 579 | 227 | 41 | 39 | 99 | 13 | 35 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0002 | 0/1 | 579 | 37 | 12 | 12 | 5 | 3 | 4 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0003 | 0/0 | 578 | 11 | 11 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0004 | 0/0 | 578 | 8 | 4 | 3 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0005 | 0/0 | 579 | 7 | 7 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0006 | 0/0 | 579 | 5 | 5 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0007 | 1/0 | 579 | 3 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0008 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0009 | 0/0 | 579 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0010 | 0/0 | 579 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| t0011 | 0/0 | 579 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 534 | 159 | 46 | 29 | 55 | 9 | 20 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0002c0002 | 1/1 | 531 | 135 | 30 | 27 | 51 | 6 | 19 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0003c0003 | 0/0 | 534 | 6 | 3 | 2 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0004c0004 | 0/0 | 531 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0005c0005 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1112 | 128 | 20 | 25 | 54 | 9 | 20 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0002 | 0/0 | 1112 | 3 | 2 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0003 | 0/0 | 1111 | 10 | 10 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0004 | 0/0 | 1111 | 3 | 2 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0005 | 0/0 | 1112 | 7 | 7 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0006 | 0/0 | 1112 | 5 | 5 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0009 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0010 | 0/0 | 1112 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0001c0001t0011 | 0/0 | 1112 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0002c0002t0001 | 0/0 | 1109 | 97 | 20 | 14 | 45 | 3 | 15 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0002c0002t0002 | 0/1 | 1109 | 34 | 10 | 11 | 5 | 3 | 4 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0002c0002t0007 | 1/0 | 1109 | 3 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0002c0002t0008 | 0/0 | 1109 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0003c0003t0003 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0003c0003t0004 | 0/0 | 1111 | 5 | 2 | 2 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0004c0004t0001 | 0/0 | 1109 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| a0005c0005t0001 | 0/0 | 1112 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | copy fasta | chr21 | 39446970 | 39520504 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0256 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0007g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0007g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0002c0002t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0003c0003t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0004c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| a0005c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00140 | hp1 | a0004 | c0004 | t0001 | g0209 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0253 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0208 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0086 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00642 | hp1 | a0003 | c0003 | t0004 | g0242 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0271 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG00735 | hp2 | a0003 | c0003 | t0004 | g0280 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01074 | hp2 | a0001 | c0001 | t0011 | g0075 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0254 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0279 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0265 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01358 | hp2 | a0002 | c0002 | t0007 | g0144 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0255 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0257 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01433 | hp2 | a0002 | c0002 | t0007 | g0145 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0278 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0277 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | IBS | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0272 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02074 | hp2 | a0002 | c0002 | t0008 | g0157 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | KHV | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0168 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | CDX | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PEL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02630 | hp1 | a0003 | c0003 | t0004 | g0281 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02717 | hp2 | a0003 | c0003 | t0004 | g0244 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0273 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0258 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0275 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0220 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0248 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0262 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0223 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03209 | hp1 | a0005 | c0005 | t0001 | g0225 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0239 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0227 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | GWD | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0263 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | MSL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03688 | hp2 | a0003 | c0003 | t0004 | g0243 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0214 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0252 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0161 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | STU | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0249 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | CHB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19010 | hp2 | a0001 | c0001 | t0010 | g0137 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ASW | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | TSI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0014 | EUR | TSI | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0207 | SAS | GIH | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | GIH | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0240 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | USA | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | LWK | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0256 | REF | REF | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0007 | g0148 | REF | REF | SH3BGR_chr21_39446970_39520504 | SH3BGR | chr21 | 39446970 | 39520504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39499884
|
T | C | 2 | a0001a0004 | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
missense_variant | MODERATE | c.374T>C | p.Val125Ala | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/7 | 501/1109 | 374/531 | 125/176 | chr21 | 39499884 | ||
| chr21:39511719
|
G | A | 1 | a0005 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.475G>A | p.Glu159Lys | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/7 | 602/1109 | 475/531 | 159/176 | chr21 | 39511719 | ||
| chr21:39511744
|
G | GAGA | 3 | a0001a0003a0005 | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
disruptive_inframe_insertion | MODERATE | c.504_506dupAGA | p.Glu169dup | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/7 | 634/1109 | 507/531 | 169/176 | INFO_REALIGN_3_PRIME | chr21 | 39511744 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39451976
|
C | G | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(2): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-121C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | 121 | chr21 | 39451976 | |||||
| chr21:39451977
|
C | T | 1 | a0001c0001t0011 | 1 | HG01074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-120C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | 120 | chr21 | 39451977 | |||||
| chr21:39452055
|
G | A | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | 42 | chr21 | 39452055 | |||||
| chr21:39452064
|
G | A | 1 | a0002c0002t0008 | 1 | HG02074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/7 | chr21 | 39452064 | ||||||
| chr21:39511785
|
T | C | 4 | a0001c0001t0003a0001c0001t0004a0003c0003t0003others(1): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/7 | 10 | chr21 | 39511785 | |||||
| chr21:39515258
|
C | A | 4 | a0001c0001t0003a0001c0001t0004a0003c0003t0003others(1): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3483 | chr21 | 39515258 | |||||
| chr21:39515296
|
T | C | 1 | a0001c0001t0009 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*243T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3521 | chr21 | 39515296 | |||||
| chr21:39515303
|
AT | A | 4 | a0001c0001t0003a0001c0001t0004a0003c0003t0003others(1): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*259delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3537 | INFO_REALIGN_3_PRIME | chr21 | 39515303 | ||||
| chr21:39515423
|
T | C | 2 | a0001c0001t0005a0001c0001t0006 | 12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*370T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3648 | chr21 | 39515423 | |||||
| chr21:39515434
|
A | T | 1 | a0001c0001t0010 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*381A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 7/7 | 3659 | chr21 | 39515434 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:39452210
|
A | G | 1 | a0001c0001t0001g0282 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.45+69A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452210 | ||||||
| chr21:39452235
|
C | T | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+94C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452235 | ||||||
| chr21:39452557
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+416G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452557 | ||||||
| chr21:39452567
|
T | G | 1 | a0002c0002t0002g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.45+426T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452567 | ||||||
| chr21:39452705
|
A | G | 5 | a0001c0001t0006g0016a0001c0001t0006g0234a0001c0001t0006g0235others(2): Show | 6 | HG02280.hp2 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+564A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452705 | ||||||
| chr21:39452716
|
C | T | 1 | a0001c0001t0003g0233 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.45+575C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452716 | ||||||
| chr21:39452806
|
C | A | 1 | a0002c0002t0002g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.45+665C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39452806 | ||||||
| chr21:39453017
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45+876G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453017 | ||||||
| chr21:39453084
|
T | A | 1 | a0002c0002t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+943T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453084 | ||||||
| chr21:39453326
|
C | T | 1 | a0003c0003t0004g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+1185C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453326 | ||||||
| chr21:39453402
|
TA | T | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+1268delA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39453402 | |||||
| chr21:39453409
|
A | T | 4 | a0001c0001t0002g0238a0001c0001t0004g0019a0001c0001t0004g0232others(1): Show | 5 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+1268A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453409 | ||||||
| chr21:39453525
|
A | G | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.45+1384A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453525 | ||||||
| chr21:39453620
|
T | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.45+1479T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453620 | ||||||
| chr21:39453629
|
T | C | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+1488T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453629 | ||||||
| chr21:39453824
|
G | T | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.45+1683G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453824 | ||||||
| chr21:39453882
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.45+1741A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453882 | ||||||
| chr21:39453957
|
A | G | 1 | a0002c0002t0001g0227 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.45+1816A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39453957 | ||||||
| chr21:39454038
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(222): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.45+1897A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454038 | ||||||
| chr21:39454089
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(223): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.45+1948A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454089 | ||||||
| chr21:39454137
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(245): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.45+1996A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454137 | ||||||
| chr21:39454198
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.45+2057A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454198 | ||||||
| chr21:39454379
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(248): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.45+2238G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454379 | ||||||
| chr21:39454574
|
C | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023 | 4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+2433C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454574 | ||||||
| chr21:39454600
|
G | A | 1 | a0001c0001t0005g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45+2459G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454600 | ||||||
| chr21:39454680
|
C | G | 1 | a0003c0003t0004g0280 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.45+2539C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454680 | ||||||
| chr21:39454689
|
T | C | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+2548T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454689 | ||||||
| chr21:39454849
|
G | A | 1 | a0002c0002t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.45+2708G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454849 | ||||||
| chr21:39454981
|
A | C | 6 | a0001c0001t0001g0169a0002c0002t0001g0166a0002c0002t0001g0167others(3): Show | 6 | HG01255.hp1 HG01346.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+2840A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39454981 | ||||||
| chr21:39455022
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45+2881G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455022 | ||||||
| chr21:39455416
|
G | A | 3 | a0001c0001t0004g0019a0001c0001t0004g0232a0002c0002t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+3275G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455416 | ||||||
| chr21:39455430
|
G | A | 43 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(40): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.45+3289G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455430 | ||||||
| chr21:39455656
|
G | A | 50 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(47): Show | 53 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.45+3515G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455656 | ||||||
| chr21:39455804
|
G | A | 6 | a0001c0001t0004g0245a0003c0003t0004g0242a0003c0003t0004g0243others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+3663G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455804 | ||||||
| chr21:39455811
|
A | T | 7 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(4): Show | 7 | HG00438.hp1 NA18983.hp2 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+3670A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39455811 | ||||||
| chr21:39456011
|
C | T | 49 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+3870C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456011 | ||||||
| chr21:39456219
|
C | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.45+4078C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456219 | ||||||
| chr21:39456330
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.45+4189C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456330 | ||||||
| chr21:39456456
|
T | C | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+4315T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456456 | ||||||
| chr21:39456526
|
A | G | 49 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+4385A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456526 | ||||||
| chr21:39456557
|
G | C | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.45+4416G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456557 | ||||||
| chr21:39456572
|
T | C | 49 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+4431T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456572 | ||||||
| chr21:39456574
|
G | A | 8 | a0002c0002t0001g0004a0002c0002t0001g0024a0002c0002t0001g0025others(5): Show | 9 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+4433G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456574 | ||||||
| chr21:39456625
|
A | AT | 49 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.45+4484_45+4485ins others(1): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39456625 | ||||||
| chr21:39456940
|
GTTAA | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.45+4804_45+4807del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39456940 | |||||
| chr21:39457142
|
A | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(224): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.45+5001A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457142 | ||||||
| chr21:39457231
|
TAA | T | 3 | a0001c0001t0004g0019a0001c0001t0004g0232a0002c0002t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+5092_45+5093del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457231 | |||||
| chr21:39457244
|
C | CTTA | 178 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.45+5108_45+5110dup others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457244 | |||||
| chr21:39457244
|
C | CTTATATG others(1): Show |
48 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(45): Show | 51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+5107_45+5108ins others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457244 | |||||
| chr21:39457249
|
T | A | 1 | a0003c0003t0004g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+5108T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457249 | ||||||
| chr21:39457250
|
