| geneid | 4436 |
|---|---|
| ensemblid | ENSG00000095002.15 |
| hgncid | 7325 |
| symbol | MSH2 |
| name | mutS homolog 2 |
| refseq_nuc | NM_000251.3 |
| refseq_prot | NP_000242.1 |
| ensembl_nuc | ENST00000233146.7 |
| ensembl_prot | ENSP00000233146.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 47403156 |
| end | 47483223 |
| strand | + |
| ver | v1.2 |
| region | chr2:47403156-47483223 |
| region5000 | chr2:47398156-47488223 |
| regionname0 | MSH2_chr2_47403156_47483223 |
| regionname5000 | MSH2_chr2_47398156_47488223 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 934 | 344 | 73 | 64 | 157 | 12 | 36 | 116 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0002 | 0/0 | 934 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0003 | 0/0 | 934 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0004 | 0/0 | 934 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0005 | 0/0 | 934 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0006 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0007 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0008 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0009 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0010 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0011 | 0/0 | 934 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2805 | 319 | 58 | 62 | 153 | 12 | 32 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0002 | 0/0 | 2805 | 12 | 11 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0003 | 0/0 | 2805 | 12 | 12 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0004 | 0/0 | 2805 | 3 | 0 | 0 | 3 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0005 | 0/0 | 2805 | 3 | 0 | 0 | 3 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0006 | 0/0 | 2805 | 3 | 0 | 1 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0007 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0008 | 0/0 | 2805 | 2 | 0 | 0 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0009 | 0/0 | 2805 | 2 | 0 | 0 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0010 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0011 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0012 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0013 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0014 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0015 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0016 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0017 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0018 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| c0019 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 311 | 366 | 84 | 63 | 167 | 12 | 38 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| t0002 | 0/0 | 311 | 3 | 2 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| t0003 | 0/0 | 267 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2805 | 319 | 58 | 62 | 153 | 12 | 32 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0002 | 0/0 | 2805 | 12 | 11 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0004 | 0/0 | 2805 | 3 | 0 | 0 | 3 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0006 | 0/0 | 2805 | 3 | 0 | 1 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0007 | 0/0 | 2805 | 3 | 3 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0009 | 0/0 | 2805 | 2 | 0 | 0 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0012 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0014 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0002c0003 | 0/0 | 2805 | 12 | 12 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0002c0019 | 0/0 | 2805 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0003c0005 | 0/0 | 2805 | 3 | 0 | 0 | 3 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0004c0010 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0005c0008 | 0/0 | 2805 | 2 | 0 | 0 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0006c0017 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0007c0013 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0008c0015 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0009c0016 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0010c0018 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0011c0011 | 0/0 | 2805 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3115 | 316 | 57 | 61 | 152 | 12 | 32 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0001t0002 | 0/0 | 3115 | 2 | 1 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0001t0003 | 0/0 | 3071 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0002t0001 | 0/0 | 3115 | 12 | 11 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0004t0001 | 0/0 | 3115 | 3 | 0 | 0 | 3 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0006t0001 | 0/0 | 3115 | 3 | 0 | 1 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0007t0001 | 0/0 | 3115 | 3 | 3 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0009t0001 | 0/0 | 3115 | 2 | 0 | 0 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0012t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0001c0014t0001 | 0/0 | 3115 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0002c0003t0001 | 0/0 | 3115 | 11 | 11 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0002c0003t0002 | 0/0 | 3115 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0002c0019t0001 | 0/0 | 3115 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0003c0005t0001 | 0/0 | 3115 | 3 | 0 | 0 | 3 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0004c0010t0001 | 0/0 | 3115 | 2 | 0 | 0 | 2 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0005c0008t0001 | 0/0 | 3115 | 2 | 0 | 0 | 0 | 0 | 2 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0006c0017t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0007c0013t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0008c0015t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0009c0016t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0010c0018t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| a0011c0011t0001 | 0/0 | 3115 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | copy fasta | chr2 | 47398156 | 47488223 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0030 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0002t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0009t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0009t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0012t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0001c0014t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0003t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0002c0019t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0003c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0003c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0003c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0004c0010t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0004c0010t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0005c0008t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0005c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0006c0017t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0007c0013t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0008c0015t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0009c0016t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0010c0018t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| a0011c0011t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0365 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0369 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01168 | hp1 | a0001 | c0006 | t0001 | g0222 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0362 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | IBS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02015 | hp1 | a0006 | c0017 | t0001 | g0335 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0235 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02132 | hp2 | a0003 | c0005 | t0001 | g0221 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CDX | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CDX | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0234 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02523 | hp2 | a0010 | c0018 | t0001 | g0339 | EAS | KHV | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02622 | hp1 | a0002 | c0019 | t0001 | g0253 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0111 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02630 | hp2 | a0001 | c0007 | t0001 | g0101 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02717 | hp2 | a0002 | c0003 | t0002 | g0171 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02809 | hp1 | a0002 | c0003 | t0001 | g0257 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0108 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0106 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0107 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03041 | hp1 | a0001 | c0014 | t0001 | g0224 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03239 | hp2 | a0001 | c0006 | t0001 | g0144 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03490 | hp1 | a0001 | c0009 | t0001 | g0274 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03492 | hp1 | a0001 | c0009 | t0001 | g0275 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | ESN | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03704 | hp2 | a0005 | c0008 | t0001 | g0212 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03834 | hp1 | a0001 | c0006 | t0001 | g0128 | SAS | BEB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04115 | hp2 | a0005 | c0008 | t0001 | g0211 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | STU | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18951 | hp2 | a0003 | c0005 | t0001 | g0247 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18959 | hp1 | a0007 | c0013 | t0001 | g0213 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18963 | hp2 | a0008 | c0015 | t0001 | g0092 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18969 | hp2 | a0009 | c0016 | t0001 | g0168 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18992 | hp2 | a0004 | c0010 | t0001 | g0351 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19011 | hp1 | a0011 | c0011 | t0001 | g0243 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | LWK | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19063 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19066 | hp1 | a0003 | c0005 | t0001 | g0173 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19074 | hp1 | a0001 | c0012 | t0001 | g0245 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19088 | hp1 | a0004 | c0010 | t0001 | g0350 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19240 | hp1 | a0001 | c0007 | t0001 | g0102 | AFR | YRI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0233 | AFR | ASW | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ASW | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | TSI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | GIH | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0252 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0349 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0103 | AFR | ACB | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03471 | hp1 | a0002 | c0003 | t0001 | g0109 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0367 | AFR | USA | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | USA | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | USA | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0110 | AFR | LWK | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0030 | REF | REF | MSH2_chr2_47398156_47488223 | MSH2 | chr2 | 47398156 | 47488223 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47403205
|
C | A | 1 | a0011 | 1 | NA19011.hp1 | missense_variant | MODERATE | c.14C>A | p.Pro5Gln | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/16 | 50/3115 | 14/2805 | 5/934 | chr2 | 47403205 | ||
| chr2:47403214
|
C | T | 1 | a0004 | 2 | NA18992.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.23C>T | p.Thr8Met | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/16 | 59/3115 | 23/2805 | 8/934 | chr2 | 47403214 | ||
| chr2:47410107
|
A | G | 1 | a0002 | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
missense_variant | MODERATE | c.380A>G | p.Asn127Ser | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/16 | 416/3115 | 380/2805 | 127/934 | chr2 | 47410107 | ||
| chr2:47410232
|
A | G | 1 | a0010 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.505A>G | p.Ile169Val | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/16 | 541/3115 | 505/2805 | 169/934 | chr2 | 47410232 | ||
| chr2:47416318
|
G | A | 1 | a0005 | 2 | HG03704.hp2 HG04115.hp2 |
missense_variant | MODERATE | c.965G>A | p.Gly322Asp | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/16 | 1001/3115 | 965/2805 | 322/934 | chr2 | 47416318 | ||
| chr2:47429833
|
C | T | 1 | a0003 | 3 | HG02132.hp2 NA18951.hp2 NA19066.hp1 |
missense_variant | MODERATE | c.1168C>T | p.Leu390Phe | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/16 | 1204/3115 | 1168/2805 | 390/934 | chr2 | 47429833 | ||
| chr2:47470993
|
A | G | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1690A>G | p.Thr564Ala | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/16 | 1726/3115 | 1690/2805 | 564/934 | chr2 | 47470993 | ||
| chr2:47475238
|
A | G | 1 | a0009 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.1973A>G | p.Glu658Gly | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/16 | 2009/3115 | 1973/2805 | 658/934 | chr2 | 47475238 | ||
| chr2:47476425
|
G | A | 1 | a0007 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.2064G>A | p.Met688Ile | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/16 | 2100/3115 | 2064/2805 | 688/934 | chr2 | 47476425 | ||
| chr2:47480770
|
A | G | 1 | a0008 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.2533A>G | p.Lys845Glu | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/16 | 2569/3115 | 2533/2805 | 845/934 | chr2 | 47480770 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47410198
|
C | A | 1 | a0001c0004 | 3 | NA18969.hp1 NA19063.hp1 NA19077.hp2 |
synonymous_variant | LOW | c.471C>A | p.Gly157Gly | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/16 | 507/3115 | 471/2805 | 157/934 | chr2 | 47410198 | ||
| chr2:47410270
|
T | C | 1 | a0002c0019 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.543T>C | p.Asn181Asn | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/16 | 579/3115 | 543/2805 | 181/934 | chr2 | 47410270 | ||
| chr2:47410300
|
C | T | 1 | a0001c0007 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.573C>T | p.Leu191Leu | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/16 | 609/3115 | 573/2805 | 191/934 | chr2 | 47410300 | ||
| chr2:47416325
|
G | A | 1 | a0001c0012 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.972G>A | p.Gln324Gln | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/16 | 1008/3115 | 972/2805 | 324/934 | chr2 | 47416325 | ||
| chr2:47416337
|
C | T | 1 | a0001c0006 | 3 | HG01168.hp1 HG03239.hp2 HG03834.hp1 |
synonymous_variant | LOW | c.984C>T | p.Ala328Ala | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/16 | 1020/3115 | 984/2805 | 328/934 | chr2 | 47416337 | ||
| chr2:47476566
|
C | T | 1 | a0001c0009 | 2 | HG03490.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.2205C>T | p.Ile735Ile | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/16 | 2241/3115 | 2205/2805 | 735/934 | chr2 | 47476566 | ||
| chr2:47482910
|
T | C | 1 | a0001c0002 | 12 | HG01109.hp1 HG02055.hp1 HG02486.hp1 others(9): Show |
synonymous_variant | LOW | c.2766T>C | p.Phe922Phe | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 16/16 | 2802/3115 | 2766/2805 | 922/934 | chr2 | 47482910 | ||
| chr2:47482946
|
G | A | 1 | a0001c0014 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.2802G>A | p.Thr934Thr | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 16/16 | 2838/3115 | 2802/2805 | 934/934 | chr2 | 47482946 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47483090
|
T | G | 2 | a0001c0001t0002a0002c0003t0002 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 16/16 | 141 | chr2 | 47483090 | |||||
| chr2:47483121
|
ATTTTGAA others(37): Show |
A | 1 | a0001c0001t0003 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173_*216delTTTTGA others(38): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 16/16 | 173 | chr2 | 47483121 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47403411
|
C | G | 270 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0112others(267): Show | 270 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.211+9C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403411 | ||||||
| chr2:47403500
|
T | C | 270 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0112others(267): Show | 270 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.211+98T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403500 | ||||||
| chr2:47403548
|
C | T | 1 | a0001c0001t0001g0370 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211+146C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403548 | ||||||
| chr2:47403565
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.211+163C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403565 | ||||||
| chr2:47403573
|
G | A | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+171G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403573 | ||||||
| chr2:47403952
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.211+550G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403952 | ||||||
| chr2:47403990
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.211+588T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47403990 | ||||||
| chr2:47404010
|
A | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.211+608A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404010 | ||||||
| chr2:47404037
|
C | G | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+635C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404037 | ||||||
| chr2:47404068
|
A | C | 1 | a0001c0002t0001g0367 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.211+666A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404068 | ||||||
| chr2:47404148
|
CTG | C | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+748_211+749del others(2): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47404148 | |||||
| chr2:47404150
|
GT | G | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+752delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47404150 | |||||
| chr2:47404213
|
C | T | 262 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0119others(259): Show | 262 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.211+811C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404213 | ||||||
| chr2:47404217
|
G | C | 1 | a0001c0001t0001g0119 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.211+815G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404217 | ||||||
| chr2:47404286
|
G | C | 1 | a0001c0001t0001g0119 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.211+884G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404286 | ||||||
| chr2:47404359
|
C | T | 12 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(9): Show | 12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.211+957C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404359 | ||||||
| chr2:47404407
|
T | A | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+1005T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404407 | ||||||
| chr2:47404464
|
G | A | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.211+1062G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404464 | ||||||
| chr2:47404525
|
G | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+1123G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404525 | ||||||
| chr2:47404592
|
G | A | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.211+1190G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404592 | ||||||
| chr2:47404621
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.211+1219T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404621 | ||||||
| chr2:47404652
|
T | C | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.211+1250T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404652 | ||||||
| chr2:47404690
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.211+1288T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404690 | ||||||
| chr2:47404705
|
G | GT | 55 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(52): Show | 55 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.211+1321dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47404705 | |||||
| chr2:47404705
|
GT | G | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 202 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.211+1321delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47404705 | |||||
| chr2:47404712
|
T | G | 1 | a0001c0001t0001g0001 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.211+1310T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404712 | ||||||
| chr2:47404748
|
C | T | 1 | a0008c0015t0001g0092 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.211+1346C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404748 | ||||||
| chr2:47404773
|
T | C | 9 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0001g0360others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+1371T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404773 | ||||||
| chr2:47404854
|
C | G | 1 | a0001c0001t0001g0285 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.211+1452C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404854 | ||||||
| chr2:47404982
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.211+1580A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404982 | ||||||
| chr2:47404996
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+1594C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47404996 | ||||||
| chr2:47405042
|
G | A | 3 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124 | 3 | HG02486.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.211+1640G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405042 | ||||||
| chr2:47405050
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211+1648T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405050 | ||||||
