| geneid | 9905 |
|---|---|
| ensemblid | ENSG00000141258.13 |
| hgncid | 29026 |
| symbol | SGSM2 |
| name | small G protein signaling modulator 2 |
| refseq_nuc | NM_014853.3 |
| refseq_prot | NP_055668.2 |
| ensembl_nuc | ENST00000268989.8 |
| ensembl_prot | ENSP00000268989.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 2337501 |
| end | 2381054 |
| strand | + |
| ver | v1.2 |
| region | chr17:2337501-2381054 |
| region5000 | chr17:2332501-2386054 |
| regionname0 | SGSM2_chr17_2337501_2381054 |
| regionname5000 | SGSM2_chr17_2332501_2386054 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1051 | 249 | 44 | 26 | 141 | 10 | 27 | 108 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002 | 1/0 | 1051 | 132 | 28 | 48 | 32 | 6 | 17 | 20 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0003 | 0/0 | 1051 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0004 | 0/0 | 1051 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0005 | 0/0 | 1051 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0006 | 0/0 | 1051 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0007 | 0/0 | 1051 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0008 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0009 | 0/0 | 1051 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0010 | 0/0 | 1051 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0011 | 0/0 | 1051 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0012 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0013 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0014 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0015 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0016 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0017 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0018 | 0/0 | 1051 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0019 | 0/0 | 1051 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0020 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0021 | 0/0 | 1051 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0022 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0023 | 0/0 | 1051 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0024 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0025 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0026 | 0/0 | 1051 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0027 | 0/0 | 1051 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0028 | 0/0 | 1051 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3156 | 184 | 20 | 22 | 119 | 6 | 17 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0002 | 1/0 | 3156 | 104 | 6 | 46 | 31 | 5 | 15 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0003 | 0/1 | 3156 | 51 | 17 | 2 | 19 | 3 | 9 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0004 | 0/0 | 3156 | 22 | 17 | 2 | 0 | 1 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0005 | 0/0 | 3156 | 5 | 5 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0006 | 0/0 | 3156 | 5 | 5 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0007 | 0/0 | 3156 | 3 | 3 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0008 | 0/0 | 3156 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0009 | 0/0 | 3156 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0010 | 0/0 | 3156 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0011 | 0/0 | 3156 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0012 | 0/0 | 3156 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0013 | 0/0 | 3156 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0014 | 0/0 | 3156 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0015 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0016 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0017 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0018 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0019 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0020 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0021 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0022 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0023 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0024 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0025 | 0/0 | 3156 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0026 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0027 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0028 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0029 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0030 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0031 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0032 | 0/0 | 3156 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0033 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0034 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0035 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0036 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0037 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0038 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0039 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0040 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0041 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0042 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0043 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0044 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0045 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0046 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| c0047 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1723 | 291 | 60 | 60 | 129 | 10 | 32 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0002 | 0/0 | 1723 | 53 | 15 | 0 | 30 | 3 | 5 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0003 | 1/0 | 1723 | 37 | 3 | 6 | 20 | 2 | 5 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0004 | 0/0 | 1723 | 5 | 0 | 5 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0005 | 0/0 | 1720 | 4 | 4 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0006 | 0/0 | 1723 | 3 | 3 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0007 | 0/0 | 1723 | 3 | 0 | 3 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0008 | 0/0 | 1723 | 3 | 0 | 0 | 2 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0009 | 0/0 | 1708 | 3 | 1 | 0 | 1 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0010 | 0/0 | 1714 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0011 | 0/0 | 1723 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0012 | 0/0 | 1723 | 2 | 0 | 0 | 0 | 1 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0013 | 0/0 | 1723 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0014 | 0/0 | 1723 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0015 | 0/0 | 1723 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0016 | 0/0 | 1723 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0017 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0018 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0019 | 0/1 | 1723 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0020 | 0/0 | 1723 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0021 | 0/0 | 1723 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0022 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0023 | 0/0 | 1705 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| t0024 | 0/0 | 1720 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0006 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3156 | 184 | 20 | 22 | 119 | 6 | 17 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0003 | 0/1 | 3156 | 51 | 17 | 2 | 19 | 3 | 9 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0005 | 0/0 | 3156 | 5 | 5 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0020 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0024 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0025 | 0/0 | 3156 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0028 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0029 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0032 | 0/0 | 3156 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0034 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0037 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0039 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002 | 1/0 | 3156 | 104 | 6 | 46 | 31 | 5 | 15 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0004 | 0/0 | 3156 | 22 | 17 | 2 | 0 | 1 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0012 | 0/0 | 3156 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0041 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0043 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0044 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0046 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0003c0006 | 0/0 | 3156 | 5 | 5 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0003c0013 | 0/0 | 3156 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0004c0010 | 0/0 | 3156 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0004c0011 | 0/0 | 3156 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0005c0009 | 0/0 | 3156 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0006c0008 | 0/0 | 3156 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0007c0007 | 0/0 | 3156 | 3 | 3 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0008c0019 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0009c0021 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0010c0033 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0011c0027 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0012c0023 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0013c0030 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0014c0031 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0015c0026 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0016c0022 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0017c0035 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0018c0036 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0019c0038 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0020c0040 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0021c0042 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0022c0045 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0023c0018 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0024c0017 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0025c0047 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0026c0016 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0027c0015 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0028c0014 | 0/0 | 3156 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4878 | 145 | 16 | 17 | 91 | 5 | 16 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0002 | 0/0 | 4878 | 17 | 1 | 0 | 16 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0003 | 0/0 | 4878 | 5 | 1 | 0 | 3 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0005 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0007 | 0/0 | 4878 | 3 | 0 | 3 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0008 | 0/0 | 4878 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0009 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0010 | 0/0 | 4869 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0011 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0012 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0013 | 0/0 | 4878 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0017 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0021 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0001t0022 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0003t0001 | 0/0 | 4878 | 28 | 8 | 2 | 11 | 1 | 6 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0003t0002 | 0/0 | 4878 | 21 | 8 | 0 | 8 | 2 | 3 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0003t0016 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0003t0019 | 0/1 | 4878 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0005t0002 | 0/0 | 4878 | 5 | 5 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0020t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0024t0005 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0025t0001 | 0/0 | 4878 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0028t0001 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0029t0001 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0032t0001 | 0/0 | 4878 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0034t0009 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0037t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0001c0039t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0001 | 0/0 | 4878 | 60 | 2 | 35 | 15 | 2 | 6 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0002 | 0/0 | 4878 | 6 | 1 | 0 | 2 | 1 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0003 | 1/0 | 4878 | 26 | 1 | 6 | 12 | 2 | 4 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0004 | 0/0 | 4878 | 5 | 0 | 5 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0005 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0009 | 0/0 | 4863 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0011 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0012 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0014 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0018 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0002t0023 | 0/0 | 4860 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0004t0001 | 0/0 | 4878 | 17 | 12 | 2 | 0 | 1 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0004t0003 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0004t0006 | 0/0 | 4878 | 3 | 3 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0004t0015 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0012t0001 | 0/0 | 4878 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0041t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0043t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0044t0003 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0002c0046t0020 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0003c0006t0001 | 0/0 | 4878 | 5 | 5 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0003c0013t0001 | 0/0 | 4878 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0004c0010t0001 | 0/0 | 4878 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0004c0011t0001 | 0/0 | 4878 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0005c0009t0002 | 0/0 | 4878 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0006c0008t0003 | 0/0 | 4878 | 3 | 0 | 0 | 3 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0007c0007t0001 | 0/0 | 4878 | 3 | 3 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0008c0019t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0009c0021t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0010c0033t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0011c0027t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0012c0023t0001 | 0/0 | 4857 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0013c0030t0024 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0014c0031t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0015c0026t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0016c0022t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0017c0035t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0018c0036t0002 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0019c0038t0008 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0020c0040t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0021c0042t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0022c0045t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0023c0018t0001 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0024c0017t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0025c0047t0001 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0026c0016t0003 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0027c0015t0005 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| a0028c0014t0001 | 0/0 | 4878 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | copy fasta | chr17 | 2332501 | 2386054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0002g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0007g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0007g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0009g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0010g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0010g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0012g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0013g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0013g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0017g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0021g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0001t0022g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0016g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0003t0019g0352 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0005t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0005t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0005t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0005t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0020t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0024t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0025t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0028t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0029t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0032t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0034t0009g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0037t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0001c0039t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0001g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0292 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0003g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0009g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0011g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0012g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0014g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0018g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0002t0023g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0004t0015g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0012t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0012t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0041t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0043t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0044t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0002c0046t0020g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0006t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0013t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0003c0013t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0004c0010t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0004c0010t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0004c0011t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0004c0011t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0005c0009t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0005c0009t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0005c0009t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0006c0008t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0006c0008t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0006c0008t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0007c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0007c0007t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0007c0007t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0008c0019t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0009c0021t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0010c0033t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0011c0027t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0012c0023t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0013c0030t0024g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0014c0031t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0015c0026t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0016c0022t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0017c0035t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0018c0036t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0019c0038t0008g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0020c0040t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0021c0042t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0022c0045t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0023c0018t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0024c0017t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0025c0047t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0026c0016t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0027c0015t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| a0028c0014t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0373 | EUR | GBR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0367 | EUR | GBR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00140 | hp2 | a0002 | c0002 | t0003 | g0291 | EUR | GBR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0370 | EUR | FIN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00280 | hp2 | a0001 | c0028 | t0001 | g0250 | EUR | FIN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0335 | EUR | FIN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00323 | hp2 | a0002 | c0002 | t0003 | g0260 | EUR | FIN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00423 | hp2 | a0001 | c0001 | t0011 | g0116 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00438 | hp1 | a0002 | c0002 | t0003 | g0209 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0353 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00558 | hp2 | a0002 | c0002 | t0003 | g0201 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00609 | hp1 | a0021 | c0042 | t0001 | g0180 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0108 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0326 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00639 | hp2 | a0028 | c0014 | t0001 | g0145 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00673 | hp1 | a0002 | c0002 | t0003 | g0222 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01070 | hp1 | a0012 | c0023 | t0001 | g0368 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0333 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0395 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0289 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0325 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01109 | hp2 | a0001 | c0025 | t0001 | g0101 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0376 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0315 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0322 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0318 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01175 | hp1 | a0002 | c0002 | t0003 | g0276 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0300 | AMR | PUR | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0016 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0337 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01346 | hp2 | a0001 | c0032 | t0001 | g0188 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0347 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01361 | hp1 | a0002 | c0002 | t0004 | g0166 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0371 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01433 | hp1 | a0002 | c0002 | t0003 | g0251 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01433 | hp2 | a0002 | c0004 | t0001 | g0137 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0043 | EUR | IBS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01515 | hp2 | a0001 | c0001 | t0012 | g0320 | EUR | IBS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01516 | hp2 | a0002 | c0004 | t0001 | g0006 | EUR | IBS | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01884 | hp1 | a0001 | c0034 | t0009 | g0396 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0089 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01891 | hp1 | a0015 | c0026 | t0001 | g0341 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01928 | hp1 | a0002 | c0002 | t0004 | g0050 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01943 | hp2 | a0002 | c0002 | t0004 | g0345 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01952 | hp1 | a0002 | c0002 | t0004 | g0342 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0184 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0173 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02004 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0164 | AMR | PEL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02015 | hp1 | a0001 | c0003 | t0002 | g0107 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02027 | hp2 | a0026 | c0016 | t0003 | g0160 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02040 | hp2 | a0001 | c0003 | t0002 | g0113 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02055 | hp1 | a0013 | c0030 | t0024 | g0149 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0389 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0119 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02071 | hp1 | a0001 | c0020 | t0001 | g0286 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02071 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02074 | hp1 | a0001 | c0003 | t0002 | g0206 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02080 | hp2 | a0002 | c0044 | t0003 | g0243 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02083 | hp1 | a0001 | c0003 | t0002 | g0380 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0264 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02132 | hp2 | a0002 | c0002 | t0011 | g0262 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02145 | hp2 | a0002 | c0004 | t0001 | g0331 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0265 | EAS | CDX | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02165 | hp2 | a0006 | c0008 | t0003 | g0187 | EAS | CDX | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02257 | hp1 | a0024 | c0017 | t0001 | g0092 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0099 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02258 | hp2 | a0001 | c0005 | t0002 | g0013 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02280 | hp1 | a0001 | c0005 | t0002 | g0013 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02280 | hp2 | a0002 | c0004 | t0006 | g0011 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02451 | hp1 | a0003 | c0006 | t0001 | g0096 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0020 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | KHV | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02572 | hp1 | a0003 | c0006 | t0001 | g0086 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0094 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0354 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0294 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02615 | hp2 | a0007 | c0007 | t0001 | g0140 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0020 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0134 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02647 | hp2 | a0027 | c0015 | t0005 | g0079 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02698 | hp1 | a0002 | c0002 | t0014 | g0346 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02698 | hp2 | a0023 | c0018 | t0001 | g0114 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0194 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02717 | hp2 | a0003 | c0013 | t0001 | g0097 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02723 | hp1 | a0002 | c0002 | t0003 | g0305 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02735 | hp2 | a0002 | c0004 | t0001 | g0132 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02809 | hp1 | a0007 | c0007 | t0001 | g0135 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0007 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02818 | hp1 | a0003 | c0006 | t0001 | g0093 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0391 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02886 | hp1 | a0017 | c0035 | t0001 | g0301 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0339 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02895 | hp2 | a0025 | c0047 | t0001 | g0282 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0090 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0007 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0340 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02922 | hp2 | a0003 | c0006 | t0001 | g0095 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02965 | hp1 | a0001 | c0024 | t0005 | g0078 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02965 | hp2 | a0001 | c0005 | t0002 | g0084 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02970 | hp2 | a0003 | c0006 | t0001 | g0024 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02976 | hp1 | a0002 | c0002 | t0023 | g0139 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0274 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03041 | hp2 | a0002 | c0004 | t0003 | g0363 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03130 | hp1 | a0007 | c0007 | t0001 | g0295 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0390 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03139 | hp1 | a0002 | c0004 | t0001 | g0091 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03139 | hp2 | a0002 | c0012 | t0001 | g0372 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03195 | hp1 | a0002 | c0004 | t0006 | g0083 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03195 | hp2 | a0016 | c0022 | t0001 | g0268 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03209 | hp1 | a0002 | c0041 | t0001 | g0312 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03209 | hp2 | a0022 | c0045 | t0001 | g0136 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0397 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0273 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03239 | hp2 | a0001 | c0029 | t0001 | g0359 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03486 | hp1 | a0001 | c0005 | t0002 | g0275 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0361 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03490 | hp2 | a0002 | c0004 | t0001 | g0069 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0008 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0314 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03492 | hp1 | a0001 | c0003 | t0002 | g0008 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0018 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0393 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03540 | hp1 | a0002 | c0004 | t0006 | g0011 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0362 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03579 | hp2 | a0002 | c0004 | t0015 | g0281 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0104 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03688 | hp1 | a0002 | c0002 | t0009 | g0280 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0302 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0308 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03831 | hp1 | a0002 | c0002 | t0012 | g0336 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0040 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0287 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03927 | hp1 | a0019 | c0038 | t0008 | g0216 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0258 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0016 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0374 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0269 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0360 | AFR | YRI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18522 | hp2 | a0002 | c0004 | t0001 | g0279 | AFR | YRI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | CHB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18747 | hp1 | a0001 | c0003 | t0002 | g0219 | EAS | CHB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | CHB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | YRI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18906 | hp2 | a0001 | c0003 | t0016 | g0266 | AFR | YRI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18939 | hp2 | a0001 | c0001 | t0017 | g0366 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0338 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0386 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18946 | hp2 | a0005 | c0009 | t0002 | g0378 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18948 | hp1 | a0002 | c0002 | t0003 | g0032 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18951 | hp2 | a0004 | c0010 | t0001 | g0117 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0387 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0235 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0298 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18969 | hp2 | a0006 | c0008 | t0003 | g0261 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18973 | hp2 | a0009 | c0021 | t0001 | g0174 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18974 | hp1 | a0001 | c0039 | t0001 | g0234 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18979 | hp2 | a0004 | c0011 | t0001 | g0155 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18981 | hp1 | a0005 | c0009 | t0002 | g0384 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18983 | hp2 | a0002 | c0002 | t0003 | g0263 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18984 | hp2 | a0002 | c0002 | t0018 | g0046 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18989 | hp2 | a0011 | c0027 | t0001 | g0240 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0381 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0382 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0394 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0175 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18998 | hp2 | a0018 | c0036 | t0002 | g0213 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18999 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19002 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19002 | hp2 | a0001 | c0037 | t0001 | g0217 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19004 | hp1 | a0008 | c0019 | t0001 | g0017 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19010 | hp2 | a0004 | c0011 | t0001 | g0385 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19030 | hp1 | a0002 | c0046 | t0020 | g0159 | AFR | LWK | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19043 | hp1 | a0001 | c0001 | t0022 | g0130 | AFR | LWK | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19043 | hp2 | a0002 | c0004 | t0001 | g0311 | AFR | LWK | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0388 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19064 | hp2 | a0006 | c0008 | t0003 | g0299 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0375 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19067 | hp1 | a0005 | c0009 | t0002 | g0383 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19067 | hp2 | a0001 | c0001 | t0010 | g0259 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19077 | hp1 | a0001 | c0001 | t0009 | g0355 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19077 | hp2 | a0001 | c0001 | t0021 | g0017 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19081 | hp1 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0014 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0379 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19240 | hp1 | a0002 | c0004 | t0001 | g0088 | AFR | YRI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | YRI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20129 | hp1 | a0014 | c0031 | t0001 | g0392 | AFR | ASW | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ASW | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0106 | EUR | TSI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0105 | EUR | TSI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0290 | EUR | TSI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0344 | EUR | TSI | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20905 | hp1 | a0001 | c0003 | t0001 | g0356 | SAS | GIH | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0288 | SAS | GIH | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG01123 | hp2 | a0002 | c0002 | t0004 | g0343 | AMR | CLM | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02109 | hp2 | a0020 | c0040 | t0001 | g0220 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0103 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02559 | hp1 | a0002 | c0043 | t0001 | g0364 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG02559 | hp2 | a0002 | c0012 | t0001 | g0129 | AFR | ACB | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03471 | hp1 | a0001 | c0005 | t0002 | g0272 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0128 | AFR | MSL | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18955 | hp1 | a0004 | c0010 | t0001 | g0350 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA18955 | hp2 | a0010 | c0033 | t0001 | g0202 | EAS | JPT | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20300 | hp1 | a0003 | c0013 | t0001 | g0087 | AFR | USA | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | USA | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0006 | AFR | LWK | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| NA21309 | hp2 | a0002 | c0002 | t0005 | g0080 | AFR | LWK | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0019 | g0352 | REF | REF | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0003 | g0292 | REF | REF | SGSM2_chr17_2332501_2386054 | SGSM2 | chr17 | 2332501 | 2386054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2343583