A | T | 1 | a0003c0003t0004g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+5109A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457250 | ||||||
| chr21:39457289
|
TTATAA | T | 46 | a0001c0001t0002g0238a0001c0001t0002g0251a0001c0001t0002g0276others(43): Show | 48 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.46-5081_46-5077del others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457289 | |||||
| chr21:39457317
|
A | G | 43 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(40): Show | 48 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.46-5058A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457317 | ||||||
| chr21:39457372
|
AGATTATT others(121): Show |
A | 4 | a0001c0001t0006g0016a0001c0001t0006g0234a0001c0001t0006g0235others(1): Show | 5 | HG02280.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-4932_46-4805del | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457372 | |||||
| chr21:39457449
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.46-4926T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457449 | ||||||
| chr21:39457460
|
AT | A | 44 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(41): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.46-4913delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457460 | |||||
| chr21:39457478
|
ATATATAT others(36): Show |
A | 2 | a0002c0002t0002g0246a0002c0002t0002g0247 | 2 | NA18950.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.46-4875_46-4833del others(43): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39457478 | |||||
| chr21:39457500
|
T | A | 1 | a0002c0002t0001g0227 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.46-4875T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457500 | ||||||
| chr21:39457856
|
T | C | 2 | a0001c0001t0003g0173a0002c0002t0002g0015 | 3 | HG01257.hp2 HG01258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.46-4519T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457856 | ||||||
| chr21:39457880
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.46-4495G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457880 | ||||||
| chr21:39457901
|
G | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46-4474G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457901 | ||||||
| chr21:39457938
|
A | C | 1 | a0001c0001t0005g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-4437A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457938 | ||||||
| chr21:39457960
|
A | G | 3 | a0002c0002t0002g0277a0002c0002t0002g0278a0002c0002t0002g0279 | 3 | HG01169.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.46-4415A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39457960 | ||||||
| chr21:39458015
|
G | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.46-4360G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458015 | ||||||
| chr21:39458096
|
G | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(244): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.46-4279G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458096 | ||||||
| chr21:39458135
|
A | G | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.46-4240A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458135 | ||||||
| chr21:39458206
|
GCT | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.46-4166_46-4165del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39458206 | |||||
| chr21:39458350
|
A | T | 48 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0019others(45): Show | 51 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.46-4025A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458350 | ||||||
| chr21:39458351
|
A | T | 3 | a0001c0001t0004g0019a0001c0001t0004g0232a0002c0002t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-4024A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458351 | ||||||
| chr21:39458412
|
C | T | 3 | a0001c0001t0004g0019a0001c0001t0004g0232a0002c0002t0002g0015 | 4 | HG01257.hp2 HG01258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3963C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458412 | ||||||
| chr21:39458431
|
C | T | 1 | a0001c0001t0002g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.46-3944C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458431 | ||||||
| chr21:39458499
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-3876A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458499 | ||||||
| chr21:39458532
|
T | C | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.46-3843T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458532 | ||||||
| chr21:39458544
|
G | A | 45 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(42): Show | 47 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.46-3831G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458544 | ||||||
| chr21:39458603
|
G | C | 2 | a0002c0002t0002g0277a0002c0002t0002g0278 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.46-3772G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458603 | ||||||
| chr21:39458647
|
C | CT | 8 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(5): Show | 8 | HG02698.hp2 HG03130.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-3711dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39458647 | |||||
| chr21:39458647
|
C | CTT | 43 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(40): Show | 45 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.46-3712_46-3711dup others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39458647 | |||||
| chr21:39458772
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-3603A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458772 | ||||||
| chr21:39458795
|
C | T | 3 | a0002c0002t0001g0020a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.46-3580C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458795 | ||||||
| chr21:39458835
|
C | T | 1 | a0002c0002t0001g0224 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-3540C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458835 | ||||||
| chr21:39458839
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-3536G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39458839 | ||||||
| chr21:39459009
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023 | 4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3366A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459009 | ||||||
| chr21:39459624
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.46-2751C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459624 | ||||||
| chr21:39459690
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.46-2685C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459690 | ||||||
| chr21:39459720
|
T | C | 1 | a0002c0002t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.46-2655T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459720 | ||||||
| chr21:39459775
|
G | T | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-2600G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459775 | ||||||
| chr21:39459996
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.46-2379A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39459996 | ||||||
| chr21:39460062
|
G | A | 8 | a0002c0002t0001g0004a0002c0002t0001g0024a0002c0002t0001g0025others(5): Show | 9 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.46-2313G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460062 | ||||||
| chr21:39460095
|
A | G | 6 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-2280A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460095 | ||||||
| chr21:39460306
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.46-2069G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460306 | ||||||
| chr21:39460439
|
T | C | 49 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.46-1936T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460439 | ||||||
| chr21:39460520
|
C | T | 40 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(37): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.46-1855C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460520 | ||||||
| chr21:39460630
|
C | T | 97 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(94): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.46-1745C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460630 | ||||||
| chr21:39460650
|
A | G | 1 | a0002c0002t0001g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.46-1725A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39460650 | ||||||
| chr21:39461082
|
A | G | 3 | a0002c0002t0001g0120a0002c0002t0001g0121a0002c0002t0001g0218 | 3 | HG02080.hp2 NA19009.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.46-1293A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461082 | ||||||
| chr21:39461113
|
T | C | 43 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(40): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.46-1262T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461113 | ||||||
| chr21:39461135
|
A | AT | 26 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(23): Show | 26 | HG01109.hp1 HG01243.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.46-1220dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39461135 | |||||
| chr21:39461135
|
AT | A | 54 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0133others(51): Show | 57 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.46-1220delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr21 | 39461135 | |||||
| chr21:39461231
|
G | C | 1 | a0002c0002t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.46-1144G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461231 | ||||||
| chr21:39461261
|
C | T | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-1114C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461261 | ||||||
| chr21:39461438
|
T | C | 2 | a0001c0001t0006g0234a0001c0001t0006g0235 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-937T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461438 | ||||||
| chr21:39461760
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.46-615G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461760 | ||||||
| chr21:39461836
|
A | T | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-539A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461836 | ||||||
| chr21:39461994
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.46-381G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39461994 | ||||||
| chr21:39462057
|
C | A | 1 | a0002c0002t0001g0215 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46-318C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462057 | ||||||
| chr21:39462138
|
C | T | 2 | a0002c0002t0001g0214a0002c0002t0001g0229 | 2 | HG03139.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.46-237C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462138 | ||||||
| chr21:39462139
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46-236G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462139 | ||||||
| chr21:39462202
|
G | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18954.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.46-173G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462202 | ||||||
| chr21:39462216
|
C | G | 4 | a0002c0002t0001g0032a0002c0002t0001g0033a0002c0002t0001g0105others(1): Show | 4 | HG01884.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-159C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462216 | ||||||
| chr21:39462268
|
C | G | 1 | a0001c0001t0005g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.46-107C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 1/6 | chr21 | 39462268 | ||||||
| chr21:39462710
|
A | G | 49 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.231+150A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39462710 | ||||||
| chr21:39462923
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.231+363A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39462923 | ||||||
| chr21:39462978
|
A | G | 98 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(95): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.231+418A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39462978 | ||||||
| chr21:39463173
|
G | A | 1 | a0002c0002t0007g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.231+613G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463173 | ||||||
| chr21:39463382
|
T | C | 1 | a0002c0002t0001g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.231+822T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463382 | ||||||
| chr21:39463632
|
T | G | 3 | a0002c0002t0001g0220a0002c0002t0001g0221a0002c0002t0001g0222 | 3 | HG01243.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.231+1072T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463632 | ||||||
| chr21:39463897
|
A | G | 98 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(95): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.231+1337A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463897 | ||||||
| chr21:39463940
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.231+1380C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39463940 | ||||||
| chr21:39464442
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.231+1882C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464442 | ||||||
| chr21:39464515
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.231+1955G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464515 | ||||||
| chr21:39464544
|
G | A | 20 | a0001c0001t0002g0251a0002c0002t0002g0017a0002c0002t0002g0018others(17): Show | 22 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.231+1984G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464544 | ||||||
| chr21:39464570
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.231+2010A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464570 | ||||||
| chr21:39464830
|
A | G | 1 | a0002c0002t0001g0218 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.231+2270A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464830 | ||||||
| chr21:39464856
|
A | G | 1 | a0002c0002t0001g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.231+2296A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464856 | ||||||
| chr21:39464948
|
G | T | 43 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(40): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.231+2388G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464948 | ||||||
| chr21:39464950
|
A | C | 98 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(95): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.231+2390A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39464950 | ||||||
| chr21:39465342
|
T | C | 98 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(95): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.231+2782T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465342 | ||||||
| chr21:39465344
|
G | A | 1 | a0002c0002t0007g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.231+2784G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465344 | ||||||
| chr21:39465418
|
G | T | 3 | a0002c0002t0001g0020a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.231+2858G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465418 | ||||||
| chr21:39465475
|
C | A | 49 | a0001c0001t0002g0251a0001c0001t0002g0276a0001c0001t0004g0245others(46): Show | 52 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.231+2915C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465475 | ||||||
| chr21:39465781
|
A | G | 43 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(40): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.231+3221A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465781 | ||||||
| chr21:39465892
|
C | T | 40 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(37): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+3332C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465892 | ||||||
| chr21:39465925
|
G | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+3365G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465925 | ||||||
| chr21:39465944
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+3384C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39465944 | ||||||
| chr21:39466241
|
C | G | 97 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(94): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.231+3681C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39466241 | ||||||
| chr21:39466516
|
A | G | 97 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(94): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.231+3956A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39466516 | ||||||
| chr21:39466900
|
A | AT | 7 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0102others(4): Show | 8 | HG00558.hp2 HG00673.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+4350dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39466900 | |||||
| chr21:39466900
|
A | ATT | 40 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(37): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.231+4349_231+4350d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39466900 | |||||
| chr21:39467041
|
T | C | 1 | a0003c0003t0004g0242 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.231+4481T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467041 | ||||||
| chr21:39467136
|
C | T | 1 | a0002c0002t0001g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.231+4576C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467136 | ||||||
| chr21:39467258
|
A | AT | 54 | a0001c0001t0001g0219a0001c0001t0002g0238a0001c0001t0002g0251others(51): Show | 57 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.231+4707dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39467258 | |||||
| chr21:39467296
|
G | T | 40 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(37): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+4736G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467296 | ||||||
| chr21:39467704
|
T | G | 40 | a0001c0001t0001g0187a0001c0001t0001g0203a0001c0001t0001g0212others(37): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.231+5144T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467704 | ||||||
| chr21:39467743
|
G | A | 1 | a0002c0002t0001g0186 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.231+5183G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467743 | ||||||
| chr21:39467747
|
A | G | 2 | a0002c0002t0002g0260a0002c0002t0002g0261 | 2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.231+5187A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467747 | ||||||
| chr21:39467822
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+5262C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467822 | ||||||
| chr21:39467853
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.231+5293A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467853 | ||||||
| chr21:39467896
|
C | A | 1 | a0001c0001t0001g0035 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.231+5336C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39467896 | ||||||
| chr21:39468282
|
T | C | 11 | a0001c0001t0005g0241a0002c0002t0001g0004a0002c0002t0001g0024others(8): Show | 12 | HG00639.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.231+5722T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468282 | ||||||
