| geneid | 64092 |
|---|---|
| ensemblid | ENSG00000155307.19 |
| hgncid | 10528 |
| symbol | SAMSN1 |
| name | SAM domain, SH3 domain and nuclear localization signals 1 |
| refseq_nuc | NM_022136.5 |
| refseq_prot | NP_071419.3 |
| ensembl_nuc | ENST00000400566.6 |
| ensembl_prot | ENSP00000383411.2 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 14485228 |
| end | 14546315 |
| strand | - |
| ver | v1.2 |
| region | chr21:14485228-14546315 |
| region5000 | chr21:14480228-14551315 |
| regionname0 | SAMSN1_chr21_14485228_14546315 |
| regionname5000 | SAMSN1_chr21_14480228_14551315 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 373 | 392 | 81 | 67 | 184 | 18 | 40 | 146 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0002 | 0/0 | 373 | 14 | 11 | 3 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0003 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0004 | 0/0 | 373 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1122 | 285 | 57 | 52 | 133 | 15 | 26 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| c0002 | 0/0 | 1122 | 107 | 24 | 15 | 51 | 3 | 14 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| c0003 | 0/0 | 1122 | 12 | 10 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| c0004 | 0/0 | 1122 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| c0005 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| c0006 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 739 | 336 | 79 | 59 | 146 | 17 | 33 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0002 | 0/0 | 739 | 44 | 8 | 6 | 26 | 0 | 4 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0003 | 0/0 | 739 | 9 | 0 | 0 | 9 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0004 | 0/0 | 739 | 4 | 3 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0005 | 0/0 | 739 | 3 | 0 | 2 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0006 | 0/0 | 739 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0007 | 0/0 | 739 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0008 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0009 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0010 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0011 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0012 | 0/0 | 739 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0013 | 0/0 | 739 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0014 | 0/0 | 739 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| t0015 | 0/0 | 739 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| 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 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0002 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1122 | 285 | 57 | 52 | 133 | 15 | 26 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002 | 0/0 | 1122 | 107 | 24 | 15 | 51 | 3 | 14 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0002c0003 | 0/0 | 1122 | 12 | 10 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0002c0004 | 0/0 | 1122 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0003c0005 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0004c0006 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1860 | 230 | 47 | 43 | 103 | 14 | 21 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0002 | 0/0 | 1860 | 34 | 5 | 5 | 21 | 0 | 3 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0003 | 0/0 | 1860 | 7 | 0 | 0 | 7 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0004 | 0/0 | 1860 | 4 | 3 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0005 | 0/0 | 1860 | 3 | 0 | 2 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0006 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0007 | 0/0 | 1860 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0010 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0011 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0012 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0001t0015 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0001 | 0/0 | 1860 | 91 | 20 | 13 | 43 | 3 | 12 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0002 | 0/0 | 1860 | 9 | 2 | 1 | 5 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0003 | 0/0 | 1860 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0006 | 0/0 | 1860 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0008 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0009 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0013 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0001c0002t0014 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0002c0003t0001 | 0/0 | 1860 | 11 | 9 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0002c0003t0002 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0002c0004t0001 | 0/0 | 1860 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0003c0005t0001 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| a0004c0006t0001 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | copy fasta | chr21 | 14480228 | 14551315 |
| 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 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0002 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0004g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0009g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0013g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0001c0002t0014g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0002c0004t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0003c0005t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| a0004c0006t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0027 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0332 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0375 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00639 | hp2 | a0001 | c0002 | t0009 | g0025 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0336 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0312 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0340 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0087 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0284 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0354 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0347 | AMR | PUR | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0330 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0352 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0351 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0023 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | IBS | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01884 | hp2 | a0004 | c0006 | t0001 | g0355 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0372 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02004 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0038 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0349 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0374 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0371 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0305 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0054 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0370 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02280 | hp1 | a0003 | c0005 | t0001 | g0362 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0359 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0345 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0053 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0329 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0339 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0358 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0342 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0052 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0381 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0292 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02970 | hp1 | a0001 | c0002 | t0008 | g0024 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0056 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0311 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0379 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03098 | hp2 | a0001 | c0002 | t0014 | g0344 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0337 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0049 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0346 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0026 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0173 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0348 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0356 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03704 | hp2 | a0001 | c0002 | t0013 | g0368 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0343 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0341 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0325 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0373 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0091 | SAS | STU | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0361 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0378 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0364 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0298 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0365 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18961 | hp1 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0380 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18977 | hp2 | a0001 | c0002 | t0006 | g0300 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0363 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0322 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0179 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0360 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0180 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0377 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0353 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0306 | AFR | ASW | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0350 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0288 | SAS | GIH | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0291 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02486 | hp2 | a0002 | c0003 | t0002 | g0044 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | ACB | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | MSL | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0367 | EAS | JPT | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0147 | REF | REF | SAMSN1_chr21_14480228_14551315 | SAMSN1 | chr21 | 14480228 | 14551315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14486000
|
C | T | 1 | a0003 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1034G>A | p.Gly345Glu | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 1088/1860 | 1034/1122 | 345/373 | chr21 | 14486000 | ||
| chr21:14500543
|
T | A | 1 | a0004 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.754A>T | p.Arg252Trp | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/8 | 808/1860 | 754/1122 | 252/373 | chr21 | 14500543 | ||
| chr21:14516983
|
C | G | 1 | a0002 | 14 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
missense_variant | MODERATE | c.188G>C | p.Gly63Ala | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/8 | 242/1860 | 188/1122 | 63/373 | chr21 | 14516983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14546256
|
G | C | 4 | a0001c0002a0002c0004a0003c0005others(1): Show | 111 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
synonymous_variant | LOW | c.6C>G | p.Leu2Leu | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/8 | 60/1860 | 6/1122 | 2/373 | chr21 | 14546256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14485271
|
G | A | 2 | a0001c0001t0004a0001c0001t0007 | 6 | HG01099.hp2 HG02145.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*641C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 641 | chr21 | 14485271 | |||||
| chr21:14485430
|
T | C | 1 | a0001c0001t0012 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 482 | chr21 | 14485430 | |||||
| chr21:14485475
|
T | C | 2 | a0001c0001t0006a0001c0002t0006 | 2 | NA18977.hp2 NA18998.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 437 | chr21 | 14485475 | |||||
| chr21:14485525
|
C | G | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0012others(3): Show | 47 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*387G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 387 | chr21 | 14485525 | |||||
| chr21:14485639
|
T | C | 1 | a0001c0002t0013 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 273 | chr21 | 14485639 | |||||
| chr21:14485816
|
C | G | 1 | a0001c0001t0011 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 96 | chr21 | 14485816 | |||||
| chr21:14485850
|
G | A | 2 | a0001c0001t0007a0001c0002t0014 | 3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 62 | chr21 | 14485850 | |||||
| chr21:14485886
|
G | A | 1 | a0001c0001t0015 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 26 | chr21 | 14485886 | |||||
| chr21:14485908
|
G | A | 2 | a0001c0001t0003a0001c0002t0003 | 9 | HG02071.hp1 HG02135.hp1 NA18952.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 8/8 | 4 | chr21 | 14485908 | |||||
| chr21:14546280
|
C | T | 2 | a0001c0001t0005a0001c0001t0010 | 4 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-19G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/8 | 19 | chr21 | 14546280 | |||||
| chr21:14546296
|
C | T | 2 | a0001c0002t0008a0001c0002t0009 | 2 | HG00639.hp2 HG02970.hp1 |
5_prime_UTR_variant | MODIFIER | c.-35G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/8 | 35 | chr21 | 14546296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:14486159
|
A | G | 15 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0075others(12): Show | 15 | HG00609.hp2 HG00735.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-45T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486159 | ||||||
| chr21:14486238
|
G | A | 85 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(82): Show | 91 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.920-124C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486238 | ||||||
| chr21:14486286
|
A | C | 1 | a0001c0002t0001g0321 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-172T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486286 | ||||||
| chr21:14486287
|
C | A | 1 | a0001c0002t0001g0321 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-173G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486287 | ||||||
| chr21:14486291
|
A | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0176others(9): Show | 14 | NA18942.hp1 NA18944.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-177T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486291 | ||||||
| chr21:14486348
|
A | ATTCC | 3 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0132 | 3 | NA18943.hp2 NA18949.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.920-235_920-234ins others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486348 | ||||||
| chr21:14486349
|
G | A | 3 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0132 | 3 | NA18943.hp2 NA18949.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.920-235C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486349 | ||||||
| chr21:14486376
|
G | A | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-262C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486376 | ||||||
| chr21:14486376
|
G | T | 60 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0033others(57): Show | 62 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.920-262C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486376 | ||||||
| chr21:14486563
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.920-449T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486563 | ||||||
| chr21:14486709
|
G | A | 1 | a0001c0002t0002g0304 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.920-595C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486709 | ||||||
| chr21:14486709
|
G | T | 1 | a0001c0001t0012g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.920-595C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486709 | ||||||
| chr21:14486768
|
G | C | 1 | a0001c0001t0001g0002 | 3 | HG00323.hp1 HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.920-654C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486768 | ||||||
| chr21:14486778
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-664A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14486778 | ||||||
| chr21:14487001
|
G | A | 17 | a0001c0001t0001g0036a0001c0001t0001g0065a0001c0001t0001g0072others(14): Show | 17 | HG00609.hp2 HG00735.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.920-887C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487001 | ||||||
| chr21:14487049
|
T | C | 93 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(90): Show | 99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-935A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487049 | ||||||
| chr21:14487110
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.920-996C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487110 | ||||||
| chr21:14487129
|
C | T | 372 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(369): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.920-1015G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487129 | ||||||
| chr21:14487231
|
G | A | 2 | a0001c0002t0001g0287a0001c0002t0001g0379 | 2 | HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.920-1117C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487231 | ||||||
| chr21:14487253
|
TTCAAAGA others(14): Show |
T | 1 | a0001c0002t0014g0344 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.920-1160_920-1140d others(23): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487253 | ||||||
| chr21:14487311
|
A | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(87): Show | 96 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.920-1197T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487311 | ||||||
| chr21:14487345
|
T | TTA | 91 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(88): Show | 97 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.920-1232_920-1231i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487345 | ||||||
| chr21:14487345
|
T | TTATA | 6 | a0001c0001t0001g0030a0001c0001t0001g0065a0001c0001t0001g0072others(3): Show | 6 | HG02055.hp1 HG02074.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-1232_920-1231i others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487345 | ||||||
| chr21:14487347
|
T | A | 128 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0030others(125): Show | 135 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.920-1233A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487347 | ||||||
| chr21:14487347
|
TTA | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0070others(18): Show | 23 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.920-1235_920-1234d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487347 | ||||||
| chr21:14487360
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-1246A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487360 | ||||||
| chr21:14487361
|
C | A | 7 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0002t0001g0284others(4): Show | 8 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.920-1247G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487361 | ||||||
| chr21:14487367
|
T | TG | 198 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(195): Show | 209 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.920-1254_920-1253i others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487367 | ||||||
| chr21:14487375
|
A | G | 2 | a0001c0001t0002g0150a0001c0001t0002g0186 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.920-1261T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487375 | ||||||
| chr21:14487486
|
T | G | 14 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG00609.hp2 HG00735.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-1372A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487486 | ||||||
| chr21:14487822
|
G | A | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-1708C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487822 | ||||||
| chr21:14487825
|
C | T | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-1711G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487825 | ||||||
| chr21:14487832
|
T | C | 43 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0033others(40): Show | 45 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.920-1718A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487832 | ||||||
| chr21:14487889
|
C | CATGGAAG others(8): Show |
1 | a0001c0002t0001g0321 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-1790_920-1776d others(17): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487889 | ||||||
| chr21:14487937
|
A | G | 13 | a0001c0001t0001g0006a0001c0001t0001g0070a0001c0001t0001g0073others(10): Show | 15 | HG01168.hp1 HG01169.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-1823T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487937 | ||||||
| chr21:14487985
|
C | G | 1 | a0001c0002t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.920-1871G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487985 | ||||||
| chr21:14487999
|
C | T | 16 | a0001c0001t0001g0093a0001c0001t0001g0111a0001c0001t0001g0177others(13): Show | 16 | HG00597.hp2 NA18951.hp2 NA18955.hp2 others(13): Show |
intron_variant | MODIFIER | c.920-1885G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14487999 | ||||||
| chr21:14488054
|
C | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0187a0001c0001t0001g0205others(3): Show | 6 | HG02015.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-1940G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488054 | ||||||
| chr21:14488079
|
A | G | 1 | a0001c0002t0001g0370 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.920-1965T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488079 | ||||||
| chr21:14488334
|
A | C | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-2220T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488334 | ||||||
| chr21:14488335
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-2221G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488335 | ||||||
| chr21:14488337
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.920-2223T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488337 | ||||||
| chr21:14488567
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.920-2453T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488567 | ||||||
| chr21:14488684
|
G | A | 4 | a0001c0001t0001g0158a0002c0003t0001g0049a0002c0004t0001g0291others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-2570C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488684 | ||||||
| chr21:14488710
|
C | A | 1 | a0001c0001t0002g0109 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.920-2596G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488710 | ||||||
| chr21:14488729
|
A | G | 21 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0057others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-2615T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488729 | ||||||
| chr21:14488806
|
C | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0057others(24): Show | 29 | HG01099.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.920-2692G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488806 | ||||||
| chr21:14488807
|
G | A | 5 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0251others(2): Show | 5 | NA18942.hp2 NA18948.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.920-2693C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488807 | ||||||
| chr21:14488886
|
C | G | 1 | a0001c0001t0003g0236 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.920-2772G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14488886 | ||||||
| chr21:14489134
|
C | T | 93 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(90): Show | 99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-3020G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489134 | ||||||
| chr21:14489232
|
AGTAACAC others(8): Show |
A | 1 | a0001c0002t0001g0321 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.920-3133_920-3119d others(17): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489232 | ||||||
| chr21:14489274
|
T | C | 175 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(172): Show | 184 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.920-3160A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489274 | ||||||