|
T | G | 1 | a0028 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.96T>G | p.Phe32Leu | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/24 | 284/4878 | 96/3156 | 32/1051 | chr17 | 2343583 | ||
| chr17:2361739
|
G | C | 2 | a0007a0027 | 4 | HG02615.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.236G>C | p.Cys79Ser | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 3/24 | 424/4878 | 236/3156 | 79/1051 | chr17 | 2361739 | ||
| chr17:2361764
|
C | A | 2 | a0006a0026 | 4 | HG02027.hp2 HG02165.hp2 NA18969.hp2 others(1): Show |
missense_variant | MODERATE | c.261C>A | p.His87Gln | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 3/24 | 449/4878 | 261/3156 | 87/1051 | chr17 | 2361764 | ||
| chr17:2362140
|
C | T | 1 | a0025 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.328C>T | p.Arg110Trp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/24 | 516/4878 | 328/3156 | 110/1051 | chr17 | 2362140 | ||
| chr17:2362161
|
G | A | 1 | a0024 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.349G>A | p.Gly117Arg | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/24 | 537/4878 | 349/3156 | 117/1051 | chr17 | 2362161 | ||
| chr17:2363466
|
T | C | 1 | a0023 | 1 | HG02698.hp2 | missense_variant&splice_region_variant | MODERATE | c.674T>C | p.Ile225Thr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/24 | 862/4878 | 674/3156 | 225/1051 | chr17 | 2363466 | ||
| chr17:2363505
|
G | A | 18 | a0001a0004a0008others(15): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
missense_variant | MODERATE | c.713G>A | p.Arg238Lys | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/24 | 901/4878 | 713/3156 | 238/1051 | chr17 | 2363505 | ||
| chr17:2364130
|
G | A | 1 | a0008 | 1 | NA19004.hp1 | stop_gained | HIGH | c.879G>A | p.Trp293* | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 8/24 | 1067/4878 | 879/3156 | 293/1051 | chr17 | 2364130 | ||
| chr17:2365017
|
G | A | 19 | a0001a0004a0007others(16): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
missense_variant | MODERATE | c.1121G>A | p.Arg374Gln | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 10/24 | 1309/4878 | 1121/3156 | 374/1051 | chr17 | 2365017 | ||
| chr17:2365260
|
G | A | 1 | a0009 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.1207G>A | p.Val403Met | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/24 | 1395/4878 | 1207/3156 | 403/1051 | chr17 | 2365260 | ||
| chr17:2367307
|
C | T | 1 | a0018 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.1325C>T | p.Ala442Val | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/24 | 1513/4878 | 1325/3156 | 442/1051 | chr17 | 2367307 | ||
| chr17:2367310
|
C | T | 2 | a0017a0027 | 2 | HG02647.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1328C>T | p.Ala443Val | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/24 | 1516/4878 | 1328/3156 | 443/1051 | chr17 | 2367310 | ||
| chr17:2367351
|
G | A | 1 | a0016 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1369G>A | p.Ala457Thr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/24 | 1557/4878 | 1369/3156 | 457/1051 | chr17 | 2367351 | ||
| chr17:2372251
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1639G>T | p.Gly547Cys | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/24 | 1827/4878 | 1639/3156 | 547/1051 | chr17 | 2372251 | ||
| chr17:2372348
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1648G>T | p.Ala550Ser | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1836/4878 | 1648/3156 | 550/1051 | chr17 | 2372348 | ||
| chr17:2372351
|
C | G | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1651C>G | p.His551Asp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1839/4878 | 1651/3156 | 551/1051 | chr17 | 2372351 | ||
| chr17:2372352
|
A | C | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1652A>C | p.His551Pro | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1840/4878 | 1652/3156 | 551/1051 | chr17 | 2372352 | ||
| chr17:2372373
|
T | G | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1673T>G | p.Val558Gly | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1861/4878 | 1673/3156 | 558/1051 | chr17 | 2372373 | ||
| chr17:2372376
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1676G>T | p.Arg559Leu | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1864/4878 | 1676/3156 | 559/1051 | chr17 | 2372376 | ||
| chr17:2372378
|
A | G | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1678A>G | p.Thr560Ala | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1866/4878 | 1678/3156 | 560/1051 | chr17 | 2372378 | ||
| chr17:2372387
|
T | C | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1687T>C | p.Ser563Pro | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1875/4878 | 1687/3156 | 563/1051 | chr17 | 2372387 | ||
| chr17:2372388
|
C | A | 1 | a0010 | 1 | NA18955.hp2 | stop_gained | HIGH | c.1688C>A | p.Ser563* | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1876/4878 | 1688/3156 | 563/1051 | chr17 | 2372388 | ||
| chr17:2372403
|
A | C | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1703A>C | p.His568Pro | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1891/4878 | 1703/3156 | 568/1051 | chr17 | 2372403 | ||
| chr17:2372406
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1706G>T | p.Ser569Ile | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1894/4878 | 1706/3156 | 569/1051 | chr17 | 2372406 | ||
| chr17:2372417
|
C | A | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1717C>A | p.Pro573Thr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1905/4878 | 1717/3156 | 573/1051 | chr17 | 2372417 | ||
| chr17:2372432
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1732G>T | p.Gly578Trp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1920/4878 | 1732/3156 | 578/1051 | chr17 | 2372432 | ||
| chr17:2372433
|
G | A | 1 | a0021 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.1733G>A | p.Gly578Glu | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1921/4878 | 1733/3156 | 578/1051 | chr17 | 2372433 | ||
| chr17:2372463
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1763G>T | p.Trp588Leu | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1951/4878 | 1763/3156 | 588/1051 | chr17 | 2372463 | ||
| chr17:2372466
|
G | T | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1766G>T | p.Ser589Ile | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1954/4878 | 1766/3156 | 589/1051 | chr17 | 2372466 | ||
| chr17:2372468
|
A | C | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1768A>C | p.Lys590Gln | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1956/4878 | 1768/3156 | 590/1051 | chr17 | 2372468 | ||
| chr17:2372471
|
T | A | 1 | a0010 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1771T>A | p.Tyr591Asn | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1959/4878 | 1771/3156 | 591/1051 | chr17 | 2372471 | ||
| chr17:2372487
|
A | C | 1 | a0010 | 1 | NA18955.hp2 | missense_variant&splice_region_variant | MODERATE | c.1787A>C | p.Lys596Thr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1975/4878 | 1787/3156 | 596/1051 | chr17 | 2372487 | ||
| chr17:2373433
|
C | T | 1 | a0011 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.2020C>T | p.Arg674Cys | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/24 | 2208/4878 | 2020/3156 | 674/1051 | chr17 | 2373433 | ||
| chr17:2373469
|
C | T | 1 | a0015 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.2056C>T | p.His686Tyr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/24 | 2244/4878 | 2056/3156 | 686/1051 | chr17 | 2373469 | ||
| chr17:2375527
|
G | T | 1 | a0005 | 3 | NA18946.hp2 NA18981.hp1 NA19067.hp1 |
missense_variant | MODERATE | c.2136G>T | p.Glu712Asp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/24 | 2324/4878 | 2136/3156 | 712/1051 | chr17 | 2375527 | ||
| chr17:2375850
|
C | T | 3 | a0003a0014a0024 | 9 | HG02257.hp1 HG02451.hp1 HG02572.hp1 others(6): Show |
missense_variant | MODERATE | c.2459C>T | p.Ala820Val | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/24 | 2647/4878 | 2459/3156 | 820/1051 | chr17 | 2375850 | ||
| chr17:2375861
|
G | A | 1 | a0004 | 4 | NA18951.hp2 NA18955.hp1 NA18979.hp2 others(1): Show |
missense_variant | MODERATE | c.2470G>A | p.Ala824Thr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/24 | 2658/4878 | 2470/3156 | 824/1051 | chr17 | 2375861 | ||
| chr17:2377047
|
CAACATGC others(194): Show |
C | 1 | a0012 | 1 | HG01070.hp1 | splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.2782_2802+180del | p.Asn928_Gln934del | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/24 | 2970/4878 | 2782/3156 | 928/1051 | chr17 | 2377047 | ||
| chr17:2379037
|
A | C | 1 | a0013 | 1 | HG02055.hp1 | missense_variant&splice_region_variant | MODERATE | c.2901A>C | p.Glu967Asp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/24 | 3089/4878 | 2901/3156 | 967/1051 | chr17 | 2379037 | ||
| chr17:2379200
|
A | C | 1 | a0013 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.3064A>C | p.Asn1022His | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/24 | 3252/4878 | 3064/3156 | 1022/1051 | chr17 | 2379200 | ||
| chr17:2379440
|
G | C | 1 | a0022 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.3076G>C | p.Glu1026Gln | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 3264/4878 | 3076/3156 | 1026/1051 | chr17 | 2379440 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2363518
|
T | C | 32 | a0001c0001a0001c0003a0001c0005others(29): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
synonymous_variant | LOW | c.726T>C | p.Cys242Cys | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/24 | 914/4878 | 726/3156 | 242/1051 | chr17 | 2363518 | ||
| chr17:2364617
|
C | T | 1 | a0001c0039 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.954C>T | p.Leu318Leu | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 9/24 | 1142/4878 | 954/3156 | 318/1051 | chr17 | 2364617 | ||
| chr17:2365036
|
G | A | 2 | a0001c0020a0002c0041 | 2 | HG02071.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.1140G>A | p.Pro380Pro | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 10/24 | 1328/4878 | 1140/3156 | 380/1051 | chr17 | 2365036 | ||
| chr17:2365295
|
C | T | 1 | a0025c0047 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.1242C>T | p.Thr414Thr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/24 | 1430/4878 | 1242/3156 | 414/1051 | chr17 | 2365295 | ||
| chr17:2365334
|
C | T | 1 | a0001c0037 | 1 | NA19002.hp2 | synonymous_variant | LOW | c.1281C>T | p.His427His | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/24 | 1469/4878 | 1281/3156 | 427/1051 | chr17 | 2365334 | ||
| chr17:2372250
|
C | T | 3 | a0001c0034a0003c0006a0024c0017 | 7 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
synonymous_variant | LOW | c.1638C>T | p.Tyr546Tyr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/24 | 1826/4878 | 1638/3156 | 546/1051 | chr17 | 2372250 | ||
| chr17:2372404
|
T | C | 1 | a0010c0033 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.1704T>C | p.His568His | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1892/4878 | 1704/3156 | 568/1051 | chr17 | 2372404 | ||
| chr17:2372407
|
C | T | 1 | a0001c0032 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1707C>T | p.Ser569Ser | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1895/4878 | 1707/3156 | 569/1051 | chr17 | 2372407 | ||
| chr17:2372434
|
G | C | 1 | a0021c0042 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.1734G>C | p.Gly578Gly | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1922/4878 | 1734/3156 | 578/1051 | chr17 | 2372434 | ||
| chr17:2372440
|
C | G | 16 | a0001c0003a0001c0005a0001c0034others(13): Show | 98 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
synonymous_variant | LOW | c.1740C>G | p.Ser580Ser | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1928/4878 | 1740/3156 | 580/1051 | chr17 | 2372440 | ||
| chr17:2372458
|
C | T | 1 | a0001c0029 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1758C>T | p.Asp586Asp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/24 | 1946/4878 | 1758/3156 | 586/1051 | chr17 | 2372458 | ||
| chr17:2373006
|
C | T | 1 | a0028c0014 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1842C>T | p.His614His | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/24 | 2030/4878 | 1842/3156 | 614/1051 | chr17 | 2373006 | ||
| chr17:2373054
|
C | T | 1 | a0001c0028 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1890C>T | p.Phe630Phe | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/24 | 2078/4878 | 1890/3156 | 630/1051 | chr17 | 2373054 | ||
| chr17:2373336
|
C | T | 1 | a0002c0044 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.1923C>T | p.Asp641Asp | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/24 | 2111/4878 | 1923/3156 | 641/1051 | chr17 | 2373336 | ||
| chr17:2375578
|
C | T | 1 | a0001c0005 | 5 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(2): Show |
synonymous_variant | LOW | c.2187C>T | p.Pro729Pro | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/24 | 2375/4878 | 2187/3156 | 729/1051 | chr17 | 2375578 | ||
| chr17:2375626
|
C | T | 1 | a0002c0046 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.2235C>T | p.Phe745Phe | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/24 | 2423/4878 | 2235/3156 | 745/1051 | chr17 | 2375626 | ||
| chr17:2375710
|
C | T | 2 | a0001c0025a0002c0043 | 2 | HG01109.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.2319C>T | p.Ser773Ser | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/24 | 2507/4878 | 2319/3156 | 773/1051 | chr17 | 2375710 | ||
| chr17:2376736
|
C | T | 1 | a0001c0024 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2613C>T | p.Tyr871Tyr | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 20/24 | 2801/4878 | 2613/3156 | 871/1051 | chr17 | 2376736 | ||
| chr17:2376790
|
G | A | 1 | a0002c0012 | 2 | HG02559.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.2667G>A | p.Ala889Ala | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 20/24 | 2855/4878 | 2667/3156 | 889/1051 | chr17 | 2376790 | ||
| chr17:2379038
|
C | T | 1 | a0013c0030 | 1 | HG02055.hp1 | splice_region_variant&synonymous_variant | LOW | c.2902C>T | p.Leu968Leu | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/24 | 3090/4878 | 2902/3156 | 968/1051 | chr17 | 2379038 | ||
| chr17:2379106
|
C | T | 1 | a0013c0030 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.2970C>T | p.His990His | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/24 | 3158/4878 | 2970/3156 | 990/1051 | chr17 | 2379106 | ||
| chr17:2379154
|
C | T | 1 | a0014c0031 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.3018C>T | p.Ile1006Ile | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/24 | 3206/4878 | 3018/3156 | 1006/1051 | chr17 | 2379154 | ||
| chr17:2379199
|
C | T | 1 | a0013c0030 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.3063C>T | p.Phe1021Phe | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/24 | 3251/4878 | 3063/3156 | 1021/1051 | chr17 | 2379199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2337548
|
TGCG | T | 7 | a0001c0001t0005a0001c0001t0022a0001c0024t0005others(4): Show | 7 | HG02055.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-121_-119delCGG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/24 | 119 | INFO_REALIGN_3_PRIME | chr17 | 2337548 | ||||
| chr17:2337548
|
TGCGGCGG others(2): Show |
T | 1 | a0001c0001t0010 | 3 | NA18999.hp1 NA19067.hp2 NA19090.hp1 |
5_prime_UTR_variant | MODIFIER | c.-127_-119delCGGCGG others(3): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/24 | 119 | INFO_REALIGN_3_PRIME | chr17 | 2337548 | ||||
| chr17:2379545
|
T | C | 9 | a0001c0001t0002a0001c0001t0022a0001c0003t0002others(6): Show | 60 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*25T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 25 | chr17 | 2379545 | |||||
| chr17:2379657
|
C | T | 1 | a0001c0001t0021 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 137 | chr17 | 2379657 | |||||
| chr17:2379658
|
G | A | 1 | a0002c0004t0006 | 3 | HG02280.hp2 HG03195.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*138G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 138 | chr17 | 2379658 | |||||
| chr17:2379665
|
G | A | 2 | a0001c0001t0011a0002c0002t0011 | 2 | HG00423.hp2 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*145G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 145 | chr17 | 2379665 | |||||
| chr17:2380005
|
A | G | 11 | a0001c0001t0002a0001c0001t0022a0001c0003t0002others(8): Show | 62 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*485A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 485 | chr17 | 2380005 | |||||
| chr17:2380029
|
G | A | 1 | a0002c0002t0014 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 509 | chr17 | 2380029 | |||||
| chr17:2380038
|
GCGGGAGA others(8): Show |
G | 4 | a0001c0001t0009a0001c0034t0009a0002c0002t0009others(1): Show | 4 | HG01884.hp1 HG02976.hp1 HG03688.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*533_*547delACGGGA others(9): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 533 | INFO_REALIGN_3_PRIME | chr17 | 2380038 | ||||
| chr17:2380226
|
G | C | 1 | a0002c0004t0015 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*706G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 706 | chr17 | 2380226 | |||||
| chr17:2380230
|
C | T | 1 | a0001c0003t0019 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*710C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 710 | chr17 | 2380230 | |||||
| chr17:2380241
|
C | T | 1 | a0002c0002t0018 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 721 | chr17 | 2380241 | |||||
| chr17:2380317
|
C | A | 1 | a0002c0002t0004 | 5 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*797C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 797 | chr17 | 2380317 | |||||
| chr17:2380373
|
A | G | 12 | a0001c0001t0002a0001c0001t0013a0001c0001t0022others(9): Show | 64 | HG01123.hp2 HG01168.hp2 HG01169.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*853A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 853 | chr17 | 2380373 | |||||
| chr17:2380374
|
G | C | 12 | a0001c0001t0002a0001c0001t0013a0001c0001t0022others(9): Show | 64 | HG01123.hp2 HG01168.hp2 HG01169.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*854G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 854 | chr17 | 2380374 | |||||
| chr17:2380481
|
A | T | 10 | a0001c0001t0002a0001c0001t0013a0001c0001t0022others(7): Show | 62 | HG01123.hp2 HG01168.hp2 HG01169.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 961 | chr17 | 2380481 | |||||
| chr17:2380594
|
T | C | 10 | a0001c0001t0002a0001c0001t0013a0001c0001t0022others(7): Show | 62 | HG01123.hp2 HG01168.hp2 HG01169.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1074T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1074 | chr17 | 2380594 | |||||
| chr17:2380597
|
G | A | 1 | a0001c0001t0007 | 3 | HG01978.hp1 HG01981.hp2 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1077G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1077 | chr17 | 2380597 | |||||
| chr17:2380706
|
G | A | 1 | a0013c0030t0024 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1186G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1186 | chr17 | 2380706 | |||||
| chr17:2380711
|
A | G | 66 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(63): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
3_prime_UTR_variant | MODIFIER | c.*1191A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1191 | chr17 | 2380711 | |||||
| chr17:2380726
|
G | A | 1 | a0001c0003t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1206 | chr17 | 2380726 | |||||
| chr17:2380873
|
G | T | 2 | a0002c0046t0020a0013c0030t0024 | 2 | HG02055.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1353G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1353 | chr17 | 2380873 | |||||
| chr17:2380890
|
T | C | 3 | a0001c0001t0008a0001c0001t0017a0019c0038t0008 | 4 | HG03927.hp1 NA18939.hp2 NA18978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1370T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1370 | chr17 | 2380890 | |||||
| chr17:2381004
|
C | T | 5 | a0001c0001t0008a0001c0001t0012a0001c0001t0017others(2): Show | 6 | HG01515.hp2 HG03831.hp1 HG03927.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1484C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 24/24 | 1484 | chr17 | 2381004 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:2337765
|
C | G | 1 | a0002c0002t0001g0397 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+20C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2337765 | ||||||
| chr17:2337813
|
C | G | 1 | a0001c0034t0009g0396 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.57+68C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2337813 | ||||||
| chr17:2337818
|
C | T | 1 | a0002c0002t0003g0395 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+73C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2337818 | ||||||
| chr17:2337901
|
C | T | 1 | a0001c0001t0001g0394 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.57+156C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2337901 | ||||||
| chr17:2337951
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0391a0001c0003t0001g0390others(4): Show | 9 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+206C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2337951 | ||||||
| chr17:2338017
|
G | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0029others(59): Show | 72 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.57+272G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338017 | ||||||
| chr17:2338121
|
G | A | 4 | a0001c0001t0005g0077a0001c0024t0005g0078a0002c0002t0005g0080others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+376G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338121 | ||||||
| chr17:2338204
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.57+459G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338204 | ||||||
| chr17:2338282
|
C | T | 1 | a0001c0001t0002g0388 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.57+537C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338282 | ||||||
| chr17:2338352
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.57+607G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338352 | ||||||
| chr17:2338354
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.57+609A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338354 | ||||||
| chr17:2338355
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.57+610G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338355 | ||||||
| chr17:2338355
|
G | GC | 16 | a0001c0001t0001g0085a0001c0005t0002g0084a0002c0004t0001g0007others(13): Show | 17 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.57+616dupC | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338355 | |||||
| chr17:2338387
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.57+642C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338387 | ||||||
| chr17:2338605
|
T | C | 253 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(250): Show | 269 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.57+860T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338605 | ||||||
| chr17:2338635
|
T | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.57+890T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338635 | ||||||
| chr17:2338756
|
T | A | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0003t0002g0099others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1011T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338756 | ||||||
| chr17:2338766
|
G | A | 21 | a0001c0001t0001g0021a0001c0001t0001g0102a0001c0001t0001g0109others(18): Show | 24 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.57+1021G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338766 | ||||||
| chr17:2338774
|
A | AATATATA others(1): Show |
4 | a0001c0001t0005g0077a0001c0024t0005g0078a0002c0002t0005g0080others(1): Show | 4 | HG02647.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1037_57+1044dup others(8): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(3): Show |
29 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0098others(26): Show | 32 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.57+1035_57+1044dup others(10): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(5): Show |
50 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0055others(47): Show | 59 | HG00609.hp2 HG01069.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.57+1033_57+1044dup others(12): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(7): Show |
29 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0070others(26): Show | 31 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.57+1031_57+1044dup others(14): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(9): Show |
8 | a0001c0001t0001g0075a0001c0001t0001g0138a0002c0002t0001g0073others(5): Show | 8 | HG00738.hp1 HG01256.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(16): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(11): Show |
1 | a0003c0013t0001g0097 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(18): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(15): Show |
3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | NA18960.hp1 NA18978.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(22): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(17): Show |
6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(24): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(19): Show |
1 | a0001c0001t0001g0150 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(26): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(21): Show |
1 | a0002c0002t0001g0151 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(28): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(23): Show |
1 | a0001c0001t0001g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(30): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(25): Show |
4 | a0001c0001t0001g0156a0001c0001t0002g0157a0001c0001t0002g0158others(1): Show | 4 | NA18970.hp2 NA18979.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(32): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(27): Show |
5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG02027.hp2 HG02083.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(34): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(29): Show |
3 | a0001c0001t0001g0165a0001c0001t0007g0164a0002c0002t0004g0166 | 3 | HG01361.hp1 HG02004.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(36): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(31): Show |
10 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 10 | HG00438.hp2 HG01981.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(38): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(33): Show |
19 | a0001c0001t0001g0009a0001c0001t0001g0178a0001c0001t0001g0179others(16): Show | 20 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(40): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(35): Show |
16 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(13): Show | 16 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(42): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(37): Show |
9 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0214others(6): Show | 9 | HG03927.hp1 HG04184.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(44): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(39): Show |
4 | a0001c0001t0001g0218a0001c0001t0002g0221a0001c0003t0002g0219others(1): Show | 4 | HG02074.hp2 HG02109.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(46): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(41): Show |
9 | a0001c0001t0001g0010a0001c0001t0001g0223a0001c0001t0001g0226others(6): Show | 10 | HG00621.hp2 HG00673.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(48): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(43): Show |
10 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG02129.hp2 NA18949.hp2 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(50): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(45): Show |
4 | a0001c0001t0001g0242a0001c0001t0002g0241a0002c0044t0003g0243others(1): Show | 4 | HG02080.hp2 NA18944.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(47): Show |
2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | NA19057.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(54): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(49): Show |
3 | a0001c0001t0001g0082a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02523.hp1 NA18941.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(56): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(51): Show |
2 | a0001c0001t0001g0248a0001c0001t0002g0249 | 2 | NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(58): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(53): Show |
1 | a0001c0028t0001g0250 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(60): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(55): Show |
1 | a0002c0002t0003g0251 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(62): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATATA others(57): Show |
1 | a0001c0003t0002g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(64): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | AATATGTA others(41): Show |
1 | a0001c0001t0003g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.57+1033_57+1034ins others(48): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338774 | |||||
| chr17:2338774
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0255 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.57+1029_57+1030ins others(35): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338774 | ||||||
| chr17:2338784
|
T | TATATATA others(27): Show |
2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA18971.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.57+1044_57+1045ins others(34): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338784 | |||||