| chr21:39468596
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(8): Show | 12 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+6036A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468596 | ||||||
| chr21:39468678
|
A | G | 113 | a0001c0001t0001g0011a0001c0001t0001g0098a0001c0001t0001g0109others(110): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.231+6118A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468678 | ||||||
| chr21:39468701
|
C | T | 30 | a0001c0001t0001g0097a0001c0001t0001g0169a0001c0001t0001g0213others(27): Show | 32 | HG00408.hp1 HG01255.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.231+6141C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468701 | ||||||
| chr21:39468889
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.232-6246T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468889 | ||||||
| chr21:39468928
|
C | T | 8 | a0002c0002t0001g0188a0002c0002t0002g0252a0002c0002t0002g0259others(5): Show | 8 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.232-6207C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468928 | ||||||
| chr21:39468952
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.232-6183T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39468952 | ||||||
| chr21:39469011
|
G | GT | 38 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(35): Show | 39 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.232-6108dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39469011 | |||||
| chr21:39469011
|
GT | G | 12 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0122others(9): Show | 12 | HG00438.hp1 HG01169.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.232-6108delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39469011 | |||||
| chr21:39469027
|
TG | T | 4 | a0001c0001t0004g0019a0002c0002t0002g0249a0002c0002t0002g0272others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-6107delG | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469027 | ||||||
| chr21:39469174
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.232-5961C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469174 | ||||||
| chr21:39469220
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0003g0003a0001c0001t0003g0022others(9): Show | 13 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.232-5915C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469220 | ||||||
| chr21:39469277
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.232-5858T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469277 | ||||||
| chr21:39469353
|
G | A | 95 | a0001c0001t0004g0245a0001c0001t0005g0241a0001c0001t0005g0264others(92): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.232-5782G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469353 | ||||||
| chr21:39469387
|
C | G | 1 | a0001c0001t0001g0094 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.232-5748C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469387 | ||||||
| chr21:39469587
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.232-5548A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469587 | ||||||
| chr21:39469629
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-5506T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469629 | ||||||
| chr21:39469638
|
TA | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.232-5494delA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39469638 | |||||
| chr21:39469639
|
A | T | 111 | a0001c0001t0001g0109a0001c0001t0001g0226a0001c0001t0002g0238others(108): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.232-5496A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469639 | ||||||
| chr21:39469803
|
C | T | 2 | a0002c0002t0002g0262a0002c0002t0002g0263 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.232-5332C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469803 | ||||||
| chr21:39469811
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.232-5324C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469811 | ||||||
| chr21:39469858
|
G | A | 18 | a0002c0002t0001g0040a0002c0002t0002g0017a0002c0002t0002g0239others(15): Show | 19 | HG00280.hp2 HG01070.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.232-5277G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469858 | ||||||
| chr21:39469943
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-5192G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469943 | ||||||
| chr21:39469947
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.232-5188T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39469947 | ||||||
| chr21:39470019
|
A | C | 1 | a0002c0002t0007g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.232-5116A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470019 | ||||||
| chr21:39470022
|
T | C | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.232-5113T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470022 | ||||||
| chr21:39470104
|
C | G | 1 | a0001c0001t0001g0093 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.232-5031C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470104 | ||||||
| chr21:39470337
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-4798C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470337 | ||||||
| chr21:39470371
|
G | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG01175.hp2 HG01261.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-4764G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470371 | ||||||
| chr21:39470534
|
T | C | 95 | a0001c0001t0005g0241a0001c0001t0005g0264a0001c0001t0005g0266others(92): Show | 104 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.232-4601T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470534 | ||||||
| chr21:39470591
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-4544A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470591 | ||||||
| chr21:39470742
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-4393T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39470742 | ||||||
| chr21:39471170
|
TTAA | T | 41 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0013others(38): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.232-3959_232-3957d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39471170 | |||||
| chr21:39471224
|
C | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.232-3911C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471224 | ||||||
| chr21:39471308
|
G | A | 130 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(127): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.232-3827G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471308 | ||||||
| chr21:39471310
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0184 | 3 | HG02922.hp2 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.232-3825G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471310 | ||||||
| chr21:39471319
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.232-3816C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471319 | ||||||
| chr21:39471379
|
G | A | 130 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(127): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.232-3756G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471379 | ||||||
| chr21:39471599
|
GTTGT | G | 107 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(104): Show | 117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.232-3517_232-3514d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39471599 | |||||
| chr21:39471622
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.232-3513A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471622 | ||||||
| chr21:39471638
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.232-3497T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471638 | ||||||
| chr21:39471639
|
A | T | 1 | a0002c0002t0002g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.232-3496A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471639 | ||||||
| chr21:39471777
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 119 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.232-3358A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471777 | ||||||
| chr21:39471811
|
G | A | 6 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-3324G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39471811 | ||||||
| chr21:39472033
|
C | T | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.232-3102C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472033 | ||||||
| chr21:39472166
|
CAG | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.232-2967_232-2966d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39472166 | |||||
| chr21:39472170
|
A | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.232-2965A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472170 | ||||||
| chr21:39472354
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-2781A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472354 | ||||||
| chr21:39472374
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.232-2761T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472374 | ||||||
| chr21:39472819
|
T | C | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.232-2316T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472819 | ||||||
| chr21:39472889
|
CAT | C | 6 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-2245_232-2244d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472889 | ||||||
| chr21:39472917
|
A | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.232-2218A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39472917 | ||||||
| chr21:39473326
|
T | G | 2 | a0001c0001t0001g0092a0001c0001t0002g0251 | 2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.232-1809T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39473326 | ||||||
| chr21:39473700
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.232-1435C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39473700 | ||||||
| chr21:39473884
|
C | CA | 137 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(134): Show | 148 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.232-1240dupA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39473884 | |||||
| chr21:39473884
|
C | CAA | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.232-1241_232-1240d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39473884 | |||||
| chr21:39473994
|
G | T | 1 | a0002c0002t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.232-1141G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39473994 | ||||||
| chr21:39474032
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232-1103A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474032 | ||||||
| chr21:39474258
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.232-877G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474258 | ||||||
| chr21:39474281
|
G | C | 1 | a0002c0002t0001g0204 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.232-854G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474281 | ||||||
| chr21:39474685
|
C | T | 1 | a0002c0002t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.232-450C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474685 | ||||||
| chr21:39474735
|
A | G | 1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.232-400A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474735 | ||||||
| chr21:39474745
|
C | G | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.232-390C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474745 | ||||||
| chr21:39474881
|
A | G | 6 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-254A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39474881 | ||||||
| chr21:39474890
|
G | GGT | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.232-229_232-228dup others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr21 | 39474890 | |||||
| chr21:39475085
|
T | C | 96 | a0001c0001t0005g0241a0001c0001t0005g0264a0001c0001t0005g0266others(93): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.232-50T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 2/6 | chr21 | 39475085 | ||||||
| chr21:39475270
|
A | G | 39 | a0001c0001t0005g0264a0001c0001t0005g0266a0001c0001t0005g0267others(36): Show | 42 | HG00280.hp2 HG00642.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.312+55A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475270 | ||||||
| chr21:39475280
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.312+65G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475280 | ||||||
| chr21:39475293
|
T | C | 1 | a0002c0002t0001g0193 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.312+78T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475293 | ||||||
| chr21:39475323
|
T | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.312+108T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475323 | ||||||
| chr21:39475439
|
C | A | 1 | a0002c0002t0002g0253 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.312+224C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475439 | ||||||
| chr21:39475465
|
G | T | 3 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023 | 4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+250G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475465 | ||||||
| chr21:39475509
|
A | G | 3 | a0002c0002t0001g0220a0002c0002t0001g0221a0002c0002t0001g0222 | 3 | HG01243.hp2 HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.312+294A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475509 | ||||||
| chr21:39475610
|
C | A | 1 | a0001c0001t0001g0110 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.312+395C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475610 | ||||||
| chr21:39475688
|
C | T | 41 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0013others(38): Show | 46 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.312+473C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39475688 | ||||||
| chr21:39476153
|
G | A | 2 | a0001c0001t0006g0234a0001c0001t0006g0235 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.312+938G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476153 | ||||||
| chr21:39476248
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.312+1033T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476248 | ||||||
| chr21:39476579
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.312+1364G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476579 | ||||||
| chr21:39476673
|
G | A | 1 | a0002c0002t0002g0239 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.312+1458G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476673 | ||||||
| chr21:39476694
|
C | T | 1 | a0002c0002t0002g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.312+1479C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476694 | ||||||
| chr21:39476741
|
T | C | 131 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(128): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.312+1526T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476741 | ||||||
| chr21:39476935
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+1720A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39476935 | ||||||
| chr21:39477501
|
A | G | 12 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(9): Show | 13 | HG01168.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.312+2286A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477501 | ||||||
| chr21:39477515
|
T | C | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+2300T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477515 | ||||||
| chr21:39477595
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+2380G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477595 | ||||||
| chr21:39477625
|
C | T | 6 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+2410C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477625 | ||||||
| chr21:39477779
|
A | G | 12 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(9): Show | 13 | HG01168.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.312+2564A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477779 | ||||||
| chr21:39477963
|
C | A | 9 | a0002c0002t0001g0014a0002c0002t0001g0123a0002c0002t0001g0124others(6): Show | 10 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+2748C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39477963 | ||||||
| chr21:39478167
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.312+2952C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478167 | ||||||
| chr21:39478373
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 5 | HG02083.hp1 NA18950.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.312+3158C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478373 | ||||||
| chr21:39478463
|
A | G | 1 | a0002c0002t0001g0215 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.312+3248A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478463 | ||||||
| chr21:39478481
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | NA18982.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.312+3266T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478481 | ||||||
| chr21:39478498
|
G | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(240): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.312+3283G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478498 | ||||||
| chr21:39478520
|
G | A | 1 | a0002c0002t0001g0193 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.312+3305G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478520 | ||||||
| chr21:39478561
|
G | A | 1 | a0001c0001t0003g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312+3346G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478561 | ||||||
| chr21:39478602
|
G | A | 18 | a0002c0002t0001g0012a0002c0002t0001g0039a0002c0002t0001g0120others(15): Show | 19 | HG00558.hp2 HG00673.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.312+3387G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39478602 | ||||||
| chr21:39479101
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.312+3886G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479101 | ||||||
| chr21:39479224
|
GGGT | G | 4 | a0001c0001t0001g0146a0001c0001t0001g0282a0001c0001t0002g0276others(1): Show | 4 | HG02895.hp2 HG03225.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+4041_312+4043d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479224 | |||||
| chr21:39479224
|
GGGTGGTG others(5): Show |
G | 1 | a0002c0002t0001g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.312+4032_312+4043d others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479224 | |||||
| chr21:39479226
|
G | GTGGTGAT others(5): Show |
4 | a0001c0001t0001g0109a0002c0002t0001g0032a0003c0003t0004g0243others(1): Show | 4 | HG01884.hp2 HG02630.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+4016_312+4017i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479226 | |||||
| chr21:39479226
|
G | GTGGTGGT others(5): Show |
2 | a0001c0001t0005g0241a0002c0002t0001g0025 | 2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.312+4022_312+4023i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479226 | |||||
| chr21:39479229
|
G | A | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312+4014G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479229 | ||||||