| chr21:14489312
|
C | T | 93 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(90): Show | 99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-3198G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489312 | ||||||
| chr21:14489319
|
G | A | 3 | a0001c0001t0007g0058a0001c0001t0007g0173a0001c0002t0014g0344 | 3 | HG03098.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.920-3205C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489319 | ||||||
| chr21:14489332
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.920-3218G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489332 | ||||||
| chr21:14489333
|
G | A | 2 | a0001c0001t0001g0028a0001c0002t0001g0020 | 3 | HG01168.hp1 HG01169.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.920-3219C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489333 | ||||||
| chr21:14489361
|
A | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0002t0001g0285 | 3 | HG02451.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920-3247T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489361 | ||||||
| chr21:14489391
|
C | CAT | 172 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0019others(169): Show | 180 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.920-3278_920-3277i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489391 | ||||||
| chr21:14489418
|
A | G | 1 | a0001c0001t0001g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.920-3304T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489418 | ||||||
| chr21:14489431
|
T | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0002t0001g0378 | 3 | NA18906.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.920-3317A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489431 | ||||||
| chr21:14489448
|
A | G | 2 | a0001c0001t0001g0184a0001c0002t0001g0380 | 2 | HG00609.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.920-3334T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489448 | ||||||
| chr21:14489491
|
C | T | 194 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(191): Show | 204 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.920-3377G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489491 | ||||||
| chr21:14489495
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.920-3381T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489495 | ||||||
| chr21:14489689
|
A | G | 13 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0176others(10): Show | 15 | NA18942.hp1 NA18944.hp1 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.920-3575T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489689 | ||||||
| chr21:14489707
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.920-3593T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489707 | ||||||
| chr21:14489755
|
C | T | 23 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0070others(20): Show | 25 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.920-3641G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489755 | ||||||
| chr21:14489807
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0272a0001c0002t0001g0315others(1): Show | 4 | NA18986.hp1 NA18995.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-3693T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489807 | ||||||
| chr21:14489853
|
G | C | 2 | a0001c0001t0007g0058a0001c0001t0007g0173 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.920-3739C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489853 | ||||||
| chr21:14489953
|
T | A | 1 | a0001c0002t0001g0335 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.920-3839A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489953 | ||||||
| chr21:14489962
|
A | G | 1 | a0001c0002t0001g0310 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.920-3848T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489962 | ||||||
| chr21:14489979
|
A | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0089a0001c0001t0001g0143others(11): Show | 14 | HG00140.hp1 HG00741.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.920-3865T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14489979 | ||||||
| chr21:14490029
|
A | G | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.920-3915T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490029 | ||||||
| chr21:14490033
|
TA | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0002t0001g0285 | 3 | HG02451.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.920-3920delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490033 | ||||||
| chr21:14490170
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(26): Show | 31 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.920-4056T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490170 | ||||||
| chr21:14490210
|
C | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0002t0001g0285others(1): Show | 4 | HG02280.hp1 HG02451.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.920-4096G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490210 | ||||||
| chr21:14490224
|
T | C | 21 | a0001c0001t0001g0014a0001c0001t0001g0050a0001c0001t0001g0057others(18): Show | 22 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.920-4110A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490224 | ||||||
| chr21:14490263
|
G | A | 372 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(369): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.920-4149C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490263 | ||||||
| chr21:14490354
|
C | G | 112 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(109): Show | 118 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.920-4240G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490354 | ||||||
| chr21:14490380
|
C | T | 93 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0035others(90): Show | 99 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.920-4266G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490380 | ||||||
| chr21:14490481
|
A | G | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.920-4367T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490481 | ||||||
| chr21:14490609
|
A | C | 11 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0075others(8): Show | 11 | HG00609.hp2 HG00735.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.920-4495T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490609 | ||||||
| chr21:14490622
|
A | G | 2 | a0002c0003t0001g0179a0002c0003t0001g0180 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.920-4508T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490622 | ||||||
| chr21:14490683
|
C | T | 13 | a0001c0001t0001g0089a0001c0001t0001g0143a0001c0001t0003g0188others(10): Show | 13 | HG00140.hp1 HG00741.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.920-4569G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490683 | ||||||
| chr21:14490806
|
G | T | 1 | a0001c0001t0003g0236 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.920-4692C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490806 | ||||||
| chr21:14490831
|
AAT | A | 14 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0037others(11): Show | 15 | HG00639.hp2 HG01081.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.920-4719_920-4718d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490831 | ||||||
| chr21:14490867
|
C | T | 1 | a0001c0002t0001g0288 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.920-4753G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490867 | ||||||
| chr21:14490960
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.920-4846G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14490960 | ||||||
| chr21:14491202
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(165): Show | 181 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.920-5088C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491202 | ||||||
| chr21:14491268
|
C | CT | 21 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(18): Show | 23 | HG01099.hp2 HG01257.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.920-5155dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491268 | ||||||
| chr21:14491278
|
T | C | 18 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0075others(15): Show | 18 | HG00323.hp2 HG00609.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.920-5164A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491278 | ||||||
| chr21:14491422
|
C | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0040others(83): Show | 92 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.920-5308G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491422 | ||||||
| chr21:14491481
|
G | C | 1 | a0001c0002t0014g0344 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.920-5367C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491481 | ||||||
| chr21:14491540
|
C | G | 1 | a0001c0002t0001g0318 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.920-5426G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491540 | ||||||
| chr21:14491569
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0002t0001g0320others(1): Show | 4 | NA18948.hp2 NA18972.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-5455G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491569 | ||||||
| chr21:14491634
|
A | G | 10 | a0001c0001t0001g0050a0001c0001t0001g0064a0001c0001t0001g0071others(7): Show | 10 | HG00639.hp2 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-5520T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491634 | ||||||
| chr21:14491640
|
T | C | 1 | a0001c0002t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.920-5526A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491640 | ||||||
| chr21:14491652
|
T | C | 9 | a0001c0001t0001g0059a0001c0001t0001g0158a0001c0001t0007g0058others(6): Show | 9 | HG00639.hp2 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.920-5538A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491652 | ||||||
| chr21:14491653
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(85): Show | 99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.920-5539T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491653 | ||||||
| chr21:14491662
|
T | A | 89 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0031others(86): Show | 93 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.920-5548A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491662 | ||||||
| chr21:14491671
|
A | G | 2 | a0001c0001t0001g0166a0001c0002t0001g0356 | 2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.920-5557T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491671 | ||||||
| chr21:14491683
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920-5569C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491683 | ||||||
| chr21:14491687
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.920-5573G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491687 | ||||||
| chr21:14491753
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.920-5639G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491753 | ||||||
| chr21:14491825
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.920-5711A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491825 | ||||||
| chr21:14491838
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.920-5724A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491838 | ||||||
| chr21:14491898
|
A | G | 1 | a0001c0001t0001g0231 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.920-5784T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491898 | ||||||
| chr21:14491956
|
A | T | 3 | a0001c0001t0001g0014a0001c0001t0007g0058a0001c0001t0007g0173 | 4 | HG03209.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.920-5842T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491956 | ||||||
| chr21:14491992
|
A | AT | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(229): Show | 248 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.920-5879dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491992 | ||||||
| chr21:14491995
|
T | C | 6 | a0001c0001t0001g0030a0001c0002t0008g0024a0002c0003t0001g0038others(3): Show | 6 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-5881A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14491995 | ||||||
| chr21:14492019
|
TACTTC | T | 3 | a0001c0001t0001g0193a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.920-5910_920-5906d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492019 | ||||||
| chr21:14492024
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 257 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.920-5910G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492024 | ||||||
| chr21:14492095
|
T | C | 10 | a0001c0001t0001g0062a0001c0001t0001g0157a0001c0001t0001g0158others(7): Show | 10 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.920-5981A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492095 | ||||||
| chr21:14492205
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.920-6091T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492205 | ||||||
| chr21:14492209
|
TTTGA | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0138a0001c0001t0002g0150others(2): Show | 6 | HG00544.hp1 HG03209.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.920-6099_920-6096d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492209 | ||||||
| chr21:14492232
|
C | A | 1 | a0001c0002t0001g0350 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.920-6118G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492232 | ||||||
| chr21:14492303
|
A | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0002t0001g0361 | 3 | HG02647.hp2 NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.919+6139T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492303 | ||||||
| chr21:14492377
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0014g0344 | 3 | HG02258.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.919+6065A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492377 | ||||||
| chr21:14492516
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.919+5926C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492516 | ||||||
| chr21:14492672
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+5770A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492672 | ||||||
| chr21:14492802
|
T | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0012others(116): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.919+5640A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14492802 | ||||||
| chr21:14493026
|
T | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG01081.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+5416A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493026 | ||||||
| chr21:14493064
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.919+5378C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493064 | ||||||
| chr21:14493069
|
C | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01081.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.919+5373G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493069 | ||||||
| chr21:14493070
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0145a0001c0001t0002g0146others(1): Show | 6 | HG00323.hp1 HG01070.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.919+5372G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493070 | ||||||
| chr21:14493106
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+5336G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493106 | ||||||
| chr21:14493148
|
G | A | 5 | a0001c0001t0001g0050a0002c0003t0001g0038a0002c0003t0001g0049others(2): Show | 5 | HG01243.hp2 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+5294C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493148 | ||||||
| chr21:14493240
|
C | G | 1 | a0001c0002t0001g0297 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.919+5202G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493240 | ||||||
| chr21:14493411
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01081.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.919+5031T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493411 | ||||||
| chr21:14493429
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01081.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.919+5013A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493429 | ||||||
| chr21:14493572
|
ACAACACA others(7): Show |
A | 1 | a0001c0002t0001g0316 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.919+4856_919+4869d others(16): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493572 | ||||||
| chr21:14493572
|
ACAACACA others(9): Show |
A | 1 | a0001c0001t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.919+4854_919+4869d others(18): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493572 | ||||||
| chr21:14493572
|
ACAACACA others(11): Show |
A | 75 | a0001c0001t0001g0019a0001c0001t0001g0029a0001c0001t0001g0080others(72): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.919+4852_919+4869d others(20): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493572 | ||||||
| chr21:14493574
|
A | AAC | 55 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0035others(52): Show | 59 | HG00323.hp2 HG00735.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.919+4866_919+4867d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
A | AACAC | 12 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0001g0075others(9): Show | 13 | HG00099.hp2 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+4864_919+4867d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
A | AACACAC | 13 | a0001c0001t0001g0046a0001c0001t0001g0061a0001c0001t0001g0068others(10): Show | 13 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.919+4862_919+4867d others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
A | AACACACA others(1): Show |
11 | a0001c0001t0001g0045a0001c0001t0001g0190a0001c0001t0002g0099others(8): Show | 12 | HG00438.hp1 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.919+4860_919+4867d others(10): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
A | AACACACA others(3): Show |
3 | a0001c0001t0001g0050a0002c0004t0001g0291a0002c0004t0001g0347 | 3 | HG01243.hp2 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.919+4858_919+4867d others(12): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
A | AACACACA others(5): Show |
2 | a0002c0003t0001g0007a0002c0003t0001g0038 | 3 | HG01168.hp2 HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.919+4856_919+4867d others(14): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
AAC | A | 14 | a0001c0001t0001g0051a0001c0001t0001g0162a0001c0001t0001g0171others(11): Show | 15 | HG01099.hp2 HG01243.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.919+4866_919+4867d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
AACAC | A | 11 | a0001c0001t0001g0014a0001c0001t0001g0163a0001c0001t0001g0207others(8): Show | 12 | HG01978.hp1 HG03209.hp2 HG03471.hp2 others(9): Show |
intron_variant | MODIFIER | c.919+4864_919+4867d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
AACACAC | A | 14 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0037others(11): Show | 14 | HG02145.hp1 HG02258.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.919+4862_919+4867d others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
AACACACA others(5): Show |
A | 2 | a0001c0001t0001g0279a0001c0002t0008g0024 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4856_919+4867d others(14): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493574
|
AACACACA others(13): Show |
A | 2 | a0001c0001t0001g0043a0003c0005t0001g0362 | 2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.919+4848_919+4867d others(22): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493574 | ||||||
| chr21:14493613
|
A | ACACACG | 6 | a0001c0001t0001g0012a0001c0001t0001g0148a0001c0001t0002g0109others(3): Show | 7 | HG02056.hp2 HG02129.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.919+4828_919+4829i others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | ||||||
| chr21:14493613
|
A | ACACG | 4 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0012g0079others(1): Show | 4 | HG02602.hp1 HG03491.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.919+4828_919+4829i others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | ||||||
| chr21:14493613
|
A | ACG | 10 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0064others(7): Show | 10 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.919+4828_919+4829i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | ||||||
| chr21:14493613
|
A | G | 2 | a0001c0001t0001g0062a0003c0005t0001g0362 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.919+4829T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493613 | ||||||
| chr21:14493635
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.919+4807A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493635 | ||||||
| chr21:14493848
|
A | G | 27 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0040others(24): Show | 28 | HG01081.hp1 HG02056.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.919+4594T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493848 | ||||||
| chr21:14493942
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(127): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.919+4500C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493942 | ||||||
| chr21:14493993
|
A | G | 130 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0019others(127): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.919+4449T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14493993 | ||||||
| chr21:14494015
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.919+4427T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494015 | ||||||
| chr21:14494092
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.919+4350T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494092 | ||||||
| chr21:14494125
|
G | A | 2 | a0001c0001t0001g0033a0001c0002t0001g0356 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.919+4317C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494125 | ||||||
| chr21:14494142
|
G | A | 2 | a0001c0001t0001g0279a0001c0002t0008g0024 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4300C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494142 | ||||||
| chr21:14494153
|
G | A | 2 | a0001c0001t0001g0279a0001c0002t0008g0024 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4289C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494153 | ||||||
| chr21:14494210
|
G | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0166a0001c0001t0001g0193others(2): Show | 5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+4232C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494210 | ||||||
| chr21:14494223
|
G | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0166a0001c0001t0001g0193others(2): Show | 5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+4219C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494223 | ||||||
| chr21:14494297
|
A | C | 380 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(377): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.919+4145T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494297 | ||||||
| chr21:14494346
|
C | A | 1 | a0001c0001t0015g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.919+4096G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494346 | ||||||
| chr21:14494373
|
C | T | 1 | a0001c0002t0001g0341 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.919+4069G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494373 | ||||||
| chr21:14494374
|
G | A | 2 | a0001c0001t0001g0279a0001c0002t0008g0024 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+4068C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494374 | ||||||
| chr21:14494482
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.919+3960A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494482 | ||||||
| chr21:14494578
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.919+3864C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494578 | ||||||
| chr21:14494708
|
C | CA | 7 | a0001c0001t0001g0107a0001c0001t0001g0170a0001c0001t0001g0172others(4): Show | 8 | HG01515.hp1 HG01517.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+3733dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494708 | ||||||
| chr21:14494803
|
C | A | 1 | a0001c0001t0001g0088 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.919+3639G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494803 | ||||||
| chr21:14494814
|