| chr17:2338786
|
T | TATATATA others(13): Show |
1 | a0007c0007t0001g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(20): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338786 | |||||
| chr17:2338786
|
T | TATATATA others(19): Show |
1 | a0007c0007t0001g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(26): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338786 | |||||
| chr17:2338788
|
T | TATATATA others(37): Show |
1 | a0001c0001t0001g0394 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(44): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2338788 | |||||
| chr17:2338789
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0072 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(13): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338789 | ||||||
| chr17:2338789
|
A | ATATATAT others(34): Show |
1 | a0002c0002t0003g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.57+1044_57+1045ins others(41): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338789 | ||||||
| chr17:2338790
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.57+1045A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338790 | ||||||
| chr17:2338790
|
A | T | 2 | a0001c0001t0001g0253a0001c0001t0002g0255 | 2 | HG04199.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.57+1045A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338790 | ||||||
| chr17:2338856
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.57+1111C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2338856 | ||||||
| chr17:2339054
|
G | C | 3 | a0001c0001t0001g0125a0001c0003t0001g0194a0002c0046t0020g0159 | 3 | HG00642.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.57+1309G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339054 | ||||||
| chr17:2339123
|
A | G | 337 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(334): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.57+1378A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339123 | ||||||
| chr17:2339153
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.57+1408C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339153 | ||||||
| chr17:2339181
|
A | G | 1 | a0002c0002t0023g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.57+1436A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339181 | ||||||
| chr17:2339198
|
C | A | 3 | a0001c0001t0001g0125a0001c0003t0001g0194a0002c0046t0020g0159 | 3 | HG00642.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.57+1453C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339198 | ||||||
| chr17:2339200
|
G | A | 87 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0055others(84): Show | 98 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.57+1455G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339200 | ||||||
| chr17:2339292
|
C | G | 84 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0055others(81): Show | 95 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.57+1547C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339292 | ||||||
| chr17:2339414
|
G | A | 1 | a0001c0003t0001g0308 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.57+1669G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339414 | ||||||
| chr17:2339451
|
A | G | 1 | a0002c0002t0001g0397 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+1706A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339451 | ||||||
| chr17:2339495
|
C | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0303others(4): Show | 7 | HG02723.hp1 HG03669.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1750C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339495 | ||||||
| chr17:2339527
|
A | G | 97 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0055others(94): Show | 108 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.57+1782A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339527 | ||||||
| chr17:2339584
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.57+1839G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339584 | ||||||
| chr17:2339707
|
C | CA | 30 | a0001c0001t0001g0025a0001c0001t0001g0102a0001c0001t0001g0125others(27): Show | 30 | HG00438.hp1 HG00544.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.57+1981dupA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2339707 | |||||
| chr17:2339756
|
C | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0062others(5): Show | 8 | HG01070.hp2 HG01884.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+2011C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339756 | ||||||
| chr17:2339757
|
G | A | 1 | a0002c0004t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57+2012G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339757 | ||||||
| chr17:2339762
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.57+2017C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339762 | ||||||
| chr17:2339820
|
T | A | 12 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0062others(9): Show | 12 | HG01070.hp2 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+2075T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339820 | ||||||
| chr17:2339842
|
C | A | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(244): Show | 263 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.57+2097C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339842 | ||||||
| chr17:2339875
|
G | C | 1 | a0001c0001t0001g0211 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.57+2130G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339875 | ||||||
| chr17:2339940
|
C | T | 8 | a0001c0001t0001g0138a0001c0001t0001g0192a0001c0001t0001g0208others(5): Show | 8 | NA18941.hp1 NA18943.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+2195C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2339940 | ||||||
| chr17:2340118
|
CT | C | 8 | a0001c0001t0001g0211a0001c0001t0001g0303a0001c0001t0002g0177others(5): Show | 8 | HG00323.hp2 HG02129.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+2387delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2340118 | |||||
| chr17:2340287
|
C | T | 336 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(333): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.57+2542C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340287 | ||||||
| chr17:2340334
|
C | T | 88 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0081others(85): Show | 93 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.57+2589C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340334 | ||||||
| chr17:2340427
|
A | G | 94 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0055others(91): Show | 105 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.57+2682A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340427 | ||||||
| chr17:2340519
|
G | A | 1 | a0002c0002t0003g0265 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.57+2774G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340519 | ||||||
| chr17:2340565
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.57+2820C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340565 | ||||||
| chr17:2340580
|
G | A | 1 | a0001c0003t0016g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.57+2835G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340580 | ||||||
| chr17:2340613
|
C | T | 9 | a0001c0001t0001g0377a0001c0001t0002g0382a0001c0003t0001g0379others(6): Show | 9 | HG02083.hp1 NA18946.hp2 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+2868C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340613 | ||||||
| chr17:2340615
|
C | T | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0003t0002g0099others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+2870C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340615 | ||||||
| chr17:2340623
|
T | C | 1 | a0001c0034t0009g0396 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.57+2878T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340623 | ||||||
| chr17:2340640
|
C | A | 17 | a0001c0001t0001g0102a0001c0001t0001g0109a0001c0001t0001g0110others(14): Show | 18 | HG00621.hp1 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.57+2895C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340640 | ||||||
| chr17:2340646
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.58-2899G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340646 | ||||||
| chr17:2340670
|
C | T | 1 | a0023c0018t0001g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.58-2875C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340670 | ||||||
| chr17:2340689
|
T | A | 1 | a0004c0010t0001g0117 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.58-2856T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340689 | ||||||
| chr17:2340726
|
A | G | 1 | a0001c0001t0022g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.58-2819A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340726 | ||||||
| chr17:2340733
|
T | C | 8 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0230others(5): Show | 8 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-2812T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340733 | ||||||
| chr17:2340734
|
G | A | 6 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0003t0001g0194others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-2811G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340734 | ||||||
| chr17:2340774
|
C | T | 1 | a0002c0002t0001g0376 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.58-2771C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340774 | ||||||
| chr17:2340783
|
A | G | 5 | a0001c0001t0002g0207a0001c0001t0002g0221a0001c0001t0002g0227others(2): Show | 5 | NA18947.hp2 NA18952.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-2762A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340783 | ||||||
| chr17:2340786
|
A | G | 21 | a0001c0001t0001g0058a0001c0001t0001g0191a0001c0001t0001g0196others(18): Show | 21 | HG00099.hp1 HG01358.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.58-2759A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340786 | ||||||
| chr17:2340791
|
A | G | 12 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0163others(9): Show | 12 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-2754A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340791 | ||||||
| chr17:2340806
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(20): Show | 25 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.58-2739G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340806 | ||||||
| chr17:2340814
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58-2731G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340814 | ||||||
| chr17:2340816
|
C | G | 1 | a0001c0001t0002g0221 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.58-2729C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340816 | ||||||
| chr17:2340817
|
C | T | 1 | a0001c0001t0003g0330 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-2728C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340817 | ||||||
| chr17:2340826
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.58-2719C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340826 | ||||||
| chr17:2340827
|
G | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.58-2718G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340827 | ||||||
| chr17:2340874
|
A | G | 1 | a0002c0002t0001g0057 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.58-2671A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340874 | ||||||
| chr17:2340908
|
T | A | 1 | a0002c0002t0003g0260 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.58-2637T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340908 | ||||||
| chr17:2340958
|
G | A | 3 | a0001c0003t0001g0390a0002c0002t0001g0389a0014c0031t0001g0392 | 3 | HG02055.hp2 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.58-2587G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340958 | ||||||
| chr17:2340998
|
C | T | 1 | a0006c0008t0003g0187 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.58-2547C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2340998 | ||||||
| chr17:2341213
|
G | GTTCAAGT others(2): Show |
5 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0270others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-2328_58-2320dup others(9): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2341213 | |||||
| chr17:2342094
|
C | T | 1 | a0002c0012t0001g0372 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.58-1451C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342094 | ||||||
| chr17:2342261
|
C | CA | 27 | a0001c0001t0001g0109a0001c0001t0001g0115a0001c0001t0001g0169others(24): Show | 28 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.58-1268dupA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | 2342261 | |||||
| chr17:2342349
|
G | A | 17 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0062others(14): Show | 17 | HG01070.hp2 HG01109.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.58-1196G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342349 | ||||||
| chr17:2342379
|
G | A | 1 | a0002c0002t0001g0333 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.58-1166G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342379 | ||||||
| chr17:2342380
|
C | T | 1 | a0002c0002t0003g0395 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-1165C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342380 | ||||||
| chr17:2342415
|
C | T | 1 | a0001c0001t0003g0330 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-1130C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342415 | ||||||
| chr17:2342441
|
A | C | 1 | a0001c0037t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.58-1104A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342441 | ||||||
| chr17:2342744
|
G | GA | 194 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0025others(191): Show | 207 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.58-801_58-800insA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342744 | ||||||
| chr17:2342758
|
C | T | 5 | a0002c0004t0001g0094a0003c0006t0001g0093a0003c0006t0001g0095others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-787C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342758 | ||||||
| chr17:2342827
|
A | G | 1 | a0002c0002t0003g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.58-718A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342827 | ||||||
| chr17:2342870
|
G | A | 10 | a0001c0001t0002g0170a0001c0001t0002g0200a0001c0001t0002g0207others(7): Show | 10 | NA18944.hp2 NA18947.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-675G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2342870 | ||||||
| chr17:2343181
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.58-364G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 1/23 | chr17 | 2343181 | ||||||
| chr17:2343663
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.133+43C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2343663 | ||||||
| chr17:2343710
|
T | G | 1 | a0002c0004t0001g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+90T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2343710 | ||||||
| chr17:2343820
|
G | A | 1 | a0002c0004t0001g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+200G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2343820 | ||||||
| chr17:2344017
|
G | T | 1 | a0001c0001t0001g0371 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.133+397G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344017 | ||||||
| chr17:2344305
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0367a0001c0001t0001g0369others(3): Show | 7 | HG00099.hp2 HG00280.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+685C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344305 | ||||||
| chr17:2344442
|
T | C | 4 | a0002c0002t0001g0131a0002c0002t0001g0133a0002c0004t0001g0069others(1): Show | 4 | HG01175.hp2 HG02735.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+822T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344442 | ||||||
| chr17:2344477
|
A | T | 1 | a0002c0002t0003g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.133+857A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344477 | ||||||
| chr17:2344559
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0391a0001c0003t0001g0390others(4): Show | 9 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+939C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344559 | ||||||
| chr17:2344562
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133+942C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344562 | ||||||
| chr17:2344688
|
T | C | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(207): Show | 223 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.133+1068T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344688 | ||||||
| chr17:2344713
|
CAT | C | 88 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0058others(85): Show | 100 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.133+1094_133+1095d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344713 | ||||||
| chr17:2344784
|
C | T | 1 | a0002c0002t0023g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.133+1164C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2344784 | ||||||
| chr17:2345006
|
T | G | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133+1386T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345006 | ||||||
| chr17:2345037
|
A | C | 110 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(107): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.133+1417A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345037 | ||||||
| chr17:2345149
|
G | T | 1 | a0001c0001t0017g0366 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.133+1529G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345149 | ||||||
| chr17:2345208
|
A | G | 4 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0270others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1588A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345208 | ||||||
| chr17:2345257
|
T | C | 1 | a0002c0004t0001g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+1637T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345257 | ||||||
| chr17:2345335
|
G | A | 1 | a0002c0004t0006g0011 | 2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.133+1715G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345335 | ||||||
| chr17:2345393
|
G | A | 1 | a0002c0004t0001g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+1773G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345393 | ||||||
| chr17:2345412
|
C | T | 4 | a0001c0001t0008g0175a0001c0001t0008g0210a0002c0002t0001g0224others(1): Show | 4 | HG00621.hp2 HG03927.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1792C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345412 | ||||||
| chr17:2345424
|
G | A | 5 | a0001c0001t0001g0125a0001c0001t0001g0154a0001c0003t0001g0194others(2): Show | 5 | HG00642.hp1 HG02040.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.133+1804G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345424 | ||||||
| chr17:2345545
|
A | G | 4 | a0001c0001t0001g0125a0001c0003t0001g0194a0001c0003t0002g0099others(1): Show | 4 | HG00642.hp1 HG02258.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1925A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345545 | ||||||
| chr17:2345593
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.133+1973C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345593 | ||||||
| chr17:2345595
|
C | CA | 181 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(178): Show | 197 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.133+1996dupA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2345595 | |||||
| chr17:2345595
|
C | CAA | 25 | a0001c0001t0001g0029a0001c0001t0001g0125a0001c0001t0001g0126others(22): Show | 25 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.133+1995_133+1996d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2345595 | |||||
| chr17:2345682
|
G | T | 1 | a0002c0002t0023g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.133+2062G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345682 | ||||||
| chr17:2345850
|
T | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0062others(12): Show | 15 | HG01070.hp2 HG01109.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.133+2230T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345850 | ||||||
| chr17:2345978
|
C | T | 7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0189others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+2358C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345978 | ||||||
| chr17:2345989
|
G | C | 7 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0306others(4): Show | 7 | HG01243.hp2 HG02723.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+2369G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2345989 | ||||||
| chr17:2346160
|
T | G | 1 | a0001c0003t0001g0373 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.133+2540T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346160 | ||||||
| chr17:2346246
|
C | T | 1 | a0002c0004t0001g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+2626C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346246 | ||||||
| chr17:2346415
|
C | CAGAGCCT others(6): Show |
1 | a0001c0001t0001g0394 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.133+2808_133+2820d others(15): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2346415 | |||||
| chr17:2346544
|
G | C | 1 | a0001c0005t0002g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+2924G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346544 | ||||||
| chr17:2346610
|
C | T | 277 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(274): Show | 294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.133+2990C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346610 | ||||||
| chr17:2346625
|
T | A | 78 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0058others(75): Show | 89 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.133+3005T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346625 | ||||||
| chr17:2346724
|
C | T | 1 | a0001c0003t0001g0356 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.133+3104C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346724 | ||||||
| chr17:2346961
|
C | T | 1 | a0001c0003t0001g0373 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.133+3341C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2346961 | ||||||
| chr17:2347210
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.133+3590A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347210 | ||||||
| chr17:2347267
|
A | G | 1 | a0026c0016t0003g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.133+3647A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347267 | ||||||
| chr17:2347343
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.133+3723G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347343 | ||||||
| chr17:2347403
|
G | T | 1 | a0002c0004t0001g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133+3783G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347403 | ||||||
| chr17:2347409
|
A | AT | 40 | a0001c0001t0001g0029a0001c0001t0001g0081a0001c0001t0001g0120others(37): Show | 40 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+3807dupT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2347409 | |||||
| chr17:2347409
|
AT | A | 22 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0161others(19): Show | 22 | HG01069.hp1 HG01074.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.133+3807delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2347409 | |||||
| chr17:2347513
|
T | G | 3 | a0001c0001t0001g0310a0001c0001t0001g0349a0004c0010t0001g0350 | 3 | HG00544.hp1 HG02132.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.133+3893T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347513 | ||||||
| chr17:2347644
|
CT | C | 6 | a0001c0001t0001g0058a0001c0001t0001g0161a0001c0001t0001g0277others(3): Show | 6 | HG01169.hp1 HG02015.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+4037delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2347644 | |||||
| chr17:2347717
|
C | G | 111 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(108): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.133+4097C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347717 | ||||||
| chr17:2347764
|
C | T | 2 | a0001c0001t0002g0157a0001c0001t0002g0158 | 2 | NA19063.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.133+4144C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347764 | ||||||
| chr17:2347765
|
G | A | 73 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0058others(70): Show | 84 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.133+4145G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347765 | ||||||
| chr17:2347893
|
A | G | 1 | a0002c0002t0003g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.133+4273A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347893 | ||||||
| chr17:2347952
|
C | T | 2 | a0001c0001t0001g0317a0002c0002t0005g0080 | 2 | HG01069.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.133+4332C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347952 | ||||||
| chr17:2347990
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.133+4370T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2347990 | ||||||
| chr17:2348045
|
C | T | 26 | a0001c0001t0001g0154a0001c0001t0001g0163a0001c0001t0001g0169others(23): Show | 26 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.133+4425C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2348045 | ||||||
| chr17:2348547
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.133+4927G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2348547 | ||||||
| chr17:2348591
|
A | G | 113 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(110): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.133+4971A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2348591 | ||||||
| chr17:2348807
|
C | A | 261 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0021others(258): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.133+5187C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2348807 | ||||||
| chr17:2348864
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133+5244C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2348864 | ||||||
| chr17:2348910
|
C | T | 27 | a0001c0001t0001g0015a0001c0001t0001g0163a0001c0001t0001g0246others(24): Show | 32 | HG01081.hp2 HG02071.hp1 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.133+5290C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2348910 | ||||||
| chr17:2349004
|
T | C | 7 | a0002c0004t0001g0094a0003c0006t0001g0086a0003c0006t0001g0093others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.133+5384T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349004 | ||||||
| chr17:2349075
|
G | A | 40 | a0001c0001t0001g0081a0001c0001t0001g0120a0001c0001t0001g0121others(37): Show | 40 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.133+5455G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349075 | ||||||
| chr17:2349087
|
G | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+5467G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349087 | ||||||
| chr17:2349196
|
C | T | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(96): Show | 101 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.133+5576C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349196 | ||||||
| chr17:2349197
|
G | A | 1 | a0001c0003t0002g0099 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.133+5577G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349197 | ||||||
| chr17:2349202
|
C | T | 133 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0062others(130): Show | 140 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.133+5582C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349202 | ||||||
| chr17:2349239
|
C | T | 2 | a0001c0001t0001g0110a0016c0022t0001g0268 | 2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.133+5619C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349239 | ||||||
| chr17:2349240
|
A | G | 252 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0023others(249): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.133+5620A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349240 | ||||||
| chr17:2349247
|
A | G | 1 | a0002c0004t0015g0281 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.133+5627A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349247 | ||||||
| chr17:2349248
|
CGCCTGTA others(1870): Show |
C | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133+5645_133+7521d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2349248 | |||||
| chr17:2349249
|
G | A | 1 | a0001c0003t0002g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.133+5629G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349249 | ||||||
| chr17:2349269
|
G | C | 172 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0025others(169): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.133+5649G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349269 | ||||||
| chr17:2349274
|
G | T | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.133+5654G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349274 | ||||||
| chr17:2349277
|
G | A | 169 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0025others(166): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.133+5657G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349277 | ||||||
| chr17:2349334
|
T | C | 250 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0023others(247): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.133+5714T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349334 | ||||||
| chr17:2349373
|
T | TA | 228 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0025others(225): Show | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.133+5764dupA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2349373 | |||||
| chr17:2349589
|
C | T | 2 | a0001c0001t0001g0303a0001c0001t0001g0306 | 2 | NA19070.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.133+5969C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349589 | ||||||
| chr17:2349638
|
C | A | 1 | a0002c0002t0003g0052 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.133+6018C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349638 | ||||||
| chr17:2349665
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.133+6045G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349665 | ||||||
| chr17:2349713
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.133+6093G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349713 | ||||||
| chr17:2349788
|
G | GA | 175 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(172): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.133+6168_133+6169i others(3): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349788 | ||||||
| chr17:2349788
|
G | GAT | 9 | a0001c0001t0001g0121a0001c0001t0001g0190a0001c0001t0001g0205others(6): Show | 9 | HG00733.hp1 HG01106.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.133+6168_133+6169i others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349788 | ||||||
| chr17:2349789
|
T | A | 27 | a0001c0001t0001g0246a0002c0002t0001g0074a0002c0002t0001g0131others(24): Show | 29 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.133+6169T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349789 | ||||||
| chr17:2349793
|
G | T | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(211): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.133+6173G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349793 | ||||||
| chr17:2349937
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.133+6317A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349937 | ||||||
| chr17:2349945
|
G | A | 208 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(205): Show | 217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.133+6325G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349945 | ||||||
| chr17:2349947
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.133+6327T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349947 | ||||||
| chr17:2349980
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.133+6360G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2349980 | ||||||
| chr17:2350022
|
C | T | 6 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0046t0020g0159others(3): Show | 7 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.133+6402C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350022 | ||||||
| chr17:2350023
|
G | A | 2 | a0002c0002t0001g0151a0002c0046t0020g0159 | 2 | NA19030.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.133+6403G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350023 | ||||||
| chr17:2350038
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.133+6418C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350038 | ||||||
| chr17:2350069
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0003g0330 | 2 | HG02523.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.133+6449A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350069 | ||||||
| chr17:2350077
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0003g0330 | 2 | HG02523.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.133+6457A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350077 | ||||||
| chr17:2350147
|
C | G | 160 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(157): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.133+6527C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350147 | ||||||
| chr17:2350174
|
G | A | 161 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(158): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.133+6554G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350174 | ||||||
| chr17:2350413
|
C | G | 1 | a0002c0002t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133+6793C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350413 | ||||||