| chr2:47405139
|
G | A | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.211+1737G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405139 | ||||||
| chr2:47405286
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.211+1884G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405286 | ||||||
| chr2:47405296
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.211+1894T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405296 | ||||||
| chr2:47405344
|
C | T | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.211+1942C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405344 | ||||||
| chr2:47405371
|
G | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02145.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.211+1969G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405371 | ||||||
| chr2:47405421
|
C | CA | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.211+2043dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47405421 | |||||
| chr2:47405421
|
C | CAA | 26 | a0001c0001t0001g0120a0001c0001t0001g0129a0001c0001t0001g0130others(23): Show | 26 | HG00597.hp2 HG00639.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+2042_211+2043d others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47405421 | |||||
| chr2:47405421
|
CA | C | 25 | a0001c0001t0001g0011a0001c0001t0001g0087a0001c0001t0001g0088others(22): Show | 25 | HG01071.hp2 HG01255.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.211+2043delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47405421 | |||||
| chr2:47405421
|
CAA | C | 18 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(15): Show | 18 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.211+2042_211+2043d others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 47405421 | |||||
| chr2:47405509
|
A | T | 1 | a0001c0006t0001g0222 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.211+2107A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405509 | ||||||
| chr2:47405615
|
C | T | 1 | a0003c0005t0001g0221 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.211+2213C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405615 | ||||||
| chr2:47405685
|
C | A | 19 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(16): Show | 19 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.211+2283C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405685 | ||||||
| chr2:47405797
|
T | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2395T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405797 | ||||||
| chr2:47405881
|
T | C | 60 | a0001c0001t0001g0020a0001c0001t0001g0104a0001c0001t0001g0120others(57): Show | 60 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.211+2479T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405881 | ||||||
| chr2:47405906
|
T | G | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02698.hp1 NA18992.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.212-2495T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405906 | ||||||
| chr2:47405950
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.212-2451C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405950 | ||||||
| chr2:47405981
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.212-2420C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47405981 | ||||||
| chr2:47406013
|
G | T | 1 | a0001c0001t0001g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.212-2388G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406013 | ||||||
| chr2:47406078
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.212-2323G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406078 | ||||||
| chr2:47406307
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.212-2094A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406307 | ||||||
| chr2:47406475
|
C | G | 1 | a0001c0001t0001g0355 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.212-1926C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406475 | ||||||
| chr2:47406477
|
C | T | 3 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284 | 3 | HG02145.hp1 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.212-1924C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406477 | ||||||
| chr2:47406578
|
C | T | 82 | a0001c0001t0001g0112a0001c0001t0001g0121a0001c0001t0001g0126others(79): Show | 82 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.212-1823C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406578 | ||||||
| chr2:47406614
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.212-1787G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406614 | ||||||
| chr2:47406627
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.212-1774A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406627 | ||||||
| chr2:47406642
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.212-1759C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406642 | ||||||
| chr2:47406879
|
A | G | 1 | a0001c0002t0001g0123 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.212-1522A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406879 | ||||||
| chr2:47406935
|
G | C | 61 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(58): Show | 61 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.212-1466G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47406935 | ||||||
| chr2:47407326
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212-1075G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407326 | ||||||
| chr2:47407423
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.212-978C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407423 | ||||||
| chr2:47407424
|
C | A | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 277 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.212-977C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407424 | ||||||
| chr2:47407458
|
G | A | 3 | a0001c0001t0001g0174a0003c0005t0001g0173a0003c0005t0001g0221 | 3 | HG02132.hp2 NA18951.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.212-943G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407458 | ||||||
| chr2:47407560
|
A | G | 7 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(4): Show | 7 | HG00639.hp1 HG01515.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-841A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407560 | ||||||
| chr2:47407622
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-779T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407622 | ||||||
| chr2:47407645
|
C | T | 4 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0263others(1): Show | 4 | NA18966.hp2 NA18983.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-756C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407645 | ||||||
| chr2:47407682
|
T | A | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.212-719T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407682 | ||||||
| chr2:47407767
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.212-634C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407767 | ||||||
| chr2:47407942
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.212-459T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407942 | ||||||
| chr2:47407993
|
G | T | 2 | a0001c0001t0002g0170a0002c0003t0002g0171 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.212-408G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407993 | ||||||
| chr2:47407996
|
A | G | 268 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0112others(265): Show | 268 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.212-405A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407996 | ||||||
| chr2:47407997
|
T | G | 268 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0112others(265): Show | 268 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.212-404T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47407997 | ||||||
| chr2:47408002
|
G | C | 1 | a0001c0001t0001g0229 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.212-399G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47408002 | ||||||
| chr2:47408159
|
A | T | 3 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124 | 3 | HG02486.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.212-242A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47408159 | ||||||
| chr2:47408286
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.212-115G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 1/15 | chr2 | 47408286 | ||||||
| chr2:47408787
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.366+232C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408787 | ||||||
| chr2:47408788
|
C | G | 10 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.366+233C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408788 | ||||||
| chr2:47408842
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.366+287T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408842 | ||||||
| chr2:47408892
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.366+337C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408892 | ||||||
| chr2:47408924
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.366+369A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408924 | ||||||
| chr2:47408925
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.366+370C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408925 | ||||||
| chr2:47408944
|
G | T | 6 | a0001c0001t0001g0132a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG02015.hp2 HG02129.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.366+389G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408944 | ||||||
| chr2:47408950
|
A | C | 1 | a0001c0001t0002g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.366+395A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47408950 | ||||||
| chr2:47409171
|
T | A | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.366+616T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409171 | ||||||
| chr2:47409176
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.366+621G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409176 | ||||||
| chr2:47409341
|
A | AGCAT | 46 | a0001c0001t0001g0120a0001c0001t0001g0264a0001c0001t0001g0286others(43): Show | 46 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.367-752_367-749dup others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 47409341 | |||||
| chr2:47409341
|
A | T | 1 | a0007c0013t0001g0213 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.367-753A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409341 | ||||||
| chr2:47409342
|
G | T | 1 | a0007c0013t0001g0213 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.367-752G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409342 | ||||||
| chr2:47409343
|
C | CATGCATT others(1): Show |
6 | a0001c0001t0001g0104a0001c0001t0001g0297a0001c0001t0001g0349others(3): Show | 6 | HG02486.hp2 HG02735.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.367-749_367-748ins others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 47409343 | |||||
| chr2:47409343
|
C | CATTT | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(85): Show | 88 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.367-713_367-710dup others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 47409343 | |||||
| chr2:47409343
|
C | CATTTATT others(1): Show |
9 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG00639.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.367-717_367-710dup others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 47409343 | |||||
| chr2:47409343
|
C | T | 1 | a0007c0013t0001g0213 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.367-751C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409343 | ||||||
| chr2:47409343
|
CATTT | C | 49 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0112others(46): Show | 49 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.367-713_367-710del others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 47409343 | |||||
| chr2:47409343
|
CATTTATT others(1): Show |
C | 6 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG02257.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-717_367-710del others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 47409343 | |||||
| chr2:47409346
|
T | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.367-748T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409346 | ||||||
| chr2:47409347
|
T | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0225others(2): Show | 5 | HG01884.hp2 HG02074.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-747T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409347 | ||||||
| chr2:47409424
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-670C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409424 | ||||||
| chr2:47409476
|
G | A | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01255.hp1 HG01346.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-618G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409476 | ||||||
| chr2:47409483
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | NA18955.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.367-611C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409483 | ||||||
| chr2:47409666
|
A | T | 1 | a0001c0001t0001g0359 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.367-428A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409666 | ||||||
| chr2:47409748
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.367-346C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409748 | ||||||
| chr2:47409788
|
A | G | 51 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(48): Show | 51 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.367-306A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409788 | ||||||
| chr2:47409886
|
C | T | 1 | a0001c0001t0001g0352 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.367-208C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409886 | ||||||
| chr2:47409926
|
C | T | 12 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(9): Show | 12 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.367-168C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47409926 | ||||||
| chr2:47410008
|
A | C | 53 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(50): Show | 53 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.367-86A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 2/15 | chr2 | 47410008 | ||||||
| chr2:47410465
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.645+93A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410465 | ||||||
| chr2:47410476
|
T | C | 1 | a0001c0001t0001g0359 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.645+104T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410476 | ||||||
| chr2:47410496
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.645+124A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410496 | ||||||
| chr2:47410594
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.645+222C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410594 | ||||||
| chr2:47410682
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.645+310C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410682 | ||||||
| chr2:47410724
|
A | G | 2 | a0005c0008t0001g0211a0005c0008t0001g0212 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.645+352A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410724 | ||||||
| chr2:47410766
|
A | AT | 8 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 8 | HG01993.hp1 HG02257.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+412dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 47410766 | |||||
| chr2:47410766
|
A | ATTT | 45 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(42): Show | 45 | HG00609.hp1 HG00735.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.645+410_645+412dup others(3): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 47410766 | |||||
| chr2:47410766
|
A | T | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.645+394A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410766 | ||||||
| chr2:47410766
|
AT | A | 177 | a0001c0001t0001g0022a0001c0001t0001g0095a0001c0001t0001g0105others(174): Show | 177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.645+412delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 47410766 | |||||
| chr2:47410788
|
A | T | 2 | a0001c0001t0001g0359a0001c0002t0001g0005 | 2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.645+416A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410788 | ||||||
| chr2:47410798
|
G | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18953.hp1 NA18964.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.645+426G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410798 | ||||||
| chr2:47410829
|
C | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.645+457C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410829 | ||||||
| chr2:47410830
|
G | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.645+458G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410830 | ||||||
| chr2:47410874
|
C | G | 195 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0119others(192): Show | 195 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.645+502C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410874 | ||||||
| chr2:47410984
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.645+612C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47410984 | ||||||
| chr2:47411030
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+658G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411030 | ||||||
| chr2:47411126
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.645+754G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411126 | ||||||
| chr2:47411148
|
GC | G | 3 | a0001c0001t0001g0295a0001c0001t0001g0319a0001c0001t0001g0320 | 3 | HG02135.hp2 HG03704.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.645+779delC | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 47411148 | |||||
| chr2:47411158
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.645+786G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411158 | ||||||
| chr2:47411168
|
G | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(8): Show | 11 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.645+796G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411168 | ||||||
| chr2:47411170
|
G | A | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(12): Show | 15 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.645+798G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411170 | ||||||
| chr2:47411228
|
C | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.645+856C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411228 | ||||||
| chr2:47411388
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+1016G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411388 | ||||||
| chr2:47411413
|
A | AT | 9 | a0001c0001t0001g0078a0001c0001t0001g0100a0001c0001t0001g0360others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-988dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | 47411413 | |||||
| chr2:47411494
|
C | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0041 | 2 | NA19066.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.646-920C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411494 | ||||||
| chr2:47411656
|
A | G | 268 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.646-758A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411656 | ||||||
| chr2:47411704
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.646-710C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411704 | ||||||
| chr2:47411752
|
T | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(11): Show | 14 | HG00642.hp1 HG01167.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.646-662T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411752 | ||||||
| chr2:47411767
|
A | G | 1 | a0001c0001t0001g0344 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.646-647A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411767 | ||||||
| chr2:47411853
|
G | A | 4 | a0001c0001t0001g0297a0001c0001t0001g0317a0001c0001t0001g0321others(1): Show | 4 | HG00408.hp2 NA18980.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-561G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411853 | ||||||
| chr2:47411967
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.646-447A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47411967 | ||||||
| chr2:47412037
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.646-377C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47412037 | ||||||
| chr2:47412190
|
A | G | 12 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(9): Show | 12 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.646-224A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47412190 | ||||||
| chr2:47412242
|
T | C | 16 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(13): Show | 16 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-172T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47412242 | ||||||
| chr2:47412276
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.646-138A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47412276 | ||||||
| chr2:47412372
|
T | C | 1 | a0001c0001t0001g0323 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.646-42T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 3/15 | chr2 | 47412372 | ||||||
| chr2:47412696
|
A | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.792+136A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412696 | ||||||
| chr2:47412732
|
T | G | 50 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.792+172T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412732 | ||||||
| chr2:47412765
|
C | T | 6 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 6 | HG02622.hp2 HG02896.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+205C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412765 | ||||||
| chr2:47412842
|
T | C | 5 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(2): Show | 5 | HG01515.hp1 HG01993.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+282T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412842 | ||||||
| chr2:47412938
|
A | G | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0083 | 3 | HG00544.hp1 NA18940.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.792+378A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412938 | ||||||