| chr21:39479229
|
G | GTGGTGGT others(8): Show |
10 | a0001c0001t0001g0116a0001c0001t0003g0022a0001c0001t0003g0119others(7): Show | 10 | HG01168.hp2 HG01361.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+4028_312+4029i others(17): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479229 | |||||
| chr21:39479232
|
G | A | 12 | a0001c0001t0001g0034a0001c0001t0001g0046a0001c0001t0001g0092others(9): Show | 12 | HG00642.hp1 HG01175.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.312+4017G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479232 | ||||||
| chr21:39479238
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(82): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312+4023G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479238 | ||||||
| chr21:39479241
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0001t0001g0185others(1): Show | 5 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+4026G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479241 | ||||||
| chr21:39479244
|
G | C | 6 | a0001c0001t0005g0241a0002c0002t0001g0025a0002c0002t0001g0032others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.312+4029G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479244 | ||||||
| chr21:39479244
|
G | GTGGTGGT others(5): Show |
1 | a0001c0001t0004g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.312+4040_312+4041i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479244 | |||||
| chr21:39479304
|
ATGGTGGT others(58): Show |
A | 7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.312+4111_312+4175d others(67): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479304 | |||||
| chr21:39479369
|
G | GTGGTGGT others(53): Show |
2 | a0001c0001t0003g0119a0001c0001t0003g0233 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312+4207_312+4208i others(62): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479369 | |||||
| chr21:39479490
|
T | C | 1 | a0002c0002t0001g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.312+4275T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479490 | ||||||
| chr21:39479630
|
T | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.312+4415T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479630 | ||||||
| chr21:39479724
|
G | A | 1 | a0003c0003t0003g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.312+4509G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479724 | ||||||
| chr21:39479858
|
C | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(142): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.312+4643C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479858 | ||||||
| chr21:39479864
|
C | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+4649C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479864 | ||||||
| chr21:39479865
|
AT | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.312+4660delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39479865 | |||||
| chr21:39479932
|
T | A | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+4717T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479932 | ||||||
| chr21:39479979
|
A | C | 2 | a0002c0002t0002g0260a0002c0002t0002g0261 | 2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.312+4764A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39479979 | ||||||
| chr21:39480150
|
A | G | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.312+4935A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480150 | ||||||
| chr21:39480323
|
A | G | 1 | a0002c0002t0001g0032 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.312+5108A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480323 | ||||||
| chr21:39480407
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.312+5192C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480407 | ||||||
| chr21:39480411
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+5196A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480411 | ||||||
| chr21:39480534
|
G | T | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.312+5319G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480534 | ||||||
| chr21:39480570
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.312+5355G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480570 | ||||||
| chr21:39480574
|
G | A | 1 | a0002c0002t0002g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.312+5359G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480574 | ||||||
| chr21:39480589
|
A | G | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+5374A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480589 | ||||||
| chr21:39480650
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0129 | 2 | NA18954.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.312+5435G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39480650 | ||||||
| chr21:39481163
|
C | T | 2 | a0002c0002t0002g0277a0002c0002t0002g0278 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.312+5948C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481163 | ||||||
| chr21:39481206
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.312+5991T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481206 | ||||||
| chr21:39481588
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.312+6373C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481588 | ||||||
| chr21:39481669
|
A | AAATTAAT others(31): Show |
1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+6465_312+6466i others(40): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39481669 | |||||
| chr21:39481780
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.312+6565C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481780 | ||||||
| chr21:39481886
|
G | A | 4 | a0002c0002t0001g0151a0002c0002t0001g0152a0002c0002t0001g0153others(1): Show | 4 | HG02040.hp2 NA18952.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+6671G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481886 | ||||||
| chr21:39481947
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.312+6732A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39481947 | ||||||
| chr21:39482021
|
G | GT | 14 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0003g0099others(11): Show | 15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.312+6807dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39482021 | |||||
| chr21:39482245
|
C | T | 1 | a0002c0002t0001g0190 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.312+7030C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482245 | ||||||
| chr21:39482313
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.312+7098A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482313 | ||||||
| chr21:39482384
|
T | C | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+7169T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482384 | ||||||
| chr21:39482574
|
G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+7359G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482574 | ||||||
| chr21:39482576
|
T | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.312+7361T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482576 | ||||||
| chr21:39482826
|
C | T | 14 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0003g0099others(11): Show | 15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.312+7611C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482826 | ||||||
| chr21:39482951
|
G | A | 1 | a0002c0002t0001g0009 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.312+7736G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39482951 | ||||||
| chr21:39483028
|
T | C | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+7813T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39483028 | ||||||
| chr21:39483331
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+8116A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39483331 | ||||||
| chr21:39483371
|
C | T | 1 | a0001c0001t0003g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312+8156C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39483371 | ||||||
| chr21:39484031
|
G | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+8816G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484031 | ||||||
| chr21:39484361
|
C | T | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.312+9146C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484361 | ||||||
| chr21:39484399
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.312+9184T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484399 | ||||||
| chr21:39484433
|
A | T | 1 | a0001c0001t0003g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.312+9218A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484433 | ||||||
| chr21:39484471
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+9256G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484471 | ||||||
| chr21:39484537
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.312+9322C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484537 | ||||||
| chr21:39484538
|
G | A | 1 | a0002c0002t0002g0260 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.312+9323G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39484538 | ||||||
| chr21:39485111
|
G | C | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+9896G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485111 | ||||||
| chr21:39485113
|
T | C | 1 | a0002c0002t0001g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.312+9898T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485113 | ||||||
| chr21:39485427
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+10212T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485427 | ||||||
| chr21:39485437
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.312+10222G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485437 | ||||||
| chr21:39485515
|
C | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+10300C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485515 | ||||||
| chr21:39485597
|
G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.312+10382G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485597 | ||||||
| chr21:39485598
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.312+10383G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485598 | ||||||
| chr21:39485605
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+10390C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485605 | ||||||
| chr21:39485686
|
CT | C | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.312+10490delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39485686 | |||||
| chr21:39485711
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+10496G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485711 | ||||||
| chr21:39485719
|
G | A | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+10504G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485719 | ||||||
| chr21:39485832
|
C | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+10617C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485832 | ||||||
| chr21:39485844
|
C | T | 2 | a0002c0002t0001g0196a0002c0002t0001g0214 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.312+10629C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485844 | ||||||
| chr21:39485889
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.312+10674T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485889 | ||||||
| chr21:39485906
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.312+10691T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485906 | ||||||
| chr21:39485930
|
C | T | 3 | a0002c0002t0002g0249a0002c0002t0002g0272a0002c0002t0002g0273 | 3 | HG02055.hp2 HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.312+10715C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485930 | ||||||
| chr21:39485978
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.312+10763A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485978 | ||||||
| chr21:39485984
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.312+10769G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39485984 | ||||||
| chr21:39486120
|
A | G | 1 | a0001c0001t0009g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.312+10905A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39486120 | ||||||
| chr21:39486830
|
G | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.312+11615G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39486830 | ||||||
| chr21:39486938
|
G | T | 2 | a0001c0001t0005g0269a0001c0001t0005g0270 | 2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.312+11723G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39486938 | ||||||
| chr21:39487168
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.312+11953G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487168 | ||||||
| chr21:39487405
|
A | G | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.312+12190A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487405 | ||||||
| chr21:39487591
|
A | G | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-12232A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487591 | ||||||
| chr21:39487704
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.313-12119A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487704 | ||||||
| chr21:39487782
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-12041G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487782 | ||||||
| chr21:39487787
|
C | T | 2 | a0002c0002t0002g0262a0002c0002t0002g0263 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.313-12036C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39487787 | ||||||
| chr21:39488085
|
T | C | 1 | a0002c0002t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.313-11738T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488085 | ||||||
| chr21:39488351
|
C | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18960.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.313-11472C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488351 | ||||||
| chr21:39488487
|
C | T | 8 | a0001c0001t0005g0264a0001c0001t0005g0266a0001c0001t0005g0267others(5): Show | 9 | HG02257.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-11336C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488487 | ||||||
| chr21:39488577
|
G | A | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-11246G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488577 | ||||||
| chr21:39488579
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG01243.hp1 HG01978.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-11244C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488579 | ||||||
| chr21:39488584
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.313-11239T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488584 | ||||||
| chr21:39488585
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.313-11238T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488585 | ||||||
| chr21:39488658
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-11165C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488658 | ||||||
| chr21:39488758
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-11065T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488758 | ||||||
| chr21:39488890
|
C | T | 14 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0003g0099others(11): Show | 15 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.313-10933C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39488890 | ||||||
| chr21:39489055
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.313-10768G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489055 | ||||||
| chr21:39489173
|
A | G | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.313-10650A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489173 | ||||||
| chr21:39489483
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-10340C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489483 | ||||||
| chr21:39489601
|
G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-10222G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489601 | ||||||
| chr21:39489750
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-10073A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489750 | ||||||
| chr21:39489784
|
C | T | 18 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(15): Show | 19 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.313-10039C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489784 | ||||||
| chr21:39489795
|
C | G | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-10028C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489795 | ||||||
| chr21:39489797
|
C | T | 1 | a0002c0002t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313-10026C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489797 | ||||||
| chr21:39489800
|
A | G | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-10023A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39489800 | ||||||
| chr21:39490023
|
A | T | 1 | a0002c0002t0002g0015 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.313-9800A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490023 | ||||||
| chr21:39490203
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-9620C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490203 | ||||||
| chr21:39490318
|
T | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-9505T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490318 | ||||||
| chr21:39490386
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-9437G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490386 | ||||||
| chr21:39490391
|
G | C | 1 | a0001c0001t0005g0241 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313-9432G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490391 | ||||||
| chr21:39490407
|
A | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.313-9416A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490407 | ||||||
| chr21:39490411
|
G | A | 1 | a0003c0003t0004g0280 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.313-9412G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490411 | ||||||
| chr21:39490603
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-9220A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490603 | ||||||
| chr21:39490653
|
G | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-9170G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490653 | ||||||
| chr21:39490663
|
C | T | 1 | a0002c0002t0002g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.313-9160C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490663 | ||||||
| chr21:39490739
|
AT | A | 12 | a0002c0002t0001g0004a0002c0002t0001g0020a0002c0002t0001g0024others(9): Show | 14 | HG00323.hp1 HG00639.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.313-9067delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39490739 | |||||
| chr21:39490739
|
ATTTT | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.313-9070_313-9067d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39490739 | |||||
| chr21:39490783
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-9040C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490783 | ||||||
| chr21:39490796
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.313-9027A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490796 | ||||||