T | A | 80 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(77): Show | 83 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.919+3628A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14494814 | ||||||
| chr21:14495080
|
T | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 17 | HG02056.hp2 HG02129.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.919+3362A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495080 | ||||||
| chr21:14495131
|
G | C | 3 | a0001c0001t0001g0279a0001c0002t0008g0024a0003c0005t0001g0362 | 3 | HG02280.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+3311C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495131 | ||||||
| chr21:14495147
|
G | A | 3 | a0001c0001t0001g0279a0001c0002t0008g0024a0003c0005t0001g0362 | 3 | HG02280.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.919+3295C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495147 | ||||||
| chr21:14495239
|
T | C | 139 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(136): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.919+3203A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495239 | ||||||
| chr21:14495416
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0059others(4): Show | 7 | HG02055.hp1 HG02630.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.919+3026C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495416 | ||||||
| chr21:14495425
|
G | A | 25 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0037others(22): Show | 27 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+3017C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495425 | ||||||
| chr21:14495505
|
C | T | 64 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(61): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.919+2937G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495505 | ||||||
| chr21:14495543
|
T | C | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.919+2899A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495543 | ||||||
| chr21:14495774
|
G | T | 25 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0037others(22): Show | 27 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.919+2668C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495774 | ||||||
| chr21:14495894
|
C | CT | 10 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0002g0169others(7): Show | 11 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+2547dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495894 | ||||||
| chr21:14495894
|
CT | C | 8 | a0001c0001t0001g0062a0001c0001t0001g0166a0001c0001t0001g0193others(5): Show | 8 | HG02280.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.919+2547delA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495894 | ||||||
| chr21:14495917
|
T | C | 133 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(130): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.919+2525A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14495917 | ||||||
| chr21:14496013
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.919+2429C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496013 | ||||||
| chr21:14496150
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+2292G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496150 | ||||||
| chr21:14496517
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.919+1925G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496517 | ||||||
| chr21:14496625
|
C | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.919+1817G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496625 | ||||||
| chr21:14496740
|
T | C | 29 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.919+1702A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496740 | ||||||
| chr21:14496851
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.919+1591C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496851 | ||||||
| chr21:14496860
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+1582C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14496860 | ||||||
| chr21:14497005
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.919+1437G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497005 | ||||||
| chr21:14497043
|
C | G | 1 | a0001c0001t0001g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.919+1399G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497043 | ||||||
| chr21:14497129
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.919+1313C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497129 | ||||||
| chr21:14497168
|
T | C | 100 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0032others(97): Show | 104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.919+1274A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497168 | ||||||
| chr21:14497184
|
G | A | 1 | a0001c0001t0002g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.919+1258C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497184 | ||||||
| chr21:14497224
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0067a0001c0001t0002g0169others(7): Show | 11 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.919+1218C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497224 | ||||||
| chr21:14497272
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.919+1170C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497272 | ||||||
| chr21:14497322
|
C | T | 1 | a0001c0002t0002g0340 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.919+1120G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497322 | ||||||
| chr21:14497364
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(298): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.919+1078T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497364 | ||||||
| chr21:14497393
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0170others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+1049C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497393 | ||||||
| chr21:14497420
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG02630.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.919+1022G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497420 | ||||||
| chr21:14497451
|
C | T | 1 | a0001c0001t0002g0109 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.919+991G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497451 | ||||||
| chr21:14497485
|
C | T | 1 | a0001c0002t0001g0329 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.919+957G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497485 | ||||||
| chr21:14497499
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919+943A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497499 | ||||||
| chr21:14497506
|
C | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0001g0287 | 3 | HG02258.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.919+936G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497506 | ||||||
| chr21:14497534
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.919+908C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497534 | ||||||
| chr21:14497565
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0170others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+877G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497565 | ||||||
| chr21:14497566
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.919+876C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497566 | ||||||
| chr21:14497628
|
G | T | 1 | a0001c0001t0003g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.919+814C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497628 | ||||||
| chr21:14497677
|
T | A | 29 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0041others(26): Show | 31 | HG00621.hp1 HG02056.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.919+765A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497677 | ||||||
| chr21:14497850
|
C | T | 47 | a0001c0001t0001g0019a0001c0001t0001g0064a0001c0001t0001g0100others(44): Show | 49 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.919+592G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497850 | ||||||
| chr21:14497940
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.919+502C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14497940 | ||||||
| chr21:14498036
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0166a0001c0001t0001g0193others(2): Show | 5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.919+406C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498036 | ||||||
| chr21:14498046
|
G | T | 1 | a0001c0002t0001g0293 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.919+396C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498046 | ||||||
| chr21:14498224
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.919+218G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498224 | ||||||
| chr21:14498298
|
C | G | 2 | a0001c0002t0001g0296a0001c0002t0001g0297 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.919+144G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498298 | ||||||
| chr21:14498306
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.919+136A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498306 | ||||||
| chr21:14498317
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 349 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.919+125G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498317 | ||||||
| chr21:14498333
|
C | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0279a0001c0002t0008g0024others(1): Show | 4 | HG02280.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.919+109G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 7/7 | chr21 | 14498333 | ||||||
| chr21:14498680
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.769-88G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498680 | ||||||
| chr21:14498703
|
T | C | 3 | a0001c0001t0001g0193a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.769-111A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498703 | ||||||
| chr21:14498732
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-140G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498732 | ||||||
| chr21:14498745
|
T | G | 14 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0068others(11): Show | 15 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.769-153A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498745 | ||||||
| chr21:14498772
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0073 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.769-180C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498772 | ||||||
| chr21:14498904
|
C | G | 1 | a0001c0002t0001g0358 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.769-312G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498904 | ||||||
| chr21:14498922
|
C | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.769-330G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14498922 | ||||||
| chr21:14499025
|
C | G | 2 | a0001c0001t0001g0033a0001c0002t0001g0356 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.769-433G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499025 | ||||||
| chr21:14499133
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.769-541T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499133 | ||||||
| chr21:14499255
|
A | G | 1 | a0001c0002t0001g0338 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.769-663T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499255 | ||||||
| chr21:14499280
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0166 | 3 | HG02965.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-688C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499280 | ||||||
| chr21:14499309
|
C | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0062a0001c0001t0001g0166 | 3 | HG02965.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.769-717G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499309 | ||||||
| chr21:14499406
|
T | C | 6 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0259others(3): Show | 6 | HG02165.hp2 NA18966.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.769-814A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499406 | ||||||
| chr21:14499467
|
G | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0033others(30): Show | 36 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.769-875C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499467 | ||||||
| chr21:14499491
|
CA | C | 63 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(60): Show | 64 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.769-900delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499491 | ||||||
| chr21:14499491
|
CAA | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.769-901_769-900del others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499491 | ||||||
| chr21:14499491
|
CAAA | C | 44 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(41): Show | 48 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.769-902_769-900del others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499491 | ||||||
| chr21:14499518
|
G | A | 2 | a0001c0001t0001g0193a0001c0002t0001g0295 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.769-926C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499518 | ||||||
| chr21:14499672
|
T | C | 3 | a0001c0001t0001g0065a0001c0001t0001g0279a0001c0002t0008g0024 | 3 | HG02451.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.768+857A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499672 | ||||||
| chr21:14499688
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.768+841T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499688 | ||||||
| chr21:14499705
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.768+824A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499705 | ||||||
| chr21:14499711
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(74): Show | 87 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.768+818C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499711 | ||||||
| chr21:14499722
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.768+807A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499722 | ||||||
| chr21:14499728
|
T | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0033others(39): Show | 45 | HG00621.hp1 HG01167.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.768+801A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499728 | ||||||
| chr21:14499932
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.768+597C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14499932 | ||||||
| chr21:14500006
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.768+523A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500006 | ||||||
| chr21:14500055
|
G | A | 1 | a0001c0002t0001g0334 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.768+474C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500055 | ||||||
| chr21:14500070
|
G | A | 1 | a0002c0003t0001g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.768+459C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500070 | ||||||
| chr21:14500130
|
G | T | 25 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(22): Show | 27 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.768+399C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500130 | ||||||
| chr21:14500223
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.768+306C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500223 | ||||||
| chr21:14500353
|
A | G | 1 | a0001c0002t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.768+176T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 6/7 | chr21 | 14500353 | ||||||
| chr21:14500794
|
T | A | 1 | a0001c0001t0012g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.562-59A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500794 | ||||||
| chr21:14500820
|
A | T | 4 | a0001c0001t0002g0099a0001c0002t0001g0021a0001c0002t0001g0323others(1): Show | 5 | HG00438.hp1 NA18997.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-85T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500820 | ||||||
| chr21:14500859
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0002t0002g0381 | 3 | HG01081.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.562-124T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500859 | ||||||
| chr21:14500967
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.562-232T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14500967 | ||||||
| chr21:14501060
|
G | A | 1 | a0001c0001t0001g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.562-325C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501060 | ||||||
| chr21:14501064
|
TG | T | 18 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 19 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.562-330delC | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501064 | ||||||
| chr21:14501127
|
A | G | 10 | a0001c0001t0001g0170a0001c0001t0001g0172a0002c0003t0001g0007others(7): Show | 11 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-392T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501127 | ||||||
| chr21:14501423
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-688T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501423 | ||||||
| chr21:14501462
|
T | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(134): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.562-727A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501462 | ||||||
| chr21:14501572
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.562-837C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501572 | ||||||
| chr21:14501577
|
T | G | 8 | a0002c0003t0001g0007a0002c0003t0001g0038a0002c0003t0001g0049others(5): Show | 9 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.562-842A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501577 | ||||||
| chr21:14501582
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.562-847C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501582 | ||||||
| chr21:14501660
|
T | G | 1 | a0001c0001t0001g0231 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.562-925A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501660 | ||||||
| chr21:14501675
|
TAAAGA | T | 25 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0077others(22): Show | 27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-945_562-941del others(5): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501675 | ||||||
| chr21:14501868
|
T | C | 2 | a0001c0001t0001g0064a0001c0002t0001g0286 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.562-1133A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501868 | ||||||
| chr21:14501913
|
G | T | 1 | a0001c0002t0001g0358 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.562-1178C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501913 | ||||||
| chr21:14501999
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.562-1264C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14501999 | ||||||
| chr21:14502104
|
C | G | 1 | a0001c0001t0002g0238 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.562-1369G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502104 | ||||||
| chr21:14502138
|
A | G | 138 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(135): Show | 143 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.562-1403T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502138 | ||||||
| chr21:14502228
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.562-1493G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502228 | ||||||
| chr21:14502247
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.562-1512T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502247 | ||||||
| chr21:14502256
|
G | GCTGGGT | 129 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(126): Show | 134 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.562-1522_562-1521i others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502256 | ||||||
| chr21:14502256
|
G | GGTGGGT | 8 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(5): Show | 8 | HG02630.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.562-1522_562-1521i others(8): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502256 | ||||||
| chr21:14502518
|
C | T | 3 | a0001c0001t0001g0037a0001c0002t0001g0361a0001c0002t0014g0344 | 3 | HG02647.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.562-1783G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502518 | ||||||
| chr21:14502548
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-1813A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502548 | ||||||
| chr21:14502561
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0003g0244 | 2 | NA18982.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.562-1826C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502561 | ||||||
| chr21:14502621
|
C | T | 1 | a0001c0002t0001g0352 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.562-1886G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502621 | ||||||
| chr21:14502710
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-1975G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502710 | ||||||
| chr21:14502784
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2049C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502784 | ||||||
| chr21:14502787
|
C | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0077others(22): Show | 27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-2052G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502787 | ||||||
| chr21:14502836
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0001g0287 | 3 | HG02258.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.562-2101C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502836 | ||||||
| chr21:14502981
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.562-2246A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14502981 | ||||||
| chr21:14503015
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.562-2280A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503015 | ||||||
| chr21:14503021
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0067others(18): Show | 22 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.562-2286G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503021 | ||||||
| chr21:14503173
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.562-2438C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503173 | ||||||
| chr21:14503189
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0064others(6): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-2454T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503189 | ||||||
| chr21:14503255
|
T | C | 1 | a0001c0002t0002g0337 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.562-2520A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503255 | ||||||
| chr21:14503258
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0043 | 3 | HG02280.hp2 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.562-2523C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503258 | ||||||
| chr21:14503259
|
T | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0120 | 2 | NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.562-2524A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503259 | ||||||
| chr21:14503343
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.562-2608C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503343 | ||||||
| chr21:14503380
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2645A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503380 | ||||||
| chr21:14503523
|
C | T | 4 | a0001c0001t0001g0198a0001c0002t0001g0370a0001c0002t0001g0371others(1): Show | 4 | HG00597.hp1 HG01123.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-2788G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503523 | ||||||
| chr21:14503607
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-2872C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503607 | ||||||
| chr21:14503659
|
C | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0002t0002g0381 | 3 | HG01081.hp1 HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.562-2924G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503659 | ||||||
| chr21:14503689
|
G | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0279a0001c0002t0008g0024 | 3 | HG02622.hp2 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.562-2954C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503689 | ||||||
| chr21:14503736
|
C | T | 10 | a0001c0001t0001g0170a0001c0001t0001g0172a0002c0003t0001g0007others(7): Show | 11 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.562-3001G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503736 | ||||||