| chr2:47412948
|
A | T | 1 | a0001c0001t0001g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.792+388A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412948 | ||||||
| chr2:47412964
|
C | T | 50 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.792+404C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47412964 | ||||||
| chr2:47413168
|
C | A | 3 | a0001c0004t0001g0045a0001c0004t0001g0046a0001c0004t0001g0047 | 3 | NA18969.hp1 NA19063.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.792+608C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413168 | ||||||
| chr2:47413267
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.792+707T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413267 | ||||||
| chr2:47413316
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.792+756G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413316 | ||||||
| chr2:47413317
|
C | T | 4 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+757C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413317 | ||||||
| chr2:47413325
|
C | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+765C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413325 | ||||||
| chr2:47413334
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.792+774T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413334 | ||||||
| chr2:47413365
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.792+805A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413365 | ||||||
| chr2:47413390
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.792+830C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413390 | ||||||
| chr2:47413460
|
C | T | 1 | a0001c0001t0001g0248 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.793-809C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413460 | ||||||
| chr2:47413514
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.793-755A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413514 | ||||||
| chr2:47413548
|
G | GGTTTTTT others(7): Show |
1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.793-721_793-720ins others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413548 | ||||||
| chr2:47413548
|
G | GGTTTTTT others(12): Show |
1 | a0001c0001t0001g0187 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.793-721_793-720ins others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413548 | ||||||
| chr2:47413548
|
G | GT | 26 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(23): Show | 26 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.793-688dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTT | 15 | a0001c0001t0001g0038a0001c0001t0001g0072a0001c0001t0001g0073others(12): Show | 15 | HG00544.hp1 HG01099.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.793-689_793-688dup others(2): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTT | 9 | a0001c0001t0001g0127a0001c0001t0001g0231a0001c0001t0001g0268others(6): Show | 9 | HG01106.hp2 HG01255.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-692_793-688dup others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTT | 17 | a0001c0001t0001g0039a0001c0001t0001g0141a0001c0001t0001g0167others(14): Show | 17 | HG01069.hp1 HG01109.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-693_793-688dup others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT | 7 | a0001c0001t0001g0112a0001c0001t0001g0142a0001c0001t0001g0273others(4): Show | 7 | HG01071.hp1 HG01071.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-694_793-688dup others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0282 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.793-697_793-688dup others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0001g0121a0001c0001t0001g0264 | 2 | HG01255.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.793-698_793-688dup others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0300 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.793-699_793-688dup others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0130a0001c0001t0001g0156a0001c0001t0001g0201others(2): Show | 5 | HG00597.hp2 HG03490.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-700_793-688dup others(13): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(7): Show |
14 | a0001c0001t0001g0040a0001c0001t0001g0136a0001c0001t0001g0147others(11): Show | 14 | HG00558.hp1 HG02080.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.793-701_793-688dup others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(8): Show |
7 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0166others(4): Show | 7 | HG01106.hp1 HG01261.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-702_793-688dup others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(9): Show |
2 | a0001c0001t0001g0129a0001c0001t0001g0311 | 2 | HG02738.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.793-703_793-688dup others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(11): Show |
3 | a0001c0001t0001g0119a0001c0001t0001g0161a0001c0001t0001g0316 | 3 | NA18973.hp2 NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.793-705_793-688dup others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(12): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0204 | 2 | HG00408.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.793-706_793-688dup others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(13): Show |
11 | a0001c0001t0001g0135a0001c0001t0001g0148a0001c0001t0001g0149others(8): Show | 11 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.793-707_793-688dup others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0207a0001c0001t0001g0210 | 2 | HG00597.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.793-708_793-688dup others(21): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0001g0208 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.793-712_793-688dup others(25): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
G | GTTTTTTT others(21): Show |
2 | a0001c0001t0001g0209a0009c0016t0001g0168 | 2 | NA18965.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.793-715_793-688dup others(28): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GT | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0014a0001c0001t0001g0022others(7): Show | 10 | HG01074.hp2 HG01928.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-688delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTT | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.793-689_793-688del others(2): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTT | G | 20 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 20 | HG00642.hp1 HG00738.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.793-690_793-688del others(3): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTT | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(3): Show | 6 | HG00609.hp2 HG00733.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-691_793-688del others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTT | G | 12 | a0001c0001t0001g0132a0001c0001t0001g0134a0001c0001t0001g0138others(9): Show | 12 | HG00438.hp2 HG02071.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.793-693_793-688del others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(3): Show |
G | 5 | a0001c0001t0001g0048a0001c0002t0001g0122a0001c0002t0001g0123others(2): Show | 5 | HG00741.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-697_793-688del others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0191 | 3 | HG00621.hp2 NA18964.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.793-698_793-688del others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(5): Show |
G | 7 | a0001c0001t0001g0019a0001c0001t0001g0087a0001c0001t0001g0091others(4): Show | 7 | HG01175.hp1 HG02602.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-699_793-688del others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(6): Show |
G | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0023others(6): Show | 9 | HG00099.hp2 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-700_793-688del others(13): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0001g0343a0001c0007t0001g0101a0001c0007t0001g0102others(1): Show | 4 | HG02559.hp2 HG02630.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-701_793-688del others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(8): Show |
G | 49 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(46): Show | 49 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.793-702_793-688del others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0001g0190a0001c0001t0001g0324 | 2 | NA18747.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.793-703_793-688del others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(10): Show |
G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-704_793-688del others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413548
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.793-705_793-688del others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 47413548 | |||||
| chr2:47413550
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.793-719T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413550 | ||||||
| chr2:47413566
|
T | C | 56 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.793-703T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413566 | ||||||
| chr2:47413593
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0158 | 2 | HG00558.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.793-676C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413593 | ||||||
| chr2:47413626
|
C | T | 5 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(2): Show | 5 | HG01515.hp1 HG01993.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-643C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413626 | ||||||
| chr2:47413832
|
A | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.793-437A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413832 | ||||||
| chr2:47413867
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.793-402C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413867 | ||||||
| chr2:47413886
|
T | G | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-383T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413886 | ||||||
| chr2:47413904
|
A | G | 52 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0264others(49): Show | 52 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.793-365A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47413904 | ||||||
| chr2:47414246
|
G | A | 6 | a0002c0003t0001g0233a0002c0003t0001g0234a0002c0003t0001g0235others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-23G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 4/15 | chr2 | 47414246 | ||||||
| chr2:47414420
|
TA | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.942+29delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47414420 | |||||
| chr2:47414420
|
TAA | T | 67 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(64): Show | 67 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.942+28_942+29delAA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47414420 | |||||
| chr2:47414420
|
TAAA | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0308a0001c0001t0001g0309others(8): Show | 11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.942+27_942+29delAA others(1): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47414420 | |||||
| chr2:47414420
|
TAAAAAAA others(6): Show |
T | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.942+17_942+29delAA others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47414420 | |||||
| chr2:47414699
|
G | A | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.942+281G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414699 | ||||||
| chr2:47414703
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.942+285G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414703 | ||||||
| chr2:47414722
|
C | A | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.942+304C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414722 | ||||||
| chr2:47414858
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.942+440T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414858 | ||||||
| chr2:47414899
|
T | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.942+481T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414899 | ||||||
| chr2:47414981
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.942+563C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414981 | ||||||
| chr2:47414984
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.942+566A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47414984 | ||||||
| chr2:47415041
|
G | T | 36 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(33): Show | 36 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.942+623G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415041 | ||||||
| chr2:47415043
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.942+625A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415043 | ||||||
| chr2:47415119
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.942+701A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415119 | ||||||
| chr2:47415128
|
G | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.942+710G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415128 | ||||||
| chr2:47415176
|
G | GC | 48 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0286others(45): Show | 48 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.942+758_942+759ins others(1): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415176 | ||||||
| chr2:47415176
|
G | GT | 41 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0021others(38): Show | 41 | HG00438.hp2 HG00741.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.942+781dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415176 | |||||
| chr2:47415176
|
G | GTT | 6 | a0001c0001t0001g0051a0001c0001t0001g0126a0001c0001t0001g0191others(3): Show | 6 | HG00735.hp2 HG01261.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.942+780_942+781dup others(2): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415176 | |||||
| chr2:47415176
|
GT | G | 38 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 38 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.942+781delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415176 | |||||
| chr2:47415176
|
GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.942+770_942+781del others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415176 | |||||
| chr2:47415177
|
T | A | 8 | a0001c0001t0001g0313a0001c0001t0001g0325a0001c0001t0001g0326others(5): Show | 8 | HG01175.hp2 NA18957.hp2 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.942+759T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415177 | ||||||
| chr2:47415179
|
T | C | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.942+761T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415179 | ||||||
| chr2:47415211
|
A | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.942+793A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415211 | ||||||
| chr2:47415288
|
A | G | 4 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+870A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415288 | ||||||
| chr2:47415337
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.942+919A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415337 | ||||||
| chr2:47415339
|
G | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18953.hp1 NA18964.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.942+921G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415339 | ||||||
| chr2:47415372
|
C | CT | 6 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(3): Show | 6 | HG01515.hp1 HG01993.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-909dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415372 | |||||
| chr2:47415372
|
C | CTTTTT | 50 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0200others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.943-913_943-909dup others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415372 | |||||
| chr2:47415372
|
CT | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(6): Show | 9 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.943-909delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415372 | |||||
| chr2:47415456
|
A | AT | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 71 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.943-818dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415456 | |||||
| chr2:47415456
|
A | ATT | 94 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0017others(91): Show | 94 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.943-819_943-818dup others(2): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415456 | |||||
| chr2:47415456
|
A | ATTT | 113 | a0001c0001t0001g0040a0001c0001t0001g0087a0001c0001t0001g0098others(110): Show | 113 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.943-820_943-818dup others(3): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415456 | |||||
| chr2:47415456
|
A | ATTTT | 14 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0143others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.943-821_943-818dup others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 47415456 | |||||
| chr2:47415484
|
G | A | 8 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(5): Show | 8 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-812G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415484 | ||||||
| chr2:47415511
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.943-785G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415511 | ||||||
| chr2:47415556
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.943-740G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415556 | ||||||
| chr2:47415585
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.943-711G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415585 | ||||||
| chr2:47415607
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.943-689T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415607 | ||||||
| chr2:47415720
|
A | C | 3 | a0001c0004t0001g0045a0001c0004t0001g0046a0001c0004t0001g0047 | 3 | NA18969.hp1 NA19063.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.943-576A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415720 | ||||||
| chr2:47415780
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.943-516G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415780 | ||||||
| chr2:47415794
|
GACGTGGC others(18): Show |
G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-501_943-477del others(25): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415794 | ||||||
| chr2:47415820
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.943-476C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415820 | ||||||
| chr2:47415880
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.943-416A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415880 | ||||||
| chr2:47415951
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.943-345C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415951 | ||||||
| chr2:47415957
|
G | A | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-339G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47415957 | ||||||
| chr2:47416052
|
C | G | 279 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.943-244C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47416052 | ||||||
| chr2:47416135
|
C | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.943-161C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47416135 | ||||||
| chr2:47416136
|
G | A | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.943-160G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 5/15 | chr2 | 47416136 | ||||||
| chr2:47416593
|
AT | A | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+171delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47416593 | |||||
| chr2:47416607
|
GT | G | 66 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(63): Show | 66 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1076+190delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47416607 | |||||
| chr2:47416634
|
A | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+205A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47416634 | ||||||
| chr2:47416718
|
C | T | 1 | a0009c0016t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1076+289C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47416718 | ||||||
| chr2:47416744
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1076+315A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47416744 | ||||||
| chr2:47416940
|
A | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1076+511A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47416940 | ||||||
| chr2:47417007
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1076+578C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417007 | ||||||
| chr2:47417008
|
G | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | NA18941.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1076+579G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417008 | ||||||
| chr2:47417151
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1076+722G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417151 | ||||||
| chr2:47417172
|
C | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1076+743C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417172 | ||||||
| chr2:47417270
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1076+841C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417270 | ||||||
| chr2:47417271
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1076+842G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417271 | ||||||
| chr2:47417435
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1076+1006A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417435 | ||||||
| chr2:47417486
|
G | C | 9 | a0001c0001t0001g0125a0001c0001t0001g0308a0001c0001t0001g0309others(6): Show | 9 | HG00738.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076+1057G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417486 | ||||||
| chr2:47417561
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1076+1132C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417561 | ||||||
| chr2:47417705
|