| chr21:39490834
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8989A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490834 | ||||||
| chr21:39490870
|
C | G | 1 | a0002c0002t0001g0211 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.313-8953C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39490870 | ||||||
| chr21:39491075
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8748A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491075 | ||||||
| chr21:39491158
|
T | TTTTA | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-8645_313-8642d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39491158 | |||||
| chr21:39491187
|
T | A | 1 | a0002c0002t0001g0215 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.313-8636T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491187 | ||||||
| chr21:39491218
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-8605C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491218 | ||||||
| chr21:39491235
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.313-8588C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491235 | ||||||
| chr21:39491297
|
G | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8526G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491297 | ||||||
| chr21:39491511
|
A | G | 3 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023 | 4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-8312A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491511 | ||||||
| chr21:39491594
|
G | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(15): Show | 19 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.313-8229G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491594 | ||||||
| chr21:39491694
|
A | G | 3 | a0002c0002t0002g0015a0002c0002t0002g0265a0002c0002t0002g0275 | 4 | HG01175.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-8129A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491694 | ||||||
| chr21:39491722
|
C | T | 1 | a0002c0002t0001g0147 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.313-8101C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491722 | ||||||
| chr21:39491788
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8035C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491788 | ||||||
| chr21:39491809
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-8014C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491809 | ||||||
| chr21:39491819
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-8004G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491819 | ||||||
| chr21:39491828
|
G | A | 1 | a0002c0002t0001g0194 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.313-7995G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39491828 | ||||||
| chr21:39492288
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-7535G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492288 | ||||||
| chr21:39492440
|
C | G | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-7383C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492440 | ||||||
| chr21:39492443
|
G | GGT | 3 | a0002c0002t0001g0106a0002c0002t0001g0120a0002c0002t0001g0121 | 3 | HG02080.hp2 HG03098.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.313-7357_313-7356d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | |||||
| chr21:39492443
|
G | GGTGGGTG others(3): Show |
1 | a0001c0001t0003g0099 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.313-7377_313-7376i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | |||||
| chr21:39492443
|
G | GGTGGGTG others(5): Show |
1 | a0001c0001t0002g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313-7377_313-7376i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | |||||
| chr21:39492443
|
G | GGTGTGTG others(1): Show |
9 | a0001c0001t0005g0264a0001c0001t0005g0266a0001c0001t0005g0267others(6): Show | 10 | HG02145.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-7363_313-7356d others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | |||||
| chr21:39492443
|
G | GGTGTGTG others(7): Show |
1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-7369_313-7356d others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492443 | |||||
| chr21:39492445
|
T | G | 1 | a0001c0001t0003g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313-7378T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492445 | ||||||
| chr21:39492447
|
T | G | 6 | a0001c0001t0004g0232a0002c0002t0002g0239a0002c0002t0002g0252others(3): Show | 6 | HG00280.hp2 HG02738.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.313-7376T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492447 | ||||||
| chr21:39492466
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0134 | 2 | HG00438.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.313-7357G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492466 | ||||||
| chr21:39492466
|
G | GTGTATA | 16 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.313-7356_313-7355i others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492466
|
G | GTGTGTAT others(1): Show |
3 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0004g0019 | 3 | HG02615.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.313-7356_313-7355i others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492466
|
G | GTGTGTAT others(3): Show |
5 | a0001c0001t0003g0119a0001c0001t0003g0230a0001c0001t0003g0231others(2): Show | 5 | HG01168.hp2 HG02145.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-7356_313-7355i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492466
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.313-7356_313-7355i others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492466
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-7356_313-7355i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492466
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0004g0232 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.313-7356_313-7355i others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492466
|
GTA | G | 6 | a0001c0001t0001g0034a0001c0001t0001g0092a0001c0001t0001g0101others(3): Show | 6 | HG01243.hp1 HG01496.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-7342_313-7341d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492466 | |||||
| chr21:39492468
|
A | G | 17 | a0001c0001t0001g0056a0001c0001t0001g0109a0001c0001t0002g0238others(14): Show | 18 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-7355A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492468 | ||||||
| chr21:39492470
|
A | G | 3 | a0001c0001t0002g0238a0001c0001t0006g0234a0001c0001t0006g0235 | 3 | HG02895.hp1 HG02897.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.313-7353A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492470 | ||||||
| chr21:39492475
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0088a0001c0001t0001g0134 | 2 | HG00438.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.313-7346_313-7337d others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492475 | |||||
| chr21:39492477
|
TATATACA others(1): Show |
T | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.313-7344_313-7337d others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492477 | |||||
| chr21:39492481
|
T | C | 7 | a0001c0001t0001g0034a0001c0001t0001g0092a0001c0001t0001g0101others(4): Show | 7 | HG01243.hp1 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.313-7342T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492481 | ||||||
| chr21:39492481
|
T | TAC | 9 | a0002c0002t0001g0167a0002c0002t0001g0189a0002c0002t0002g0249others(6): Show | 9 | HG00642.hp1 HG00735.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-7325_313-7324d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39492481 | |||||
| chr21:39492483
|
C | T | 43 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(40): Show | 46 | HG01168.hp2 HG01346.hp2 HG02055.hp1 others(43): Show |
intron_variant | MODIFIER | c.313-7340C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492483 | ||||||
| chr21:39492485
|
C | T | 26 | a0001c0001t0001g0109a0001c0001t0001g0226a0001c0001t0002g0238others(23): Show | 28 | HG01168.hp2 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.313-7338C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492485 | ||||||
| chr21:39492487
|
CACACACA others(11): Show |
C | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-7335_313-7318d others(20): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492487 | ||||||
| chr21:39492493
|
C | G | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-7330C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492493 | ||||||
| chr21:39492569
|
T | C | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-7254T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492569 | ||||||
| chr21:39492636
|
C | G | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-7187C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492636 | ||||||
| chr21:39492703
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.313-7120T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492703 | ||||||
| chr21:39492794
|
G | T | 11 | a0001c0001t0001g0109a0001c0001t0005g0264a0001c0001t0005g0266others(8): Show | 12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-7029G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39492794 | ||||||
| chr21:39493077
|
C | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-6746C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493077 | ||||||
| chr21:39493145
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-6678G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493145 | ||||||
| chr21:39493298
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313-6525G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493298 | ||||||
| chr21:39493306
|
A | T | 1 | a0001c0001t0003g0119 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.313-6517A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493306 | ||||||
| chr21:39493446
|
G | C | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-6377G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493446 | ||||||
| chr21:39493523
|
T | C | 1 | a0001c0001t0005g0266 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.313-6300T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493523 | ||||||
| chr21:39493781
|
A | G | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-6042A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39493781 | ||||||
| chr21:39494112
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.313-5711A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494112 | ||||||
| chr21:39494160
|
C | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.313-5663C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494160 | ||||||
| chr21:39494225
|
T | G | 2 | a0002c0002t0002g0265a0002c0002t0002g0275 | 2 | HG01175.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.313-5598T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494225 | ||||||
| chr21:39494228
|
TTCC | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.313-5592_313-5590d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39494228 | |||||
| chr21:39494231
|
C | CTCT | 97 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0012others(94): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.313-5572_313-5570d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39494231 | |||||
| chr21:39494231
|
C | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0065a0001c0001t0001g0066others(50): Show | 56 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(53): Show |
intron_variant | MODIFIER | c.313-5592C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494231 | ||||||
| chr21:39494238
|
T | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-5585T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494238 | ||||||
| chr21:39494247
|
TCTTC | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG01109.hp1 HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.313-5575_313-5572d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494247 | ||||||
| chr21:39494251
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.313-5572C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494251 | ||||||
| chr21:39494342
|
T | C | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-5481T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494342 | ||||||
| chr21:39494443
|
G | A | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-5380G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494443 | ||||||
| chr21:39494481
|
G | A | 4 | a0002c0002t0001g0105a0002c0002t0001g0220a0002c0002t0001g0221others(1): Show | 4 | HG01243.hp2 HG02647.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-5342G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494481 | ||||||
| chr21:39494697
|
T | A | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-5126T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494697 | ||||||
| chr21:39494851
|
T | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-4972T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39494851 | ||||||
| chr21:39495090
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-4733G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495090 | ||||||
| chr21:39495130
|
G | GT | 281 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(278): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.313-4690dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39495130 | |||||
| chr21:39495229
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-4594A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495229 | ||||||
| chr21:39495482
|
C | CT | 36 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(33): Show | 38 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.313-4326dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39495482 | |||||
| chr21:39495487
|
T | TG | 11 | a0001c0001t0005g0241a0001c0001t0005g0264a0001c0001t0005g0266others(8): Show | 12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-4336_313-4335i others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495487 | ||||||
| chr21:39495633
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-4190C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495633 | ||||||
| chr21:39495653
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.313-4170A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495653 | ||||||
| chr21:39495654
|
A | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 162 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.313-4169A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495654 | ||||||
| chr21:39495707
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.313-4116C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495707 | ||||||
| chr21:39495806
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0092a0001c0001t0001g0101others(3): Show | 6 | HG01243.hp1 HG01496.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-4017C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495806 | ||||||
| chr21:39495807
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-4016G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495807 | ||||||
| chr21:39495972
|
A | C | 18 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0035others(15): Show | 19 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.313-3851A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39495972 | ||||||
| chr21:39496137
|
CG | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-3685delG | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496137 | ||||||
| chr21:39496226
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-3597C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496226 | ||||||
| chr21:39496229
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313-3594G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496229 | ||||||
| chr21:39496236
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3587C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496236 | ||||||
| chr21:39496296
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3527C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496296 | ||||||
| chr21:39496317
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.313-3506G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496317 | ||||||
| chr21:39496327
|
C | T | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-3496C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496327 | ||||||
| chr21:39496356
|
C | T | 1 | a0003c0003t0004g0242 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.313-3467C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496356 | ||||||
| chr21:39496357
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.313-3466G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496357 | ||||||
| chr21:39496360
|
T | C | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-3463T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496360 | ||||||
| chr21:39496362
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3461C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496362 | ||||||
| chr21:39496364
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.313-3459G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496364 | ||||||
| chr21:39496368
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-3455C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496368 | ||||||
| chr21:39496392
|
C | G | 1 | a0002c0002t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.313-3431C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496392 | ||||||
| chr21:39496392
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.313-3431C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496392 | ||||||
| chr21:39496425
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3398A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496425 | ||||||
| chr21:39496439
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.313-3384G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496439 | ||||||
| chr21:39496456
|
C | T | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-3367C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496456 | ||||||
| chr21:39496486
|
G | A | 3 | a0001c0001t0002g0276a0001c0001t0003g0099a0001c0001t0004g0232 | 3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.313-3337G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496486 | ||||||
| chr21:39496489
|
A | G | 2 | a0001c0001t0006g0234a0001c0001t0006g0235 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.313-3334A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496489 | ||||||
| chr21:39496495
|
A | G | 1 | a0002c0002t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.313-3328A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496495 | ||||||
| chr21:39496501
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-3322C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496501 | ||||||
| chr21:39496506
|
C | CA | 10 | a0001c0001t0003g0230a0002c0002t0001g0039a0002c0002t0001g0124others(7): Show | 10 | HG01168.hp1 HG01358.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-3294dupA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | |||||
| chr21:39496506
|