| chr21:14503806
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.562-3071T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503806 | ||||||
| chr21:14503928
|
G | C | 50 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0029others(47): Show | 53 | HG00621.hp1 HG01168.hp2 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.562-3193C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503928 | ||||||
| chr21:14503947
|
T | C | 132 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(129): Show | 137 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.562-3212A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503947 | ||||||
| chr21:14503979
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.562-3244C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14503979 | ||||||
| chr21:14504048
|
G | A | 135 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0014others(132): Show | 140 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.562-3313C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504048 | ||||||
| chr21:14504077
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.562-3342G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504077 | ||||||
| chr21:14504088
|
A | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-3353T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504088 | ||||||
| chr21:14504126
|
C | T | 1 | a0001c0002t0001g0310 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.562-3391G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504126 | ||||||
| chr21:14504142
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0136 | 2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.562-3407G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504142 | ||||||
| chr21:14504210
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.562-3475T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504210 | ||||||
| chr21:14504241
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.562-3506G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504241 | ||||||
| chr21:14504277
|
G | A | 25 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0077others(22): Show | 27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-3542C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504277 | ||||||
| chr21:14504389
|
T | C | 2 | a0001c0002t0001g0320a0001c0002t0001g0321 | 2 | NA18972.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.562-3654A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504389 | ||||||
| chr21:14504485
|
A | T | 1 | a0001c0002t0001g0309 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.562-3750T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504485 | ||||||
| chr21:14504486
|
A | G | 25 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0077others(22): Show | 27 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(24): Show |
intron_variant | MODIFIER | c.562-3751T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504486 | ||||||
| chr21:14504605
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-3870A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504605 | ||||||
| chr21:14504664
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.562-3929C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504664 | ||||||
| chr21:14504724
|
T | G | 1 | a0001c0001t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.562-3989A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504724 | ||||||
| chr21:14504789
|
C | T | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-4054G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504789 | ||||||
| chr21:14504918
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.562-4183G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504918 | ||||||
| chr21:14504936
|
C | G | 1 | a0001c0001t0002g0209 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.562-4201G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14504936 | ||||||
| chr21:14505067
|
C | T | 16 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0043others(13): Show | 17 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.562-4332G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505067 | ||||||
| chr21:14505155
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.562-4420G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505155 | ||||||
| chr21:14505194
|
C | CA | 9 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0064others(6): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-4460dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505194 | ||||||
| chr21:14505259
|
A | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(24): Show | 29 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.562-4524T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505259 | ||||||
| chr21:14505451
|
T | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0037others(26): Show | 31 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.562-4716A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505451 | ||||||
| chr21:14505555
|
C | T | 11 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0002t0001g0356others(8): Show | 12 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.561+4755G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505555 | ||||||
| chr21:14505599
|
A | G | 1 | a0001c0002t0002g0373 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.561+4711T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505599 | ||||||
| chr21:14505614
|
C | T | 9 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0064others(6): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+4696G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505614 | ||||||
| chr21:14505754
|
C | A | 24 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0057others(21): Show | 25 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.561+4556G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505754 | ||||||
| chr21:14505777
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.561+4533G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505777 | ||||||
| chr21:14505848
|
A | C | 139 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0028others(136): Show | 143 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.561+4462T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505848 | ||||||
| chr21:14505895
|
G | A | 14 | a0001c0001t0001g0177a0001c0001t0001g0200a0001c0001t0001g0202others(11): Show | 16 | HG00642.hp2 HG01074.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.561+4415C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505895 | ||||||
| chr21:14505979
|
G | A | 1 | a0001c0002t0001g0023 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.561+4331C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14505979 | ||||||
| chr21:14506003
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.561+4307T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506003 | ||||||
| chr21:14506044
|
C | G | 2 | a0001c0001t0001g0070a0001c0001t0001g0273 | 2 | HG01106.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.561+4266G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506044 | ||||||
| chr21:14506091
|
G | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0125others(5): Show | 8 | HG01106.hp1 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+4219C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506091 | ||||||
| chr21:14506118
|
G | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0028others(152): Show | 161 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.561+4192C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506118 | ||||||
| chr21:14506267
|
T | G | 23 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(20): Show | 23 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+4043A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506267 | ||||||
| chr21:14506293
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561+4017T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506293 | ||||||
| chr21:14506344
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 4 | HG02630.hp1 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+3966A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506344 | ||||||
| chr21:14506356
|
C | CAG | 22 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(19): Show | 22 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.561+3953_561+3954i others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506356 | ||||||
| chr21:14506389
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0070a0001c0002t0001g0361others(1): Show | 4 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+3921T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506389 | ||||||
| chr21:14506480
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+3830G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506480 | ||||||
| chr21:14506507
|
C | G | 1 | a0001c0001t0001g0171 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.561+3803G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506507 | ||||||
| chr21:14506518
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561+3792G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506518 | ||||||
| chr21:14506571
|
A | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.561+3739T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506571 | ||||||
| chr21:14506680
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 28 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.561+3630G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14506680 | ||||||
| chr21:14507162
|
C | T | 17 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0157others(14): Show | 17 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.561+3148G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507162 | ||||||
| chr21:14507165
|
C | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0070a0001c0002t0001g0361others(1): Show | 4 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+3145G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507165 | ||||||
| chr21:14507243
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.561+3067T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507243 | ||||||
| chr21:14507423
|
G | T | 1 | a0001c0002t0008g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.561+2887C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507423 | ||||||
| chr21:14507575
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.561+2735G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507575 | ||||||
| chr21:14507656
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.561+2654T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507656 | ||||||
| chr21:14507665
|
C | T | 3 | a0001c0001t0001g0037a0001c0002t0001g0361a0001c0002t0014g0344 | 3 | HG02647.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.561+2645G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507665 | ||||||
| chr21:14507838
|
T | TA | 81 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0071others(78): Show | 85 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.561+2471dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507838 | ||||||
| chr21:14507838
|
T | TAA | 8 | a0001c0001t0001g0125a0001c0001t0002g0034a0001c0002t0001g0346others(5): Show | 8 | HG02109.hp2 HG02129.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+2470_561+2471d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507838 | ||||||
| chr21:14507838
|
TA | T | 74 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0039others(71): Show | 77 | HG00621.hp1 HG01081.hp1 HG01167.hp2 others(74): Show |
intron_variant | MODIFIER | c.561+2471delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507838 | ||||||
| chr21:14507853
|
T | A | 1 | a0001c0002t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.561+2457A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507853 | ||||||
| chr21:14507886
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.561+2424G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507886 | ||||||
| chr21:14507894
|
T | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0273 | 2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.561+2416A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507894 | ||||||
| chr21:14507903
|
A | G | 1 | a0001c0002t0001g0349 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.561+2407T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14507903 | ||||||
| chr21:14508016
|
G | A | 1 | a0001c0002t0001g0351 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.561+2294C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508016 | ||||||
| chr21:14508080
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+2230G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508080 | ||||||
| chr21:14508166
|
G | T | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+2144C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508166 | ||||||
| chr21:14508170
|
A | C | 20 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(17): Show | 20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+2140T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508170 | ||||||
| chr21:14508183
|
C | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+2127G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508183 | ||||||
| chr21:14508186
|
T | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0070a0001c0002t0001g0361others(1): Show | 4 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+2124A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508186 | ||||||
| chr21:14508270
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.561+2040T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508270 | ||||||
| chr21:14508276
|
C | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.561+2034G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508276 | ||||||
| chr21:14508357
|
G | GA | 32 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(29): Show | 34 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(31): Show |
intron_variant | MODIFIER | c.561+1952dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508357 | ||||||
| chr21:14508363
|
A | T | 4 | a0001c0001t0002g0099a0001c0002t0001g0021a0001c0002t0001g0323others(1): Show | 5 | HG00438.hp1 NA18997.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+1947T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508363 | ||||||
| chr21:14508366
|
A | C | 20 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(17): Show | 20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1944T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508366 | ||||||
| chr21:14508367
|
C | T | 1 | a0001c0002t0001g0322 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.561+1943G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508367 | ||||||
| chr21:14508427
|
C | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(17): Show | 20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1883G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508427 | ||||||
| chr21:14508451
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.561+1859T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508451 | ||||||
| chr21:14508602
|
C | G | 18 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1708G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508602 | ||||||
| chr21:14508674
|
A | G | 20 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(17): Show | 20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1636T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508674 | ||||||
| chr21:14508675
|
C | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG02683.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.561+1635G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508675 | ||||||
| chr21:14508738
|
A | G | 18 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1572T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508738 | ||||||
| chr21:14508772
|
T | C | 20 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(17): Show | 20 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.561+1538A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508772 | ||||||
| chr21:14508855
|
C | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1455G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508855 | ||||||
| chr21:14508870
|
C | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1440G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508870 | ||||||
| chr21:14508914
|
G | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0067others(15): Show | 18 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+1396C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508914 | ||||||
| chr21:14508933
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.561+1377A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508933 | ||||||
| chr21:14508993
|
T | A | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.561+1317A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14508993 | ||||||
| chr21:14509051
|
G | A | 2 | a0001c0001t0001g0039a0001c0002t0002g0381 | 2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.561+1259C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509051 | ||||||
| chr21:14509139
|
A | AAAAAG | 27 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0077others(24): Show | 29 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+1166_561+1170d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509139 | ||||||
| chr21:14509139
|
AAAAAG | A | 15 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0067others(12): Show | 15 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.561+1166_561+1170d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509139 | ||||||
| chr21:14509158
|
A | AGAAAG | 17 | a0001c0001t0001g0176a0001c0001t0001g0195a0001c0001t0001g0206others(14): Show | 17 | HG01975.hp2 HG02155.hp2 NA18612.hp1 others(14): Show |
intron_variant | MODIFIER | c.561+1147_561+1151d others(7): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509158 | ||||||
| chr21:14509319
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.561+991C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509319 | ||||||
| chr21:14509335
|
A | G | 1 | a0001c0002t0001g0349 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.561+975T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509335 | ||||||
| chr21:14509342
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.561+968T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509342 | ||||||
| chr21:14509834
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0136 | 2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.561+476T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509834 | ||||||
| chr21:14509867
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0273 | 2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.561+443A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509867 | ||||||
| chr21:14509877
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0273 | 2 | HG01106.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.561+433G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509877 | ||||||
| chr21:14509941
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.561+369G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509941 | ||||||
| chr21:14509981
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.561+329A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14509981 | ||||||
| chr21:14510023
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+287G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510023 | ||||||
| chr21:14510032
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.561+278C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510032 | ||||||
| chr21:14510064
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(19): Show | 23 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.561+246C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510064 | ||||||
| chr21:14510070
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.561+240A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510070 | ||||||
| chr21:14510093
|
T | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.561+217A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510093 | ||||||
| chr21:14510097
|
C | T | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.561+213G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510097 | ||||||
| chr21:14510144
|
G | GAA | 8 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01106.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.561+164_561+165dup others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510144 | ||||||
| chr21:14510144
|
G | GAAA | 14 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0002g0169others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.561+163_561+165dup others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510144 | ||||||
| chr21:14510144
|
GA | G | 27 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0043others(24): Show | 29 | HG00621.hp1 HG02056.hp2 HG02602.hp1 others(26): Show |
intron_variant | MODIFIER | c.561+165delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510144 | ||||||
| chr21:14510165
|
G | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01106.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.561+145C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510165 | ||||||
| chr21:14510301
|
T | C | 8 | a0001c0001t0001g0138a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG02071.hp1 HG02074.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+9A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 5/7 | chr21 | 14510301 | ||||||
| chr21:14510528
|
CAACT | C | 5 | a0001c0001t0001g0125a0001c0001t0001g0157a0001c0001t0001g0158others(2): Show | 5 | HG01106.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-71_410-68delAG others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510528 | ||||||
| chr21:14510535
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.410-74C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510535 | ||||||
| chr21:14510535
|
G | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.410-74C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510535 | ||||||
| chr21:14510617
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.410-156A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510617 | ||||||
| chr21:14510627
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.410-166A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510627 | ||||||
| chr21:14510677
|
A | ACT | 137 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(134): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.410-218_410-217dup others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510677 | ||||||
| chr21:14510722
|
G | A | 1 | a0001c0002t0001g0297 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.410-261C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510722 | ||||||
| chr21:14510761
|
C | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.410-300G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510761 | ||||||
| chr21:14510892
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273others(1): Show | 4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-431C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510892 | ||||||
| chr21:14510910
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0007g0058a0001c0001t0007g0173 | 4 | HG03209.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-449G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510910 | ||||||
| chr21:14510931
|
T | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0066 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.410-470A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510931 | ||||||
| chr21:14510961
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.410-500T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510961 | ||||||
| chr21:14510971
|
A | G | 14 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0002g0169others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.410-510T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14510971 | ||||||
| chr21:14511671
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.409+773C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511671 | ||||||
| chr21:14511777
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0007g0058a0001c0001t0007g0173 | 4 | HG03209.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+667G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511777 | ||||||
| chr21:14511803
|
T | A | 1 | a0001c0002t0009g0025 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.409+641A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511803 | ||||||