A | G | 55 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0285others(52): Show | 55 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076+1276A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417705 | ||||||
| chr2:47417788
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1076+1359A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417788 | ||||||
| chr2:47417878
|
A | C | 55 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0285others(52): Show | 55 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076+1449A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47417878 | ||||||
| chr2:47418110
|
G | T | 276 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(273): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1076+1681G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418110 | ||||||
| chr2:47418132
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0013 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+1703C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418132 | ||||||
| chr2:47418146
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1076+1717T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418146 | ||||||
| chr2:47418347
|
C | G | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1076+1918C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418347 | ||||||
| chr2:47418510
|
G | A | 11 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(8): Show | 11 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1076+2081G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418510 | ||||||
| chr2:47418737
|
A | G | 1 | a0001c0001t0001g0355 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1076+2308A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418737 | ||||||
| chr2:47418767
|
A | G | 1 | a0001c0001t0001g0248 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1076+2338A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418767 | ||||||
| chr2:47418806
|
T | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1076+2377T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418806 | ||||||
| chr2:47418879
|
G | C | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(8): Show | 11 | HG02257.hp2 HG02615.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1076+2450G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418879 | ||||||
| chr2:47418935
|
G | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG02895.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1076+2506G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418935 | ||||||
| chr2:47418993
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1076+2564T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47418993 | ||||||
| chr2:47419007
|
G | C | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1076+2578G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419007 | ||||||
| chr2:47419011
|
C | A | 1 | a0001c0001t0001g0286 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1076+2582C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419011 | ||||||
| chr2:47419086
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1076+2657C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419086 | ||||||
| chr2:47419142
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1076+2713G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419142 | ||||||
| chr2:47419418
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1076+2989C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419418 | ||||||
| chr2:47419444
|
G | T | 1 | a0001c0001t0001g0037 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1076+3015G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419444 | ||||||
| chr2:47419460
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1076+3031C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419460 | ||||||
| chr2:47419474
|
C | G | 1 | a0001c0001t0001g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1076+3045C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419474 | ||||||
| chr2:47419536
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004 | 3 | HG02895.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1076+3107C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419536 | ||||||
| chr2:47419542
|
T | C | 25 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0146others(22): Show | 25 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.1076+3113T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419542 | ||||||
| chr2:47419543
|
C | G | 51 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0136others(48): Show | 51 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1076+3114C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419543 | ||||||
| chr2:47419610
|
C | CT | 50 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0229others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1076+3193dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47419610 | |||||
| chr2:47419610
|
CT | C | 9 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(6): Show | 9 | HG02559.hp1 HG02622.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076+3193delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47419610 | |||||
| chr2:47419636
|
T | A | 1 | a0002c0003t0001g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1076+3207T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419636 | ||||||
| chr2:47419755
|
C | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(97): Show | 100 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1076+3326C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419755 | ||||||
| chr2:47419766
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0276 | 2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1076+3337C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419766 | ||||||
| chr2:47419829
|
C | T | 63 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0225others(60): Show | 63 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1076+3400C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47419829 | ||||||
| chr2:47420002
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1076+3573C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420002 | ||||||
| chr2:47420168
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+3739G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420168 | ||||||
| chr2:47420390
|
A | G | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1076+3961A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420390 | ||||||
| chr2:47420407
|
C | A | 1 | a0001c0001t0001g0343 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1076+3978C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420407 | ||||||
| chr2:47420489
|
C | T | 5 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(2): Show | 5 | HG01515.hp1 HG01993.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+4060C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420489 | ||||||
| chr2:47420598
|
A | C | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4169A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420598 | ||||||
| chr2:47420640
|
T | G | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1076+4211T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420640 | ||||||
| chr2:47420699
|
C | T | 11 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(8): Show | 11 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.1076+4270C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420699 | ||||||
| chr2:47420737
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0013 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+4308C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420737 | ||||||
| chr2:47420759
|
C | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1076+4330C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420759 | ||||||
| chr2:47420838
|
G | A | 289 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1076+4409G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420838 | ||||||
| chr2:47420901
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1076+4472C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420901 | ||||||
| chr2:47420951
|
G | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+4522G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47420951 | ||||||
| chr2:47421167
|
C | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4738C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421167 | ||||||
| chr2:47421196
|
C | T | 5 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+4767C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421196 | ||||||
| chr2:47421209
|
G | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4780G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421209 | ||||||
| chr2:47421225
|
C | CA | 85 | a0001c0001t0001g0015a0001c0001t0001g0020a0001c0001t0001g0044others(82): Show | 85 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1076+4819dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421225 | |||||
| chr2:47421225
|
C | CAA | 21 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 21 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1076+4818_1076+481 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421225 | |||||
| chr2:47421225
|
C | CAAAAA | 34 | a0001c0001t0001g0120a0001c0001t0001g0285a0001c0001t0001g0286others(31): Show | 34 | HG00408.hp2 HG01346.hp1 HG02015.hp1 others(31): Show |
intron_variant | MODIFIER | c.1076+4815_1076+481 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421225 | |||||
| chr2:47421225
|
C | CAAAAAA | 10 | a0001c0001t0001g0296a0001c0001t0001g0318a0001c0001t0001g0330others(7): Show | 10 | HG00609.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076+4814_1076+481 others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421225 | |||||
| chr2:47421225
|
CA | C | 23 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(20): Show | 23 | HG01168.hp1 HG01358.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1076+4819delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421225 | |||||
| chr2:47421225
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0115others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4812_1076+481 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421225 | |||||
| chr2:47421264
|
C | CT | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+4837dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47421264 | |||||
| chr2:47421264
|
C | T | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1076+4835C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421264 | ||||||
| chr2:47421271
|
A | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(1): Show | 4 | HG01175.hp1 HG02683.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+4842A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421271 | ||||||
| chr2:47421373
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1076+4944G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421373 | ||||||
| chr2:47421383
|
C | T | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1076+4954C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421383 | ||||||
| chr2:47421415
|
G | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4986G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421415 | ||||||
| chr2:47421693
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1076+5264C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421693 | ||||||
| chr2:47421696
|
A | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1076+5267A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421696 | ||||||
| chr2:47421825
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1076+5396C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421825 | ||||||
| chr2:47421916
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1076+5487C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421916 | ||||||
| chr2:47421923
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1076+5494C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421923 | ||||||
| chr2:47421938
|
A | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1076+5509A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421938 | ||||||
| chr2:47421942
|
A | T | 10 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(7): Show | 10 | HG01884.hp1 HG02145.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1076+5513A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47421942 | ||||||
| chr2:47422010
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1076+5581G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422010 | ||||||
| chr2:47422040
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1076+5611A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422040 | ||||||
| chr2:47422045
|
A | AACCT | 36 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0017others(33): Show | 36 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.1076+5638_1076+564 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47422045 | |||||
| chr2:47422063
|
CCTACCTA others(5): Show |
C | 1 | a0001c0001t0001g0301 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1076+5638_1076+564 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47422063 | |||||
| chr2:47422176
|
C | G | 46 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1076+5747C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422176 | ||||||
| chr2:47422179
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1076+5750G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422179 | ||||||
| chr2:47422214
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1076+5785G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422214 | ||||||
| chr2:47422227
|
G | C | 1 | a0001c0001t0001g0310 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1076+5798G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422227 | ||||||
| chr2:47422229
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1076+5800G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422229 | ||||||
| chr2:47422230
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1076+5801T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422230 | ||||||
| chr2:47422250
|
A | G | 50 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0285others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1076+5821A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422250 | ||||||
| chr2:47422263
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1076+5834C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422263 | ||||||
| chr2:47422295
|
AAG | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+5869_1076+587 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47422295 | |||||
| chr2:47422374
|
C | G | 9 | a0001c0001t0001g0125a0001c0001t0001g0368a0001c0001t0002g0170others(6): Show | 9 | HG00738.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076+5945C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422374 | ||||||
| chr2:47422434
|
G | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+6005G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422434 | ||||||
| chr2:47422447
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+6018C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422447 | ||||||
| chr2:47422457
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1076+6028C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422457 | ||||||
| chr2:47422465
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1076+6036C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422465 | ||||||
| chr2:47422483
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1076+6054C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422483 | ||||||
| chr2:47422518
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1076+6089C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422518 | ||||||
| chr2:47422642
|
T | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0146a0001c0001t0001g0151others(2): Show | 5 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+6213T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422642 | ||||||
| chr2:47422650
|
CA | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(95): Show | 98 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1076+6233delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47422650 | |||||
| chr2:47422708
|
A | G | 6 | a0001c0001t0002g0170a0001c0001t0002g0258a0001c0007t0001g0101others(3): Show | 6 | HG00738.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+6279A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422708 | ||||||
| chr2:47422745
|
A | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+6316A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422745 | ||||||
| chr2:47422974
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1076+6545T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47422974 | ||||||
| chr2:47423085
|
G | A | 5 | a0001c0001t0001g0240a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | NA18966.hp2 NA18983.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+6656G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423085 | ||||||
| chr2:47423105
|
C | A | 45 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1077-6637C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423105 | ||||||
| chr2:47423141
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1077-6601C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423141 | ||||||
| chr2:47423150
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1077-6592G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423150 | ||||||
| chr2:47423150
|
G | C | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1077-6592G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423150 | ||||||
| chr2:47423171
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1077-6571G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423171 | ||||||
| chr2:47423248
|
C | A | 3 | a0003c0005t0001g0173a0003c0005t0001g0221a0003c0005t0001g0247 | 3 | HG02132.hp2 NA18951.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1077-6494C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423248 | ||||||
| chr2:47423264
|
C | A | 49 | a0001c0001t0001g0104a0001c0001t0001g0120a0001c0001t0001g0285others(46): Show | 49 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1077-6478C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423264 | ||||||
| chr2:47423278
|
T | G | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1077-6464T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423278 | ||||||
| chr2:47423321
|
T | A | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1077-6421T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423321 | ||||||
| chr2:47423343
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1077-6399C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423343 | ||||||
| chr2:47423347
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1077-6395C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423347 | ||||||
| chr2:47423353
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-6389G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423353 | ||||||
| chr2:47423562
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077-6180C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423562 | ||||||
| chr2:47423563
|
T | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-6179T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423563 | ||||||
| chr2:47423570
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077-6172C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423570 | ||||||
| chr2:47423571
|
C | A | 1 | a0001c0001t0001g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1077-6171C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423571 | ||||||
| chr2:47423794
|
A | G | 38 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(35): Show | 38 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1077-5948A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423794 | ||||||
| chr2:47423861
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1077-5881G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423861 | ||||||
| chr2:47423911
|
G | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077-5831G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423911 | ||||||
| chr2:47423955
|
A | T | 1 | a0001c0001t0001g0132 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1077-5787A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423955 | ||||||
| chr2:47423976
|
A | G | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1077-5766A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47423976 | ||||||
| chr2:47424109
|
T | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1077-5633T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424109 | ||||||
| chr2:47424142
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1077-5600G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424142 | ||||||
| chr2:47424244
|
C | A | 1 | a0001c0001t0001g0303 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1077-5498C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424244 | ||||||
| chr2:47424340
|
C | T | 1 | a0010c0018t0001g0339 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1077-5402C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424340 | ||||||
| chr2:47424366
|
G | A | 2 | a0004c0010t0001g0350a0004c0010t0001g0351 | 2 | NA18992.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1077-5376G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424366 | ||||||
| chr2:47424429
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1077-5313G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424429 | ||||||
| chr2:47424447
|
G | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1077-5295G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424447 | ||||||
| chr2:47424502
|
ATTACAGG others(20): Show |
A | 1 | a0001c0001t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1077-5236_1077-521 others(31): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47424502 | |||||
| chr2:47424647
|
G | C | 20 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(17): Show | 20 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1077-5095G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424647 | ||||||
| chr2:47424661
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1077-5081G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424661 | ||||||
| chr2:47424690
|
A | G | 3 | a0003c0005t0001g0173a0003c0005t0001g0221a0003c0005t0001g0247 | 3 | HG02132.hp2 NA18951.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1077-5052A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424690 | ||||||