| chr17:2350416
|
C | A | 1 | a0002c0002t0001g0060 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133+6796C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350416 | ||||||
| chr17:2350469
|
G | A | 34 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(31): Show | 37 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.133+6849G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350469 | ||||||
| chr17:2350499
|
G | A | 274 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(271): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.133+6879G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350499 | ||||||
| chr17:2350652
|
G | A | 1 | a0002c0002t0012g0336 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.133+7032G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350652 | ||||||
| chr17:2350715
|
A | C | 1 | a0002c0046t0020g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133+7095A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350715 | ||||||
| chr17:2350732
|
G | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.133+7112G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350732 | ||||||
| chr17:2350843
|
T | C | 34 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(31): Show | 37 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.133+7223T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350843 | ||||||
| chr17:2350922
|
T | C | 1 | a0001c0001t0012g0320 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.133+7302T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350922 | ||||||
| chr17:2350979
|
G | A | 174 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(171): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.133+7359G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2350979 | ||||||
| chr17:2351027
|
T | C | 273 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(270): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.133+7407T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351027 | ||||||
| chr17:2351082
|
T | C | 209 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(206): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.133+7462T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351082 | ||||||
| chr17:2351194
|
A | G | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.133+7574A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351194 | ||||||
| chr17:2351238
|
T | G | 35 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(32): Show | 38 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.133+7618T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351238 | ||||||
| chr17:2351247
|
A | G | 34 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(31): Show | 37 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.133+7627A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351247 | ||||||
| chr17:2351468
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.133+7848C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351468 | ||||||
| chr17:2351570
|
C | G | 1 | a0006c0008t0003g0299 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.133+7950C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351570 | ||||||
| chr17:2351844
|
A | C | 177 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(174): Show | 185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.133+8224A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351844 | ||||||
| chr17:2351899
|
A | G | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(207): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.133+8279A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2351899 | ||||||
| chr17:2352029
|
G | A | 1 | a0002c0002t0003g0298 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.133+8409G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352029 | ||||||
| chr17:2352057
|
C | T | 207 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(204): Show | 216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.133+8437C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352057 | ||||||
| chr17:2352124
|
G | A | 1 | a0001c0001t0022g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.133+8504G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352124 | ||||||
| chr17:2352149
|
C | A | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133+8529C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352149 | ||||||
| chr17:2352390
|
C | T | 58 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(55): Show | 60 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.133+8770C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352390 | ||||||
| chr17:2352410
|
C | T | 1 | a0001c0003t0002g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.133+8790C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352410 | ||||||
| chr17:2352450
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.133+8830G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352450 | ||||||
| chr17:2352732
|
C | A | 174 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(171): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.134-8905C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352732 | ||||||
| chr17:2352767
|
C | CT | 28 | a0001c0001t0001g0126a0001c0001t0001g0256a0001c0001t0001g0296others(25): Show | 29 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-8842dupT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
C | CTT | 6 | a0002c0002t0001g0048a0002c0002t0001g0151a0002c0002t0003g0030others(3): Show | 6 | HG01891.hp1 HG01934.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-8843_134-8842d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CT | C | 166 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(163): Show | 172 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.134-8842delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CTT | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0154a0001c0001t0001g0176others(5): Show | 8 | HG01516.hp1 HG02040.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-8843_134-8842d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CTTTTT | C | 6 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0046t0020g0159others(3): Show | 7 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-8846_134-8842d others(7): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CTTTTTT | C | 28 | a0002c0002t0001g0074a0002c0002t0001g0131a0002c0002t0001g0133others(25): Show | 30 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.134-8847_134-8842d others(8): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CTTTTTTT others(3): Show |
C | 56 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(53): Show | 58 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.134-8851_134-8842d others(12): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0003t0001g0308a0001c0003t0001g0339a0001c0003t0002g0273others(2): Show | 5 | HG02895.hp1 HG02895.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-8852_134-8842d others(13): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352767
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-8858_134-8842d others(19): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2352767 | |||||
| chr17:2352775
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0218a0001c0001t0001g0246others(2): Show | 5 | HG02074.hp2 HG02523.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-8862T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352775 | ||||||
| chr17:2352776
|
T | C | 160 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(157): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.134-8861T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352776 | ||||||
| chr17:2352777
|
T | C | 8 | a0001c0001t0001g0115a0001c0001t0001g0154a0001c0001t0001g0176others(5): Show | 8 | HG01516.hp1 HG02040.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-8860T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352777 | ||||||
| chr17:2352778
|
T | C | 2 | a0001c0025t0001g0101a0002c0002t0002g0103 | 2 | HG01109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.134-8859T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352778 | ||||||
| chr17:2352779
|
T | C | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-8858T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352779 | ||||||
| chr17:2352780
|
T | C | 6 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0046t0020g0159others(3): Show | 7 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-8857T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352780 | ||||||
| chr17:2352781
|
T | C | 30 | a0001c0001t0001g0161a0002c0002t0001g0074a0002c0002t0001g0131others(27): Show | 32 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.134-8856T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352781 | ||||||
| chr17:2352783
|
T | C | 1 | a0001c0001t0001g0357 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.134-8854T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352783 | ||||||
| chr17:2352800
|
C | T | 1 | a0001c0034t0009g0396 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.134-8837C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352800 | ||||||
| chr17:2352808
|
C | T | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8829C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352808 | ||||||
| chr17:2352817
|
G | A | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8820G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352817 | ||||||
| chr17:2352840
|
C | T | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8797C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352840 | ||||||
| chr17:2352846
|
C | G | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8791C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352846 | ||||||
| chr17:2352864
|
G | T | 5 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0031others(2): Show | 7 | HG01192.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-8773G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352864 | ||||||
| chr17:2352870
|
C | T | 65 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(62): Show | 67 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.134-8767C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352870 | ||||||
| chr17:2352878
|
C | T | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8759C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352878 | ||||||
| chr17:2352900
|
C | A | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8737C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352900 | ||||||
| chr17:2352922
|
C | T | 1 | a0001c0005t0002g0013 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.134-8715C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352922 | ||||||
| chr17:2352924
|
T | C | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8713T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352924 | ||||||
| chr17:2352927
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-8710G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352927 | ||||||
| chr17:2352932
|
C | T | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8705C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352932 | ||||||
| chr17:2352933
|
A | G | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8704A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352933 | ||||||
| chr17:2352934
|
C | T | 275 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(272): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.134-8703C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352934 | ||||||
| chr17:2352963
|
G | C | 1 | a0001c0001t0001g0334 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.134-8674G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352963 | ||||||
| chr17:2352967
|
C | T | 144 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(141): Show | 149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.134-8670C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352967 | ||||||
| chr17:2352977
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-8660C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2352977 | ||||||
| chr17:2353029
|
G | A | 281 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(278): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.134-8608G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353029 | ||||||
| chr17:2353218
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.134-8419A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353218 | ||||||
| chr17:2353245
|
A | T | 1 | a0002c0002t0001g0314 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.134-8392A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353245 | ||||||
| chr17:2353391
|
G | T | 34 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(31): Show | 37 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.134-8246G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353391 | ||||||
| chr17:2353534
|
G | A | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(219): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.134-8103G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353534 | ||||||
| chr17:2353545
|
T | A | 1 | a0002c0002t0003g0052 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.134-8092T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353545 | ||||||
| chr17:2353650
|
A | C | 5 | a0002c0002t0023g0139a0002c0004t0001g0279a0002c0004t0001g0300others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-7987A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353650 | ||||||
| chr17:2353651
|
G | C | 5 | a0002c0002t0023g0139a0002c0004t0001g0279a0002c0004t0001g0300others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-7986G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353651 | ||||||
| chr17:2353749
|
GACTGAGA others(10): Show |
G | 1 | a0001c0003t0001g0374 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.134-7886_134-7870d others(19): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2353749 | |||||
| chr17:2353766
|
T | TA | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(211): Show | 223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.134-7861dupA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2353766 | |||||
| chr17:2353766
|
T | TAA | 9 | a0001c0001t0001g0186a0001c0001t0001g0256a0001c0001t0001g0257others(6): Show | 9 | HG02698.hp2 HG03669.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-7862_134-7861d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2353766 | |||||
| chr17:2353796
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.134-7841A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353796 | ||||||
| chr17:2353815
|
T | C | 1 | a0001c0001t0022g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.134-7822T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353815 | ||||||
| chr17:2353913
|
T | G | 1 | a0021c0042t0001g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.134-7724T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353913 | ||||||
| chr17:2353926
|
T | A | 1 | a0020c0040t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.134-7711T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353926 | ||||||
| chr17:2353994
|
C | CG | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-7643_134-7642i others(3): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353994 | ||||||
| chr17:2353997
|
G | T | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-7640G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2353997 | ||||||
| chr17:2354023
|
T | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | NA18971.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.134-7614T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354023 | ||||||
| chr17:2354106
|
T | C | 1 | a0002c0002t0005g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.134-7531T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354106 | ||||||
| chr17:2354215
|
T | TTTGTTTG others(9): Show |
1 | a0001c0001t0002g0157 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.134-7420_134-7419i others(18): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354215 | |||||
| chr17:2354215
|
T | TTTTGTTT others(9): Show |
1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.134-7408_134-7407i others(18): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354215 | |||||
| chr17:2354215
|
T | TTTTGTTT others(10): Show |
218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 227 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.134-7408_134-7407i others(19): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354215 | |||||
| chr17:2354215
|
T | TTTTGTTT others(11): Show |
1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.134-7408_134-7407i others(20): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354215 | |||||
| chr17:2354238
|
C | T | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-7399C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354238 | ||||||
| chr17:2354269
|
C | T | 1 | a0001c0003t0002g0128 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.134-7368C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354269 | ||||||
| chr17:2354321
|
T | G | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-7316T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354321 | ||||||
| chr17:2354332
|
G | A | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-7305G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354332 | ||||||
| chr17:2354338
|
G | A | 1 | a0002c0002t0001g0035 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.134-7299G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354338 | ||||||
| chr17:2354367
|
A | C | 35 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(32): Show | 38 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.134-7270A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354367 | ||||||
| chr17:2354525
|
T | A | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-7112T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354525 | ||||||
| chr17:2354570
|
A | G | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-7067A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354570 | ||||||
| chr17:2354594
|
CTAAA | C | 3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0296 | 3 | HG03669.hp1 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.134-7039_134-7036d others(6): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354594 | |||||
| chr17:2354619
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.134-7018T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354619 | ||||||
| chr17:2354699
|
C | T | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-6938C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354699 | ||||||
| chr17:2354723
|
A | C | 1 | a0001c0001t0001g0370 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.134-6914A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354723 | ||||||
| chr17:2354853
|
C | T | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(218): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.134-6784C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354853 | ||||||
| chr17:2354855
|
T | TATATCTT others(684): Show |
1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-6751_134-6750i others(693): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354855 | |||||
| chr17:2354855
|
T | TATATCTT others(139): Show |
1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6758_134-6757i others(148): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354855 | |||||
| chr17:2354887
|
C | G | 359 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(356): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.134-6750C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354887 | ||||||
| chr17:2354900
|
A | ACCCCATA others(535): Show |
1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.134-6689_134-6688i others(544): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354900 | |||||
| chr17:2354936
|
C | CGTTGGGG others(783): Show |
1 | a0002c0002t0004g0345 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.134-6689_134-6688i others(792): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354936 | |||||
| chr17:2354936
|
C | CGTTGGGG others(586): Show |
1 | a0001c0003t0001g0258 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.134-6689_134-6688i others(595): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354936 | |||||
| chr17:2354936
|
C | CGTTGGGG others(586): Show |
44 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(41): Show | 46 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.134-6689_134-6688i others(595): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354936 | |||||
| chr17:2354936
|
C | G | 35 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0033others(32): Show | 38 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.134-6701C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354936 | ||||||
| chr17:2354939
|
T | TG | 34 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0074others(31): Show | 37 | HG01175.hp2 HG01243.hp2 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.134-6694dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(833): Show |
1 | a0002c0002t0002g0018 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.134-6689_134-6688i others(842): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(833): Show |
63 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0098others(60): Show | 73 | HG00609.hp2 HG00642.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.134-6689_134-6688i others(842): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(833): Show |
1 | a0002c0002t0014g0346 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-6689_134-6688i others(842): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(833): Show |
1 | a0002c0002t0018g0046 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.134-6689_134-6688i others(842): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(784): Show |
3 | a0001c0001t0022g0130a0007c0007t0001g0135a0027c0015t0005g0079 | 3 | HG02647.hp2 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.134-6689_134-6688i others(793): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(190): Show |
6 | a0001c0001t0002g0382a0004c0011t0001g0155a0004c0011t0001g0385others(3): Show | 6 | NA18946.hp2 NA18979.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-6689_134-6688i others(199): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354939
|
T | TGGGGAAG others(784): Show |
1 | a0002c0002t0004g0166 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.134-6689_134-6688i others(793): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354939 | |||||
| chr17:2354949
|
A | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(10): Show | 14 | HG01167.hp1 HG01358.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-6688A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354949 | ||||||
| chr17:2354949
|
A | GCCCCATA others(784): Show |
1 | a0007c0007t0001g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.134-6689_134-6688i others(793): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354949 | ||||||
| chr17:2354988
|
TG | T | 18 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0070others(15): Show | 19 | HG01167.hp1 HG01358.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.134-6644delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354988 | |||||
| chr17:2354989
|
G | GGGAAAGG others(90): Show |
1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.134-6646_134-6645i others(99): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354989 | |||||
| chr17:2354989
|
G | GGGAAAGG others(684): Show |
1 | a0016c0022t0001g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.134-6646_134-6645i others(693): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354989 | |||||
| chr17:2354989
|
GGGGGAAG others(42): Show |
G | 2 | a0001c0003t0002g0105a0002c0002t0002g0103 | 2 | HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.134-6594_134-6546d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2354989 | |||||
| chr17:2354993
|
G | A | 11 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0070others(8): Show | 12 | HG01167.hp1 HG01358.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-6644G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354993 | ||||||
| chr17:2354994
|
A | C | 2 | a0001c0001t0001g0023a0002c0002t0001g0033 | 2 | HG03540.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.134-6643A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2354994 | ||||||
| chr17:2355035
|
GGTTGGGG others(391): Show |
G | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.134-6594_134-6197d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355035 | |||||
| chr17:2355038
|
T | TG | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(223): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.134-6595dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355038 | |||||
| chr17:2355038
|
T | TGGGGAAG others(289): Show |
1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-6546_134-6545i others(298): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355038 | |||||
| chr17:2355042
|
G | A | 2 | a0001c0001t0001g0023a0002c0002t0001g0033 | 2 | HG03540.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.134-6595G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355042 | ||||||
| chr17:2355043
|
A | C | 71 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0098others(68): Show | 82 | HG00609.hp2 HG00642.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.134-6594A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355043 | ||||||
| chr17:2355048
|
A | ACCCCATA others(934): Show |
1 | a0002c0002t0001g0028 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.134-6546_134-6545i others(943): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355048 | |||||
| chr17:2355048
|
A | ACCCCATA others(143): Show |
1 | a0004c0010t0001g0350 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.134-6510_134-6509i others(152): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355048 | |||||
| chr17:2355048
|
A | ACCCCATA others(142): Show |
59 | a0001c0001t0001g0110a0001c0001t0001g0351a0001c0001t0009g0355others(56): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.134-6495_134-6494i others(151): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355048 | |||||
| chr17:2355048
|
A | ACCCCATA others(142): Show |
1 | a0001c0003t0001g0325 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.134-6490_134-6489i others(151): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355048 | |||||
| chr17:2355048
|
A | G | 72 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0098others(69): Show | 83 | HG00609.hp2 HG00642.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.134-6589A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355048 | ||||||
| chr17:2355053
|
A | ATATCTTA others(289): Show |
1 | a0002c0002t0001g0347 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.134-6546_134-6545i others(298): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355053 | |||||
| chr17:2355065
|
G | GGTGGAAT others(142): Show |
2 | a0002c0002t0003g0276a0002c0002t0003g0289 | 2 | HG01099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.134-6495_134-6494i others(151): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355065 | |||||
| chr17:2355084
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0391 | 3 | HG01070.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.134-6553G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355084 | ||||||
| chr17:2355084
|
G | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(214): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.134-6553G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355084 | ||||||
| chr17:2355085
|
G | A | 1 | a0014c0031t0001g0392 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.134-6552G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355085 | ||||||
| chr17:2355085
|
GT | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0200a0001c0001t0002g0255 | 3 | NA18950.hp2 NA18994.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.134-6550delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355085 | |||||
| chr17:2355087
|
TG | T | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(220): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.134-6545delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355087 | |||||
| chr17:2355088
|
G | C | 3 | a0001c0001t0002g0170a0001c0001t0002g0200a0001c0001t0002g0255 | 3 | NA18950.hp2 NA18994.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.134-6549G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355088 | ||||||
| chr17:2355090
|
G | C | 1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6547G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355090 | ||||||
| chr17:2355093
|
A | C | 21 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0070others(18): Show | 21 | HG00642.hp1 HG01070.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-6544A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355093 | ||||||
| chr17:2355098
|
A | ACCCCATA others(192): Show |
4 | a0001c0003t0001g0054a0001c0003t0001g0354a0001c0003t0001g0379others(1): Show | 4 | HG02602.hp1 NA18990.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-6495_134-6494i others(201): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355098 | |||||
| chr17:2355098
|
A | G | 183 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(180): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.134-6539A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355098 | ||||||
| chr17:2355134
|
G | C | 2 | a0001c0003t0002g0105a0002c0002t0002g0103 | 2 | HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.134-6503G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355134 | ||||||
| chr17:2355135
|
GT | G | 183 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(180): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.134-6500delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355135 | |||||
| chr17:2355137
|
TG | T | 22 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(19): Show | 23 | HG00558.hp2 HG01167.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-6495delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355137 | |||||
| chr17:2355138
|
G | C | 183 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(180): Show | 189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.134-6499G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355138 | ||||||
| chr17:2355138
|
G | GGGGGAAG others(42): Show |
15 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(12): Show | 15 | HG02056.hp1 HG02083.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.134-6495_134-6494i others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355138 | |||||
| chr17:2355142
|
G | A | 5 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0085others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-6495G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355142 | ||||||
| chr17:2355143
|
C | A | 226 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(223): Show | 235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.134-6494C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355143 | ||||||
| chr17:2355148
|
G | A | 44 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0070others(41): Show | 48 | HG01167.hp1 HG01175.hp2 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.134-6489G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355148 | ||||||
| chr17:2355185
|
GT | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(182): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.134-6450delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355185 | |||||
| chr17:2355187
|
TG | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0348a0001c0001t0003g0324others(1): Show | 5 | HG01261.hp1 HG02257.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-6445delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355187 | |||||
| chr17:2355188
|
G | C | 185 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(182): Show | 191 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.134-6449G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355188 | ||||||
| chr17:2355190
|
G | GAAAGGGA others(42): Show |
3 | a0002c0002t0001g0376a0002c0002t0001g0397a0002c0043t0001g0364 | 3 | HG01167.hp1 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.134-6447_134-6446i others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355190 | ||||||
| chr17:2355192
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-6445G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355192 | ||||||
| chr17:2355193
|
A | C | 37 | a0001c0001t0001g0110a0001c0001t0001g0348a0001c0001t0001g0351others(34): Show | 39 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.134-6444A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355193 | ||||||
| chr17:2355198
|
A | ACCCCATA others(93): Show |
18 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(15): Show | 18 | HG02056.hp1 HG02083.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.134-6345_134-6344i others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355198 | |||||
| chr17:2355198
|
A | G | 72 | a0001c0001t0001g0110a0001c0001t0001g0348a0001c0001t0001g0351others(69): Show | 77 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(74): Show |
intron_variant | MODIFIER | c.134-6439A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355198 | ||||||
| chr17:2355202
|
C | CATATCTT others(93): Show |
2 | a0001c0003t0002g0274a0001c0005t0002g0272 | 2 | HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.134-6345_134-6344i others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355202 | |||||
| chr17:2355202
|
C | T | 5 | a0001c0003t0002g0012a0001c0003t0002g0273a0001c0003t0016g0266others(2): Show | 7 | HG02258.hp2 HG02280.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-6435C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355202 | ||||||
| chr17:2355203
|