| chr21:14511834
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273others(1): Show | 4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+610G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511834 | ||||||
| chr21:14511855
|
A | G | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.409+589T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511855 | ||||||
| chr21:14511884
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273others(1): Show | 4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.409+560C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511884 | ||||||
| chr21:14511958
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.409+486C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511958 | ||||||
| chr21:14511960
|
G | A | 1 | a0001c0002t0001g0346 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.409+484C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14511960 | ||||||
| chr21:14512001
|
C | T | 62 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0100others(59): Show | 64 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.409+443G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512001 | ||||||
| chr21:14512023
|
A | G | 1 | a0001c0002t0001g0308 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.409+421T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512023 | ||||||
| chr21:14512024
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.409+420G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512024 | ||||||
| chr21:14512025
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0139 | 3 | HG01255.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.409+419C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512025 | ||||||
| chr21:14512103
|
C | T | 63 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0100others(60): Show | 65 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.409+341G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512103 | ||||||
| chr21:14512133
|
G | C | 89 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0064others(86): Show | 92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.409+311C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512133 | ||||||
| chr21:14512154
|
G | T | 89 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0064others(86): Show | 92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.409+290C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512154 | ||||||
| chr21:14512260
|
T | A | 1 | a0001c0001t0001g0256 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.409+184A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512260 | ||||||
| chr21:14512302
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.409+142T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512302 | ||||||
| chr21:14512304
|
A | C | 1 | a0001c0002t0003g0374 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.409+140T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512304 | ||||||
| chr21:14512428
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.409+16C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512428 | ||||||
| chr21:14512437
|
G | A | 3 | a0001c0001t0001g0037a0001c0002t0001g0361a0001c0002t0014g0344 | 3 | HG02647.hp2 HG03098.hp2 NA18906.hp1 |
splice_region_variant&intron_variant | LOW | c.409+7C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 4/7 | chr21 | 14512437 | ||||||
| chr21:14512578
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.280-5T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512578 | ||||||
| chr21:14512628
|
A | T | 231 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(228): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.280-55T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512628 | ||||||
| chr21:14512634
|
A | T | 95 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(92): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.280-61T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512634 | ||||||
| chr21:14512653
|
C | CAAG | 95 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(92): Show | 98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.280-81_280-80insCT others(1): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512653 | ||||||
| chr21:14512713
|
T | A | 17 | a0001c0001t0001g0064a0001c0001t0001g0170a0001c0001t0001g0172others(14): Show | 18 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-140A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512713 | ||||||
| chr21:14512744
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280-171G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512744 | ||||||
| chr21:14512783
|
C | T | 219 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(216): Show | 228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.280-210G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512783 | ||||||
| chr21:14512868
|
G | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0042 | 3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.280-295C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512868 | ||||||
| chr21:14512917
|
T | C | 19 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0170others(16): Show | 20 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(17): Show |
intron_variant | MODIFIER | c.280-344A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512917 | ||||||
| chr21:14512953
|
C | T | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-380G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14512953 | ||||||
| chr21:14513195
|
T | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273others(1): Show | 4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-622A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513195 | ||||||
| chr21:14513262
|
G | A | 2 | a0002c0003t0001g0049a0002c0004t0001g0291 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.280-689C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513262 | ||||||
| chr21:14513327
|
A | T | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-754T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513327 | ||||||
| chr21:14513428
|
T | G | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-855A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513428 | ||||||
| chr21:14513484
|
A | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 7 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-911T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513484 | ||||||
| chr21:14513498
|
T | C | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-925A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513498 | ||||||
| chr21:14513520
|
CGT | C | 107 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(104): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.280-949_280-948del others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513520 | ||||||
| chr21:14513747
|
A | G | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-1174T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14513747 | ||||||
| chr21:14514295
|
T | C | 221 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.280-1722A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514295 | ||||||
| chr21:14514545
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280-1972T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514545 | ||||||
| chr21:14514552
|
G | T | 3 | a0001c0001t0004g0008a0001c0001t0004g0047a0001c0001t0004g0048 | 4 | HG01099.hp2 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1979C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514552 | ||||||
| chr21:14514598
|
T | G | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.280-2025A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514598 | ||||||
| chr21:14514611
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.280-2038C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514611 | ||||||
| chr21:14514629
|
A | G | 20 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(17): Show | 21 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.280-2056T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514629 | ||||||
| chr21:14514670
|
A | C | 229 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(226): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.280-2097T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514670 | ||||||
| chr21:14514793
|
A | G | 1 | a0001c0002t0009g0025 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.279+2099T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514793 | ||||||
| chr21:14514819
|
C | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0262a0001c0001t0001g0264others(4): Show | 7 | HG02129.hp2 NA18974.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+2073G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514819 | ||||||
| chr21:14514902
|
T | C | 17 | a0001c0001t0001g0064a0001c0001t0001g0170a0001c0001t0001g0172others(14): Show | 18 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.279+1990A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514902 | ||||||
| chr21:14514908
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.279+1984T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514908 | ||||||
| chr21:14514958
|
A | G | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.279+1934T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514958 | ||||||
| chr21:14514977
|
G | A | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.279+1915C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14514977 | ||||||
| chr21:14515198
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 7 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.279+1694G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515198 | ||||||
| chr21:14515224
|
A | G | 225 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(222): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.279+1668T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515224 | ||||||
| chr21:14515424
|
G | A | 14 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0002g0169others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+1468C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515424 | ||||||
| chr21:14515426
|
A | T | 225 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(222): Show | 234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.279+1466T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515426 | ||||||
| chr21:14515481
|
T | A | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+1411A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515481 | ||||||
| chr21:14515515
|
C | T | 5 | a0001c0001t0002g0099a0001c0002t0001g0021a0001c0002t0001g0323others(2): Show | 6 | HG00438.hp1 HG04115.hp2 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1377G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515515 | ||||||
| chr21:14515575
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279+1317A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515575 | ||||||
| chr21:14515638
|
T | A | 1 | a0001c0002t0001g0329 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.279+1254A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515638 | ||||||
| chr21:14515660
|
C | T | 2 | a0001c0001t0001g0039a0001c0002t0002g0381 | 2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.279+1232G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515660 | ||||||
| chr21:14515915
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279+977C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14515915 | ||||||
| chr21:14516054
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0178a0001c0001t0001g0187others(7): Show | 12 | HG00597.hp2 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.279+838C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516054 | ||||||
| chr21:14516207
|
C | A | 14 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0002g0169others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.279+685G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516207 | ||||||
| chr21:14516274
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0166a0001c0002t0009g0025 | 3 | HG00639.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.279+618A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516274 | ||||||
| chr21:14516374
|
T | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0220 | 2 | HG00597.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.279+518A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516374 | ||||||
| chr21:14516396
|
T | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.279+496A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516396 | ||||||
| chr21:14516415
|
C | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+477G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516415 | ||||||
| chr21:14516440
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.279+452C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516440 | ||||||
| chr21:14516536
|
C | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+356G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516536 | ||||||
| chr21:14516581
|
G | A | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.279+311C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516581 | ||||||
| chr21:14516641
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.279+251G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516641 | ||||||
| chr21:14516643
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.279+249G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516643 | ||||||
| chr21:14516719
|
C | A | 11 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0116others(8): Show | 11 | HG01433.hp1 HG01928.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.279+173G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516719 | ||||||
| chr21:14516805
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0002t0001g0287 | 3 | HG02258.hp1 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.279+87A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 3/7 | chr21 | 14516805 | ||||||
| chr21:14517213
|
C | G | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130-172G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517213 | ||||||
| chr21:14517232
|
G | A | 135 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130-191C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517232 | ||||||
| chr21:14517450
|
C | A | 1 | a0001c0002t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130-409G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517450 | ||||||
| chr21:14517503
|
G | A | 14 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0002g0169others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-462C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517503 | ||||||
| chr21:14517562
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.130-521C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517562 | ||||||
| chr21:14517747
|
T | A | 363 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(360): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.130-706A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517747 | ||||||
| chr21:14517750
|
G | C | 1 | a0001c0002t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.130-709C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517750 | ||||||
| chr21:14517821
|
GA | G | 62 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0100others(59): Show | 64 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.130-781delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517821 | ||||||
| chr21:14517899
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 152 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.130-858A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517899 | ||||||
| chr21:14517912
|
C | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.130-871G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517912 | ||||||
| chr21:14517921
|
T | C | 1 | a0001c0002t0001g0369 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.130-880A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14517921 | ||||||
| chr21:14518119
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.130-1078G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518119 | ||||||
| chr21:14518150
|
C | T | 69 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0100others(66): Show | 71 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.130-1109G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518150 | ||||||
| chr21:14518222
|
AC | A | 13 | a0002c0003t0001g0007a0002c0003t0001g0038a0002c0003t0001g0049others(10): Show | 14 | HG01168.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.130-1182delG | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518222 | ||||||
| chr21:14518256
|
C | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0116others(1): Show | 4 | HG01433.hp1 HG01928.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-1215G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518256 | ||||||
| chr21:14518320
|
T | C | 2 | a0002c0003t0001g0049a0002c0004t0001g0291 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.130-1279A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518320 | ||||||
| chr21:14518355
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.130-1314A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518355 | ||||||
| chr21:14518438
|
G | A | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-1397C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518438 | ||||||
| chr21:14518445
|
A | AT | 224 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(221): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.130-1405dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518445 | ||||||
| chr21:14518551
|
T | C | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0259 | 3 | HG02165.hp2 NA18966.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.130-1510A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518551 | ||||||
| chr21:14518553
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(221): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.130-1512C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518553 | ||||||
| chr21:14518570
|
CATTCACT others(5): Show |
C | 1 | a0001c0002t0001g0327 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.130-1541_130-1530d others(14): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518570 | ||||||
| chr21:14518659
|
T | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273others(1): Show | 4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1618A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518659 | ||||||
| chr21:14518695
|
C | A | 1 | a0001c0002t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-1654G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518695 | ||||||
| chr21:14518879
|
A | C | 1 | a0001c0002t0001g0023 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.130-1838T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518879 | ||||||
| chr21:14518882
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01081.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-1841A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518882 | ||||||
| chr21:14518885
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.130-1844G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518885 | ||||||
| chr21:14518895
|
A | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0134others(3): Show | 6 | HG00323.hp2 HG01515.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-1854T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518895 | ||||||
| chr21:14518938
|
C | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(112): Show | 120 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.130-1897G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14518938 | ||||||
| chr21:14519019
|
G | T | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.130-1978C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519019 | ||||||
| chr21:14519077
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273others(1): Show | 4 | HG01106.hp1 HG02258.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2036G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519077 | ||||||
| chr21:14519093
|
A | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01081.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-2052T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519093 | ||||||
| chr21:14519101
|
A | G | 1 | a0001c0002t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.129+2049T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519101 | ||||||
| chr21:14519265
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG00280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.129+1885A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519265 | ||||||
| chr21:14519416
|
T | A | 1 | a0001c0001t0001g0163 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.129+1734A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519416 | ||||||
| chr21:14519472
|
T | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1678A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519472 | ||||||
| chr21:14519488
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1662G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519488 | ||||||
| chr21:14519555
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1595A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519555 | ||||||
| chr21:14519602
|
A | G | 14 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0002g0169others(11): Show | 14 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.129+1548T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519602 | ||||||
| chr21:14519695
|
GAT | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1453_129+1454d others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519695 | ||||||
| chr21:14519721
|
GGATCTAA others(9): Show |
G | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0267 | 3 | NA18974.hp2 NA19000.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.129+1413_129+1428d others(18): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519721 | ||||||
| chr21:14519759
|
A | G | 2 | a0001c0001t0001g0039a0001c0002t0002g0381 | 2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.129+1391T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519759 | ||||||
| chr21:14519818
|
A | G | 15 | a0001c0001t0001g0177a0001c0001t0001g0200a0001c0001t0001g0202others(12): Show | 17 | HG00642.hp2 HG01074.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.129+1332T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519818 | ||||||
| chr21:14519919
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01081.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1231T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519919 | ||||||
| chr21:14519923
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+1227G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519923 | ||||||
| chr21:14519932
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0139a0001c0001t0001g0161others(2): Show | 6 | HG00735.hp1 HG01255.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1218C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14519932 | ||||||
| chr21:14520094
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+1056G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520094 | ||||||
| chr21:14520189
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(23): Show | 27 | HG01081.hp1 HG01106.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+961G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520189 | ||||||
| chr21:14520233
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.129+917G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520233 | ||||||
| chr21:14520238
|
G | C | 3 | a0001c0001t0001g0193a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.129+912C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520238 | ||||||
| chr21:14520255
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.129+895A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520255 | ||||||
| chr21:14520478
|
C | G | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.129+672G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520478 | ||||||
| chr21:14520499
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.129+651C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520499 | ||||||
| chr21:14520616
|
C | A | 1 | a0001c0001t0001g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.129+534G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520616 | ||||||
| chr21:14520659
|
A | C | 2 | a0001c0001t0001g0039a0001c0002t0002g0381 | 2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.129+491T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520659 | ||||||