| chr2:47424728
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1077-5014T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424728 | ||||||
| chr2:47424751
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077-4991A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424751 | ||||||
| chr2:47424797
|
C | G | 4 | a0001c0001t0001g0313a0001c0001t0001g0329a0001c0001t0001g0344others(1): Show | 4 | HG01175.hp2 NA18957.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-4945C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424797 | ||||||
| chr2:47424892
|
CA | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1077-4837delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47424892 | |||||
| chr2:47424999
|
CCTT | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1077-4742_1077-474 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47424999 | ||||||
| chr2:47425101
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077-4641A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425101 | ||||||
| chr2:47425175
|
A | C | 38 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(35): Show | 38 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1077-4567A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425175 | ||||||
| chr2:47425281
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1077-4461C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425281 | ||||||
| chr2:47425316
|
C | T | 36 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0146others(33): Show | 36 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1077-4426C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425316 | ||||||
| chr2:47425351
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077-4391A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425351 | ||||||
| chr2:47425431
|
G | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(34): Show | 37 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1077-4311G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425431 | ||||||
| chr2:47425447
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0368 | 2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1077-4295A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425447 | ||||||
| chr2:47425458
|
A | G | 7 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0115others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077-4284A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425458 | ||||||
| chr2:47425636
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1077-4106C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425636 | ||||||
| chr2:47425695
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1077-4047C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425695 | ||||||
| chr2:47425704
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1077-4038C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425704 | ||||||
| chr2:47425796
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1077-3946A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425796 | ||||||
| chr2:47425837
|
GTTTT | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1077-3891_1077-388 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47425837 | |||||
| chr2:47425858
|
A | C | 67 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1077-3884A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425858 | ||||||
| chr2:47425926
|
T | C | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-3816T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425926 | ||||||
| chr2:47425986
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1077-3756G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47425986 | ||||||
| chr2:47426076
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1077-3666G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426076 | ||||||
| chr2:47426141
|
T | TA | 23 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0093others(20): Show | 23 | HG00423.hp1 HG00597.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1077-3599dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47426141 | |||||
| chr2:47426143
|
A | AAT | 7 | a0001c0001t0001g0360a0001c0001t0001g0362a0001c0001t0001g0363others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077-3599_1077-359 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426143 | ||||||
| chr2:47426143
|
A | AATTT | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-3599_1077-359 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426143 | ||||||
| chr2:47426143
|
AT | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 63 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1077-3577delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47426143 | |||||
| chr2:47426144
|
T | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1077-3598T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426144 | ||||||
| chr2:47426145
|
T | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0249a0002c0003t0001g0106 | 3 | HG01515.hp2 HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1077-3597T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426145 | ||||||
| chr2:47426217
|
G | A | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02698.hp1 NA18992.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1077-3525G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426217 | ||||||
| chr2:47426217
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077-3525G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426217 | ||||||
| chr2:47426221
|
T | C | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1077-3521T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426221 | ||||||
| chr2:47426249
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1077-3493G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426249 | ||||||
| chr2:47426254
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1077-3488T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426254 | ||||||
| chr2:47426293
|
A | C | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1077-3449A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426293 | ||||||
| chr2:47426304
|
T | A | 1 | a0001c0001t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1077-3438T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426304 | ||||||
| chr2:47426334
|
C | T | 11 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(8): Show | 11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1077-3408C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426334 | ||||||
| chr2:47426360
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1077-3382G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426360 | ||||||
| chr2:47426466
|
A | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1077-3276A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426466 | ||||||
| chr2:47426506
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1077-3236C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426506 | ||||||
| chr2:47426519
|
T | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG02083.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1077-3223T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426519 | ||||||
| chr2:47426530
|
C | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 17 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1077-3212C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426530 | ||||||
| chr2:47426561
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077-3181C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426561 | ||||||
| chr2:47426571
|
CA | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077-3170delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426571 | ||||||
| chr2:47426917
|
GATGTTTG others(72): Show |
G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1077-2744_1077-266 others(83): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47426917 | |||||
| chr2:47426993
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1077-2749A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47426993 | ||||||
| chr2:47427194
|
A | G | 94 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1077-2548A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427194 | ||||||
| chr2:47427291
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1077-2451G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427291 | ||||||
| chr2:47427400
|
G | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1077-2342G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427400 | ||||||
| chr2:47427437
|
A | G | 1 | a0002c0003t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1077-2305A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427437 | ||||||
| chr2:47427524
|
T | C | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1077-2218T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427524 | ||||||
| chr2:47427551
|
T | G | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1077-2191T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427551 | ||||||
| chr2:47427646
|
G | T | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1077-2096G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427646 | ||||||
| chr2:47427700
|
G | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1077-2042G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427700 | ||||||
| chr2:47427705
|
G | T | 5 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-2037G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427705 | ||||||
| chr2:47427955
|
A | C | 6 | a0001c0001t0002g0170a0001c0001t0002g0258a0001c0007t0001g0101others(3): Show | 6 | HG00738.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-1787A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47427955 | ||||||
| chr2:47428004
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1077-1738G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428004 | ||||||
| chr2:47428105
|
TGGCAGGT others(9): Show |
T | 1 | a0001c0002t0001g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077-1620_1077-160 others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47428105 | |||||
| chr2:47428158
|
G | T | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1077-1584G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428158 | ||||||
| chr2:47428191
|
A | T | 1 | a0001c0001t0001g0320 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1077-1551A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428191 | ||||||
| chr2:47428224
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1077-1518G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428224 | ||||||
| chr2:47428238
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1077-1504C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428238 | ||||||
| chr2:47428327
|
A | G | 231 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1077-1415A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428327 | ||||||
| chr2:47428348
|
C | CA | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0040others(121): Show | 124 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1077-1373dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47428348 | |||||
| chr2:47428348
|
C | CAA | 7 | a0001c0001t0001g0125a0001c0001t0001g0136a0001c0001t0001g0142others(4): Show | 7 | HG00140.hp2 HG02080.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077-1374_1077-137 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47428348 | |||||
| chr2:47428348
|
CA | C | 7 | a0001c0001t0001g0036a0001c0001t0001g0050a0001c0001t0001g0089others(4): Show | 7 | HG00140.hp1 HG01069.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-1373delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47428348 | |||||
| chr2:47428348
|
CAAA | C | 13 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(10): Show | 13 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1077-1375_1077-137 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47428348 | |||||
| chr2:47428366
|
A | AG | 56 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1077-1376_1077-137 others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428366 | ||||||
| chr2:47428366
|
A | G | 5 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-1376A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428366 | ||||||
| chr2:47428374
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1077-1368G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428374 | ||||||
| chr2:47428653
|
C | G | 46 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1077-1089C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428653 | ||||||
| chr2:47428671
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077-1071T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428671 | ||||||
| chr2:47428700
|
G | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0318a0001c0001t0001g0349 | 3 | HG01258.hp2 HG02486.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1077-1042G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428700 | ||||||
| chr2:47428752
|
C | G | 1 | a0001c0004t0001g0047 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1077-990C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428752 | ||||||
| chr2:47428760
|
A | G | 94 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(91): Show | 94 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1077-982A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428760 | ||||||
| chr2:47428784
|
A | G | 93 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1077-958A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428784 | ||||||
| chr2:47428797
|
G | A | 11 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(8): Show | 11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1077-945G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47428797 | ||||||
| chr2:47429015
|
T | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(20): Show | 23 | HG00099.hp2 HG01168.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1077-727T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429015 | ||||||
| chr2:47429092
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077-650C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429092 | ||||||
| chr2:47429223
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1077-519C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429223 | ||||||
| chr2:47429227
|
T | A | 8 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(5): Show | 8 | HG00738.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077-515T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429227 | ||||||
| chr2:47429259
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-483G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429259 | ||||||
| chr2:47429266
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1077-476C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429266 | ||||||
| chr2:47429324
|
T | G | 27 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(24): Show | 27 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1077-418T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429324 | ||||||
| chr2:47429325
|
CT | C | 349 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(346): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1077-400delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47429325 | |||||
| chr2:47429325
|
CTT | C | 6 | a0001c0001t0001g0044a0001c0001t0001g0166a0001c0001t0001g0197others(3): Show | 6 | HG01167.hp2 HG03130.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-401_1077-400d others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 47429325 | |||||
| chr2:47429368
|
C | G | 8 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(5): Show | 8 | HG00738.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077-374C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429368 | ||||||
| chr2:47429483
|
G | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-259G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429483 | ||||||
| chr2:47429513
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077-229C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429513 | ||||||
| chr2:47429637
|
T | G | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1077-105T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429637 | ||||||
| chr2:47429662
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1077-80G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429662 | ||||||
| chr2:47429732
|
T | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-10T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 6/15 | chr2 | 47429732 | ||||||
| chr2:47429962
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1276+21T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47429962 | ||||||
| chr2:47429988
|
T | A | 4 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | NA18970.hp1 NA18979.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+47T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47429988 | ||||||
| chr2:47429992
|
C | A | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1276+51C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47429992 | ||||||
| chr2:47430047
|
A | T | 1 | a0001c0002t0001g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1276+106A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430047 | ||||||
| chr2:47430057
|
C | CT | 8 | a0001c0001t0001g0369a0001c0002t0001g0114a0001c0002t0001g0116others(5): Show | 8 | HG01074.hp1 HG01109.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+132dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47430057 | |||||
| chr2:47430057
|
CT | C | 33 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(30): Show | 33 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1276+132delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47430057 | |||||
| chr2:47430127
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1276+186C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430127 | ||||||
| chr2:47430128
|
T | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0083 | 3 | HG00544.hp1 NA18940.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1276+187T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430128 | ||||||
| chr2:47430324
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1276+383C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430324 | ||||||
| chr2:47430526
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1276+585C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430526 | ||||||
| chr2:47430545
|
G | A | 35 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(32): Show | 35 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1276+604G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430545 | ||||||
| chr2:47430576
|
A | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(19): Show | 22 | HG00099.hp2 HG00738.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1276+635A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430576 | ||||||
| chr2:47430711
|
TTCTC | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276+775_1276+778d others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47430711 | |||||
| chr2:47430760
|
C | T | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1276+819C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430760 | ||||||
| chr2:47430808
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1276+867G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430808 | ||||||
| chr2:47430850
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1276+909A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430850 | ||||||
| chr2:47430952
|
A | G | 29 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(26): Show | 29 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1276+1011A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47430952 | ||||||
| chr2:47431085
|
A | G | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+1144A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431085 | ||||||
| chr2:47431121
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+1180A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431121 | ||||||
| chr2:47431127
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+1186A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431127 | ||||||
| chr2:47431285
|
T | TTTTTATA others(8): Show |
1 | a0001c0001t0001g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1276+1348_1276+134 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47431285 | |||||
| chr2:47431290
|
T | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1276+1349T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431290 | ||||||
| chr2:47431291
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1276+1350A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431291 | ||||||
| chr2:47431313
|
G | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276+1372G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431313 | ||||||
| chr2:47431326
|
TA | T | 13 | a0001c0001t0001g0044a0001c0001t0001g0225a0001c0001t0001g0226others(10): Show | 13 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1276+1394delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47431326 | |||||
| chr2:47431335
|
A | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1276+1394A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431335 | ||||||
| chr2:47431643
|
C | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+1702C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431643 | ||||||
| chr2:47431667
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1276+1726G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431667 | ||||||
| chr2:47431711
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1276+1770C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431711 | ||||||
| chr2:47431730
|
G | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+1789G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431730 | ||||||
| chr2:47431885
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1276+1944A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431885 | ||||||
| chr2:47431912
|
C | T | 12 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(9): Show | 12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276+1971C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431912 | ||||||
| chr2:47431925
|
C | CA | 15 | a0001c0001t0001g0015a0001c0001t0001g0083a0001c0001t0001g0138others(12): Show | 15 | HG00597.hp1 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1276+2004dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47431925 | |||||