A | G | 1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6434A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355203 | ||||||
| chr17:2355223
|
C | T | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-6414C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355223 | ||||||
| chr17:2355235
|
GT | G | 3 | a0001c0001t0001g0357a0001c0003t0002g0105a0002c0002t0002g0103 | 3 | HG02486.hp1 NA18612.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.134-6400delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355235 | |||||
| chr17:2355235
|
GTTGGGGG others(94): Show |
G | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.134-6400_134-6300d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355235 | |||||
| chr17:2355237
|
TG | T | 187 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(184): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.134-6395delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355237 | |||||
| chr17:2355237
|
TGGGGGCA others(44): Show |
T | 1 | a0001c0001t0001g0150 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.134-6395_134-6345d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355237 | |||||
| chr17:2355237
|
TGGGGGCA others(193): Show |
T | 3 | a0001c0001t0001g0138a0001c0001t0003g0254a0001c0037t0001g0217 | 3 | HG02015.hp2 NA19002.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.134-6395_134-6196d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355237 | |||||
| chr17:2355238
|
G | C | 3 | a0001c0001t0001g0357a0001c0003t0002g0105a0002c0002t0002g0103 | 3 | HG02486.hp1 NA18612.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.134-6399G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355238 | ||||||
| chr17:2355240
|
G | C | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-6397G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355240 | ||||||
| chr17:2355243
|
C | A | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(215): Show | 228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.134-6394C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355243 | ||||||
| chr17:2355244
|
A | G | 1 | a0002c0004t0001g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-6393A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355244 | ||||||
| chr17:2355248
|
G | A | 183 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(180): Show | 190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.134-6389G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355248 | ||||||
| chr17:2355249
|
CCCCATAT others(1631): Show |
C | 33 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0131others(30): Show | 36 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.134-6339_134-4702d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355249 | |||||
| chr17:2355273
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.134-6364C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355273 | ||||||
| chr17:2355284
|
G | C | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.134-6353G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355284 | ||||||
| chr17:2355286
|
T | G | 1 | a0001c0001t0001g0303 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.134-6351T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355286 | ||||||
| chr17:2355287
|
TG | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0304a0023c0018t0001g0114 | 4 | HG02257.hp2 HG02698.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-6345delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355287 | |||||
| chr17:2355288
|
G | C | 1 | a0001c0003t0002g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-6349G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355288 | ||||||
| chr17:2355288
|
G | GGGGCAGG others(94): Show |
1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6346_134-6345i others(103): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355288 | |||||
| chr17:2355293
|
A | AAGGGACC others(42): Show |
5 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0085others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-6340_134-6339i others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355293 | |||||
| chr17:2355293
|
A | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 6 | HG02132.hp1 HG02165.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-6344A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355293 | ||||||
| chr17:2355298
|
G | A | 187 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(184): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.134-6339G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355298 | ||||||
| chr17:2355299
|
CCCCATAT others(1581): Show |
C | 1 | a0002c0002t0001g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.134-6303_134-4716d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355299 | |||||
| chr17:2355303
|
A | G | 3 | a0002c0002t0001g0376a0002c0002t0001g0397a0002c0043t0001g0364 | 3 | HG01167.hp1 HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.134-6334A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355303 | ||||||
| chr17:2355334
|
A | C | 182 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(179): Show | 188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.134-6303A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355334 | ||||||
| chr17:2355334
|
A | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0150a0001c0001t0001g0256others(10): Show | 14 | HG00558.hp2 HG01167.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-6303A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355334 | ||||||
| chr17:2355336
|
T | G | 1 | a0001c0003t0002g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-6301T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355336 | ||||||
| chr17:2355337
|
TG | T | 173 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(170): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.134-6295delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355337 | |||||
| chr17:2355337
|
TGGGGGAA others(93): Show |
T | 3 | a0001c0001t0001g0211a0001c0001t0001g0256a0001c0003t0002g0219 | 3 | HG04228.hp2 NA18747.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.134-6295_134-6196d others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355337 | |||||
| chr17:2355338
|
G | C | 2 | a0001c0001t0002g0022a0001c0003t0002g0105 | 2 | HG02622.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.134-6299G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355338 | ||||||
| chr17:2355338
|
G | GGGGGAAG others(141): Show |
3 | a0007c0007t0001g0135a0007c0007t0001g0140a0027c0015t0005g0079 | 3 | HG02615.hp2 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.134-6245_134-6098d others(150): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355338 | |||||
| chr17:2355338
|
G | GGGGGCAG others(141): Show |
2 | a0001c0001t0001g0110a0001c0001t0022g0130 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-6295_134-6294i others(150): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355338 | |||||
| chr17:2355338
|
G | GGGGGCAG others(241): Show |
1 | a0016c0022t0001g0268 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.134-6295_134-6294i others(250): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355338 | |||||
| chr17:2355342
|
G | A | 1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6295G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355342 | ||||||
| chr17:2355343
|
A | C | 53 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(50): Show | 55 | HG00099.hp1 HG00140.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-6294A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355343 | ||||||
| chr17:2355344
|
A | G | 1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6293A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355344 | ||||||
| chr17:2355348
|
A | G | 1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-6289A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355348 | ||||||
| chr17:2355353
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-6284A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355353 | ||||||
| chr17:2355384
|
G | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(9): Show | 12 | HG00733.hp1 HG01891.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-6253G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355384 | ||||||
| chr17:2355387
|
T | TG | 63 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0055others(60): Show | 66 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.134-6246dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355387 | |||||
| chr17:2355387
|
TGGGGCAG others(43): Show |
T | 56 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(53): Show | 57 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.134-6245_134-6196d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355387 | |||||
| chr17:2355387
|
TGGGGCAG others(92): Show |
T | 20 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(17): Show | 21 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.134-6245_134-6147d others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355387 | |||||
| chr17:2355392
|
C | A | 59 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0023others(56): Show | 61 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-6245C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355392 | ||||||
| chr17:2355397
|
G | A | 112 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0021others(109): Show | 116 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.134-6240G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355397 | ||||||
| chr17:2355397
|
GCCCCATA others(43): Show |
G | 1 | a0001c0001t0001g0329 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.134-6204_134-6155d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355397 | |||||
| chr17:2355399
|
C | T | 54 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(51): Show | 56 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.134-6238C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355399 | ||||||
| chr17:2355401
|
C | T | 55 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(52): Show | 57 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.134-6236C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355401 | ||||||
| chr17:2355402
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-6235A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355402 | ||||||
| chr17:2355432
|
G | GGTTGGGG others(38): Show |
1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6205_134-6204i others(47): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355432 | ||||||
| chr17:2355433
|
A | C | 9 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0085others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-6204A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355433 | ||||||
| chr17:2355433
|
A | G | 106 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0021others(103): Show | 110 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.134-6204A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355433 | ||||||
| chr17:2355435
|
T | G | 1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6202T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355435 | ||||||
| chr17:2355436
|
TG | T | 62 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0055others(59): Show | 65 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.134-6196delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355436 | |||||
| chr17:2355437
|
G | GGGGGAAG others(92): Show |
2 | a0002c0002t0001g0376a0002c0002t0001g0397 | 2 | HG01167.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.134-6155_134-6154i others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355437 | |||||
| chr17:2355437
|
G | T | 1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-6200G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355437 | ||||||
| chr17:2355442
|
A | C | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-6195A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355442 | ||||||
| chr17:2355447
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0348 | 3 | HG02257.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.134-6190A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355447 | ||||||
| chr17:2355483
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-6154G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355483 | ||||||
| chr17:2355483
|
G | C | 62 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0055others(59): Show | 65 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.134-6154G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355483 | ||||||
| chr17:2355486
|
T | TG | 67 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0021others(64): Show | 69 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.134-6147dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355486 | |||||
| chr17:2355486
|
TGGGGAAG others(93): Show |
T | 1 | a0001c0001t0001g0161 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.134-6097_134-5998d others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355486 | |||||
| chr17:2355491
|
A | C | 2 | a0002c0002t0001g0027a0002c0002t0003g0201 | 2 | HG00558.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.134-6146A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355491 | ||||||
| chr17:2355496
|
A | G | 2 | a0001c0025t0001g0101a0002c0002t0003g0201 | 2 | HG00558.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.134-6141A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355496 | ||||||
| chr17:2355532
|
G | A | 1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-6105G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355532 | ||||||
| chr17:2355532
|
G | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0138a0001c0001t0001g0321others(4): Show | 8 | HG02015.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-6105G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355532 | ||||||
| chr17:2355532
|
GGTTGGGG others(43): Show |
G | 56 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(53): Show | 58 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.134-6071_134-6022d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355532 | |||||
| chr17:2355535
|
TG | T | 62 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0081others(59): Show | 64 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(61): Show |
intron_variant | MODIFIER | c.134-6097delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355535 | |||||
| chr17:2355535
|
TGGGGGAA others(44): Show |
T | 103 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0025others(100): Show | 105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.134-6097_134-6047d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355535 | |||||
| chr17:2355536
|
G | C | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.134-6101G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355536 | ||||||
| chr17:2355541
|
A | C | 52 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(49): Show | 54 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.134-6096A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355541 | ||||||
| chr17:2355546
|
A | G | 52 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(49): Show | 54 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.134-6091A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355546 | ||||||
| chr17:2355566
|
A | G | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(99): Show | 108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.134-6071A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355566 | ||||||
| chr17:2355571
|
CGGGGTGT others(44): Show |
C | 1 | a0001c0001t0001g0215 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.134-6062_134-6012d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355571 | |||||
| chr17:2355582
|
A | C | 2 | a0001c0001t0001g0021a0002c0043t0001g0364 | 3 | HG02257.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.134-6055A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355582 | ||||||
| chr17:2355582
|
A | G | 37 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(34): Show | 38 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.134-6055A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355582 | ||||||
| chr17:2355585
|
TG | T | 9 | a0001c0001t0001g0021a0001c0001t0001g0329a0001c0001t0002g0228others(6): Show | 10 | HG00558.hp2 HG00733.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-6047delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355585 | |||||
| chr17:2355632
|
G | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0143others(2): Show | 6 | HG00642.hp2 HG01261.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-6005G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355632 | ||||||
| chr17:2355635
|
T | TG | 63 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(60): Show | 65 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.134-5998dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355635 | |||||
| chr17:2355635
|
TGGGGAAG others(43): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.134-5956_134-5907d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355635 | |||||
| chr17:2355640
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.134-5997A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355640 | ||||||
| chr17:2355645
|
A | G | 27 | a0001c0001t0001g0023a0001c0001t0001g0120a0001c0001t0001g0143others(24): Show | 27 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.134-5992A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355645 | ||||||
| chr17:2355665
|
G | A | 1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-5972G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355665 | ||||||
| chr17:2355681
|
A | C | 53 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(50): Show | 55 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-5956A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355681 | ||||||
| chr17:2355681
|
A | G | 195 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(192): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.134-5956A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355681 | ||||||
| chr17:2355681
|
A | T | 6 | a0001c0001t0001g0110a0001c0001t0022g0130a0007c0007t0001g0135others(3): Show | 6 | HG02615.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-5956A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355681 | ||||||
| chr17:2355683
|
T | G | 2 | a0001c0001t0001g0358a0010c0033t0001g0202 | 2 | HG00642.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.134-5954T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355683 | ||||||
| chr17:2355684
|
TG | T | 146 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(143): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.134-5948delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355684 | |||||
| chr17:2355685
|
G | C | 3 | a0001c0001t0001g0143a0001c0001t0001g0358a0010c0033t0001g0202 | 3 | HG00642.hp2 NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.134-5952G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355685 | ||||||
| chr17:2355690
|
A | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0085others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-5947A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355690 | ||||||
| chr17:2355695
|
A | G | 112 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(109): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.134-5942A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355695 | ||||||
| chr17:2355715
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-5922G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355715 | ||||||
| chr17:2355731
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-5906G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355731 | ||||||
| chr17:2355731
|
G | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0144others(1): Show | 4 | NA18964.hp2 NA18978.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-5906G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355731 | ||||||
| chr17:2355734
|
T | C | 55 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(52): Show | 57 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.134-5903T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355734 | ||||||
| chr17:2355734
|
T | TG | 110 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0023others(107): Show | 112 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.134-5899dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355734 | |||||
| chr17:2355739
|
A | C | 54 | a0001c0001t0001g0023a0001c0001t0001g0081a0001c0001t0001g0122others(51): Show | 56 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.134-5898A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355739 | ||||||
| chr17:2355744
|
A | G | 133 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(130): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.134-5893A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355744 | ||||||
| chr17:2355770
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.134-5867G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355770 | ||||||
| chr17:2355780
|
G | A | 1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-5857G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355780 | ||||||
| chr17:2355781
|
GT | G | 52 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(49): Show | 54 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.134-5854delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355781 | |||||
| chr17:2355783
|
TG | T | 7 | a0001c0001t0001g0138a0001c0001t0001g0348a0001c0001t0002g0228others(4): Show | 7 | HG01109.hp2 HG02015.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-5849delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355783 | |||||
| chr17:2355783
|
TGGGGGAA others(44): Show |
T | 1 | a0001c0003t0002g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-5849_134-5799d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355783 | |||||
| chr17:2355784
|
G | C | 52 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(49): Show | 54 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.134-5853G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355784 | ||||||
| chr17:2355784
|
G | GGGGGAAG others(191): Show |
1 | a0002c0002t0009g0280 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.134-5800_134-5799i others(200): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355784 | |||||
| chr17:2355789
|
A | C | 6 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-5848A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355789 | ||||||
| chr17:2355794
|
A | ACCCCATA others(42): Show |
1 | a0002c0043t0001g0364 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134-5800_134-5799i others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355794 | |||||
| chr17:2355794
|
A | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(5): Show | 8 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-5843A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355794 | ||||||
| chr17:2355820
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.134-5817G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355820 | ||||||
| chr17:2355830
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-5807G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355830 | ||||||
| chr17:2355830
|
G | GGTTGGGG others(292): Show |
1 | a0001c0001t0001g0123 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.134-5799_134-5798i others(301): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355830 | |||||
| chr17:2355830
|
G | GGTTGGGG others(440): Show |
46 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0332others(43): Show | 48 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.134-5799_134-5798i others(449): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355830 | |||||
| chr17:2355830
|
G | GGTTGGGG others(440): Show |
2 | a0002c0012t0001g0129a0002c0012t0001g0372 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.134-5799_134-5798i others(449): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355830 | |||||
| chr17:2355830
|
G | GGTTGGGG others(440): Show |
1 | a0001c0003t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.134-5799_134-5798i others(449): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355830 | |||||
| chr17:2355833
|
TG | T | 33 | a0001c0001t0001g0109a0001c0001t0001g0138a0001c0001t0001g0143others(30): Show | 34 | HG00558.hp2 HG00597.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.134-5799delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355833 | |||||
| chr17:2355833
|
TGGGGGAA others(43): Show |
T | 15 | a0001c0001t0001g0154a0001c0001t0001g0162a0001c0001t0001g0163others(12): Show | 15 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-5799_134-5750d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355833 | |||||
| chr17:2355834
|
G | C | 1 | a0001c0001t0001g0317 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.134-5803G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355834 | ||||||
| chr17:2355834
|
G | GGGGGAAG others(42): Show |
2 | a0007c0007t0001g0140a0027c0015t0005g0079 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.134-5749_134-5701d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355834 | |||||
| chr17:2355834
|
G | GGGGGCAG others(530): Show |
1 | a0002c0002t0001g0033 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.134-5799_134-5798i others(539): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355834 | |||||
| chr17:2355834
|
G | GGGGGCAG others(341): Show |
1 | a0001c0003t0001g0354 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134-5799_134-5798i others(350): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355834 | |||||
| chr17:2355839
|
A | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(5): Show | 8 | HG01167.hp1 HG01891.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-5798A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355839 | ||||||
| chr17:2355844
|
A | G | 11 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(8): Show | 11 | HG01167.hp1 HG01891.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-5793A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355844 | ||||||
| chr17:2355870
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.134-5767G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355870 | ||||||
| chr17:2355883
|
T | TG | 59 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(56): Show | 61 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-5750dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355883 | |||||
| chr17:2355883
|
T | TGGGGAAG others(92): Show |
3 | a0001c0001t0001g0110a0001c0001t0022g0130a0016c0022t0001g0268 | 3 | HG03195.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-5701_134-5700i others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355883 | |||||
| chr17:2355883
|
T | TGGGGGAA others(291): Show |
1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.134-5750_134-5749i others(300): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355883 | |||||
| chr17:2355883
|
T | TGGGGGCA others(341): Show |
5 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0085others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-5750_134-5749i others(350): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355883 | |||||
| chr17:2355883
|
TGGGGAAG others(93): Show |
T | 11 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0001t0001g0247others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-5700_134-5601d others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355883 | |||||
| chr17:2355888
|
A | C | 3 | a0001c0001t0001g0021a0001c0003t0001g0354a0002c0043t0001g0364 | 4 | HG02257.hp2 HG02559.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-5749A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355888 | ||||||
| chr17:2355893
|
A | G | 3 | a0001c0001t0001g0021a0001c0003t0001g0354a0002c0043t0001g0364 | 4 | HG02257.hp2 HG02559.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-5744A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355893 | ||||||
| chr17:2355929
|
G | A | 1 | a0001c0003t0001g0354 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134-5708G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355929 | ||||||
| chr17:2355929
|
G | GGTTGGGG others(92): Show |
1 | a0007c0007t0001g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.134-5701_134-5700i others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355929 | |||||
| chr17:2355929
|
GGTTGGGG others(43): Show |
G | 14 | a0001c0001t0001g0115a0001c0001t0001g0257a0001c0001t0001g0296others(11): Show | 14 | HG02055.hp1 HG02622.hp1 HG03669.hp1 others(11): Show |
intron_variant | MODIFIER | c.134-5674_134-5625d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355929 | |||||
| chr17:2355932
|
TG | T | 8 | a0001c0001t0001g0123a0001c0001t0001g0143a0001c0001t0001g0256others(5): Show | 8 | HG02015.hp1 HG02040.hp2 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-5700delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355932 | |||||
| chr17:2355932
|
TGGGGGAA others(44): Show |
T | 88 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(85): Show | 92 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.134-5700_134-5650d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355932 | |||||
| chr17:2355938
|
A | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0123a0002c0002t0001g0376others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-5699A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355938 | ||||||
| chr17:2355943
|
A | G | 3 | a0001c0001t0001g0123a0002c0002t0001g0376a0002c0002t0001g0397 | 3 | HG01167.hp1 HG03225.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.134-5694A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355943 | ||||||
| chr17:2355963
|
A | G | 88 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0021others(85): Show | 90 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.134-5674A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355963 | ||||||
| chr17:2355969
|
G | A | 3 | a0001c0001t0001g0138a0001c0001t0003g0254a0001c0037t0001g0217 | 3 | HG02015.hp2 NA19002.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.134-5668G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355969 | ||||||
| chr17:2355979
|
A | G | 87 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0021others(84): Show | 89 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.134-5658A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355979 | ||||||
| chr17:2355982
|
TG | T | 7 | a0001c0001t0001g0110a0001c0001t0001g0143a0001c0001t0022g0130others(4): Show | 7 | HG00558.hp2 HG02602.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.134-5650delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355982 | |||||
| chr17:2355983
|
G | GGGGGAAG others(42): Show |
2 | a0007c0007t0001g0140a0027c0015t0005g0079 | 2 | HG02615.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.134-5608_134-5560d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2355983 | |||||
| chr17:2355988
|
A | C | 2 | a0001c0001t0001g0021a0002c0043t0001g0364 | 3 | HG02257.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.134-5649A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355988 | ||||||
| chr17:2355993
|
A | G | 4 | a0001c0001t0001g0021a0002c0002t0001g0376a0002c0002t0001g0397others(1): Show | 5 | HG01167.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-5644A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2355993 | ||||||
| chr17:2356029
|
G | A | 2 | a0002c0002t0001g0376a0002c0002t0001g0397 | 2 | HG01167.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.134-5608G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356029 | ||||||
| chr17:2356029
|
G | T | 1 | a0001c0003t0001g0054 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.134-5608G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356029 | ||||||
| chr17:2356029
|
GGTTGGGG others(42): Show |
G | 1 | a0001c0003t0002g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.134-5600_134-5552d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356029 | |||||
| chr17:2356032
|
T | TG | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(29): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.134-5601dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356032 | |||||
| chr17:2356032
|
TGGGGAAG others(43): Show |
T | 12 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0171others(9): Show | 12 | HG00597.hp2 HG00733.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-5559_134-5510d others(52): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356032 | |||||
| chr17:2356042
|
A | G | 1 | a0002c0043t0001g0364 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134-5595A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356042 | ||||||
| chr17:2356062
|
G | A | 2 | a0001c0003t0001g0354a0002c0002t0003g0201 | 2 | HG00558.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.134-5575G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356062 | ||||||
| chr17:2356078
|
A | C | 2 | a0001c0001t0001g0143a0013c0030t0024g0149 | 2 | HG02055.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.134-5559A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356078 | ||||||
| chr17:2356078
|
A | G | 180 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(177): Show | 186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.134-5559A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356078 | ||||||
| chr17:2356078
|
A | T | 53 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(50): Show | 55 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.134-5559A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356078 | ||||||
| chr17:2356081
|
TG | T | 163 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0055others(160): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.134-5551delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356081 | |||||
| chr17:2356081
|
TGGGGGAA others(44): Show |