| chr21:14520669
|
T | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129+481A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520669 | ||||||
| chr21:14520703
|
T | G | 1 | a0001c0002t0001g0351 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.129+447A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520703 | ||||||
| chr21:14520760
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 7 | HG02280.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.129+390C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520760 | ||||||
| chr21:14520763
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.129+387C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520763 | ||||||
| chr21:14520805
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.129+345T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520805 | ||||||
| chr21:14520813
|
G | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 107 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.129+337C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520813 | ||||||
| chr21:14520865
|
T | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.129+285A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520865 | ||||||
| chr21:14520883
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.129+267A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520883 | ||||||
| chr21:14520907
|
C | T | 84 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(81): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.129+243G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14520907 | ||||||
| chr21:14521034
|
C | T | 1 | a0001c0001t0001g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.129+116G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14521034 | ||||||
| chr21:14521088
|
G | A | 1 | a0001c0002t0009g0025 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.129+62C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 2/7 | chr21 | 14521088 | ||||||
| chr21:14521224
|
A | T | 3 | a0001c0001t0001g0193a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.58-3T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521224 | ||||||
| chr21:14521246
|
A | T | 85 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(82): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.58-25T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521246 | ||||||
| chr21:14521262
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.58-41A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521262 | ||||||
| chr21:14521273
|
T | C | 199 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.58-52A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521273 | ||||||
| chr21:14521323
|
C | A | 1 | a0001c0002t0001g0348 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.58-102G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521323 | ||||||
| chr21:14521420
|
T | C | 1 | a0002c0003t0001g0007 | 2 | HG01168.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.58-199A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521420 | ||||||
| chr21:14521709
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273 | 3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-488C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521709 | ||||||
| chr21:14521859
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.58-638C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521859 | ||||||
| chr21:14521900
|
T | TA | 114 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(111): Show | 119 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.58-680dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521900 | ||||||
| chr21:14521900
|
TA | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0062a0001c0001t0001g0139others(6): Show | 10 | HG00735.hp1 HG01255.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-680delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521900 | ||||||
| chr21:14521957
|
G | A | 208 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.58-736C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14521957 | ||||||
| chr21:14522042
|
G | A | 85 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0071others(82): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.58-821C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522042 | ||||||
| chr21:14522043
|
G | A | 85 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0071others(82): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.58-822C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522043 | ||||||
| chr21:14522052
|
A | C | 117 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(114): Show | 123 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.58-831T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522052 | ||||||
| chr21:14522197
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0279 | 2 | HG02622.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58-976C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522197 | ||||||
| chr21:14522205
|
A | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0189 | 2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.58-984T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522205 | ||||||
| chr21:14522253
|
G | A | 14 | a0001c0001t0001g0138a0001c0001t0001g0176a0001c0001t0001g0206others(11): Show | 14 | HG02155.hp2 NA18612.hp1 NA18942.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-1032C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522253 | ||||||
| chr21:14522262
|
A | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(95): Show | 102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-1041T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522262 | ||||||
| chr21:14522517
|
T | C | 228 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(225): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.58-1296A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522517 | ||||||
| chr21:14522659
|
T | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(205): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.58-1438A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522659 | ||||||
| chr21:14522666
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(3): Show | 7 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1445G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522666 | ||||||
| chr21:14522667
|
A | C | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(3): Show | 7 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1446T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522667 | ||||||
| chr21:14522733
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1512C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522733 | ||||||
| chr21:14522776
|
A | G | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-1555T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522776 | ||||||
| chr21:14522983
|
G | T | 1 | a0001c0002t0003g0298 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.58-1762C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14522983 | ||||||
| chr21:14523007
|
G | A | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-1786C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523007 | ||||||
| chr21:14523199
|
A | G | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG02165.hp2 NA18948.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1978T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523199 | ||||||
| chr21:14523257
|
A | C | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2036T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523257 | ||||||
| chr21:14523361
|
TGACTTGC others(11): Show |
T | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.58-2158_58-2141del others(18): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523361 | ||||||
| chr21:14523364
|
C | T | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2143G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523364 | ||||||
| chr21:14523370
|
A | G | 1 | a0001c0002t0001g0293 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.58-2149T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523370 | ||||||
| chr21:14523428
|
C | A | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2207G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523428 | ||||||
| chr21:14523574
|
C | A | 1 | a0001c0002t0001g0343 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.58-2353G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523574 | ||||||
| chr21:14523575
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0002g0135 | 2 | HG01515.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.58-2354C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523575 | ||||||
| chr21:14523690
|
A | G | 1 | a0001c0002t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58-2469T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523690 | ||||||
| chr21:14523691
|
T | C | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2470A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523691 | ||||||
| chr21:14523694
|
A | G | 93 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(90): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.58-2473T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523694 | ||||||
| chr21:14523718
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273 | 3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-2497C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523718 | ||||||
| chr21:14523728
|
G | T | 86 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0071others(83): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.58-2507C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523728 | ||||||
| chr21:14523804
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0172 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.58-2583T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523804 | ||||||
| chr21:14523839
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.58-2618A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523839 | ||||||
| chr21:14523890
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.58-2669T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523890 | ||||||
| chr21:14523915
|
A | C | 1 | a0001c0001t0001g0032 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.58-2694T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523915 | ||||||
| chr21:14523960
|
A | G | 86 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0071others(83): Show | 89 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.58-2739T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14523960 | ||||||
| chr21:14524101
|
A | G | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2880T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524101 | ||||||
| chr21:14524186
|
G | C | 2 | a0001c0001t0001g0062a0001c0001t0001g0166 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.58-2965C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524186 | ||||||
| chr21:14524195
|
T | C | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-2974A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524195 | ||||||
| chr21:14524226
|
A | T | 1 | a0001c0001t0001g0019 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.58-3005T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524226 | ||||||
| chr21:14524243
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58-3022T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524243 | ||||||
| chr21:14524263
|
A | G | 1 | a0001c0002t0001g0303 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.58-3042T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524263 | ||||||
| chr21:14524274
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 5 | HG00639.hp2 HG02280.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-3053A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524274 | ||||||
| chr21:14524375
|
G | GC | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-3155_58-3154ins others(1): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524375 | ||||||
| chr21:14524389
|
A | T | 1 | a0001c0002t0001g0023 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.58-3168T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524389 | ||||||
| chr21:14524390
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273 | 3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-3169A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524390 | ||||||
| chr21:14524463
|
T | C | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0273 | 3 | HG01106.hp1 HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.58-3242A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524463 | ||||||
| chr21:14524676
|
T | C | 2 | a0001c0001t0001g0187a0001c0002t0001g0326 | 2 | NA18950.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.58-3455A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524676 | ||||||
| chr21:14524705
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.58-3484C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524705 | ||||||
| chr21:14524761
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0042 | 3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58-3540A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14524761 | ||||||
| chr21:14525036
|
T | A | 1 | a0001c0002t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58-3815A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525036 | ||||||
| chr21:14525047
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.58-3826T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525047 | ||||||
| chr21:14525123
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG02630.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.58-3902A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525123 | ||||||
| chr21:14525152
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.58-3931A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525152 | ||||||
| chr21:14525252
|
T | C | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-4031A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525252 | ||||||
| chr21:14525369
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.58-4148G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525369 | ||||||
| chr21:14525486
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.58-4265T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525486 | ||||||
| chr21:14525536
|
A | G | 85 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0073others(82): Show | 88 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.58-4315T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525536 | ||||||
| chr21:14525550
|
C | G | 1 | a0001c0001t0002g0118 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.58-4329G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525550 | ||||||
| chr21:14525608
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 141 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.58-4387C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525608 | ||||||
| chr21:14525651
|
C | T | 3 | a0001c0001t0001g0193a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG02615.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.58-4430G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525651 | ||||||
| chr21:14525670
|
G | A | 10 | a0001c0001t0001g0064a0001c0001t0001g0170a0001c0001t0001g0172others(7): Show | 10 | HG02257.hp2 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-4449C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525670 | ||||||
| chr21:14525718
|
T | C | 114 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(111): Show | 118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.58-4497A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525718 | ||||||
| chr21:14525745
|
T | C | 1 | a0001c0002t0001g0349 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58-4524A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525745 | ||||||
| chr21:14525776
|
T | C | 1 | a0001c0001t0007g0173 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-4555A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525776 | ||||||
| chr21:14525779
|
A | T | 1 | a0001c0002t0001g0336 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.58-4558T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525779 | ||||||
| chr21:14525821
|
T | C | 18 | a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0174others(15): Show | 19 | HG01081.hp1 HG01168.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-4600A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525821 | ||||||
| chr21:14525831
|
T | G | 112 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(109): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-4610A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525831 | ||||||
| chr21:14525853
|
C | T | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.58-4632G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525853 | ||||||
| chr21:14525863
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4642A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525863 | ||||||
| chr21:14525933
|
C | T | 111 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0031others(108): Show | 115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.58-4712G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525933 | ||||||
| chr21:14525934
|
G | C | 2 | a0001c0001t0001g0043a0001c0002t0001g0356 | 2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58-4713C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525934 | ||||||
| chr21:14525963
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(96): Show | 111 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.58-4742C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525963 | ||||||
| chr21:14525985
|
C | A | 2 | a0001c0001t0001g0039a0001c0002t0002g0381 | 2 | HG01081.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.58-4764G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14525985 | ||||||
| chr21:14526077
|
AG | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4857delC | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526077 | ||||||
| chr21:14526114
|
C | G | 108 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(105): Show | 112 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.58-4893G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526114 | ||||||
| chr21:14526133
|
G | T | 1 | a0001c0001t0001g0234 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.58-4912C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526133 | ||||||
| chr21:14526146
|
G | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0002t0014g0344 | 3 | HG02647.hp2 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58-4925C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526146 | ||||||
| chr21:14526156
|
C | G | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.58-4935G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526156 | ||||||
| chr21:14526270
|
C | T | 99 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(96): Show | 103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.58-5049G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526270 | ||||||
| chr21:14526271
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58-5050C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526271 | ||||||
| chr21:14526271
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.58-5050C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526271 | ||||||
| chr21:14526295
|
T | A | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(319): Show | 346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.58-5074A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526295 | ||||||
| chr21:14526360
|
C | G | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(97): Show | 104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.58-5139G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526360 | ||||||
| chr21:14526388
|
C | T | 4 | a0001c0002t0001g0334a0001c0002t0001g0366a0001c0002t0001g0367others(1): Show | 4 | HG02129.hp1 NA18953.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-5167G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526388 | ||||||
| chr21:14526454
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-5233C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526454 | ||||||
| chr21:14526470
|
T | C | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.58-5249A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526470 | ||||||
| chr21:14526499
|
C | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.58-5278G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526499 | ||||||
| chr21:14526505
|
T | G | 1 | a0001c0001t0002g0112 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.58-5284A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526505 | ||||||
| chr21:14526540
|
A | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG00735.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.58-5319T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526540 | ||||||
| chr21:14526543
|
T | C | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(94): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.58-5322A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526543 | ||||||
| chr21:14526599
|
G | A | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.58-5378C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526599 | ||||||
| chr21:14526764
|
G | A | 110 | a0001c0001t0001g0051a0001c0001t0001g0064a0001c0001t0001g0100others(107): Show | 116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-5543C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526764 | ||||||
| chr21:14526852
|
C | G | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(95): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-5631G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526852 | ||||||
| chr21:14526885
|
G | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.58-5664C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526885 | ||||||
| chr21:14526902
|
A | T | 119 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0043others(116): Show | 125 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.58-5681T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526902 | ||||||
| chr21:14526931
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.58-5710T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526931 | ||||||
| chr21:14526954
|
G | A | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(95): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-5733C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14526954 | ||||||
| chr21:14527000
|
G | A | 1 | a0001c0001t0003g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.58-5779C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527000 | ||||||
| chr21:14527043
|
T | A | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(95): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-5822A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527043 | ||||||
| chr21:14527053
|
C | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0065a0001c0001t0001g0157others(5): Show | 8 | HG02258.hp1 HG02451.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-5832G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527053 | ||||||
| chr21:14527076
|
T | C | 97 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(94): Show | 101 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.58-5855A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527076 | ||||||
| chr21:14527147
|
G | A | 1 | a0001c0002t0001g0331 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.58-5926C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527147 | ||||||
| chr21:14527184
|
T | A | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-5963A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527184 | ||||||
| chr21:14527185
|
C | A | 4 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(1): Show | 4 | HG00741.hp1 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-5964G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527185 | ||||||
| chr21:14527250
|
T | C | 1 | a0001c0002t0001g0380 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.58-6029A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527250 | ||||||
| chr21:14527291
|
G | A | 58 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0036others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.58-6070C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527291 | ||||||
| chr21:14527399
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.58-6178C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527399 | ||||||
| chr21:14527420