CA | C | 57 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(54): Show | 61 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.313-3294delA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | |||||
| chr21:39496506
|
CAA | C | 21 | a0001c0001t0001g0047a0001c0001t0001g0064a0001c0001t0001g0077others(18): Show | 22 | HG00558.hp1 HG01978.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.313-3295_313-3294d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | |||||
| chr21:39496506
|
CAAA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.313-3296_313-3294d others(5): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | |||||
| chr21:39496506
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3303_313-3294d others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39496506 | |||||
| chr21:39496519
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-3304A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496519 | ||||||
| chr21:39496527
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3296A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496527 | ||||||
| chr21:39496556
|
T | C | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-3267T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496556 | ||||||
| chr21:39496557
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-3266G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496557 | ||||||
| chr21:39496796
|
T | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-3027T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39496796 | ||||||
| chr21:39497024
|
T | C | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-2799T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497024 | ||||||
| chr21:39497215
|
G | C | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-2608G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497215 | ||||||
| chr21:39497320
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-2503G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497320 | ||||||
| chr21:39497343
|
C | T | 2 | a0002c0002t0001g0161a0002c0002t0001g0162 | 2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.313-2480C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497343 | ||||||
| chr21:39497344
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.313-2479G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497344 | ||||||
| chr21:39497425
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-2398C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497425 | ||||||
| chr21:39497746
|
A | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.313-2077A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497746 | ||||||
| chr21:39497822
|
A | G | 1 | a0002c0002t0001g0160 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.313-2001A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39497822 | ||||||
| chr21:39498037
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-1786A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498037 | ||||||
| chr21:39498200
|
T | C | 2 | a0001c0001t0004g0019a0002c0002t0001g0229 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.313-1623T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498200 | ||||||
| chr21:39498234
|
A | ACCGT | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1588_313-1585d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39498234 | |||||
| chr21:39498237
|
G | C | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-1586G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498237 | ||||||
| chr21:39498345
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.313-1478C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498345 | ||||||
| chr21:39498387
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-1436A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498387 | ||||||
| chr21:39498449
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313-1374T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498449 | ||||||
| chr21:39498506
|
G | T | 1 | a0002c0002t0001g0202 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.313-1317G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498506 | ||||||
| chr21:39498508
|
T | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1315T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498508 | ||||||
| chr21:39498532
|
T | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.313-1291T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498532 | ||||||
| chr21:39498709
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.313-1114T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498709 | ||||||
| chr21:39498718
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-1105C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498718 | ||||||
| chr21:39498775
|
T | C | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-1048T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498775 | ||||||
| chr21:39498837
|
C | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-986C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498837 | ||||||
| chr21:39498857
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-966A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39498857 | ||||||
| chr21:39499009
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.313-814C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499009 | ||||||
| chr21:39499062
|
T | A | 3 | a0002c0002t0002g0015a0002c0002t0002g0265a0002c0002t0002g0275 | 4 | HG01175.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.313-761T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499062 | ||||||
| chr21:39499106
|
G | A | 1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.313-717G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499106 | ||||||
| chr21:39499113
|
A | G | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.313-710A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499113 | ||||||
| chr21:39499137
|
C | G | 3 | a0001c0001t0002g0276a0001c0001t0003g0099a0001c0001t0004g0232 | 3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.313-686C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499137 | ||||||
| chr21:39499210
|
A | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-613A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499210 | ||||||
| chr21:39499240
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-583C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499240 | ||||||
| chr21:39499255
|
C | CATCT | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.313-567_313-564dup others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(1): Show |
3 | a0001c0001t0002g0276a0001c0001t0003g0099a0001c0001t0004g0232 | 3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.313-564_313-563ins others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(5): Show |
34 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(31): Show | 36 | HG00642.hp1 HG00735.hp2 HG01346.hp2 others(33): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(9): Show |
2 | a0001c0001t0001g0046a0001c0001t0002g0238 | 2 | HG02735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.313-564_313-563ins others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(13): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0068others(4): Show | 7 | HG01123.hp2 HG01243.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(20): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(17): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0031others(48): Show | 53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(24): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(21): Show |
30 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 33 | HG01070.hp1 HG01109.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(28): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(25): Show |
12 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0056others(9): Show | 13 | HG00408.hp2 HG01261.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.313-564_313-563ins others(32): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(29): Show |
2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02074.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.313-564_313-563ins others(36): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499255
|
C | CATCTATC others(33): Show |
1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.313-564_313-563ins others(40): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499255 | |||||
| chr21:39499258
|
C | CTATCTAT others(17): Show |
1 | a0001c0001t0001g0059 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.313-564_313-563ins others(24): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499258 | |||||
| chr21:39499260
|
G | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.313-563G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499260 | ||||||
| chr21:39499260
|
GTCTA | G | 3 | a0002c0002t0001g0167a0002c0002t0001g0168a0002c0002t0001g0170 | 3 | HG01255.hp1 HG01346.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.313-559_313-556del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499260 | |||||
| chr21:39499268
|
G | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0109a0001c0001t0001g0146others(1): Show | 4 | HG02809.hp2 HG03239.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-555G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499268 | ||||||
| chr21:39499272
|
A | ATCTATCT others(17): Show |
1 | a0001c0001t0001g0146 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.313-542_313-541ins others(24): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499272 | |||||
| chr21:39499276
|
A | G | 1 | a0002c0002t0002g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313-547A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499276 | ||||||
| chr21:39499280
|
A | G | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-543A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499280 | ||||||
| chr21:39499326
|
CTCCG | C | 11 | a0001c0001t0005g0241a0001c0001t0005g0264a0001c0001t0005g0266others(8): Show | 12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-494_313-491del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499326 | |||||
| chr21:39499329
|
C | T | 4 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0003g0099others(1): Show | 4 | HG02109.hp2 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-494C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499329 | ||||||
| chr21:39499463
|
ATCT | A | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-355_313-353del others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr21 | 39499463 | |||||
| chr21:39499591
|
A | G | 1 | a0002c0002t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.313-232A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499591 | ||||||
| chr21:39499641
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.313-182C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499641 | ||||||
| chr21:39499687
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.313-136C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499687 | ||||||
| chr21:39499785
|
G | C | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.313-38G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499785 | ||||||
| chr21:39499800
|
T | C | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.313-23T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 3/6 | chr21 | 39499800 | ||||||
| chr21:39500159
|
G | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.405+244G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500159 | ||||||
| chr21:39500202
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.405+287T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500202 | ||||||
| chr21:39500257
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+342C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500257 | ||||||
| chr21:39500274
|
A | C | 1 | a0002c0002t0001g0201 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.405+359A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500274 | ||||||
| chr21:39500335
|
G | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.405+420G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500335 | ||||||
| chr21:39500462
|
T | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(277): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.405+547T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500462 | ||||||
| chr21:39500509
|
G | A | 4 | a0002c0002t0002g0017a0002c0002t0002g0254a0002c0002t0002g0255others(1): Show | 5 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+594G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500509 | ||||||
| chr21:39500519
|
A | G | 4 | a0001c0001t0003g0119a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | HG02145.hp2 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.405+604A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500519 | ||||||
| chr21:39500546
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+631C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500546 | ||||||
| chr21:39500589
|
G | A | 1 | a0002c0002t0002g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.405+674G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500589 | ||||||
| chr21:39500751
|
G | A | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405+836G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500751 | ||||||
| chr21:39500779
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0179a0001c0001t0001g0180others(6): Show | 10 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.405+864C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39500779 | ||||||
| chr21:39501157
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.405+1242C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501157 | ||||||
| chr21:39501211
|
A | G | 1 | a0002c0002t0001g0159 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.405+1296A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501211 | ||||||
| chr21:39501385
|
C | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405+1470C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501385 | ||||||
| chr21:39501497
|
T | C | 1 | a0002c0002t0002g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.405+1582T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501497 | ||||||
| chr21:39501561
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+1646A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501561 | ||||||
| chr21:39501600
|
A | G | 1 | a0002c0002t0007g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.405+1685A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501600 | ||||||
| chr21:39501639
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.405+1724A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501639 | ||||||
| chr21:39501744
|
T | G | 2 | a0001c0001t0003g0099a0001c0001t0004g0232 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.405+1829T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501744 | ||||||
| chr21:39501837
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.405+1922A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501837 | ||||||
| chr21:39501900
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0095a0001c0001t0001g0096others(14): Show | 18 | HG01346.hp2 HG02559.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.405+1985G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501900 | ||||||
| chr21:39501973
|
G | C | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+2058G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501973 | ||||||
| chr21:39501976
|
C | G | 1 | a0001c0001t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.405+2061C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39501976 | ||||||
| chr21:39502046
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0002g0251 | 2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.405+2131G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502046 | ||||||
| chr21:39502067
|
G | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.405+2152G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502067 | ||||||
| chr21:39502112
|
G | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+2197G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502112 | ||||||
| chr21:39502113
|
C | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+2198C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502113 | ||||||
| chr21:39502166
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.405+2251A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502166 | ||||||
| chr21:39502199
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.405+2284T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502199 | ||||||
| chr21:39502259
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.405+2344C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502259 | ||||||
| chr21:39502498
|
A | G | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+2583A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502498 | ||||||
| chr21:39502596
|
C | G | 3 | a0002c0002t0001g0205a0002c0002t0001g0206a0002c0002t0001g0208 | 3 | HG00323.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.405+2681C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502596 | ||||||
| chr21:39502690
|
C | T | 1 | a0002c0002t0002g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.405+2775C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502690 | ||||||
| chr21:39502715
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+2800G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502715 | ||||||
| chr21:39502719
|
G | A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.405+2804G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502719 | ||||||
| chr21:39502733
|
G | A | 1 | a0002c0002t0001g0208 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.405+2818G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502733 | ||||||
| chr21:39502806
|
C | T | 29 | a0002c0002t0001g0040a0002c0002t0001g0186a0002c0002t0001g0237others(26): Show | 31 | HG00280.hp2 HG00642.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.405+2891C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502806 | ||||||
| chr21:39502826
|
G | A | 3 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023 | 4 | HG02055.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.405+2911G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39502826 | ||||||
| chr21:39502985
|
C | CT | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.405+3083dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 39502985 | |||||
| chr21:39503090
|
C | T | 2 | a0001c0001t0003g0230a0001c0001t0003g0231 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.405+3175C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503090 | ||||||
| chr21:39503248
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.405+3333A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503248 | ||||||
| chr21:39503359
|
T | C | 6 | a0001c0001t0004g0019a0003c0003t0004g0242a0003c0003t0004g0243others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.405+3444T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503359 | ||||||
| chr21:39503385
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.405+3470A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503385 | ||||||