T | 42 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(39): Show | 43 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.134-5551_134-5501d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356081 | |||||
| chr17:2356082
|
G | GGGGAAGG others(41): Show |
1 | a0017c0035t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.134-5552_134-5551i others(50): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356082 | |||||
| chr17:2356082
|
G | GGGGGAAG others(42): Show |
1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-5550_134-5502d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356082 | |||||
| chr17:2356087
|
A | C | 3 | a0001c0001t0001g0021a0002c0002t0001g0376a0002c0002t0001g0397 | 4 | HG01167.hp1 HG02257.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-5550A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356087 | ||||||
| chr17:2356092
|
A | G | 4 | a0001c0001t0001g0021a0001c0025t0001g0101a0002c0002t0001g0376others(1): Show | 5 | HG01109.hp2 HG01167.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-5545A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356092 | ||||||
| chr17:2356112
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-5525G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356112 | ||||||
| chr17:2356128
|
G | A | 3 | a0001c0001t0001g0348a0002c0002t0001g0376a0002c0002t0001g0397 | 3 | HG01167.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.134-5509G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356128 | ||||||
| chr17:2356128
|
G | C | 3 | a0001c0001t0001g0143a0001c0001t0003g0324a0013c0030t0024g0149 | 3 | HG02055.hp1 HG02486.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.134-5509G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356128 | ||||||
| chr17:2356131
|
TG | T | 195 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(192): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.134-5501delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356131 | |||||
| chr17:2356132
|
G | GGGGAAGG others(41): Show |
1 | a0001c0001t0001g0123 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.134-5502_134-5501i others(50): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356132 | |||||
| chr17:2356137
|
A | C | 1 | a0002c0043t0001g0364 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134-5500A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356137 | ||||||
| chr17:2356142
|
A | G | 2 | a0001c0001t0001g0021a0002c0043t0001g0364 | 3 | HG02257.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.134-5495A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356142 | ||||||
| chr17:2356143
|
C | A | 1 | a0001c0001t0001g0321 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.134-5494C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356143 | ||||||
| chr17:2356178
|
G | A | 2 | a0001c0001t0001g0021a0002c0043t0001g0364 | 3 | HG02257.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.134-5459G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356178 | ||||||
| chr17:2356178
|
G | C | 44 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(41): Show | 46 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.134-5459G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356178 | ||||||
| chr17:2356178
|
G | T | 1 | a0001c0003t0001g0354 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134-5459G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356178 | ||||||
| chr17:2356181
|
T | TG | 59 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(56): Show | 62 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.134-5452dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356181 | |||||
| chr17:2356227
|
A | C | 84 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(81): Show | 87 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.134-5410A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356227 | ||||||
| chr17:2356227
|
A | G | 164 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(161): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.134-5410A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356227 | ||||||
| chr17:2356230
|
TG | T | 187 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(184): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.134-5402delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356230 | |||||
| chr17:2356230
|
TGGGGGAA others(93): Show |
T | 6 | a0001c0001t0001g0156a0001c0001t0001g0172a0001c0001t0001g0189others(3): Show | 6 | HG00280.hp1 HG01106.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-5402_134-5303d others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356230 | |||||
| chr17:2356231
|
G | GGGGGAAG others(42): Show |
22 | a0001c0001t0001g0122a0001c0001t0001g0351a0001c0003t0001g0054others(19): Show | 22 | HG00558.hp1 HG02895.hp1 HG02897.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-5401_134-5353d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356231 | |||||
| chr17:2356236
|
A | C | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-5401A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356236 | ||||||
| chr17:2356241
|
A | G | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-5396A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356241 | ||||||
| chr17:2356261
|
G | A | 2 | a0002c0002t0001g0376a0002c0002t0001g0397 | 2 | HG01167.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.134-5376G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356261 | ||||||
| chr17:2356267
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134-5370G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356267 | ||||||
| chr17:2356269
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.134-5368G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356269 | ||||||
| chr17:2356269
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134-5368G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356269 | ||||||
| chr17:2356272
|
G | A | 1 | a0002c0002t0001g0042 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.134-5365G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356272 | ||||||
| chr17:2356277
|
G | A | 3 | a0001c0001t0001g0021a0002c0002t0001g0376a0002c0002t0001g0397 | 4 | HG01167.hp1 HG02257.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-5360G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356277 | ||||||
| chr17:2356277
|
G | C | 42 | a0001c0001t0001g0075a0001c0001t0001g0115a0001c0001t0001g0154others(39): Show | 42 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.134-5360G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356277 | ||||||
| chr17:2356278
|
GTTGGGGC others(589): Show |
G | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.134-5352_134-4757d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356278 | |||||
| chr17:2356280
|
T | TG | 7 | a0001c0001t0001g0021a0001c0001t0001g0123a0001c0001t0001g0348others(4): Show | 8 | HG01167.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-5353dupG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356280 | |||||
| chr17:2356285
|
C | A | 242 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(239): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.134-5352C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356285 | ||||||
| chr17:2356290
|
G | A | 242 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(239): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.134-5347G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356290 | ||||||
| chr17:2356310
|
G | A | 1 | a0002c0043t0001g0364 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134-5327G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356310 | ||||||
| chr17:2356317
|
G | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.134-5320G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356317 | ||||||
| chr17:2356326
|
A | C | 74 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0025others(71): Show | 75 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.134-5311A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356326 | ||||||
| chr17:2356326
|
A | G | 168 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(165): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.134-5311A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356326 | ||||||
| chr17:2356329
|
TG | T | 215 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(212): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.134-5303delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356329 | |||||
| chr17:2356330
|
G | GGGGGAAG others(42): Show |
1 | a0002c0043t0001g0364 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134-5302_134-5254d others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356330 | |||||
| chr17:2356353
|
GAATGGTG others(93): Show |
G | 1 | a0001c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.134-5234_134-5135d others(102): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356353 | |||||
| chr17:2356360
|
G | A | 25 | a0001c0001t0001g0122a0001c0001t0001g0349a0001c0001t0001g0351others(22): Show | 25 | HG00558.hp1 HG02132.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-5277G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356360 | ||||||
| chr17:2356366
|
G | A | 57 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 60 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.134-5271G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356366 | ||||||
| chr17:2356366
|
GGGGTGTA others(92): Show |
G | 1 | a0001c0037t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.134-5267_134-5169d others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356366 | |||||
| chr17:2356368
|
G | T | 57 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 60 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.134-5269G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356368 | ||||||
| chr17:2356376
|
G | A | 1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-5261G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356376 | ||||||
| chr17:2356376
|
G | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(69): Show | 75 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.134-5261G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356376 | ||||||
| chr17:2356379
|
TG | T | 145 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(142): Show | 149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.134-5253delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356379 | |||||
| chr17:2356379
|
TGGGGGAA others(94): Show |
T | 41 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0075others(38): Show | 42 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.134-5253_134-5153d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356379 | |||||
| chr17:2356392
|
C | A | 1 | a0002c0002t0001g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.134-5245C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356392 | ||||||
| chr17:2356410
|
G | A | 30 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(27): Show | 33 | HG00099.hp1 HG01099.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.134-5227G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356410 | ||||||
| chr17:2356416
|
G | A | 3 | a0001c0001t0001g0115a0001c0001t0001g0357a0001c0001t0002g0227 | 3 | NA18612.hp1 NA18947.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.134-5221G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356416 | ||||||
| chr17:2356418
|
G | T | 3 | a0001c0001t0001g0115a0001c0001t0001g0357a0001c0001t0002g0227 | 3 | NA18612.hp1 NA18947.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.134-5219G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356418 | ||||||
| chr17:2356426
|
G | A | 1 | a0001c0001t0001g0021 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.134-5211G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356426 | ||||||
| chr17:2356426
|
G | C | 2 | a0001c0001t0001g0138a0001c0001t0003g0254 | 2 | HG02015.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.134-5211G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356426 | ||||||
| chr17:2356426
|
G | GGTTGGGG others(141): Show |
1 | a0001c0003t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.134-5203_134-5202i others(150): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356426 | |||||
| chr17:2356427
|
GTTGGGGG others(292): Show |
G | 43 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(40): Show | 44 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.134-5203_134-4905d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356427 | |||||
| chr17:2356427
|
GTTGGGGG others(391): Show |
G | 2 | a0001c0001t0001g0115a0001c0001t0002g0227 | 2 | NA18947.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.134-5203_134-4806d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356427 | |||||
| chr17:2356427
|
GTTGGGGG others(440): Show |
G | 59 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0056others(56): Show | 62 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.134-5203_134-4757d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356427 | |||||
| chr17:2356429
|
TG | T | 150 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0098others(147): Show | 162 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.134-5203delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356429 | |||||
| chr17:2356429
|
TGGGGGCA others(44): Show |
T | 31 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0138others(28): Show | 31 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.134-5203_134-5153d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356429 | |||||
| chr17:2356429
|
TGGGGGCA others(342): Show |
T | 2 | a0001c0001t0001g0357a0001c0001t0002g0022 | 2 | HG02622.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.134-5203_134-4855d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356429 | |||||
| chr17:2356430
|
G | GGGGGAAG others(91): Show |
1 | a0002c0012t0001g0129 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.134-5203_134-5202i others(100): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356430 | |||||
| chr17:2356430
|
GGGGGCAG others(539): Show |
G | 1 | a0001c0001t0001g0143 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.134-5203_134-4658d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356430 | |||||
| chr17:2356435
|
C | A | 63 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(60): Show | 66 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.134-5202C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356435 | ||||||
| chr17:2356440
|
G | A | 64 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(61): Show | 67 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.134-5197G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356440 | ||||||
| chr17:2356453
|
A | G | 182 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0061others(179): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.134-5184A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356453 | ||||||
| chr17:2356460
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.134-5177G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356460 | ||||||
| chr17:2356466
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0370a0001c0020t0001g0286 | 3 | HG00280.hp1 HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.134-5171G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356466 | ||||||
| chr17:2356468
|
G | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0370a0001c0020t0001g0286 | 3 | HG00280.hp1 HG01106.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.134-5169G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356468 | ||||||
| chr17:2356476
|
G | A | 3 | a0001c0001t0001g0348a0001c0003t0001g0354a0002c0012t0001g0129 | 3 | HG02559.hp2 HG02602.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.134-5161G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356476 | ||||||
| chr17:2356476
|
G | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0172a0001c0003t0001g0108 | 3 | HG00621.hp1 NA18951.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.134-5161G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356476 | ||||||
| chr17:2356476
|
G | GGTTGGGG others(91): Show |
23 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0332others(20): Show | 25 | HG00099.hp1 HG01099.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-5154_134-5153i others(100): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356476 | |||||
| chr17:2356477
|
GTTGGGGG others(143): Show |
G | 1 | a0001c0001t0001g0189 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.134-5153_134-5004d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356477 | |||||
| chr17:2356477
|
GTTGGGGG others(242): Show |
G | 1 | a0001c0003t0002g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.134-5153_134-4905d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356477 | |||||
| chr17:2356477
|
GTTGGGGG others(341): Show |
G | 2 | a0001c0001t0001g0370a0001c0020t0001g0286 | 2 | HG00280.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.134-5153_134-4806d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356477 | |||||
| chr17:2356479
|
TG | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0156others(3): Show | 7 | HG00621.hp1 HG02257.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-5153delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356479 | |||||
| chr17:2356480
|
G | GGGGAAGG others(41): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0005t0002g0084others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-5154_134-5153i others(50): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356480 | |||||
| chr17:2356503
|
A | G | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(248): Show | 268 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.134-5134A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356503 | ||||||
| chr17:2356516
|
G | A | 39 | a0001c0001t0001g0075a0001c0001t0001g0154a0001c0001t0001g0161others(36): Show | 39 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.134-5121G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356516 | ||||||
| chr17:2356518
|
G | T | 39 | a0001c0001t0001g0075a0001c0001t0001g0154a0001c0001t0001g0161others(36): Show | 39 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.134-5119G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356518 | ||||||
| chr17:2356526
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0070others(2): Show | 6 | HG02257.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-5111G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356526 | ||||||
| chr17:2356526
|
G | C | 27 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(24): Show | 28 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.134-5111G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356526 | ||||||
| chr17:2356527
|
GTTGGGGG others(291): Show |
G | 24 | a0001c0001t0001g0075a0001c0001t0001g0161a0001c0001t0001g0163others(21): Show | 24 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.134-5103_134-4806d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356527 | |||||
| chr17:2356529
|
TG | T | 191 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0061others(188): Show | 205 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.134-5103delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356529 | |||||
| chr17:2356529
|
TGGGGGAA others(44): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.134-5103_134-5053d others(53): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356529 | |||||
| chr17:2356529
|
TGGGGGAA others(143): Show |
T | 1 | a0001c0003t0002g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.134-5103_134-4954d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356529 | |||||
| chr17:2356529
|
TGGGGGAA others(242): Show |
T | 2 | a0001c0001t0001g0304a0023c0018t0001g0114 | 2 | HG02698.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.134-5103_134-4855d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356529 | |||||
| chr17:2356530
|
G | GGGGAAGG others(190): Show |
1 | a0001c0001t0001g0123 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.134-5104_134-5103i others(199): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356530 | |||||
| chr17:2356540
|
A | ACCCCATA others(42): Show |
1 | a0001c0001t0001g0348 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.134-5085_134-5084i others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356540 | |||||
| chr17:2356553
|
A | G | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(220): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.134-5084A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356553 | ||||||
| chr17:2356566
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0176others(3): Show | 6 | HG00733.hp1 HG01106.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-5071G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356566 | ||||||
| chr17:2356568
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0171a0001c0001t0001g0176others(3): Show | 6 | HG00733.hp1 HG01106.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-5069G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356568 | ||||||
| chr17:2356576
|
G | A | 28 | a0001c0001t0001g0061a0001c0001t0001g0122a0001c0001t0001g0123others(25): Show | 28 | HG00558.hp1 HG02132.hp1 HG02602.hp2 others(25): Show |
intron_variant | MODIFIER | c.134-5061G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356576 | ||||||
| chr17:2356576
|
G | C | 1 | a0001c0037t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.134-5061G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356576 | ||||||
| chr17:2356576
|
G | GGTTGGGG others(42): Show |
25 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0332others(22): Show | 27 | HG00099.hp1 HG01099.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.134-5054_134-5053i others(51): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356576 | |||||
| chr17:2356576
|
G | GGTTGGGG others(92): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0005t0002g0084others(1): Show | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-5035_134-5034i others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356576 | |||||
| chr17:2356579
|
TG | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(44): Show | 49 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.134-5053delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356579 | |||||
| chr17:2356603
|
A | G | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(221): Show | 241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.134-5034A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356603 | ||||||
| chr17:2356616
|
G | A | 1 | a0001c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.134-5021G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356616 | ||||||
| chr17:2356618
|
G | T | 1 | a0001c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.134-5019G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356618 | ||||||
| chr17:2356627
|
A | G | 49 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(46): Show | 51 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.134-5010A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356627 | ||||||
| chr17:2356652
|
A | G | 225 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(222): Show | 242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.134-4985A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356652 | ||||||
| chr17:2356665
|
G | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(21): Show | 25 | HG00280.hp2 HG00597.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-4972G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356665 | ||||||
| chr17:2356667
|
G | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(21): Show | 25 | HG00280.hp2 HG00597.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-4970G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356667 | ||||||
| chr17:2356676
|
GTTGGGGG others(142): Show |
G | 3 | a0001c0001t0001g0156a0001c0001t0001g0172a0001c0001t0008g0210 | 3 | NA18951.hp1 NA18970.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.134-4954_134-4806d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356676 | |||||
| chr17:2356676
|
GTTGGGGG others(191): Show |
G | 1 | a0001c0003t0001g0108 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.134-4954_134-4757d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356676 | |||||
| chr17:2356678
|
TG | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(22): Show | 26 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.134-4954delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356678 | |||||
| chr17:2356678
|
TGGGGGAA others(241): Show |
T | 7 | a0001c0001t0001g0010a0001c0001t0001g0120a0001c0001t0001g0171others(4): Show | 7 | HG00733.hp1 HG01106.hp2 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-4954_134-4707d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356678 | |||||
| chr17:2356679
|
GGGGGAAG others(290): Show |
G | 14 | a0001c0001t0001g0154a0001c0001t0001g0162a0001c0001t0001g0183others(11): Show | 14 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-4954_134-4658d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356679 | |||||
| chr17:2356702
|
A | G | 202 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0021others(199): Show | 218 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.134-4935A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356702 | ||||||
| chr17:2356715
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.134-4922G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356715 | ||||||
| chr17:2356717
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.134-4920G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356717 | ||||||
| chr17:2356726
|
A | G | 26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(23): Show | 27 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.134-4911A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356726 | ||||||
| chr17:2356751
|
A | G | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(243): Show | 263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.134-4886A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356751 | ||||||
| chr17:2356775
|
GTTGGGGG others(92): Show |
G | 2 | a0001c0001t0001g0198a0001c0037t0001g0217 | 2 | HG00408.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.134-4855_134-4757d others(101): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356775 | |||||
| chr17:2356777
|
TG | T | 46 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(43): Show | 47 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.134-4855delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356777 | |||||
| chr17:2356777
|
TGGGGGAA others(142): Show |
T | 22 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(19): Show | 23 | HG00280.hp2 HG00597.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.134-4855_134-4707d others(2): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356777 | |||||
| chr17:2356782
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.134-4855G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356782 | ||||||
| chr17:2356801
|
A | G | 226 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(223): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.134-4836A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356801 | ||||||
| chr17:2356813
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.134-4824C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356813 | ||||||
| chr17:2356814
|
G | A | 47 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(44): Show | 48 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.134-4823G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356814 | ||||||
| chr17:2356816
|
G | T | 47 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(44): Show | 48 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.134-4821G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356816 | ||||||
| chr17:2356825
|
A | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(47): Show | 51 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.134-4812A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356825 | ||||||
| chr17:2356831
|
G | A | 1 | a0001c0001t0008g0210 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.134-4806G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356831 | ||||||
| chr17:2356850
|
A | G | 257 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0023others(254): Show | 273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.134-4787A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356850 | ||||||
| chr17:2356863
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0304 | 2 | HG03688.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.134-4774G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356863 | ||||||
| chr17:2356868
|
G | A | 1 | a0017c0035t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.134-4769G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356868 | ||||||
| chr17:2356874
|
A | G | 81 | a0001c0001t0001g0015a0001c0001t0001g0025a0001c0001t0001g0029others(78): Show | 82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.134-4763A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356874 | ||||||
| chr17:2356887
|
T | C | 144 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0025others(141): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.134-4750T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356887 | ||||||
| chr17:2356906
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.134-4731G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356906 | ||||||
| chr17:2356925
|
TG | T | 144 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0025others(141): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.134-4707delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2356925 | |||||
| chr17:2356961
|
T | C | 203 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(200): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.134-4676T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356961 | ||||||
| chr17:2356962
|
G | C | 1 | a0001c0001t0001g0231 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.134-4675G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356962 | ||||||
| chr17:2356963
|
G | T | 1 | a0001c0001t0002g0157 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.134-4674G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356963 | ||||||
| chr17:2356967
|
G | A | 1 | a0001c0003t0002g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.134-4670G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356967 | ||||||
| chr17:2356976
|
A | G | 171 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(168): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.134-4661A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356976 | ||||||
| chr17:2356979
|
G | A | 164 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0019others(161): Show | 169 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.134-4658G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356979 | ||||||
| chr17:2356984
|
G | C | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-4653G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2356984 | ||||||
| chr17:2357068
|
T | C | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(217): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.134-4569T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357068 | ||||||
| chr17:2357080
|
G | A | 1 | a0025c0047t0001g0282 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-4557G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357080 | ||||||
| chr17:2357452
|
C | G | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-4185C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357452 | ||||||
| chr17:2357457
|
C | T | 33 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0131others(30): Show | 36 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.134-4180C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357457 | ||||||
| chr17:2357554
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0001g0182a0001c0001t0001g0394 | 3 | HG00597.hp2 NA18984.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.134-4083A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357554 | ||||||
| chr17:2357616
|
A | G | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-4021A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357616 | ||||||
| chr17:2357669
|
T | C | 1 | a0004c0010t0001g0350 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.134-3968T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357669 | ||||||
| chr17:2357863
|
G | T | 1 | a0001c0001t0001g0153 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.134-3774G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2357863 | ||||||
| chr17:2358060
|
C | T | 1 | a0002c0002t0001g0397 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.134-3577C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358060 | ||||||
| chr17:2358257
|
G | A | 33 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0002t0001g0131others(30): Show | 36 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.134-3380G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358257 | ||||||
| chr17:2358277
|
G | A | 2 | a0002c0002t0001g0376a0002c0043t0001g0364 | 2 | HG01167.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.134-3360G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358277 | ||||||
| chr17:2358348
|
G | A | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.134-3289G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358348 | ||||||
| chr17:2358364
|
A | C | 1 | a0002c0002t0003g0291 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.134-3273A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358364 | ||||||
| chr17:2358383
|
A | G | 284 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(281): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.134-3254A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358383 | ||||||
| chr17:2358459
|
C | T | 13 | a0001c0001t0001g0009a0001c0001t0001g0082a0001c0001t0001g0152others(10): Show | 14 | HG00408.hp1 HG02074.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-3178C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358459 | ||||||