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58-6199T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527420 | ||||||
| chr21:14527443
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 118 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.58-6222G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527443 | ||||||
| chr21:14527549
|
G | T | 1 | a0002c0003t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58-6328C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527549 | ||||||
| chr21:14527625
|
T | C | 3 | a0001c0001t0001g0064a0001c0002t0001g0286a0001c0002t0001g0287 | 3 | HG02257.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.58-6404A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527625 | ||||||
| chr21:14527634
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.58-6413C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527634 | ||||||
| chr21:14527760
|
TA | T | 6 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0065others(3): Show | 6 | HG01081.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-6540delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527760 | ||||||
| chr21:14527760
|
TAAA | T | 99 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0033others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.58-6542_58-6540del others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527760 | ||||||
| chr21:14527760
|
TAAAA | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(96): Show | 112 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.58-6543_58-6540del others(4): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527760 | ||||||
| chr21:14527799
|
A | G | 7 | a0001c0001t0001g0195a0001c0002t0001g0004a0001c0002t0001g0299others(4): Show | 9 | HG00408.hp2 HG00438.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-6578T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527799 | ||||||
| chr21:14527806
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.58-6585T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527806 | ||||||
| chr21:14527876
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.58-6655G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527876 | ||||||
| chr21:14527877
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.58-6656T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527877 | ||||||
| chr21:14527901
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.58-6680A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14527901 | ||||||
| chr21:14528101
|
C | A | 2 | a0001c0001t0001g0114a0001c0001t0002g0113 | 2 | HG00621.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58-6880G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528101 | ||||||
| chr21:14528203
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.58-6982C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528203 | ||||||
| chr21:14528380
|
T | C | 1 | a0001c0002t0001g0327 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.58-7159A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528380 | ||||||
| chr21:14528549
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.58-7328A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528549 | ||||||
| chr21:14528633
|
C | G | 1 | a0001c0002t0002g0373 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58-7412G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528633 | ||||||
| chr21:14528839
|
G | T | 1 | a0001c0001t0001g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.58-7618C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528839 | ||||||
| chr21:14528883
|
C | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0136 | 2 | HG00099.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.58-7662G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528883 | ||||||
| chr21:14528896
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-7675G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528896 | ||||||
| chr21:14528939
|
G | C | 1 | a0001c0001t0001g0225 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-7718C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14528939 | ||||||
| chr21:14529023
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-7802G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529023 | ||||||
| chr21:14529271
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.58-8050G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529271 | ||||||
| chr21:14529346
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0042 | 3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58-8125C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529346 | ||||||
| chr21:14529415
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-8194T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529415 | ||||||
| chr21:14529471
|
A | C | 1 | a0001c0001t0001g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.58-8250T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529471 | ||||||
| chr21:14529594
|
A | C | 1 | a0001c0002t0001g0352 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.58-8373T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529594 | ||||||
| chr21:14529656
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0232a0001c0001t0001g0233 | 5 | HG01256.hp2 HG01258.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-8435T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529656 | ||||||
| chr21:14529689
|
A | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58-8468T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529689 | ||||||
| chr21:14529694
|
T | C | 1 | a0001c0002t0003g0374 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.58-8473A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529694 | ||||||
| chr21:14529814
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58-8593A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529814 | ||||||
| chr21:14529965
|
C | A | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0032others(97): Show | 104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.58-8744G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529965 | ||||||
| chr21:14529966
|
C | T | 111 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0001g0100others(108): Show | 117 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.58-8745G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14529966 | ||||||
| chr21:14530034
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0042 | 3 | HG02723.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58-8813A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530034 | ||||||
| chr21:14530057
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.58-8836G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530057 | ||||||
| chr21:14530071
|
C | T | 1 | a0001c0002t0001g0022 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.58-8850G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530071 | ||||||
| chr21:14530098
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.58-8877G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530098 | ||||||
| chr21:14530174
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(89): Show | 103 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.58-8953C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530174 | ||||||
| chr21:14530181
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-8960C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530181 | ||||||
| chr21:14530188
|
G | A | 1 | a0001c0002t0001g0287 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-8967C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530188 | ||||||
| chr21:14530189
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-8968A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530189 | ||||||
| chr21:14530241
|
T | C | 5 | a0001c0002t0001g0284a0001c0002t0001g0352a0001c0002t0001g0353others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-9020A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530241 | ||||||
| chr21:14530278
|
A | C | 380 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(377): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.58-9057T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530278 | ||||||
| chr21:14530300
|
G | C | 6 | a0001c0002t0001g0369a0001c0002t0001g0370a0001c0002t0001g0371others(3): Show | 6 | HG00597.hp1 HG02135.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-9079C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530300 | ||||||
| chr21:14530311
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.58-9090G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530311 | ||||||
| chr21:14530312
|
G | A | 1 | a0001c0002t0001g0356 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58-9091C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530312 | ||||||
| chr21:14530316
|
C | CA | 15 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0061others(12): Show | 15 | HG02258.hp1 HG02622.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-9096dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530316 | ||||||
| chr21:14530333
|
A | AAAAAAG | 12 | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0137others(9): Show | 13 | HG00438.hp1 HG01081.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-9113_58-9112ins others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530333 | ||||||
| chr21:14530333
|
A | AAAAAG | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.58-9113_58-9112ins others(5): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530333 | ||||||
| chr21:14530333
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-9112T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530333 | ||||||
| chr21:14530337
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0172a0001c0001t0007g0173 | 4 | HG02895.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9116C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530337 | ||||||
| chr21:14530339
|
A | AAGAAATA others(3): Show |
34 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0077others(31): Show | 37 | HG00621.hp1 HG00621.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.58-9128_58-9119dup others(10): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530339 | ||||||
| chr21:14530339
|
A | AATAATC | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.58-9119_58-9118ins others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530339 | ||||||
| chr21:14530339
|
A | AGAAAGAA others(6): Show |
3 | a0001c0001t0001g0014a0001c0001t0001g0172a0001c0001t0007g0173 | 4 | HG02895.hp1 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9119_58-9118ins others(13): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530339 | ||||||
| chr21:14530358
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 114 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.58-9137G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530358 | ||||||
| chr21:14530378
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.58-9157C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530378 | ||||||
| chr21:14530522
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-9301G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530522 | ||||||
| chr21:14530657
|
G | T | 215 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0033others(212): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.58-9436C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530657 | ||||||
| chr21:14530764
|
T | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0275 | 4 | HG00639.hp1 HG01433.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-9543A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530764 | ||||||
| chr21:14530922
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0003g0266 | 2 | NA18979.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.58-9701A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530922 | ||||||
| chr21:14530994
|
T | A | 2 | a0001c0002t0001g0330a0001c0002t0001g0331 | 2 | HG01256.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.58-9773A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14530994 | ||||||
| chr21:14531073
|
T | C | 1 | a0001c0002t0002g0373 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58-9852A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531073 | ||||||
| chr21:14531287
|
T | C | 1 | a0001c0002t0001g0349 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58-10066A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531287 | ||||||
| chr21:14531521
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-10300A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531521 | ||||||
| chr21:14531528
|
T | C | 1 | a0001c0002t0003g0374 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.58-10307A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531528 | ||||||
| chr21:14531897
|
C | A | 36 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(33): Show | 38 | HG00639.hp2 HG01099.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.58-10676G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531897 | ||||||
| chr21:14531907
|
G | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0281others(2): Show | 5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-10686C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531907 | ||||||
| chr21:14531999
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-10778C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14531999 | ||||||
| chr21:14532071
|
G | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG00735.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.58-10850C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532071 | ||||||
| chr21:14532099
|
G | A | 1 | a0001c0002t0001g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58-10878C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532099 | ||||||
| chr21:14532182
|
G | A | 3 | a0001c0001t0001g0064a0001c0002t0001g0286a0001c0002t0001g0287 | 3 | HG02257.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.58-10961C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532182 | ||||||
| chr21:14532263
|
T | C | 1 | a0001c0002t0002g0332 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.58-11042A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532263 | ||||||
| chr21:14532295
|
C | A | 1 | a0001c0002t0001g0333 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.58-11074G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532295 | ||||||
| chr21:14532674
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.58-11453A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532674 | ||||||
| chr21:14532901
|
ATTAT | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 8 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-11684_58-11681d others(6): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532901 | ||||||
| chr21:14532921
|
T | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0067a0001c0001t0001g0068others(1): Show | 4 | HG02630.hp1 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-11700A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532921 | ||||||
| chr21:14532936
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.58-11715A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14532936 | ||||||
| chr21:14533138
|
T | A | 1 | a0001c0001t0001g0231 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.58-11917A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533138 | ||||||
| chr21:14533194
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 8 | HG01256.hp2 HG01258.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-11973C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533194 | ||||||
| chr21:14533232
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0106 | 3 | NA18945.hp2 NA18962.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.58-12011T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533232 | ||||||
| chr21:14533259
|
C | T | 54 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0154others(51): Show | 58 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.58-12038G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533259 | ||||||
| chr21:14533887
|
A | C | 2 | a0001c0002t0001g0296a0001c0002t0001g0297 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.57+12318T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533887 | ||||||
| chr21:14533959
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+12246C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14533959 | ||||||
| chr21:14534015
|
A | C | 1 | a0001c0001t0001g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.57+12190T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534015 | ||||||
| chr21:14534214
|
A | T | 1 | a0001c0001t0001g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.57+11991T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534214 | ||||||
| chr21:14534253
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+11952G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534253 | ||||||
| chr21:14534269
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(244): Show | 266 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+11936C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534269 | ||||||
| chr21:14534326
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.57+11879G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534326 | ||||||
| chr21:14534378
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0062 | 2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.57+11827T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534378 | ||||||
| chr21:14534399
|
G | C | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0281others(2): Show | 5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+11806C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534399 | ||||||
| chr21:14534477
|
T | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0273 | 2 | HG01106.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.57+11728A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534477 | ||||||
| chr21:14534523
|
TC | T | 7 | a0001c0001t0001g0037a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG02258.hp1 HG02647.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+11681delG | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534523 | ||||||
| chr21:14534524
|
C | CT | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(235): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.57+11680dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534524 | ||||||
| chr21:14534524
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(5): Show | 9 | HG01106.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+11681G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534524 | ||||||
| chr21:14534594
|
C | A | 2 | a0001c0001t0002g0238a0001c0001t0002g0239 | 2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.57+11611G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534594 | ||||||
| chr21:14534608
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0066 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57+11597G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534608 | ||||||
| chr21:14534665
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.57+11540C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534665 | ||||||
| chr21:14534728
|
A | C | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+11477T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534728 | ||||||
| chr21:14534974
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+11231G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534974 | ||||||
| chr21:14534986
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01081.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+11219G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14534986 | ||||||
| chr21:14535134
|
C | T | 9 | a0001c0001t0002g0169a0001c0001t0002g0175a0001c0002t0001g0294others(6): Show | 9 | HG01884.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+11071G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535134 | ||||||
| chr21:14535198
|
C | A | 1 | a0001c0002t0001g0350 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.57+11007G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535198 | ||||||
| chr21:14535224
|
T | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0273a0001c0002t0002g0381 | 3 | HG01106.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.57+10981A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535224 | ||||||
| chr21:14535590
|
T | A | 2 | a0002c0003t0001g0049a0002c0004t0001g0291 | 2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.57+10615A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535590 | ||||||
| chr21:14535759
|
T | C | 1 | a0001c0001t0002g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.57+10446A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535759 | ||||||
| chr21:14535998
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+10207G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14535998 | ||||||
| chr21:14536054
|
C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(95): Show | 109 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.57+10151G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536054 | ||||||
| chr21:14536088
|
A | G | 1 | a0002c0003t0002g0044 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.57+10117T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536088 | ||||||
| chr21:14536141
|
T | C | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+10064A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536141 | ||||||
| chr21:14536158
|
G | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0281others(2): Show | 5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+10047C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536158 | ||||||
| chr21:14536243
|
A | C | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+9962T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536243 | ||||||
| chr21:14536318
|
T | C | 1 | a0001c0002t0001g0351 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.57+9887A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536318 | ||||||
| chr21:14536321
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.57+9884G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536321 | ||||||
| chr21:14536407
|
C | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0070a0001c0001t0001g0157others(7): Show | 10 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+9798G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536407 | ||||||
| chr21:14536570
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.57+9635C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536570 | ||||||
| chr21:14536649
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.57+9556A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536649 | ||||||
| chr21:14536685
|
AAAG | A | 4 | a0001c0001t0001g0033a0001c0001t0002g0034a0001c0001t0002g0164others(1): Show | 5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+9517_57+9519del others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536685 | ||||||
| chr21:14536702
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+9503G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536702 | ||||||
| chr21:14536702
|
C | T | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+9503G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536702 | ||||||
| chr21:14536707
|
C | G | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(264): Show | 287 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.57+9498G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536707 | ||||||
| chr21:14536752
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.57+9453G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536752 | ||||||
| chr21:14536777
|
G | A | 2 | a0002c0003t0001g0179a0002c0003t0001g0180 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.57+9428C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536777 | ||||||
| chr21:14536888
|
G | A | 5 | a0001c0002t0001g0284a0001c0002t0001g0352a0001c0002t0001g0353others(2): Show | 5 | HG01167.hp2 HG01169.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+9317C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536888 | ||||||
| chr21:14536930
|
A | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(112): Show | 128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.57+9275T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536930 | ||||||
| chr21:14536947
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.57+9258A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536947 | ||||||
| chr21:14536969
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+9236A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536969 | ||||||