| chr21:39503417
|
T | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.405+3502T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503417 | ||||||
| chr21:39503418
|
T | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.405+3503T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503418 | ||||||
| chr21:39503418
|
T | TA | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.405+3510dupA | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 39503418 | |||||
| chr21:39503482
|
C | T | 15 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(12): Show | 16 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+3567C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503482 | ||||||
| chr21:39503487
|
A | C | 15 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(12): Show | 16 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+3572A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503487 | ||||||
| chr21:39503561
|
C | T | 3 | a0002c0002t0001g0020a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.405+3646C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503561 | ||||||
| chr21:39503718
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.405+3803T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503718 | ||||||
| chr21:39503788
|
C | T | 15 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(12): Show | 16 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+3873C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503788 | ||||||
| chr21:39503915
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0129 | 2 | NA18954.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.405+4000C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39503915 | ||||||
| chr21:39504098
|
G | T | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.405+4183G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504098 | ||||||
| chr21:39504323
|
G | A | 9 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(6): Show | 10 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.405+4408G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504323 | ||||||
| chr21:39504416
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.405+4501A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504416 | ||||||
| chr21:39504459
|
C | G | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-4539C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504459 | ||||||
| chr21:39504557
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.406-4441A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504557 | ||||||
| chr21:39504708
|
C | T | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-4290C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504708 | ||||||
| chr21:39504709
|
C | T | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-4289C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504709 | ||||||
| chr21:39504726
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.406-4272C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39504726 | ||||||
| chr21:39505070
|
C | A | 12 | a0001c0001t0001g0109a0001c0001t0005g0241a0001c0001t0005g0264others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.406-3928C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505070 | ||||||
| chr21:39505104
|
C | T | 40 | a0002c0002t0001g0002a0002c0002t0001g0012a0002c0002t0001g0013others(37): Show | 45 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.406-3894C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505104 | ||||||
| chr21:39505264
|
C | G | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-3734C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505264 | ||||||
| chr21:39505276
|
C | T | 1 | a0002c0002t0001g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.406-3722C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505276 | ||||||
| chr21:39505286
|
G | T | 12 | a0001c0001t0001g0109a0001c0001t0005g0241a0001c0001t0005g0264others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.406-3712G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505286 | ||||||
| chr21:39505398
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.406-3600C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505398 | ||||||
| chr21:39505451
|
T | C | 1 | a0002c0002t0002g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.406-3547T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505451 | ||||||
| chr21:39505540
|
A | G | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-3458A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505540 | ||||||
| chr21:39505571
|
G | A | 12 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0005g0264others(9): Show | 13 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.406-3427G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505571 | ||||||
| chr21:39505665
|
T | G | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406-3333T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505665 | ||||||
| chr21:39505722
|
G | A | 1 | a0002c0002t0002g0015 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.406-3276G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505722 | ||||||
| chr21:39505760
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.406-3238C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505760 | ||||||
| chr21:39505879
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.406-3119G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505879 | ||||||
| chr21:39505879
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.406-3119G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39505879 | ||||||
| chr21:39506089
|
C | A | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-2909C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506089 | ||||||
| chr21:39506524
|
G | A | 10 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(7): Show | 11 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.406-2474G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506524 | ||||||
| chr21:39506554
|
G | T | 1 | a0002c0002t0001g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.406-2444G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506554 | ||||||
| chr21:39506665
|
T | C | 16 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(13): Show | 17 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.406-2333T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506665 | ||||||
| chr21:39506682
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.406-2316C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506682 | ||||||
| chr21:39506695
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.406-2303A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506695 | ||||||
| chr21:39506834
|
T | A | 17 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(14): Show | 18 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.406-2164T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506834 | ||||||
| chr21:39506887
|
T | C | 11 | a0001c0001t0005g0241a0001c0001t0005g0264a0001c0001t0005g0266others(8): Show | 12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.406-2111T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39506887 | ||||||
| chr21:39507026
|
A | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1972A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507026 | ||||||
| chr21:39507124
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1874G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507124 | ||||||
| chr21:39507132
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406-1866C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507132 | ||||||
| chr21:39507274
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1724A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507274 | ||||||
| chr21:39507315
|
A | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0097 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.406-1683A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507315 | ||||||
| chr21:39507394
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.406-1604C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507394 | ||||||
| chr21:39507407
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0004g0232 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.406-1591C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507407 | ||||||
| chr21:39507410
|
C | T | 2 | a0001c0001t0001g0176a0002c0002t0002g0246 | 2 | HG03195.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.406-1588C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507410 | ||||||
| chr21:39507451
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1547A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507451 | ||||||
| chr21:39507459
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1539A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507459 | ||||||
| chr21:39507480
|
T | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1518T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507480 | ||||||
| chr21:39507508
|
T | G | 1 | a0005c0005t0001g0225 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.406-1490T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507508 | ||||||
| chr21:39507521
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.406-1477C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507521 | ||||||
| chr21:39507569
|
G | A | 1 | a0002c0002t0001g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.406-1429G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507569 | ||||||
| chr21:39507659
|
C | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1339C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507659 | ||||||
| chr21:39507728
|
C | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-1270C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507728 | ||||||
| chr21:39507813
|
G | A | 2 | a0002c0002t0002g0271a0003c0003t0004g0280 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.406-1185G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507813 | ||||||
| chr21:39507894
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406-1104T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39507894 | ||||||
| chr21:39508003
|
T | C | 2 | a0002c0002t0001g0032a0002c0002t0001g0033 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.406-995T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508003 | ||||||
| chr21:39508145
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-853A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508145 | ||||||
| chr21:39508158
|
C | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-840C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508158 | ||||||
| chr21:39508212
|
G | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-786G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508212 | ||||||
| chr21:39508223
|
C | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-775C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508223 | ||||||
| chr21:39508248
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 167 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.406-750G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508248 | ||||||
| chr21:39508290
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0002g0251 | 2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.406-708C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508290 | ||||||
| chr21:39508464
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-534A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508464 | ||||||
| chr21:39508554
|
C | G | 1 | a0002c0002t0001g0216 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.406-444C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508554 | ||||||
| chr21:39508784
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.406-214T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508784 | ||||||
| chr21:39508951
|
G | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.406-47G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | chr21 | 39508951 | ||||||
| chr21:39508954
|
CTTGAA | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.406-41_406-37delGA others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr21 | 39508954 | |||||
| chr21:39509169
|
A | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+142A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509169 | ||||||
| chr21:39509271
|
G | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+244G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509271 | ||||||
| chr21:39509280
|
G | A | 1 | a0002c0002t0002g0258 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.435+253G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509280 | ||||||
| chr21:39509301
|
G | A | 1 | a0002c0002t0002g0246 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.435+274G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509301 | ||||||
| chr21:39509339
|
C | T | 2 | a0001c0001t0003g0119a0001c0001t0003g0233 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.435+312C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509339 | ||||||
| chr21:39509471
|
G | GT | 23 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(20): Show | 25 | HG00408.hp1 HG01070.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.435+465dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509471 | |||||
| chr21:39509471
|
GT | G | 13 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0037others(10): Show | 15 | HG02080.hp1 HG02155.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.435+465delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509471 | |||||
| chr21:39509471
|
GTT | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 103 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.435+464_435+465del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509471 | |||||
| chr21:39509552
|
G | A | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+525G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509552 | ||||||
| chr21:39509594
|
C | T | 1 | a0002c0002t0002g0265 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.435+567C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509594 | ||||||
| chr21:39509726
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.435+699C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509726 | ||||||
| chr21:39509854
|
C | T | 2 | a0002c0002t0001g0039a0002c0002t0001g0132 | 2 | HG02698.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.435+827C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509854 | ||||||
| chr21:39509913
|
C | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+886C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39509913 | ||||||
| chr21:39509937
|
TTTTGTTA others(297): Show |
T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.435+924_435+1227de others(1): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39509937 | |||||
| chr21:39510034
|
C | T | 1 | a0002c0002t0001g0132 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.435+1007C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510034 | ||||||
| chr21:39510133
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.435+1106G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510133 | ||||||
| chr21:39510154
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1127A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510154 | ||||||
| chr21:39510156
|
AT | A | 3 | a0002c0002t0001g0004a0002c0002t0001g0024a0002c0002t0002g0274 | 4 | HG00639.hp1 HG00735.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1130delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510156 | ||||||
| chr21:39510164
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1137G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510164 | ||||||
| chr21:39510177
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1150T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510177 | ||||||
| chr21:39510217
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1190C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510217 | ||||||
| chr21:39510222
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.435+1195G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510222 | ||||||
| chr21:39510261
|
A | G | 6 | a0002c0002t0001g0020a0002c0002t0001g0032a0002c0002t0001g0033others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+1234A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510261 | ||||||
| chr21:39510365
|
T | TAC | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(109): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.436-1290_436-1289d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510365
|
T | TACAC | 4 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0005g0269others(1): Show | 5 | HG00099.hp1 HG00323.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-1292_436-1289d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510365
|
T | TACACAC | 7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0109others(4): Show | 7 | HG00438.hp1 HG02080.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1294_436-1289d others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510365
|
T | TACGCGCA others(1): Show |
6 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(3): Show | 7 | HG02055.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1313_436-1312i others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510365
|
T | TACGCGCA others(3): Show |
2 | a0001c0001t0003g0119a0001c0001t0004g0245 | 2 | HG01168.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.436-1313_436-1312i others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510365
|
T | TACGCGCG others(1): Show |
4 | a0003c0003t0004g0242a0003c0003t0004g0244a0003c0003t0004g0280others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1313_436-1312i others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510365
|
TAC | T | 7 | a0001c0001t0010g0137a0002c0002t0001g0020a0002c0002t0001g0032others(4): Show | 7 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1290_436-1289d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510365 | |||||
| chr21:39510366
|
A | ACGCGCG | 3 | a0001c0001t0003g0099a0001c0001t0004g0019a0001c0001t0004g0232 | 3 | HG02109.hp2 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1313_436-1312i others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510366 | |||||
| chr21:39510368
|
A | G | 3 | a0001c0001t0003g0173a0003c0003t0003g0223a0003c0003t0004g0243 | 3 | HG03195.hp1 HG03540.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.436-1312A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510368 | ||||||
| chr21:39510369
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.436-1311C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510369 | ||||||
| chr21:39510370
|
A | G | 3 | a0001c0001t0003g0173a0003c0003t0003g0223a0003c0003t0004g0243 | 3 | HG03195.hp1 HG03540.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.436-1310A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510370 | ||||||
| chr21:39510372
|
A | G | 1 | a0003c0003t0004g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.436-1308A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510372 | ||||||
| chr21:39510373
|
CACACACA others(49): Show |