| chr2:47431925
|
CA | C | 33 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG00099.hp2 HG00738.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1276+2004delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47431925 | |||||
| chr2:47431925
|
CAA | C | 8 | a0001c0001t0001g0226a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+2003_1276+200 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47431925 | |||||
| chr2:47431925
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(7): Show | 10 | HG02257.hp2 HG02615.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1276+1997_1276+200 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47431925 | |||||
| chr2:47431936
|
A | G | 2 | a0001c0001t0001g0334a0001c0001t0001g0341 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1276+1995A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431936 | ||||||
| chr2:47431945
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1276+2004A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431945 | ||||||
| chr2:47431945
|
AG | A | 125 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1276+2005delG | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431945 | ||||||
| chr2:47431946
|
G | A | 66 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0126others(63): Show | 66 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1276+2005G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431946 | ||||||
| chr2:47431948
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276+2007A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47431948 | ||||||
| chr2:47432105
|
C | T | 1 | a0001c0001t0001g0354 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1276+2164C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432105 | ||||||
| chr2:47432119
|
G | T | 7 | a0001c0001t0001g0295a0001c0001t0001g0319a0001c0001t0001g0320others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+2178G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432119 | ||||||
| chr2:47432174
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1276+2233C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432174 | ||||||
| chr2:47432205
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1276+2264G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432205 | ||||||
| chr2:47432285
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+2344T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432285 | ||||||
| chr2:47432321
|
A | T | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1276+2380A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432321 | ||||||
| chr2:47432326
|
C | T | 1 | a0010c0018t0001g0339 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1276+2385C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432326 | ||||||
| chr2:47432389
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1276+2448C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432389 | ||||||
| chr2:47432390
|
G | A | 1 | a0001c0014t0001g0224 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1276+2449G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432390 | ||||||
| chr2:47432395
|
C | CTTTG | 137 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0017others(134): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1276+2486_1276+248 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47432395 | |||||
| chr2:47432395
|
C | CTTTGTTT others(1): Show |
5 | a0001c0001t0001g0013a0001c0001t0001g0206a0001c0001t0001g0237others(2): Show | 5 | HG00140.hp2 HG03516.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+2482_1276+248 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47432395 | |||||
| chr2:47432395
|
CTTTG | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(33): Show | 36 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1276+2486_1276+248 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47432395 | |||||
| chr2:47432395
|
CTTTGTTT others(5): Show |
C | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | NA18970.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1276+2478_1276+248 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47432395 | |||||
| chr2:47432437
|
G | C | 3 | a0001c0001t0001g0206a0005c0008t0001g0211a0005c0008t0001g0212 | 3 | HG00140.hp2 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1276+2496G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432437 | ||||||
| chr2:47432568
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0086 | 2 | HG04204.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1276+2627G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432568 | ||||||
| chr2:47432626
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1276+2685G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432626 | ||||||
| chr2:47432631
|
G | T | 12 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(9): Show | 12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276+2690G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432631 | ||||||
| chr2:47432669
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1276+2728A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432669 | ||||||
| chr2:47432680
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1276+2739G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432680 | ||||||
| chr2:47432683
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1276+2742C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432683 | ||||||
| chr2:47432683
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1276+2742C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432683 | ||||||
| chr2:47432814
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1276+2873C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432814 | ||||||
| chr2:47432829
|
C | T | 14 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(11): Show | 14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1276+2888C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432829 | ||||||
| chr2:47432872
|
C | G | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(4): Show | 7 | HG00642.hp1 HG01167.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1276+2931C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432872 | ||||||
| chr2:47432935
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1276+2994C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432935 | ||||||
| chr2:47432943
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1276+3002C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432943 | ||||||
| chr2:47432955
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1276+3014C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432955 | ||||||
| chr2:47432980
|
A | G | 12 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(9): Show | 12 | HG00738.hp2 HG01109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1276+3039A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432980 | ||||||
| chr2:47432987
|
G | C | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276+3046G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47432987 | ||||||
| chr2:47433017
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+3076G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433017 | ||||||
| chr2:47433026
|
G | C | 1 | a0001c0001t0001g0183 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1276+3085G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433026 | ||||||
| chr2:47433033
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1276+3092C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433033 | ||||||
| chr2:47433038
|
G | A | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241others(1): Show | 4 | NA18941.hp1 NA19012.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1276+3097G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433038 | ||||||
| chr2:47433038
|
G | C | 1 | a0001c0001t0001g0304 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1276+3097G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433038 | ||||||
| chr2:47433047
|
A | AC | 47 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(44): Show | 47 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.1276+3118dupC | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47433047 | |||||
| chr2:47433047
|
AC | A | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1276+3118delC | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47433047 | |||||
| chr2:47433053
|
C | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1276+3112C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433053 | ||||||
| chr2:47433059
|
C | A | 1 | a0001c0001t0001g0052 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1276+3118C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433059 | ||||||
| chr2:47433060
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0264a0001c0001t0001g0368 | 3 | HG02109.hp2 NA18747.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+3119G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433060 | ||||||
| chr2:47433071
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02083.hp2 NA18982.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1276+3130G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433071 | ||||||
| chr2:47433106
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1276+3165C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433106 | ||||||
| chr2:47433120
|
G | A | 12 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(9): Show | 12 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276+3179G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433120 | ||||||
| chr2:47433144
|
G | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+3203G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433144 | ||||||
| chr2:47433157
|
G | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1276+3216G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433157 | ||||||
| chr2:47433170
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1276+3229G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433170 | ||||||
| chr2:47433179
|
G | A | 15 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(12): Show | 15 | HG00738.hp2 HG01109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1276+3238G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433179 | ||||||
| chr2:47433224
|
GGGCAGAG others(120): Show |
G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+3310_1276+343 others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47433224 | |||||
| chr2:47433234
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1276+3293G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433234 | ||||||
| chr2:47433265
|
G | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(3): Show | 6 | HG02895.hp1 HG03041.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276+3324G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433265 | ||||||
| chr2:47433290
|
G | C | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1276+3349G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433290 | ||||||
| chr2:47433322
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1276+3381C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433322 | ||||||
| chr2:47433369
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(6): Show | 9 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276+3428C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433369 | ||||||
| chr2:47433409
|
TCTTCCCA others(120): Show |
T | 1 | a0001c0001t0001g0050 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1276+3515_1276+364 others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47433409 | |||||
| chr2:47433428
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1276+3487C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433428 | ||||||
| chr2:47433469
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1276+3528C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433469 | ||||||
| chr2:47433505
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1276+3564C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433505 | ||||||
| chr2:47433529
|
T | G | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1276+3588T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433529 | ||||||
| chr2:47433551
|
C | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1276+3610C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433551 | ||||||
| chr2:47433685
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1276+3744C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433685 | ||||||
| chr2:47433738
|
T | C | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+3797T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433738 | ||||||
| chr2:47433745
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1276+3804C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433745 | ||||||
| chr2:47433746
|
G | C | 2 | a0001c0001t0001g0288a0001c0001t0001g0292 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1276+3805G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433746 | ||||||
| chr2:47433747
|
C | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1276+3806C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433747 | ||||||
| chr2:47433759
|
A | G | 1 | a0001c0001t0001g0355 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1276+3818A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433759 | ||||||
| chr2:47433772
|
AGTGGCTG others(33): Show |
A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+3871_1276+391 others(44): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47433772 | |||||
| chr2:47433781
|
C | T | 3 | a0001c0001t0001g0311a0001c0009t0001g0274a0001c0009t0001g0275 | 3 | HG02738.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1276+3840C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433781 | ||||||
| chr2:47433790
|
G | C | 34 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0132others(31): Show | 34 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1276+3849G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433790 | ||||||
| chr2:47433816
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1276+3875G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433816 | ||||||
| chr2:47433823
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(1): Show | 4 | HG00738.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+3882G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433823 | ||||||
| chr2:47433874
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1276+3933T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433874 | ||||||
| chr2:47433931
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0028 | 2 | HG01928.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.1276+3990C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47433931 | ||||||
| chr2:47434014
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1276+4073C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434014 | ||||||
| chr2:47434015
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0027 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1276+4074G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434015 | ||||||
| chr2:47434076
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1276+4135G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434076 | ||||||
| chr2:47434118
|
C | T | 1 | a0001c0001t0001g0285 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1276+4177C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434118 | ||||||
| chr2:47434126
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+4185C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434126 | ||||||
| chr2:47434210
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1276+4269C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434210 | ||||||
| chr2:47434299
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+4358G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434299 | ||||||
| chr2:47434315
|
G | T | 1 | a0001c0001t0001g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1276+4374G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434315 | ||||||
| chr2:47434324
|
G | C | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1276+4383G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434324 | ||||||
| chr2:47434371
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1276+4430C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434371 | ||||||
| chr2:47434372
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1276+4431C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434372 | ||||||
| chr2:47434396
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1276+4455C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434396 | ||||||
| chr2:47434414
|
C | G | 2 | a0002c0003t0001g0109a0002c0003t0001g0110 | 2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1276+4473C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434414 | ||||||
| chr2:47434505
|
G | A | 8 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(5): Show | 8 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1276+4564G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434505 | ||||||
| chr2:47434523
|
A | AGGGAGAG others(10): Show |
229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1276+4595_1276+461 others(21): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47434523 | |||||
| chr2:47434523
|
A | AGGGAGAG others(27): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0267 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1276+4611_1276+461 others(38): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47434523 | |||||
| chr2:47434532
|
G | A | 1 | a0001c0001t0001g0353 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1276+4591G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434532 | ||||||
| chr2:47434552
|
A | ACC | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0228 | 3 | HG02055.hp1 HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1276+4611_1276+461 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434552 | ||||||
| chr2:47434554
|
G | T | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0228 | 3 | HG02055.hp1 HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1276+4613G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434554 | ||||||
| chr2:47434555
|
A | G | 3 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0228 | 3 | HG02055.hp1 HG02145.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1276+4614A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434555 | ||||||
| chr2:47434667
|
C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1276+4726C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434667 | ||||||
| chr2:47434683
|
C | T | 5 | a0001c0001t0001g0240a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | NA18966.hp2 NA18983.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276+4742C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434683 | ||||||
| chr2:47434684
|
A | T | 5 | a0001c0001t0001g0240a0001c0001t0001g0260a0001c0001t0001g0261others(2): Show | 5 | NA18966.hp2 NA18983.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276+4743A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434684 | ||||||
| chr2:47434692
|
A | T | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1276+4751A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434692 | ||||||
| chr2:47434716
|
T | C | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1276+4775T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434716 | ||||||
| chr2:47434905
|
C | A | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1276+4964C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434905 | ||||||
| chr2:47434913
|
TA | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+4978delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47434913 | |||||
| chr2:47434920
|
G | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+4979G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47434920 | ||||||
| chr2:47435000
|
G | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+5059G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435000 | ||||||
| chr2:47435019
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1276+5078C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435019 | ||||||
| chr2:47435032
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+5091A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435032 | ||||||
| chr2:47435094
|
T | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1276+5153T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435094 | ||||||
| chr2:47435095
|
T | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1276+5154T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435095 | ||||||
| chr2:47435124
|
C | T | 6 | a0001c0001t0001g0313a0001c0001t0001g0344a0001c0001t0001g0352others(3): Show | 6 | HG01168.hp1 HG01175.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276+5183C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435124 | ||||||
| chr2:47435125
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1276+5184C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435125 | ||||||
| chr2:47435138
|
C | CT | 21 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0125others(18): Show | 21 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1276+5210dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435138 | |||||
| chr2:47435138
|
CT | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0264a0001c0001t0001g0289others(5): Show | 8 | HG01074.hp1 HG01515.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276+5210delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435138 | |||||
| chr2:47435145
|
TTTTTTTG | T | 11 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(8): Show | 11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1276+5225_1276+523 others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435145 | |||||
| chr2:47435226
|
G | T | 5 | a0001c0001t0001g0120a0001c0001t0001g0296a0001c0001t0001g0323others(2): Show | 5 | NA18952.hp1 NA18970.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1276+5285G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435226 | ||||||
| chr2:47435233
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(25): Show | 28 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1276+5292G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435233 | ||||||
| chr2:47435239
|