| chr17:2358526
|
T | A | 1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-3111T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358526 | ||||||
| chr17:2358546
|
C | A | 1 | a0002c0002t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.134-3091C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358546 | ||||||
| chr17:2358551
|
A | C | 1 | a0002c0002t0003g0291 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.134-3086A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358551 | ||||||
| chr17:2358711
|
C | CA | 181 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(178): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.134-2918dupA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358711 | |||||
| chr17:2358711
|
C | CAA | 11 | a0001c0001t0001g0169a0001c0001t0001g0176a0001c0001t0001g0196others(8): Show | 11 | HG00438.hp2 HG01515.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-2919_134-2918d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358711 | |||||
| chr17:2358801
|
T | C | 3 | a0007c0007t0001g0135a0007c0007t0001g0140a0027c0015t0005g0079 | 3 | HG02615.hp2 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.134-2836T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358801 | ||||||
| chr17:2358872
|
TG | T | 2 | a0002c0004t0006g0011a0002c0004t0006g0083 | 3 | HG02280.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.134-2764delG | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358872 | ||||||
| chr17:2358873
|
G | GT | 17 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0085others(14): Show | 17 | HG00438.hp1 HG01243.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.134-2743dupT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358873 | |||||
| chr17:2358873
|
G | GTT | 40 | a0001c0001t0001g0070a0001c0001t0001g0081a0001c0001t0001g0123others(37): Show | 42 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.134-2744_134-2743d others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358873 | |||||
| chr17:2358873
|
G | GTTT | 14 | a0001c0001t0001g0122a0001c0001t0001g0332a0001c0001t0002g0382others(11): Show | 15 | HG00558.hp1 HG01361.hp1 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.134-2745_134-2743d others(5): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358873 | |||||
| chr17:2358873
|
GT | G | 13 | a0001c0001t0001g0110a0002c0002t0001g0043a0002c0002t0001g0376others(10): Show | 13 | HG01167.hp1 HG01515.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.134-2743delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358873 | |||||
| chr17:2358875
|
T | TTTTG | 26 | a0002c0002t0001g0133a0002c0002t0023g0139a0002c0004t0001g0006others(23): Show | 28 | HG01243.hp2 HG01433.hp2 HG01516.hp2 others(25): Show |
intron_variant | MODIFIER | c.134-2759_134-2758i others(6): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358875 | |||||
| chr17:2358876
|
T | G | 1 | a0001c0024t0005g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.134-2761T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358876 | ||||||
| chr17:2358876
|
T | TTTG | 5 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0046t0020g0159others(2): Show | 6 | HG02451.hp2 HG02622.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-2759_134-2758i others(5): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2358876 | |||||
| chr17:2358878
|
T | TG | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(183): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.134-2759_134-2758i others(3): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358878 | ||||||
| chr17:2358883
|
T | G | 1 | a0001c0037t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.134-2754T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358883 | ||||||
| chr17:2358884
|
T | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(183): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.134-2753T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2358884 | ||||||
| chr17:2359078
|
C | T | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-2559C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359078 | ||||||
| chr17:2359156
|
C | T | 1 | a0002c0046t0020g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.134-2481C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359156 | ||||||
| chr17:2359168
|
C | T | 27 | a0002c0002t0001g0131a0002c0002t0001g0133a0002c0002t0023g0139others(24): Show | 29 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-2469C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359168 | ||||||
| chr17:2359283
|
C | T | 1 | a0001c0003t0001g0258 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.134-2354C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359283 | ||||||
| chr17:2359317
|
G | A | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(248): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.134-2320G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359317 | ||||||
| chr17:2359409
|
C | T | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(247): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.134-2228C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359409 | ||||||
| chr17:2359521
|
G | A | 1 | a0001c0003t0002g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.134-2116G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359521 | ||||||
| chr17:2359666
|
C | T | 16 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0071others(13): Show | 17 | HG00642.hp1 HG01070.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.134-1971C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359666 | ||||||
| chr17:2359682
|
G | GCCGGCCA others(12): Show |
1 | a0001c0001t0001g0329 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.134-1953_134-1935d others(21): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr17 | 2359682 | |||||
| chr17:2359703
|
A | C | 285 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(282): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.134-1934A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359703 | ||||||
| chr17:2359704
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.134-1933C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359704 | ||||||
| chr17:2359730
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.134-1907A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359730 | ||||||
| chr17:2359747
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.134-1890G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2359747 | ||||||
| chr17:2360069
|
G | A | 1 | a0001c0001t0001g0394 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.134-1568G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360069 | ||||||
| chr17:2360122
|
C | A | 94 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(91): Show | 97 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.134-1515C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360122 | ||||||
| chr17:2360154
|
C | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0358a0001c0001t0013g0318others(1): Show | 4 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1483C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360154 | ||||||
| chr17:2360171
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0197a0001c0001t0001g0231others(2): Show | 6 | HG00408.hp2 NA18953.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.134-1466C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360171 | ||||||
| chr17:2360250
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.134-1387G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360250 | ||||||
| chr17:2360360
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.134-1277A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360360 | ||||||
| chr17:2360453
|
C | T | 4 | a0001c0003t0001g0390a0001c0003t0002g0020a0002c0046t0020g0159others(1): Show | 5 | HG02451.hp2 HG02622.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-1184C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360453 | ||||||
| chr17:2360572
|
G | A | 96 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(93): Show | 99 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.134-1065G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360572 | ||||||
| chr17:2360729
|
C | T | 27 | a0002c0002t0001g0131a0002c0002t0001g0133a0002c0002t0023g0139others(24): Show | 29 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-908C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360729 | ||||||
| chr17:2360869
|
C | T | 5 | a0002c0002t0001g0057a0002c0002t0001g0063a0002c0002t0001g0072others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-768C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360869 | ||||||
| chr17:2360921
|
T | C | 95 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(92): Show | 98 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.134-716T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360921 | ||||||
| chr17:2360955
|
C | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0028c0014t0001g0145 | 3 | HG00140.hp1 HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.134-682C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360955 | ||||||
| chr17:2360957
|
C | A | 86 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(83): Show | 89 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.134-680C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2360957 | ||||||
| chr17:2361155
|
C | G | 1 | a0002c0002t0001g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.134-482C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361155 | ||||||
| chr17:2361185
|
A | G | 95 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(92): Show | 98 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.134-452A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361185 | ||||||
| chr17:2361254
|
G | A | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134-383G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361254 | ||||||
| chr17:2361275
|
G | A | 53 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(50): Show | 55 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.134-362G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361275 | ||||||
| chr17:2361282
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-355G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361282 | ||||||
| chr17:2361413
|
G | A | 1 | a0001c0003t0001g0374 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.134-224G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361413 | ||||||
| chr17:2361474
|
G | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.134-163G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361474 | ||||||
| chr17:2361480
|
C | T | 286 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(283): Show | 305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.134-157C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361480 | ||||||
| chr17:2361500
|
G | A | 285 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(282): Show | 304 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.134-137G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361500 | ||||||
| chr17:2361526
|
C | A | 1 | a0002c0046t0020g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.134-111C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361526 | ||||||
| chr17:2361563
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0085a0025c0047t0001g0282 | 3 | HG01891.hp2 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.134-74A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 2/23 | chr17 | 2361563 | ||||||
| chr17:2361819
|
C | A | 168 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(165): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.296+20C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 3/23 | chr17 | 2361819 | ||||||
| chr17:2361907
|
G | A | 1 | a0002c0002t0003g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.296+108G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 3/23 | chr17 | 2361907 | ||||||
| chr17:2361961
|
C | T | 1 | a0001c0003t0016g0266 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.297-148C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 3/23 | chr17 | 2361961 | ||||||
| chr17:2361982
|
T | C | 47 | a0001c0001t0001g0081a0001c0001t0001g0122a0001c0001t0001g0123others(44): Show | 49 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.297-127T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 3/23 | chr17 | 2361982 | ||||||
| chr17:2362298
|
A | G | 94 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(91): Show | 98 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.458+28A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362298 | ||||||
| chr17:2362319
|
C | A | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.458+49C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362319 | ||||||
| chr17:2362365
|
G | A | 5 | a0002c0002t0004g0050a0002c0002t0004g0166a0002c0002t0004g0342others(2): Show | 5 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.458+95G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362365 | ||||||
| chr17:2362426
|
C | CCCCGTTC others(22): Show |
1 | a0001c0001t0001g0179 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.458+158_458+159ins others(29): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr17 | 2362426 | |||||
| chr17:2362428
|
C | T | 1 | a0002c0002t0003g0298 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.458+158C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362428 | ||||||
| chr17:2362431
|
T | TCCCAAAA others(22): Show |
29 | a0002c0002t0001g0131a0002c0002t0001g0133a0002c0002t0002g0103others(26): Show | 31 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.458+243_458+271dup others(29): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr17 | 2362431 | |||||
| chr17:2362431
|
T | TCCCAAAA others(22): Show |
42 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0025others(39): Show | 42 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.458+183_458+184ins others(29): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr17 | 2362431 | |||||
| chr17:2362431
|
T | TCCCAAAA others(171): Show |
1 | a0017c0035t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.458+173_458+174ins others(178): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr17 | 2362431 | |||||
| chr17:2362454
|
C | T | 123 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(120): Show | 126 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.458+184C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362454 | ||||||
| chr17:2362457
|
G | A | 1 | a0001c0001t0011g0116 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.458+187G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362457 | ||||||
| chr17:2362457
|
G | GTTCCCCA others(22): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0236 | 2 | HG01516.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.458+215_458+216ins others(29): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr17 | 2362457 | |||||
| chr17:2362507
|
A | ACCGCCCC others(22): Show |
125 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(122): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.458+265_458+266ins others(29): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr17 | 2362507 | |||||
| chr17:2362507
|
A | G | 45 | a0001c0001t0001g0010a0001c0001t0001g0021a0001c0001t0001g0025others(42): Show | 45 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.458+237A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362507 | ||||||
| chr17:2362619
|
G | A | 95 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(92): Show | 99 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.459-219G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362619 | ||||||
| chr17:2362629
|
G | A | 1 | a0002c0044t0003g0243 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.459-209G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362629 | ||||||
| chr17:2362650
|
C | T | 95 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(92): Show | 99 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.459-188C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362650 | ||||||
| chr17:2362761
|
T | C | 95 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(92): Show | 99 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.459-77T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 4/23 | chr17 | 2362761 | ||||||
| chr17:2363154
|
C | G | 1 | a0001c0001t0001g0335 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.672+20C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363154 | ||||||
| chr17:2363196
|
G | A | 2 | a0001c0003t0001g0379a0001c0003t0001g0381 | 2 | NA18990.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.672+62G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363196 | ||||||
| chr17:2363269
|
C | T | 2 | a0002c0002t0002g0103a0002c0046t0020g0159 | 2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.672+135C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363269 | ||||||
| chr17:2363282
|
T | C | 4 | a0007c0007t0001g0135a0007c0007t0001g0140a0007c0007t0001g0295others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+148T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363282 | ||||||
| chr17:2363331
|
G | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.673-134G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363331 | ||||||
| chr17:2363398
|
G | A | 1 | a0002c0046t0020g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673-67G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363398 | ||||||
| chr17:2363415
|
T | C | 295 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(292): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.673-50T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | chr17 | 2363415 | ||||||
| chr17:2363446
|
G | GC | 20 | a0002c0002t0001g0151a0002c0002t0002g0026a0002c0002t0002g0124others(17): Show | 20 | HG00323.hp2 HG00438.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.673-15dupC | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr17 | 2363446 | |||||
| chr17:2363753
|
C | T | 1 | a0002c0002t0003g0298 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.807+154C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/23 | chr17 | 2363753 | ||||||
| chr17:2363754
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.807+155G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/23 | chr17 | 2363754 | ||||||
| chr17:2363755
|
C | A | 2 | a0002c0002t0001g0036a0002c0002t0001g0037 | 2 | HG02135.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.807+156C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/23 | chr17 | 2363755 | ||||||
| chr17:2363970
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.808-89C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/23 | chr17 | 2363970 | ||||||
| chr17:2363981
|
G | A | 1 | a0001c0001t0009g0355 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.808-78G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 7/23 | chr17 | 2363981 | ||||||
| chr17:2364352
|
C | T | 2 | a0001c0003t0001g0361a0001c0003t0001g0362 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.932+169C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 8/23 | chr17 | 2364352 | ||||||
| chr17:2364400
|
C | T | 207 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(204): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.933-196C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 8/23 | chr17 | 2364400 | ||||||
| chr17:2364429
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.933-167G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 8/23 | chr17 | 2364429 | ||||||
| chr17:2364579
|
G | A | 2 | a0001c0001t0001g0147a0028c0014t0001g0145 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.933-17G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 8/23 | chr17 | 2364579 | ||||||
| chr17:2364682
|
C | T | 4 | a0007c0007t0001g0135a0007c0007t0001g0140a0007c0007t0001g0295others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000+19C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 9/23 | chr17 | 2364682 | ||||||
| chr17:2364774
|
A | G | 1 | a0002c0002t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1000+111A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 9/23 | chr17 | 2364774 | ||||||
| chr17:2364845
|
G | C | 293 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(290): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1001-52G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 9/23 | chr17 | 2364845 | ||||||
| chr17:2364846
|
T | C | 1 | a0001c0001t0001g0349 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1001-51T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 9/23 | chr17 | 2364846 | ||||||
| chr17:2365098
|
G | T | 28 | a0002c0002t0001g0131a0002c0002t0001g0133a0002c0002t0023g0139others(25): Show | 30 | HG01175.hp2 HG01243.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.1161+41G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 10/23 | chr17 | 2365098 | ||||||
| chr17:2365365
|
G | C | 3 | a0005c0009t0002g0378a0005c0009t0002g0383a0005c0009t0002g0384 | 3 | NA18946.hp2 NA18981.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1288+24G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365365 | ||||||
| chr17:2365387
|
T | C | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(260): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1288+46T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365387 | ||||||
| chr17:2365394
|
C | T | 1 | a0002c0004t0001g0137 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1288+53C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365394 | ||||||
| chr17:2365402
|
G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288+61G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365402 | ||||||
| chr17:2365433
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1288+92C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365433 | ||||||
| chr17:2365590
|
G | A | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1288+249G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365590 | ||||||
| chr17:2365743
|
C | CT | 35 | a0001c0001t0001g0055a0001c0001t0001g0098a0001c0001t0001g0110others(32): Show | 37 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1288+423dupT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 2365743 | |||||
| chr17:2365743
|
CT | C | 20 | a0001c0001t0001g0019a0001c0001t0001g0082a0001c0001t0001g0100others(17): Show | 21 | HG01109.hp2 HG01167.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1288+423delT | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | 2365743 | |||||
| chr17:2365778
|
G | A | 21 | a0001c0001t0001g0115a0001c0001t0002g0157a0001c0001t0002g0158others(18): Show | 21 | HG02015.hp1 HG02040.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1288+437G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365778 | ||||||
| chr17:2365785
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1288+444T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365785 | ||||||
| chr17:2365795
|
G | A | 15 | a0002c0002t0001g0063a0002c0002t0001g0072a0002c0002t0001g0073others(12): Show | 16 | HG01074.hp1 HG01123.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1288+454G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365795 | ||||||
| chr17:2365807
|
C | T | 3 | a0001c0003t0001g0390a0001c0003t0002g0020a0014c0031t0001g0392 | 4 | HG02451.hp2 HG02622.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+466C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365807 | ||||||
| chr17:2365894
|
C | A | 3 | a0001c0003t0001g0339a0001c0003t0001g0340a0001c0003t0001g0360 | 3 | HG02895.hp1 HG02897.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1288+553C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2365894 | ||||||
| chr17:2366391
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1289-880G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366391 | ||||||
| chr17:2366413
|
C | T | 21 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0082others(18): Show | 23 | HG00280.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1289-858C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366413 | ||||||
| chr17:2366456
|
T | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1289-815T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366456 | ||||||
| chr17:2366475
|
C | T | 232 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(229): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1289-796C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366475 | ||||||
| chr17:2366593
|
G | A | 1 | a0001c0003t0002g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1289-678G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366593 | ||||||
| chr17:2366843
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1289-428C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366843 | ||||||
| chr17:2366951
|
G | A | 2 | a0002c0002t0001g0041a0005c0009t0002g0378 | 2 | HG03704.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1289-320G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366951 | ||||||
| chr17:2366990
|
G | A | 175 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(172): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1289-281G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2366990 | ||||||
| chr17:2367063
|
T | G | 1 | a0001c0025t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1289-208T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2367063 | ||||||
| chr17:2367221
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1289-50C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 11/23 | chr17 | 2367221 | ||||||
| chr17:2367483
|
T | C | 265 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(262): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1423+78T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2367483 | ||||||
| chr17:2367591
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1423+186G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2367591 | ||||||
| chr17:2367663
|
C | T | 5 | a0001c0003t0001g0390a0002c0002t0002g0103a0002c0041t0001g0312others(2): Show | 5 | HG02486.hp1 HG03130.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423+258C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2367663 | ||||||
| chr17:2367734
|
C | CCAGACAG others(32): Show |
1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1423+330_1423+368d others(41): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 2367734 | |||||
| chr17:2367825
|
T | C | 3 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159 | 3 | HG02486.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1423+420T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2367825 | ||||||
| chr17:2367944
|
C | T | 3 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159 | 3 | HG02486.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1423+539C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2367944 | ||||||
| chr17:2368022
|
T | C | 3 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159 | 3 | HG02486.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1423+617T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368022 | ||||||
| chr17:2368038
|
C | T | 3 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159 | 3 | HG02486.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1423+633C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368038 | ||||||
| chr17:2368217
|
C | T | 3 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159 | 3 | HG02486.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1423+812C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368217 | ||||||
| chr17:2368313
|
C | T | 1 | a0003c0006t0001g0095 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1423+908C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368313 | ||||||
| chr17:2368344
|
A | G | 3 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159 | 3 | HG02486.hp1 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1423+939A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368344 | ||||||
| chr17:2368489
|
C | G | 1 | a0002c0002t0003g0265 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1423+1084C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368489 | ||||||
| chr17:2368513
|
G | A | 1 | a0002c0002t0003g0326 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1423+1108G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368513 | ||||||
| chr17:2368552
|
T | A | 4 | a0002c0002t0002g0103a0002c0041t0001g0312a0002c0046t0020g0159others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1423+1147T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368552 | ||||||
| chr17:2368666
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1423+1261C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368666 | ||||||
| chr17:2368730
|
T | C | 137 | a0001c0001t0001g0064a0001c0001t0001g0267a0001c0001t0022g0130others(134): Show | 151 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1423+1325T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368730 | ||||||
| chr17:2368736
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1423+1331G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368736 | ||||||
| chr17:2368763
|
T | C | 396 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(393): Show | 420 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(417): Show |
intron_variant | MODIFIER | c.1423+1358T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368763 | ||||||
| chr17:2368983
|
C | G | 90 | a0001c0001t0001g0081a0001c0001t0001g0115a0001c0001t0001g0121others(87): Show | 99 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1423+1578C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2368983 | ||||||
| chr17:2369051
|
G | T | 31 | a0001c0001t0002g0022a0001c0001t0002g0157a0001c0001t0002g0158others(28): Show | 32 | HG02015.hp1 HG02040.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1423+1646G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369051 | ||||||
| chr17:2369175
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1423+1770T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369175 | ||||||
| chr17:2369370
|
A | G | 4 | a0001c0003t0002g0107a0001c0003t0002g0112a0001c0003t0002g0113others(1): Show | 4 | HG02015.hp1 HG02040.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424-1892A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369370 | ||||||
| chr17:2369496
|
C | A | 1 | a0001c0001t0001g0313 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1424-1766C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369496 | ||||||
| chr17:2369545
|
A | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1424-1717A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369545 | ||||||
| chr17:2369571
|
G | A | 1 | a0001c0003t0002g0105 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1424-1691G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369571 | ||||||
| chr17:2369683
|
C | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0062a0001c0001t0001g0071others(12): Show | 16 | HG00642.hp1 HG01070.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1424-1579C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369683 | ||||||
| chr17:2369715
|
C | T | 4 | a0007c0007t0001g0135a0007c0007t0001g0140a0007c0007t0001g0295others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1424-1547C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369715 | ||||||
| chr17:2369758
|
C | T | 1 | a0002c0002t0023g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1424-1504C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369758 | ||||||
| chr17:2369770
|
G | A | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(244): Show | 258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1424-1492G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369770 | ||||||
| chr17:2369877
|
G | A | 221 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0021others(218): Show | 229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1424-1385G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369877 | ||||||
| chr17:2369894
|
C | T | 1 | a0001c0003t0002g0219 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1424-1368C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369894 | ||||||
| chr17:2369912
|
C | T | 1 | a0001c0039t0001g0234 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1424-1350C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369912 | ||||||
| chr17:2369973
|
G | C | 1 | a0007c0007t0001g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1424-1289G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369973 | ||||||
| chr17:2369997
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1424-1265C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2369997 | ||||||
| chr17:2370151
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1424-1111G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370151 | ||||||
| chr17:2370240
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1424-1022C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370240 | ||||||
| chr17:2370240
|
C | T | 1 | a0002c0002t0014g0346 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1424-1022C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370240 | ||||||
| chr17:2370287
|
G | C | 49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0005g0077others(46): Show | 51 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1424-975G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370287 | ||||||
| chr17:2370341
|
G | T | 49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(46): Show | 51 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1424-921G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370341 | ||||||
| chr17:2370344
|
G | A | 12 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(9): Show | 12 | HG01891.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1424-918G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370344 | ||||||
| chr17:2370398
|