C | 1 | a0003c0003t0004g0243 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.436-1288_436-1233d others(58): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510373 | |||||
| chr21:39510375
|
CACACACA others(16): Show |
C | 1 | a0001c0001t0003g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.436-1288_436-1266d others(25): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510375 | |||||
| chr21:39510377
|
CACACACA others(14): Show |
C | 1 | a0003c0003t0003g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.436-1288_436-1268d others(23): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510377 | |||||
| chr21:39510398
|
T | TAC | 11 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0044others(8): Show | 11 | HG00597.hp1 HG02015.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.436-1259_436-1258d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | |||||
| chr21:39510398
|
TAC | T | 88 | a0001c0001t0001g0034a0001c0001t0001g0092a0001c0001t0001g0101others(85): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.436-1259_436-1258d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | |||||
| chr21:39510398
|
TACACAC | T | 3 | a0001c0001t0003g0099a0001c0001t0004g0019a0001c0001t0004g0232 | 3 | HG02109.hp2 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1263_436-1258d others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | |||||
| chr21:39510398
|
TACACACA others(28): Show |
T | 1 | a0002c0002t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.436-1259_436-1225d others(37): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510398 | |||||
| chr21:39510408
|
CACACACA others(47): Show |
C | 4 | a0003c0003t0004g0242a0003c0003t0004g0244a0003c0003t0004g0280others(1): Show | 4 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1257_436-1204d others(56): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510408 | |||||
| chr21:39510429
|
T | TAC | 3 | a0002c0002t0001g0154a0002c0002t0001g0172a0003c0003t0003g0223 | 3 | HG01981.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.436-1226_436-1225d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | |||||
| chr21:39510429
|
TAC | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.436-1226_436-1225d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | |||||
| chr21:39510429
|
TACAC | T | 7 | a0001c0001t0001g0067a0001c0001t0002g0238a0002c0002t0001g0028others(4): Show | 7 | HG01346.hp1 HG02559.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-1228_436-1225d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | |||||
| chr21:39510429
|
TACACACA others(1): Show |
T | 13 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0005g0241others(10): Show | 14 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.436-1232_436-1225d others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510429 | |||||
| chr21:39510435
|
CACACACA others(20): Show |
C | 8 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(5): Show | 9 | HG01168.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.436-1226_436-1200d others(29): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510435 | |||||
| chr21:39510437
|
C | CACACACA others(18): Show |
6 | a0002c0002t0001g0020a0002c0002t0001g0032a0002c0002t0001g0033others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-1224_436-1200d others(27): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510437 | |||||
| chr21:39510437
|
CACACACA others(18): Show |
C | 2 | a0001c0001t0003g0099a0001c0001t0004g0232 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1224_436-1200d others(27): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510437 | |||||
| chr21:39510454
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1226A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510454 | ||||||
| chr21:39510454
|
ACTGTAGC others(20): Show |
A | 1 | a0001c0001t0004g0019 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.436-1224_436-1198d others(29): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510454 | |||||
| chr21:39510462
|
T | TAC | 134 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.436-1201_436-1200d others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510462 | |||||
| chr21:39510462
|
T | TACAC | 3 | a0001c0001t0001g0045a0001c0001t0001g0060a0003c0003t0004g0243 | 3 | HG03492.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.436-1203_436-1200d others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510462 | |||||
| chr21:39510481
|
C | A | 2 | a0001c0001t0003g0099a0001c0001t0004g0232 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.436-1199C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510481 | ||||||
| chr21:39510513
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1167T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510513 | ||||||
| chr21:39510514
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1166C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510514 | ||||||
| chr21:39510516
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.436-1164T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510516 | ||||||
| chr21:39510569
|
T | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-1111T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510569 | ||||||
| chr21:39510664
|
A | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0110a0001c0001t0001g0169 | 3 | HG01943.hp2 HG02074.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.436-1016A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510664 | ||||||
| chr21:39510908
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.436-772_436-771ins others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510908 | ||||||
| chr21:39510909
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.436-771C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510909 | ||||||
| chr21:39510909
|
C | CTA | 30 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0070others(27): Show | 33 | HG00323.hp2 HG00558.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.436-734_436-733dup others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATA | 70 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0036others(67): Show | 77 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.436-736_436-733dup others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATA | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(63): Show | 70 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.436-738_436-733dup others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(1): Show |
20 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0062others(17): Show | 21 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.436-740_436-733dup others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(3): Show |
4 | a0001c0001t0001g0282a0002c0002t0001g0202a0002c0002t0001g0211others(1): Show | 4 | HG02809.hp1 NA18981.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.436-742_436-733dup others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(5): Show |
5 | a0001c0001t0001g0117a0002c0002t0001g0121a0002c0002t0001g0150others(2): Show | 5 | HG00408.hp1 NA18981.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-744_436-733dup others(12): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0043a0001c0001t0001g0074a0001c0001t0001g0133 | 3 | HG04204.hp1 NA19011.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.436-746_436-733dup others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0044 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.436-748_436-733dup others(16): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(13): Show |
1 | a0001c0001t0001g0213 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.436-752_436-733dup others(20): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
C | CTATATAT others(23): Show |
1 | a0001c0001t0001g0089 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.436-762_436-733dup others(30): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTA | C | 18 | a0001c0001t0001g0130a0001c0001t0001g0175a0001c0001t0001g0176others(15): Show | 18 | HG00735.hp2 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.436-734_436-733del others(2): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTATA | C | 11 | a0001c0001t0001g0103a0001c0001t0001g0226a0002c0002t0001g0237others(8): Show | 13 | HG01070.hp2 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.436-736_436-733del others(4): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTATATA | C | 15 | a0001c0001t0001g0057a0002c0002t0001g0040a0002c0002t0001g0156others(12): Show | 15 | HG00280.hp2 HG00642.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.436-738_436-733del others(6): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTATATAT others(1): Show |
C | 7 | a0001c0001t0001g0035a0001c0001t0001g0174a0001c0001t0003g0003others(4): Show | 8 | HG02055.hp1 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.436-740_436-733del others(8): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTATATAT others(3): Show |
C | 2 | a0001c0001t0001g0055a0002c0002t0001g0197 | 2 | HG00099.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.436-742_436-733del others(10): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTATATAT others(7): Show |
C | 1 | a0002c0002t0001g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-746_436-733del others(14): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510909
|
CTATATAT others(15): Show |
C | 2 | a0001c0001t0001g0109a0002c0002t0001g0120 | 2 | HG02080.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.436-754_436-733del others(22): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39510909 | |||||
| chr21:39510980
|
A | C | 2 | a0002c0002t0001g0028a0002c0002t0001g0029 | 2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.436-700A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510980 | ||||||
| chr21:39510984
|
T | G | 1 | a0002c0002t0002g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436-696T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39510984 | ||||||
| chr21:39511097
|
AT | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.436-575delT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39511097 | |||||
| chr21:39511110
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436-570G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511110 | ||||||
| chr21:39511215
|
G | A | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-465G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511215 | ||||||
| chr21:39511309
|
TGTG | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0097a0005c0005t0001g0225 | 3 | HG03209.hp1 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.436-367_436-365del others(3): Show |
SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr21 | 39511309 | |||||
| chr21:39511325
|
T | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-355T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511325 | ||||||
| chr21:39511335
|
T | A | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-345T>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511335 | ||||||
| chr21:39511425
|
G | T | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-255G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511425 | ||||||
| chr21:39511444
|
A | T | 2 | a0002c0002t0001g0200a0002c0002t0001g0216 | 2 | NA18970.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.436-236A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511444 | ||||||
| chr21:39511587
|
T | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-93T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511587 | ||||||
| chr21:39511610
|
A | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.436-70A>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511610 | ||||||
| chr21:39511638
|
C | A | 11 | a0001c0001t0005g0241a0001c0001t0005g0264a0001c0001t0005g0266others(8): Show | 12 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.436-42C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 5/6 | chr21 | 39511638 | ||||||
| chr21:39511867
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*34+58C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39511867 | ||||||
| chr21:39511873
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+64A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39511873 | ||||||
| chr21:39511983
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*34+174C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39511983 | ||||||
| chr21:39512055
|
T | G | 2 | a0001c0001t0001g0092a0001c0001t0002g0251 | 2 | HG01496.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.*34+246T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512055 | ||||||
| chr21:39512101
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0177others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+292T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512101 | ||||||
| chr21:39512102
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0177others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+293T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512102 | ||||||
| chr21:39512131
|
T | G | 1 | a0002c0002t0001g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*34+322T>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512131 | ||||||
| chr21:39512344
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG01346.hp2 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.*34+535C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512344 | ||||||
| chr21:39512345
|
C | T | 1 | a0001c0001t0011g0075 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.*34+536C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512345 | ||||||
| chr21:39512384
|
G | T | 2 | a0001c0001t0003g0099a0001c0001t0004g0232 | 2 | HG02109.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.*34+575G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512384 | ||||||
| chr21:39512436
|
T | C | 1 | a0002c0002t0002g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.*34+627T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512436 | ||||||
| chr21:39512895
|
A | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0125 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*34+1086A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512895 | ||||||
| chr21:39512944
|
A | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0065a0001c0001t0001g0066others(29): Show | 34 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.*34+1135A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512944 | ||||||
| chr21:39512997
|
C | T | 4 | a0001c0001t0003g0119a0001c0001t0003g0230a0001c0001t0003g0231others(1): Show | 4 | HG02145.hp2 HG02922.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.*34+1188C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39512997 | ||||||
| chr21:39513017
|
A | G | 5 | a0003c0003t0004g0242a0003c0003t0004g0243a0003c0003t0004g0244others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.*34+1208A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513017 | ||||||
| chr21:39513176
|
C | T | 8 | a0001c0001t0003g0099a0001c0001t0004g0019a0001c0001t0004g0232others(5): Show | 8 | HG00642.hp1 HG00735.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.*34+1367C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513176 | ||||||
| chr21:39513181
|
G | A | 32 | a0001c0001t0001g0109a0001c0001t0002g0276a0001c0001t0003g0003others(29): Show | 34 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.*34+1372G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513181 | ||||||
| chr21:39513232
|
A | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1423A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513232 | ||||||
| chr21:39513255
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1446A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513255 | ||||||
| chr21:39513257
|
G | C | 1 | a0002c0002t0001g0207 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.*34+1448G>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513257 | ||||||
| chr21:39513265
|
C | A | 1 | a0002c0002t0001g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*34+1456C>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513265 | ||||||
| chr21:39513272
|
A | G | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1463A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513272 | ||||||
| chr21:39513280
|
T | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1471T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513280 | ||||||
| chr21:39513354
|
T | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*34+1545T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513354 | ||||||
| chr21:39513364
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.*34+1555A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513364 | ||||||
| chr21:39513391
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.*34+1582C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513391 | ||||||
| chr21:39513525
|
G | GT | 11 | a0002c0002t0001g0004a0002c0002t0001g0024a0002c0002t0001g0025others(8): Show | 12 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.*35-1559dupT | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr21 | 39513525 | |||||
| chr21:39513621
|
C | G | 1 | a0002c0002t0001g0191 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.*35-1467C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513621 | ||||||
| chr21:39513795
|
A | G | 3 | a0002c0002t0001g0020a0002c0002t0001g0141a0002c0002t0001g0142 | 3 | HG02647.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.*35-1293A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39513795 | ||||||
| chr21:39514099
|
A | G | 4 | a0002c0002t0002g0017a0002c0002t0002g0254a0002c0002t0002g0255others(1): Show | 5 | HG01070.hp2 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35-989A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514099 | ||||||
| chr21:39514142
|
C | T | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*35-946C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514142 | ||||||
| chr21:39514237
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.*35-851C>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514237 | ||||||
| chr21:39514393
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0125 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.*35-695G>T | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514393 | ||||||
| chr21:39514398
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.*35-690A>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514398 | ||||||
| chr21:39514610
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.*35-478C>G | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514610 | ||||||
| chr21:39514642
|
A | C | 18 | a0001c0001t0003g0003a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 19 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.*35-446A>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514642 | ||||||
| chr21:39514889
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.*35-199T>C | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514889 | ||||||
| chr21:39514989
|
G | A | 1 | a0001c0001t0002g0238 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*35-99G>A | SH3BGR | ENSG00000185437.16 | transcript | ENST00000333634.10 | protein_coding | 6/6 | chr21 | 39514989 |