| chr21:14536970
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(82): Show | 94 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.57+9235G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14536970 | ||||||
| chr21:14537042
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(108): Show | 124 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.57+9163T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537042 | ||||||
| chr21:14537128
|
C | T | 1 | a0001c0002t0001g0292 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.57+9077G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537128 | ||||||
| chr21:14537155
|
C | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+9050G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537155 | ||||||
| chr21:14537208
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.57+8997T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537208 | ||||||
| chr21:14537247
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0002g0034a0001c0001t0002g0164others(1): Show | 5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+8958G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537247 | ||||||
| chr21:14537282
|
A | C | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0281others(2): Show | 5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+8923T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537282 | ||||||
| chr21:14537355
|
C | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.57+8850G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537355 | ||||||
| chr21:14537375
|
A | AT | 30 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(27): Show | 31 | HG01081.hp1 HG01099.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+8829dupA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537375 | ||||||
| chr21:14537460
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(214): Show | 236 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.57+8745G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537460 | ||||||
| chr21:14537492
|
G | A | 1 | a0001c0002t0002g0377 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.57+8713C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537492 | ||||||
| chr21:14537499
|
T | C | 2 | a0001c0001t0001g0062a0001c0002t0001g0356 | 2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57+8706A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537499 | ||||||
| chr21:14537536
|
G | A | 1 | a0001c0002t0001g0357 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.57+8669C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537536 | ||||||
| chr21:14537557
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(103): Show | 118 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.57+8648G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537557 | ||||||
| chr21:14537715
|
T | A | 107 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0154others(104): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.57+8490A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537715 | ||||||
| chr21:14537854
|
G | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01081.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+8351C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537854 | ||||||
| chr21:14537952
|
C | A | 1 | a0001c0001t0002g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.57+8253G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14537952 | ||||||
| chr21:14538034
|
T | A | 1 | a0001c0001t0001g0267 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.57+8171A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538034 | ||||||
| chr21:14538072
|
G | A | 7 | a0001c0001t0002g0169a0001c0001t0002g0175a0001c0002t0001g0358others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+8133C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538072 | ||||||
| chr21:14538158
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0098 | 3 | HG00099.hp2 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.57+8047G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538158 | ||||||
| chr21:14538194
|
T | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+8011A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538194 | ||||||
| chr21:14538233
|
ACATTTTA others(6): Show |
A | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7959_57+7971del others(13): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538233 | ||||||
| chr21:14538246
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(281): Show | 304 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.57+7959A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538246 | ||||||
| chr21:14538247
|
G | A | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7958C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538247 | ||||||
| chr21:14538248
|
T | C | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7957A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538248 | ||||||
| chr21:14538251
|
T | A | 1 | a0003c0005t0001g0362 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+7954A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538251 | ||||||
| chr21:14538606
|
T | G | 10 | a0001c0001t0001g0167a0001c0001t0001g0259a0001c0001t0001g0260others(7): Show | 10 | HG02129.hp2 NA18943.hp1 NA18974.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+7599A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538606 | ||||||
| chr21:14538916
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.57+7289C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14538916 | ||||||
| chr21:14539008
|
A | C | 1 | a0001c0001t0003g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.57+7197T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539008 | ||||||
| chr21:14539015
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+7190A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539015 | ||||||
| chr21:14539112
|
G | A | 4 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | HG02615.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+7093C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539112 | ||||||
| chr21:14539149
|
C | A | 107 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0001g0154others(104): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.57+7056G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539149 | ||||||
| chr21:14539286
|
T | G | 1 | a0001c0001t0004g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.57+6919A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539286 | ||||||
| chr21:14539412
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.57+6793T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539412 | ||||||
| chr21:14539463
|
G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+6742C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539463 | ||||||
| chr21:14539566
|
A | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+6639T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539566 | ||||||
| chr21:14539567
|
A | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+6638T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539567 | ||||||
| chr21:14539624
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+6581A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539624 | ||||||
| chr21:14539641
|
A | T | 3 | a0001c0001t0001g0033a0001c0001t0002g0034a0002c0003t0001g0007 | 4 | HG01168.hp2 HG02004.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+6564T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539641 | ||||||
| chr21:14539686
|
A | G | 1 | a0001c0002t0001g0288 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.57+6519T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539686 | ||||||
| chr21:14539698
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.57+6507G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539698 | ||||||
| chr21:14539712
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 8 | HG00423.hp1 HG00609.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+6493G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539712 | ||||||
| chr21:14539746
|
A | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(244): Show | 266 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.57+6459T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539746 | ||||||
| chr21:14539781
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 8 | HG01106.hp1 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+6424G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539781 | ||||||
| chr21:14539835
|
A | G | 13 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0088others(10): Show | 14 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+6370T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539835 | ||||||
| chr21:14539890
|
A | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178 | 3 | NA18942.hp1 NA19010.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.57+6315T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14539890 | ||||||
| chr21:14540233
|
C | G | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+5972G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540233 | ||||||
| chr21:14540404
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.57+5801C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540404 | ||||||
| chr21:14540475
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+5730C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540475 | ||||||
| chr21:14540479
|
A | G | 3 | a0001c0001t0001g0064a0001c0002t0001g0286a0001c0002t0001g0287 | 3 | HG02257.hp2 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.57+5726T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540479 | ||||||
| chr21:14540538
|
A | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0170a0001c0001t0001g0171others(5): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+5667T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540538 | ||||||
| chr21:14540743
|
G | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 261 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.57+5462C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540743 | ||||||
| chr21:14540750
|
T | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 261 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.57+5455A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540750 | ||||||
| chr21:14540807
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.57+5398G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540807 | ||||||
| chr21:14540832
|
A | G | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0281others(2): Show | 5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+5373T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540832 | ||||||
| chr21:14540853
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(239): Show | 261 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.57+5352C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14540853 | ||||||
| chr21:14541024
|
T | C | 2 | a0002c0003t0001g0038a0002c0003t0001g0049 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.57+5181A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541024 | ||||||
| chr21:14541025
|
G | T | 2 | a0002c0003t0001g0038a0002c0003t0001g0049 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.57+5180C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541025 | ||||||
| chr21:14541074
|
T | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA18939.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.57+5131A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541074 | ||||||
| chr21:14541116
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+5089G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541116 | ||||||
| chr21:14541145
|
G | T | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+5060C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541145 | ||||||
| chr21:14541147
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+5058C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541147 | ||||||
| chr21:14541187
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+5018C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541187 | ||||||
| chr21:14541239
|
C | A | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+4966G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541239 | ||||||
| chr21:14541323
|
T | TA | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+4881dupT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541323 | ||||||
| chr21:14541323
|
TAA | T | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.57+4880_57+4881del others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541323 | ||||||
| chr21:14541372
|
C | A | 3 | a0001c0002t0001g0363a0001c0002t0001g0364a0001c0002t0002g0365 | 3 | NA18944.hp1 NA18953.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.57+4833G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541372 | ||||||
| chr21:14541380
|
A | G | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.57+4825T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541380 | ||||||
| chr21:14541448
|
C | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+4757G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541448 | ||||||
| chr21:14541458
|
C | G | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0004g0008others(3): Show | 7 | HG01099.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+4747G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541458 | ||||||
| chr21:14541515
|
G | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(243): Show | 265 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.57+4690C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541515 | ||||||
| chr21:14541520
|
T | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.57+4685A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541520 | ||||||
| chr21:14541603
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+4602A>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541603 | ||||||
| chr21:14541649
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0002g0034a0001c0001t0002g0164others(1): Show | 5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+4556T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541649 | ||||||
| chr21:14541699
|
C | T | 10 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(7): Show | 13 | HG02683.hp1 HG04184.hp1 NA18944.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+4506G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541699 | ||||||
| chr21:14541918
|
A | C | 1 | a0001c0001t0002g0169 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.57+4287T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541918 | ||||||
| chr21:14541958
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.57+4247G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541958 | ||||||
| chr21:14541965
|
CTGGGTAA others(5): Show |
C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.57+4228_57+4239del others(12): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541965 | ||||||
| chr21:14541987
|
G | GAA | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(219): Show | 240 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.57+4216_57+4217dup others(2): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541987 | ||||||
| chr21:14541987
|
G | GAAA | 21 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(18): Show | 22 | HG00597.hp1 HG01981.hp1 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+4215_57+4217dup others(3): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14541987 | ||||||
| chr21:14542059
|
G | C | 1 | a0001c0001t0002g0155 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.57+4146C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542059 | ||||||
| chr21:14542077
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.57+4128C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542077 | ||||||
| chr21:14542154
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG00735.hp2 NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.57+4051G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542154 | ||||||
| chr21:14542565
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.57+3640A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542565 | ||||||
| chr21:14542619
|
A | C | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.57+3586T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542619 | ||||||
| chr21:14542690
|
T | C | 1 | a0001c0002t0001g0378 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.57+3515A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542690 | ||||||
| chr21:14542990
|
C | A | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG02615.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.57+3215G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14542990 | ||||||
| chr21:14543153
|
C | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | NA18962.hp2 NA18982.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.57+3052G>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543153 | ||||||
| chr21:14543159
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+3046C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543159 | ||||||
| chr21:14543185
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(133): Show | 148 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.57+3020T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543185 | ||||||
| chr21:14543278
|
T | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.57+2927A>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543278 | ||||||
| chr21:14543402
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 259 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.57+2803G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543402 | ||||||
| chr21:14543417
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.57+2788A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543417 | ||||||
| chr21:14543480
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.57+2725T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543480 | ||||||
| chr21:14543533
|
C | T | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+2672G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543533 | ||||||
| chr21:14543732
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.57+2473A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543732 | ||||||
| chr21:14543751
|
A | C | 108 | a0001c0001t0001g0033a0001c0001t0001g0167a0001c0001t0002g0034others(105): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.57+2454T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543751 | ||||||
| chr21:14543813
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(281): Show | 304 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.57+2392T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543813 | ||||||
| chr21:14543905
|
C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG01081.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+2300G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14543905 | ||||||
| chr21:14544015
|
T | C | 1 | a0001c0002t0001g0379 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57+2190A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544015 | ||||||
| chr21:14544044
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+2161G>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544044 | ||||||
| chr21:14544231
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0274a0001c0001t0001g0275 | 4 | HG00639.hp1 HG01433.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+1974A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544231 | ||||||
| chr21:14544270
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(242): Show | 264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.57+1935C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544270 | ||||||
| chr21:14544285
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.57+1920T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544285 | ||||||
| chr21:14544302
|
C | T | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+1903G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544302 | ||||||
| chr21:14544303
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.57+1902C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544303 | ||||||
| chr21:14544309
|
GCAAAGTG others(28): Show |
G | 1 | a0002c0003t0001g0038 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.57+1861_57+1895del others(35): Show |
SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544309 | ||||||
| chr21:14544394
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0002g0034a0001c0001t0002g0164others(1): Show | 5 | HG01168.hp2 HG02004.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+1811T>C | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544394 | ||||||
| chr21:14544660
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57+1545T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544660 | ||||||
| chr21:14544738
|
A | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | NA18941.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.57+1467T>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14544738 | ||||||
| chr21:14545091
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0036 | 2 | HG02165.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.57+1114G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545091 | ||||||
| chr21:14545240
|
A | T | 108 | a0001c0001t0001g0033a0001c0001t0002g0034a0001c0002t0001g0004others(105): Show | 115 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.57+965T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545240 | ||||||
| chr21:14545254
|
C | T | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0281others(2): Show | 5 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+951G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545254 | ||||||
| chr21:14545499
|
G | A | 1 | a0001c0002t0001g0380 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.57+706C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545499 | ||||||
| chr21:14545536
|
CT | C | 8 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(5): Show | 8 | HG02258.hp1 HG02738.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+668delA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545536 | ||||||
| chr21:14545536
|
CTT | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(129): Show | 144 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.57+667_57+668delAA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545536 | ||||||
| chr21:14545547
|
TA | T | 107 | a0001c0001t0001g0033a0001c0001t0002g0034a0001c0002t0001g0004others(104): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.57+657delT | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545547 | ||||||
| chr21:14545548
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0279 | 2 | HG02886.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.57+657T>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545548 | ||||||
| chr21:14545626
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00735.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.57+579C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545626 | ||||||
| chr21:14545627
|
G | T | 1 | a0001c0001t0001g0031 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.57+578C>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545627 | ||||||
| chr21:14545629
|
G | C | 1 | a0001c0001t0001g0278 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.57+576C>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545629 | ||||||
| chr21:14545655
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57+550G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545655 | ||||||
| chr21:14545714
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG02280.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+491G>A | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545714 | ||||||
| chr21:14545808
|
G | A | 1 | a0001c0002t0002g0381 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.57+397C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545808 | ||||||
| chr21:14545820
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.57+385A>G | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545820 | ||||||
| chr21:14545887
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.57+318C>T | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14545887 | ||||||
| chr21:14546046
|
CTT | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0001g0283 | 3 | HG02738.hp1 HG03017.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.57+157_57+158delAA | SAMSN1 | ENSG00000155307.19 | transcript | ENST00000400566.6 | protein_coding | 1/7 | chr21 | 14546046 |