T | G | 1 | a0002c0041t0001g0312 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1424-864T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370398 | ||||||
| chr17:2370433
|
T | C | 48 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(45): Show | 50 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1424-829T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370433 | ||||||
| chr17:2370489
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1424-773A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370489 | ||||||
| chr17:2370493
|
G | GGCCTCTG others(24): Show |
49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(46): Show | 51 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1424-748_1424-747i others(33): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 2370493 | |||||
| chr17:2370681
|
G | A | 1 | a0002c0004t0001g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1424-581G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370681 | ||||||
| chr17:2370745
|
C | T | 1 | a0023c0018t0001g0114 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1424-517C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370745 | ||||||
| chr17:2370768
|
G | A | 9 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1424-494G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370768 | ||||||
| chr17:2370781
|
A | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1424-481A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370781 | ||||||
| chr17:2370899
|
G | GCA | 49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(46): Show | 51 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1424-362_1424-361i others(4): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 2370899 | |||||
| chr17:2370971
|
C | T | 1 | a0001c0001t0007g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1424-291C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370971 | ||||||
| chr17:2370998
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1424-264C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2370998 | ||||||
| chr17:2371028
|
CAGA | C | 48 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(45): Show | 50 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1424-231_1424-229d others(5): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr17 | 2371028 | |||||
| chr17:2371043
|
C | T | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(243): Show | 257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.1424-219C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2371043 | ||||||
| chr17:2371046
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1424-216C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2371046 | ||||||
| chr17:2371084
|
G | A | 48 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(45): Show | 50 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1424-178G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 12/23 | chr17 | 2371084 | ||||||
| chr17:2371475
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1577+60G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371475 | ||||||
| chr17:2371491
|
C | T | 2 | a0001c0001t0001g0147a0028c0014t0001g0145 | 2 | HG00639.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1577+76C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371491 | ||||||
| chr17:2371497
|
A | G | 1 | a0002c0002t0005g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1577+82A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371497 | ||||||
| chr17:2371505
|
G | C | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1577+90G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371505 | ||||||
| chr17:2371506
|
A | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1577+91A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371506 | ||||||
| chr17:2371508
|
A | C | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1577+93A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371508 | ||||||
| chr17:2371538
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1577+123G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371538 | ||||||
| chr17:2371550
|
C | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1577+135C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371550 | ||||||
| chr17:2371563
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1577+148C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371563 | ||||||
| chr17:2371564
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1577+149G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371564 | ||||||
| chr17:2371575
|
G | A | 48 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(45): Show | 50 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1577+160G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371575 | ||||||
| chr17:2371579
|
T | C | 48 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(45): Show | 50 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1577+164T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371579 | ||||||
| chr17:2371646
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1577+231A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371646 | ||||||
| chr17:2371667
|
T | A | 3 | a0005c0009t0002g0378a0005c0009t0002g0383a0005c0009t0002g0384 | 3 | NA18946.hp2 NA18981.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1577+252T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371667 | ||||||
| chr17:2371695
|
G | A | 110 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(107): Show | 117 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.1577+280G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371695 | ||||||
| chr17:2371723
|
T | C | 124 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(121): Show | 131 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.1577+308T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371723 | ||||||
| chr17:2371813
|
C | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-377C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371813 | ||||||
| chr17:2371836
|
T | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-354T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371836 | ||||||
| chr17:2371842
|
T | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-348T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371842 | ||||||
| chr17:2371873
|
C | T | 1 | a0001c0001t0022g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1578-317C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371873 | ||||||
| chr17:2371874
|
G | A | 49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0003t0001g0054others(46): Show | 52 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1578-316G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371874 | ||||||
| chr17:2371880
|
C | T | 1 | a0002c0004t0001g0300 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1578-310C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371880 | ||||||
| chr17:2371894
|
G | A | 49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0003t0001g0054others(46): Show | 52 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1578-296G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371894 | ||||||
| chr17:2371895
|
A | T | 49 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0003t0001g0054others(46): Show | 52 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1578-295A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371895 | ||||||
| chr17:2371905
|
G | A | 51 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(48): Show | 54 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1578-285G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371905 | ||||||
| chr17:2371909
|
C | T | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-281C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371909 | ||||||
| chr17:2371936
|
C | G | 60 | a0001c0001t0001g0081a0001c0001t0001g0110a0001c0001t0001g0123others(57): Show | 63 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1578-254C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371936 | ||||||
| chr17:2371946
|
T | C | 89 | a0001c0001t0001g0081a0001c0001t0001g0110a0001c0001t0001g0123others(86): Show | 93 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1578-244T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2371946 | ||||||
| chr17:2372009
|
A | AG | 48 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0123others(45): Show | 51 | HG00099.hp1 HG00558.hp1 HG01099.hp2 others(48): Show |
intron_variant | MODIFIER | c.1578-181_1578-180i others(3): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372009 | ||||||
| chr17:2372078
|
G | T | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-112G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372078 | ||||||
| chr17:2372087
|
C | T | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-103C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372087 | ||||||
| chr17:2372113
|
A | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-77A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372113 | ||||||
| chr17:2372118
|
C | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-72C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372118 | ||||||
| chr17:2372119
|
T | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-71T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372119 | ||||||
| chr17:2372120
|
C | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-70C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372120 | ||||||
| chr17:2372127
|
T | C | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1578-63T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 13/23 | chr17 | 2372127 | ||||||
| chr17:2372274
|
GGCTGTGG others(20): Show |
G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1642+21_1643-42del others(27): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372274 | ||||||
| chr17:2372300
|
C | T | 8 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0125others(5): Show | 8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1643-43C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372300 | ||||||
| chr17:2372314
|
C | T | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1643-29C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372314 | ||||||
| chr17:2372315
|
T | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1643-28T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372315 | ||||||
| chr17:2372316
|
C | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1643-27C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372316 | ||||||
| chr17:2372318
|
TGCTGCCC others(3): Show |
T | 2 | a0001c0001t0001g0211a0002c0041t0001g0312 | 2 | HG03209.hp1 NA19070.hp2 |
splice_region_variant&intron_variant | LOW | c.1643-12_1643-3delT others(9): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | 2372318 | |||||
| chr17:2372323
|
C | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1643-20C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372323 | ||||||
| chr17:2372326
|
A | C | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1643-17A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372326 | ||||||
| chr17:2372336
|
A | T | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.1643-7A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 14/23 | chr17 | 2372336 | ||||||
| chr17:2372494
|
A | C | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.1788+6A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372494 | ||||||
| chr17:2372503
|
G | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1788+15G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372503 | ||||||
| chr17:2372504
|
T | G | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1788+16T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372504 | ||||||
| chr17:2372505
|
T | A | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1788+17T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372505 | ||||||
| chr17:2372528
|
T | C | 1 | a0010c0033t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1788+40T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372528 | ||||||
| chr17:2372550
|
T | C | 94 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(91): Show | 101 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.1788+62T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372550 | ||||||
| chr17:2372735
|
C | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1789-218C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372735 | ||||||
| chr17:2372791
|
G | T | 93 | a0001c0001t0001g0081a0001c0001t0001g0123a0001c0001t0002g0022others(90): Show | 100 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1789-162G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372791 | ||||||
| chr17:2372903
|
G | T | 5 | a0002c0002t0001g0376a0007c0007t0001g0135a0007c0007t0001g0140others(2): Show | 5 | HG01167.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1789-50G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372903 | ||||||
| chr17:2372927
|
C | G | 3 | a0001c0003t0001g0308a0001c0003t0001g0356a0001c0003t0001g0374 | 3 | HG03710.hp1 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1789-26C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372927 | ||||||
| chr17:2372935
|
A | G | 3 | a0002c0012t0001g0129a0002c0012t0001g0372a0003c0006t0001g0095 | 3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1789-18A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 15/23 | chr17 | 2372935 | ||||||
| chr17:2373107
|
CTGA | C | 146 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0021others(143): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1917+30_1917+32del others(3): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr17 | 2373107 | |||||
| chr17:2373138
|
C | T | 36 | a0001c0001t0001g0115a0001c0001t0007g0164a0001c0001t0007g0173others(33): Show | 43 | HG00609.hp2 HG00621.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1917+57C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/23 | chr17 | 2373138 | ||||||
| chr17:2373154
|
G | A | 1 | a0001c0003t0001g0379 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1917+73G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/23 | chr17 | 2373154 | ||||||
| chr17:2373162
|
C | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0100a0001c0001t0001g0102others(12): Show | 16 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1917+81C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/23 | chr17 | 2373162 | ||||||
| chr17:2373206
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1917+125C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/23 | chr17 | 2373206 | ||||||
| chr17:2373249
|
C | G | 3 | a0001c0003t0001g0308a0001c0003t0001g0356a0001c0003t0001g0374 | 3 | HG03710.hp1 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1918-82C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 16/23 | chr17 | 2373249 | ||||||
| chr17:2373646
|
T | C | 30 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0190others(27): Show | 32 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.2100+133T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2373646 | ||||||
| chr17:2373829
|
G | A | 8 | a0001c0034t0009g0396a0002c0004t0001g0088a0003c0006t0001g0024others(5): Show | 8 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2100+316G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2373829 | ||||||
| chr17:2373848
|
T | A | 1 | a0002c0002t0004g0342 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2100+335T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2373848 | ||||||
| chr17:2374273
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(2): Show | 5 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2100+760T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374273 | ||||||
| chr17:2374374
|
T | C | 296 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(293): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2100+861T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374374 | ||||||
| chr17:2374398
|
G | A | 1 | a0002c0002t0001g0028 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2100+885G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374398 | ||||||
| chr17:2374426
|
C | A | 294 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(291): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2100+913C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374426 | ||||||
| chr17:2374450
|
G | A | 2 | a0001c0001t0001g0367a0028c0014t0001g0145 | 2 | HG00099.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.2100+937G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374450 | ||||||
| chr17:2374483
|
G | C | 2 | a0002c0046t0020g0159a0013c0030t0024g0149 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2100+970G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374483 | ||||||
| chr17:2374526
|
G | A | 1 | a0001c0003t0001g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2101-966G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374526 | ||||||
| chr17:2374540
|
G | A | 41 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0170others(38): Show | 43 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(40): Show |
intron_variant | MODIFIER | c.2101-952G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374540 | ||||||
| chr17:2374635
|
G | A | 1 | a0002c0002t0001g0042 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2101-857G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374635 | ||||||
| chr17:2374770
|
T | G | 295 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(292): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2101-722T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374770 | ||||||
| chr17:2374991
|
G | A | 1 | a0002c0002t0014g0346 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2101-501G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2374991 | ||||||
| chr17:2375091
|
C | T | 2 | a0001c0001t0001g0348a0015c0026t0001g0341 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2101-401C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375091 | ||||||
| chr17:2375092
|
C | G | 2 | a0002c0046t0020g0159a0013c0030t0024g0149 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2101-400C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375092 | ||||||
| chr17:2375098
|
G | C | 291 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(288): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2101-394G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375098 | ||||||
| chr17:2375207
|
C | G | 1 | a0002c0002t0001g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2101-285C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375207 | ||||||
| chr17:2375261
|
T | C | 102 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0061others(99): Show | 106 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.2101-231T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375261 | ||||||
| chr17:2375263
|
C | T | 100 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0061others(97): Show | 104 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2101-229C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375263 | ||||||
| chr17:2375315
|
C | T | 280 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(277): Show | 301 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.2101-177C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375315 | ||||||
| chr17:2375350
|
C | T | 311 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0019others(308): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.2101-142C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375350 | ||||||
| chr17:2375391
|
G | T | 81 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0061others(78): Show | 83 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2101-101G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 17/23 | chr17 | 2375391 | ||||||
| chr17:2376060
|
T | C | 44 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0170others(41): Show | 46 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(43): Show |
intron_variant | MODIFIER | c.2485-77T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 18/23 | chr17 | 2376060 | ||||||
| chr17:2376276
|
G | A | 1 | a0002c0002t0001g0051 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2609+15G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376276 | ||||||
| chr17:2376303
|
G | GCCGCGCA others(7): Show |
52 | a0001c0001t0002g0022a0001c0001t0002g0157a0001c0001t0002g0158others(49): Show | 54 | HG01123.hp2 HG01167.hp1 HG01361.hp1 others(51): Show |
intron_variant | MODIFIER | c.2609+46_2609+47ins others(14): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | INFO_REALIGN_3_PRIME | chr17 | 2376303 | |||||
| chr17:2376324
|
A | C | 9 | a0001c0001t0001g0358a0002c0002t0001g0003a0002c0002t0001g0043others(6): Show | 11 | HG00642.hp2 HG00735.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.2609+63A>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376324 | ||||||
| chr17:2376327
|
A | G | 56 | a0001c0001t0001g0019a0001c0001t0001g0055a0001c0001t0001g0064others(53): Show | 58 | HG00099.hp2 HG00280.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2609+66A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376327 | ||||||
| chr17:2376364
|
G | T | 1 | a0001c0001t0001g0309 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2609+103G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376364 | ||||||
| chr17:2376374
|
T | C | 1 | a0002c0002t0002g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2609+113T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376374 | ||||||
| chr17:2376397
|
T | C | 2 | a0001c0025t0001g0101a0002c0043t0001g0364 | 2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2609+136T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376397 | ||||||
| chr17:2376401
|
T | C | 63 | a0001c0001t0001g0064a0001c0001t0002g0022a0001c0001t0002g0157others(60): Show | 68 | HG01123.hp2 HG01167.hp1 HG01261.hp2 others(65): Show |
intron_variant | MODIFIER | c.2609+140T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376401 | ||||||
| chr17:2376465
|
C | T | 1 | a0001c0003t0002g0020 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2609+204C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376465 | ||||||
| chr17:2376519
|
G | A | 2 | a0001c0003t0001g0361a0001c0003t0001g0362 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2610-214G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376519 | ||||||
| chr17:2376524
|
G | A | 1 | a0001c0001t0022g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2610-209G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376524 | ||||||
| chr17:2376619
|
G | T | 1 | a0002c0002t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2610-114G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376619 | ||||||
| chr17:2376621
|
C | A | 1 | a0002c0004t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2610-112C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376621 | ||||||
| chr17:2376622
|
G | A | 6 | a0002c0004t0001g0007a0002c0004t0001g0088a0002c0004t0001g0089others(3): Show | 7 | HG01884.hp2 HG02145.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2610-111G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376622 | ||||||
| chr17:2376658
|
G | C | 7 | a0001c0003t0002g0012a0001c0003t0002g0273a0001c0003t0002g0274others(4): Show | 9 | HG02258.hp2 HG02280.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2610-75G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 19/23 | chr17 | 2376658 | ||||||
| chr17:2376847
|
C | T | 1 | a0017c0035t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2692+32C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 20/23 | chr17 | 2376847 | ||||||
| chr17:2376858
|
G | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0049 | 4 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2692+43G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 20/23 | chr17 | 2376858 | ||||||
| chr17:2377154
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2802+86C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377154 | ||||||
| chr17:2377168
|
A | G | 2 | a0001c0001t0009g0355a0002c0002t0009g0280 | 2 | HG03688.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2802+100A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377168 | ||||||
| chr17:2377243
|
T | G | 2 | a0002c0046t0020g0159a0013c0030t0024g0149 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2802+175T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377243 | ||||||
| chr17:2377251
|
C | T | 1 | a0001c0001t0007g0164 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2802+183C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377251 | ||||||
| chr17:2377252
|
G | A | 2 | a0002c0046t0020g0159a0013c0030t0024g0149 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2802+184G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377252 | ||||||
| chr17:2377309
|
C | A | 1 | a0002c0002t0001g0068 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2802+241C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377309 | ||||||
| chr17:2377320
|
C | T | 11 | a0001c0001t0022g0130a0001c0003t0002g0012a0001c0003t0002g0020others(8): Show | 14 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.2802+252C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377320 | ||||||
| chr17:2377415
|
TGGA | T | 4 | a0006c0008t0003g0187a0006c0008t0003g0261a0006c0008t0003g0299others(1): Show | 4 | HG02027.hp2 HG02165.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2802+350_2802+352d others(5): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 2377415 | |||||
| chr17:2377483
|
CA | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(235): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.2803-357delA | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 2377483 | |||||
| chr17:2377486
|
A | AAAAAAAA others(16): Show |
9 | a0001c0001t0022g0130a0001c0003t0002g0012a0001c0003t0002g0020others(6): Show | 12 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2803-359_2803-358i others(25): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 2377486 | |||||
| chr17:2377498
|
A | AACGAAAA others(18): Show |
4 | a0001c0001t0002g0207a0001c0001t0002g0388a0002c0002t0004g0050others(1): Show | 4 | HG01928.hp1 NA18965.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2803-358_2803-357i others(27): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 2377498 | |||||
| chr17:2377498
|
A | ACGAAAAA others(17): Show |
42 | a0001c0001t0002g0022a0001c0001t0002g0157a0001c0001t0002g0158others(39): Show | 44 | HG01123.hp2 HG01361.hp1 HG01943.hp2 others(41): Show |
intron_variant | MODIFIER | c.2803-359_2803-358i others(26): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377498 | ||||||
| chr17:2377501
|
C | A | 47 | a0001c0001t0001g0010a0001c0001t0001g0056a0001c0001t0001g0115others(44): Show | 57 | HG00280.hp2 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.2803-356C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377501 | ||||||
| chr17:2377523
|
TGAG | T | 5 | a0002c0002t0001g0376a0007c0007t0001g0135a0007c0007t0001g0140others(2): Show | 5 | HG01167.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2803-327_2803-325d others(5): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr17 | 2377523 | |||||
| chr17:2377640
|
T | C | 390 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(387): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.2803-217T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377640 | ||||||
| chr17:2377718
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2803-139G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377718 | ||||||
| chr17:2377754
|
T | C | 1 | a0001c0001t0022g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2803-103T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377754 | ||||||
| chr17:2377769
|
A | G | 15 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0125others(12): Show | 15 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2803-88A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377769 | ||||||
| chr17:2377785
|
G | A | 1 | a0001c0003t0001g0353 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2803-72G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 21/23 | chr17 | 2377785 | ||||||
| chr17:2377973
|
A | G | 11 | a0001c0001t0001g0010a0001c0001t0001g0156a0001c0001t0001g0167others(8): Show | 15 | HG00280.hp2 HG01192.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.2899+20A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2377973 | ||||||
| chr17:2377984
|
G | A | 1 | a0001c0003t0001g0308 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2899+31G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2377984 | ||||||
| chr17:2378304
|
G | A | 2 | a0001c0001t0001g0335a0002c0002t0001g0151 | 2 | HG00323.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2899+351G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378304 | ||||||
| chr17:2378402
|
T | A | 1 | a0001c0001t0001g0186 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2899+449T>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378402 | ||||||
| chr17:2378433
|
G | A | 6 | a0001c0003t0001g0353a0002c0002t0001g0376a0007c0007t0001g0135others(3): Show | 6 | HG00558.hp1 HG01167.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2899+480G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378433 | ||||||
| chr17:2378444
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0233 | 2 | HG00673.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2899+491C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378444 | ||||||
| chr17:2378539
|
A | G | 7 | a0001c0001t0001g0168a0001c0001t0001g0278a0001c0001t0001g0283others(4): Show | 8 | HG02071.hp1 NA18941.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.2900-497A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378539 | ||||||
| chr17:2378702
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0156a0001c0001t0001g0167others(3): Show | 7 | HG00280.hp2 NA18942.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2900-334G>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378702 | ||||||
| chr17:2378779
|
C | T | 6 | a0001c0001t0001g0023a0001c0001t0001g0061a0001c0001t0001g0070others(3): Show | 6 | HG01891.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2900-257C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378779 | ||||||
| chr17:2378921
|
CCAGCCTC others(5): Show |
C | 1 | a0006c0008t0003g0261 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2900-103_2900-92de others(13): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr17 | 2378921 | |||||
| chr17:2378921
|
CCAGCCTC others(11): Show |
C | 55 | a0001c0001t0002g0022a0001c0001t0002g0157a0001c0001t0002g0158others(52): Show | 60 | HG01123.hp2 HG01361.hp1 HG01928.hp1 others(57): Show |
intron_variant | MODIFIER | c.2900-109_2900-92de others(19): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr17 | 2378921 | |||||
| chr17:2378924
|
G | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-112G>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378924 | ||||||
| chr17:2378927
|
T | C | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-109T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378927 | ||||||
| chr17:2378933
|
T | C | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-103T>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378933 | ||||||
| chr17:2378945
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-91C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378945 | ||||||
| chr17:2378946
|
C | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-90C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378946 | ||||||
| chr17:2378947
|
A | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-89A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378947 | ||||||
| chr17:2378959
|
A | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-77A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378959 | ||||||
| chr17:2378960
|
G | C | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-76G>C | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2378960 | ||||||
| chr17:2379019
|
C | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2900-17C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 22/23 | chr17 | 2379019 | ||||||
| chr17:2379254
|
C | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3067+51C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379254 | ||||||
| chr17:2379288
|
T | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3067+85T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379288 | ||||||
| chr17:2379334
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-98C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379334 | ||||||
| chr17:2379341
|
A | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-91A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379341 | ||||||
| chr17:2379352
|
A | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0244 | 2 | HG00408.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.3068-80A>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379352 | ||||||
| chr17:2379355
|
GAGCAGGG others(16): Show |
G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-73_3068-51del others(23): Show |
SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | 2379355 | |||||
| chr17:2379381
|
C | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-51C>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379381 | ||||||
| chr17:2379390
|
C | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-42C>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379390 | ||||||
| chr17:2379397
|
T | G | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-35T>G | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379397 | ||||||
| chr17:2379408
|
A | T | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3068-24A>T | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379408 | ||||||
| chr17:2379429
|
C | A | 1 | a0013c0030t0024g0149 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.3068-3C>A | SGSM2 | ENSG00000141258.13 | transcript | ENST00000268989.8 | protein_coding | 23/23 | chr17 | 2379429 |