C | G | 4 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(1): Show | 4 | HG00738.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+5298C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435239 | ||||||
| chr2:47435241
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1276+5300A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435241 | ||||||
| chr2:47435373
|
T | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0368a0001c0001t0001g0369 | 3 | HG01074.hp1 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+5432T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435373 | ||||||
| chr2:47435502
|
C | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1276+5561C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435502 | ||||||
| chr2:47435511
|
C | CT | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1276+5596dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
C | CTT | 76 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 76 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1276+5595_1276+559 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
C | CTTT | 44 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0087others(41): Show | 44 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1276+5594_1276+559 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
C | CTTTT | 9 | a0001c0001t0001g0012a0001c0001t0001g0242a0001c0001t0001g0261others(6): Show | 9 | HG00438.hp1 HG02027.hp2 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276+5593_1276+559 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
CT | C | 23 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0033others(20): Show | 23 | HG01361.hp1 HG02015.hp1 HG03492.hp2 others(20): Show |
intron_variant | MODIFIER | c.1276+5596delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
CTTTTTTT | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0025others(6): Show | 9 | HG00642.hp1 HG01928.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1276+5590_1276+559 others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
CTTTTTTT others(3): Show |
C | 12 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(9): Show | 12 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1276+5587_1276+559 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435511
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0011a0001c0001t0001g0267 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1276+5585_1276+559 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47435511 | |||||
| chr2:47435589
|
A | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1276+5648A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435589 | ||||||
| chr2:47435600
|
A | T | 6 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0137others(3): Show | 6 | HG00438.hp2 HG02071.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1276+5659A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435600 | ||||||
| chr2:47435618
|
C | G | 3 | a0001c0001t0001g0267a0001c0009t0001g0274a0001c0009t0001g0275 | 3 | HG03225.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1276+5677C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435618 | ||||||
| chr2:47435647
|
G | T | 17 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1276+5706G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435647 | ||||||
| chr2:47435668
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5727C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435668 | ||||||
| chr2:47435670
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5729C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435670 | ||||||
| chr2:47435673
|
C | G | 2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1276+5732C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435673 | ||||||
| chr2:47435673
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5732C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435673 | ||||||
| chr2:47435674
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5733C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435674 | ||||||
| chr2:47435675
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5734A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435675 | ||||||
| chr2:47435679
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5738C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435679 | ||||||
| chr2:47435682
|
G | T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5741G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435682 | ||||||
| chr2:47435683
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1276+5742C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435683 | ||||||
| chr2:47435735
|
A | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0368a0001c0001t0001g0369 | 3 | HG01074.hp1 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+5794A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435735 | ||||||
| chr2:47435806
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1276+5865G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435806 | ||||||
| chr2:47435834
|
T | C | 89 | a0001c0001t0001g0040a0001c0001t0001g0112a0001c0001t0001g0119others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.1276+5893T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435834 | ||||||
| chr2:47435973
|
G | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+6032G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47435973 | ||||||
| chr2:47436061
|
T | A | 1 | a0001c0001t0001g0072 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1276+6120T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436061 | ||||||
| chr2:47436092
|
G | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+6151G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436092 | ||||||
| chr2:47436122
|
G | A | 2 | a0001c0001t0001g0361a0001c0001t0001g0363 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1276+6181G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436122 | ||||||
| chr2:47436176
|
A | T | 1 | a0001c0001t0001g0354 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1276+6235A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436176 | ||||||
| chr2:47436265
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+6324A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436265 | ||||||
| chr2:47436350
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1276+6409A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436350 | ||||||
| chr2:47436351
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0161 | 2 | NA18973.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1276+6410T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436351 | ||||||
| chr2:47436395
|
G | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1276+6454G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436395 | ||||||
| chr2:47436439
|
C | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1276+6498C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436439 | ||||||
| chr2:47436524
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+6583A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436524 | ||||||
| chr2:47436530
|
C | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+6589C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436530 | ||||||
| chr2:47436578
|
C | T | 9 | a0001c0001t0001g0125a0001c0002t0001g0005a0001c0002t0001g0113others(6): Show | 9 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1276+6637C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436578 | ||||||
| chr2:47436616
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1276+6675G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436616 | ||||||
| chr2:47436680
|
C | G | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1276+6739C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436680 | ||||||
| chr2:47436706
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1276+6765G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436706 | ||||||
| chr2:47436718
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1276+6777G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436718 | ||||||
| chr2:47436753
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1276+6812G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436753 | ||||||
| chr2:47436777
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1276+6836C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436777 | ||||||
| chr2:47436837
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1276+6896G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436837 | ||||||
| chr2:47436838
|
C | T | 1 | a0001c0001t0001g0353 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1276+6897C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436838 | ||||||
| chr2:47436899
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1276+6958A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47436899 | ||||||
| chr2:47437131
|
A | C | 1 | a0001c0001t0001g0303 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1276+7190A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437131 | ||||||
| chr2:47437223
|
C | A | 5 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(2): Show | 5 | HG00738.hp2 HG02451.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1276+7282C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437223 | ||||||
| chr2:47437280
|
T | C | 1 | a0001c0007t0001g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1276+7339T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437280 | ||||||
| chr2:47437295
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1276+7354T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437295 | ||||||
| chr2:47437419
|
C | CAAAT | 52 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(49): Show | 52 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.1276+7510_1276+751 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437419
|
C | CAAATAAA others(1): Show |
101 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0012others(98): Show | 101 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1276+7506_1276+751 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437419
|
C | CAAATAAA others(5): Show |
78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 78 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1276+7502_1276+751 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437419
|
C | CAAATAAA others(9): Show |
2 | a0001c0001t0001g0369a0002c0003t0001g0110 | 2 | HG01074.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1276+7498_1276+751 others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437419
|
CAAAT | C | 10 | a0001c0001t0001g0008a0001c0001t0001g0104a0001c0001t0001g0184others(7): Show | 10 | HG00597.hp1 HG01258.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1276+7510_1276+751 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437419
|
CAAATAAA others(1): Show |
C | 6 | a0001c0001t0001g0041a0001c0001t0001g0289a0001c0001t0001g0290others(3): Show | 6 | HG01515.hp1 HG01993.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276+7506_1276+751 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437419
|
CAAATAAA others(9): Show |
C | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1276+7498_1276+751 others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47437419 | |||||
| chr2:47437488
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1276+7547G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437488 | ||||||
| chr2:47437518
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1276+7577A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437518 | ||||||
| chr2:47437556
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1276+7615A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437556 | ||||||
| chr2:47437680
|
A | G | 6 | a0001c0001t0001g0174a0001c0001t0001g0237a0001c0001t0001g0238others(3): Show | 6 | NA18941.hp1 NA18951.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1276+7739A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437680 | ||||||
| chr2:47437765
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1277-7783C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437765 | ||||||
| chr2:47437769
|
G | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1277-7779G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437769 | ||||||
| chr2:47437817
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1277-7731G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437817 | ||||||
| chr2:47437850
|
A | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-7698A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437850 | ||||||
| chr2:47437914
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1277-7634A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437914 | ||||||
| chr2:47437917
|
C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(6): Show | 9 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1277-7631C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437917 | ||||||
| chr2:47437927
|
C | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-7621C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47437927 | ||||||
| chr2:47438001
|
T | C | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-7547T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438001 | ||||||
| chr2:47438077
|
C | T | 1 | a0002c0003t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1277-7471C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438077 | ||||||
| chr2:47438109
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1277-7439C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438109 | ||||||
| chr2:47438110
|
T | G | 1 | a0001c0001t0001g0307 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1277-7438T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438110 | ||||||
| chr2:47438111
|
G | C | 1 | a0001c0001t0001g0307 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1277-7437G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438111 | ||||||
| chr2:47438123
|
C | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-7425C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438123 | ||||||
| chr2:47438132
|
T | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0223 | 3 | HG02896.hp1 NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1277-7416T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438132 | ||||||
| chr2:47438218
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1277-7330A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438218 | ||||||
| chr2:47438246
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1277-7302A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438246 | ||||||
| chr2:47438294
|
TC | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-7249delC | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47438294 | |||||
| chr2:47438397
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1277-7151A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438397 | ||||||
| chr2:47438437
|
A | G | 1 | a0002c0003t0001g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1277-7111A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438437 | ||||||
| chr2:47438480
|
T | G | 116 | a0001c0001t0001g0040a0001c0001t0001g0112a0001c0001t0001g0119others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1277-7068T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438480 | ||||||
| chr2:47438558
|
T | G | 13 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(10): Show | 13 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1277-6990T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438558 | ||||||
| chr2:47438639
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1277-6909G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438639 | ||||||
| chr2:47438651
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1277-6897C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438651 | ||||||
| chr2:47438655
|
G | A | 1 | a0001c0001t0001g0313 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1277-6893G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438655 | ||||||
| chr2:47438658
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1277-6890A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438658 | ||||||
| chr2:47438659
|
C | G | 1 | a0001c0001t0001g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1277-6889C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438659 | ||||||
| chr2:47438782
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1277-6766C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438782 | ||||||
| chr2:47438880
|
C | G | 1 | a0001c0001t0001g0314 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1277-6668C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438880 | ||||||
| chr2:47438883
|
T | C | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1277-6665T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47438883 | ||||||
| chr2:47439162
|
C | T | 1 | a0002c0003t0001g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1277-6386C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439162 | ||||||
| chr2:47439169
|
G | A | 13 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1277-6379G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439169 | ||||||
| chr2:47439223
|
C | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1277-6325C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439223 | ||||||
| chr2:47439253
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1277-6295T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439253 | ||||||
| chr2:47439275
|
G | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1277-6273G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439275 | ||||||
| chr2:47439284
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1277-6264C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439284 | ||||||
| chr2:47439298
|
C | A | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1277-6250C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439298 | ||||||
| chr2:47439318
|
T | TA | 95 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1277-6221dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47439318 | |||||
| chr2:47439339
|
A | G | 2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1277-6209A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439339 | ||||||
| chr2:47439373
|
C | G | 1 | a0001c0002t0001g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1277-6175C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439373 | ||||||
| chr2:47439379
|
G | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0154a0001c0001t0001g0157others(3): Show | 6 | HG00558.hp1 NA18973.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1277-6169G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439379 | ||||||
| chr2:47439480
|
C | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-6068C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439480 | ||||||
| chr2:47439485
|
C | CA | 15 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | HG00099.hp2 HG01168.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1277-6048dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47439485 | |||||
| chr2:47439495
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(204): Show | 207 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1277-6053A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439495 | ||||||
| chr2:47439513
|
G | T | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1277-6035G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439513 | ||||||
| chr2:47439531
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1277-6017C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439531 | ||||||
| chr2:47439583
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1277-5965A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439583 | ||||||
| chr2:47439652
|
C | G | 1 | a0002c0003t0001g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1277-5896C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439652 | ||||||
| chr2:47439699
|
T | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(27): Show | 30 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1277-5849T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439699 | ||||||
| chr2:47439921
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-5627G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439921 | ||||||
| chr2:47439947
|
A | C | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1277-5601A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439947 | ||||||
| chr2:47439988
|
G | C | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1277-5560G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47439988 | ||||||
| chr2:47440090
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1277-5458G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440090 | ||||||
| chr2:47440166
|
C | A | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1277-5382C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440166 | ||||||
| chr2:47440166
|
C | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-5382C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440166 | ||||||
| chr2:47440198
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1277-5350T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440198 | ||||||
| chr2:47440270
|
A | G | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1277-5278A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440270 | ||||||
| chr2:47440299
|
C | CT | 11 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0067others(8): Show | 11 | HG00423.hp2 HG01081.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1277-5231dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47440299 | |||||
| chr2:47440299
|
CT | C | 37 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(34): Show | 37 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1277-5231delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47440299 | |||||
| chr2:47440322
|
C | T | 1 | a0001c0004t0001g0047 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1277-5226C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440322 | ||||||
| chr2:47440363
|
G | C | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1277-5185G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440363 | ||||||
| chr2:47440364
|
A | T | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1277-5184A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440364 | ||||||
| chr2:47440427
|
C | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0278a0001c0001t0001g0281 | 3 | HG01884.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1277-5121C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440427 | ||||||
| chr2:47440537
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1277-5011C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440537 | ||||||
| chr2:47440576
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 2 | HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1277-4972A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440576 | ||||||
| chr2:47440600
|
C | T | 3 | a0002c0003t0001g0233a0002c0003t0001g0252a0002c0003t0001g0257 | 3 | HG02109.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1277-4948C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440600 | ||||||
| chr2:47440832
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18953.hp1 NA18964.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1277-4716C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440832 | ||||||
| chr2:47440854
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1277-4694T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440854 | ||||||
| chr2:47440959
|
G | A | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1277-4589G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440959 | ||||||
| chr2:47440961
|
C | T | 1 | a0001c0001t0001g0087 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1277-4587C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440961 | ||||||
| chr2:47440990
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1277-4558G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47440990 | ||||||
| chr2:47441003
|
G | T | 1 | a0002c0003t0001g0234 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1277-4545G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441003 | ||||||
| chr2:47441094
|
C | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | NA18970.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1277-4454C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441094 | ||||||
| chr2:47441276
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1277-4272C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441276 | ||||||
| chr2:47441416
|
A | G | 8 | a0001c0002t0001g0005a0001c0002t0001g0113a0001c0002t0001g0114others(5): Show | 8 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1277-4132A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441416 | ||||||
| chr2:47441422
|
G | A | 9 | a0001c0001t0001g0264a0001c0001t0001g0360a0001c0001t0001g0361others(6): Show | 9 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1277-4126G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441422 | ||||||
| chr2:47441499
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1277-4049T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441499 | ||||||
| chr2:47441577
|
C | T | 3 | a0001c0001t0001g0311a0001c0009t0001g0274a0001c0009t0001g0275 | 3 | HG02738.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1277-3971C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441577 | ||||||
| chr2:47441601
|
C | T | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1277-3947C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441601 | ||||||
| chr2:47441610
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1277-3938C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441610 | ||||||
| chr2:47441676
|
A | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-3872A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441676 | ||||||
| chr2:47441680
|
C | G | 5 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(2): Show | 5 | HG01515.hp1 HG01993.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1277-3868C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441680 | ||||||
| chr2:47441718
|
A | AT | 22 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(19): Show | 22 | HG00099.hp2 HG00738.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1277-3811dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47441718 | |||||
| chr2:47441718
|
A | ATT | 9 | a0001c0001t0001g0125a0001c0002t0001g0005a0001c0002t0001g0113others(6): Show | 9 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1277-3812_1277-381 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47441718 | |||||
| chr2:47441718
|
AT | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(180): Show | 183 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1277-3811delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47441718 | |||||
| chr2:47441830
|
G | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1277-3718G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441830 | ||||||
| chr2:47441830
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1277-3718G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441830 | ||||||
| chr2:47441961
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1277-3587A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47441961 | ||||||
| chr2:47442042
|
T | TTG | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1277-3494_1277-349 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442042 | |||||
| chr2:47442114
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1277-3434G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442114 | ||||||
| chr2:47442151
|
CAT | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1277-3389_1277-338 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442151 | |||||
| chr2:47442164
|
CTATATAT others(12): Show |
C | 29 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(26): Show | 29 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1277-3367_1277-334 others(23): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442164 | |||||
| chr2:47442168
|
A | G | 3 | a0001c0002t0001g0122a0001c0002t0001g0124a0002c0003t0001g0107 | 3 | HG02486.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1277-3380A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442168 | ||||||
| chr2:47442180
|
TGTATATA others(23): Show |
T | 1 | a0001c0006t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1277-3348_1277-331 others(34): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442180 | |||||
| chr2:47442251
|
GTA | G | 191 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0028others(188): Show | 191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1277-3287_1277-328 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442251 | |||||
| chr2:47442253
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1277-3295A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442253 | ||||||
| chr2:47442287
|
T | G | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1277-3261T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442287 | ||||||
| chr2:47442290
|
GTA | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0358others(8): Show | 11 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1277-3248_1277-324 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442290 | |||||
| chr2:47442292
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1277-3256A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442292 | ||||||
| chr2:47442294
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1277-3235_1277-321 others(27): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442294 | |||||
| chr2:47442308
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1277-3240A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442308 | ||||||
| chr2:47442313
|
GTATGTAT others(1): Show |
G | 35 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(32): Show | 35 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1277-3221_1277-321 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442313 | |||||
| chr2:47442359
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1277-3189G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442359 | ||||||
| chr2:47442359
|
G | GTATATAT others(37): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1277-3182_1277-313 others(48): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442359 | |||||
| chr2:47442393
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1277-3155A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442393 | ||||||
| chr2:47442399
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1277-3149G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442399 | ||||||
| chr2:47442400
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1277-3148T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442400 | ||||||
| chr2:47442421
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-3127A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442421 | ||||||
| chr2:47442428
|
T | C | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277-3120T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442428 | ||||||
| chr2:47442474
|
C | CAT | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1277-3062_1277-306 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47442474 | |||||
| chr2:47442479
|
A | G | 1 | a0001c0006t0001g0222 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1277-3069A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442479 | ||||||
| chr2:47442613
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1277-2935T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442613 | ||||||
| chr2:47442676
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1277-2872G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442676 | ||||||
| chr2:47442896
|
A | T | 1 | a0001c0001t0001g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1277-2652A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47442896 | ||||||
| chr2:47443032
|
G | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-2516G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443032 | ||||||
| chr2:47443081
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1277-2467C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443081 | ||||||
| chr2:47443106
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1277-2442A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443106 | ||||||
| chr2:47443115
|
T | A | 1 | a0001c0001t0001g0051 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1277-2433T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443115 | ||||||
| chr2:47443139
|
T | C | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1277-2409T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443139 | ||||||
| chr2:47443165
|
G | C | 182 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0105others(179): Show | 182 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1277-2383G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443165 | ||||||
| chr2:47443188
|
C | T | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1277-2360C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443188 | ||||||
| chr2:47443213
|
G | A | 14 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1277-2335G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443213 | ||||||
| chr2:47443251
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1277-2297G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443251 | ||||||
| chr2:47443284
|
A | G | 3 | a0001c0001t0001g0267a0001c0001t0001g0287a0001c0001t0001g0312 | 3 | HG02976.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-2264A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443284 | ||||||
| chr2:47443418
|
G | A | 4 | a0001c0001t0001g0297a0001c0001t0001g0317a0001c0001t0001g0321others(1): Show | 4 | HG00408.hp2 NA18980.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-2130G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443418 | ||||||
| chr2:47443434
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-2114T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443434 | ||||||
| chr2:47443509
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(1): Show | 4 | HG00738.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-2039G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443509 | ||||||
| chr2:47443550
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1277-1998A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443550 | ||||||
| chr2:47443650
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1277-1898G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443650 | ||||||
| chr2:47443659
|
G | C | 1 | a0001c0001t0001g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1277-1889G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443659 | ||||||
| chr2:47443720
|
A | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-1828A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443720 | ||||||
| chr2:47443768
|
A | G | 4 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | NA18970.hp1 NA18979.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-1780A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443768 | ||||||
| chr2:47443815
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(1): Show | 4 | HG00738.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1277-1733G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443815 | ||||||
| chr2:47443882
|
G | T | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1277-1666G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443882 | ||||||
| chr2:47443897
|
C | CT | 10 | a0001c0001t0001g0302a0001c0001t0001g0313a0001c0001t0001g0325others(7): Show | 10 | HG01074.hp1 HG01175.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.1277-1639dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47443897 | |||||
| chr2:47443922
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1277-1626C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47443922 | ||||||
| chr2:47444353
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1277-1195C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444353 | ||||||
| chr2:47444361
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1277-1187C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444361 | ||||||
| chr2:47444426
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0040others(195): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1277-1122A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444426 | ||||||
| chr2:47444564
|
A | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1277-984A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444564 | ||||||
| chr2:47444594
|
G | C | 4 | a0001c0001t0001g0267a0001c0007t0001g0101a0001c0007t0001g0102others(1): Show | 4 | HG02559.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1277-954G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444594 | ||||||
| chr2:47444603
|
A | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1277-945A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444603 | ||||||
| chr2:47444608
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1277-940G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444608 | ||||||
| chr2:47444640
|
A | G | 1 | a0001c0001t0001g0332 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1277-908A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444640 | ||||||
| chr2:47444756
|
C | T | 1 | a0009c0016t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1277-792C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444756 | ||||||
| chr2:47444768
|
C | CT | 15 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0090others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1277-758dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47444768 | |||||
| chr2:47444768
|
C | CTTT | 14 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00099.hp2 HG01175.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1277-760_1277-758d others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47444768 | |||||
| chr2:47444768
|
C | CTTTT | 7 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(4): Show | 7 | HG00738.hp2 HG01515.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1277-761_1277-758d others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47444768 | |||||
| chr2:47444768
|
CTTTTTTT others(2): Show |
C | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1277-766_1277-758d others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47444768 | |||||
| chr2:47444768
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0167a0001c0006t0001g0128a0001c0006t0001g0222others(1): Show | 4 | HG01168.hp1 HG03834.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1277-767_1277-758d others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 47444768 | |||||
| chr2:47444787
|
T | G | 1 | a0001c0001t0001g0130 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1277-761T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444787 | ||||||
| chr2:47444927
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1277-621A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444927 | ||||||
| chr2:47444967
|
A | C | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1277-581A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444967 | ||||||
| chr2:47444997
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1277-551C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47444997 | ||||||
| chr2:47445011
|
C | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1277-537C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445011 | ||||||
| chr2:47445035
|
C | T | 1 | a0001c0002t0001g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1277-513C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445035 | ||||||
| chr2:47445062
|
G | GTCCGGC | 18 | a0001c0001t0001g0003a0001c0001t0001g0112a0001c0001t0001g0126others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1277-486_1277-485i others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445062 | ||||||
| chr2:47445063
|
A | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0112a0001c0001t0001g0126others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1277-485A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445063 | ||||||
| chr2:47445064
|
G | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0112a0001c0001t0001g0126others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1277-484G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445064 | ||||||
| chr2:47445222
|
G | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1277-326G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445222 | ||||||
| chr2:47445241
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1277-307A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445241 | ||||||
| chr2:47445309
|
C | T | 1 | a0009c0016t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1277-239C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445309 | ||||||
| chr2:47445336
|
T | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(200): Show | 203 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1277-212T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445336 | ||||||
| chr2:47445430
|
G | A | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1277-118G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445430 | ||||||
| chr2:47445481
|
A | G | 2 | a0001c0002t0001g0122a0001c0002t0001g0124 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1277-67A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445481 | ||||||
| chr2:47445540
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA21309.hp2 | splice_region_variant&intron_variant | LOW | c.1277-8T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 7/15 | chr2 | 47445540 | ||||||
| chr2:47445761
|
C | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+104C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47445761 | ||||||
| chr2:47445804
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1386+147G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47445804 | ||||||
| chr2:47445811
|
T | A | 10 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0067others(7): Show | 10 | NA18949.hp1 NA18955.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+154T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47445811 | ||||||
| chr2:47445812
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1386+155A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47445812 | ||||||
| chr2:47445819
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1386+162T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47445819 | ||||||
| chr2:47445958
|
G | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+301G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47445958 | ||||||
| chr2:47446012
|
A | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+355A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446012 | ||||||
| chr2:47446028
|
T | A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1386+371T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446028 | ||||||
| chr2:47446260
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1386+603T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446260 | ||||||
| chr2:47446265
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1386+608C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446265 | ||||||
| chr2:47446350
|
C | G | 5 | a0001c0001t0001g0296a0001c0001t0001g0323a0001c0001t0001g0330others(2): Show | 5 | NA18952.hp1 NA18970.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+693C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446350 | ||||||
| chr2:47446366
|
T | TAG | 3 | a0001c0001t0001g0264a0001c0001t0001g0309a0001c0001t0001g0368 | 3 | HG02109.hp2 HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+712_1386+713d others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47446366 | |||||
| chr2:47446376
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1386+719T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446376 | ||||||
| chr2:47446472
|
T | TTTC | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1386+817_1386+818i others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47446472 | |||||
| chr2:47446518
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1386+861T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446518 | ||||||
| chr2:47446574
|
T | A | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1386+917T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446574 | ||||||
| chr2:47446784
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1386+1127G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446784 | ||||||
| chr2:47446813
|
C | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+1156C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446813 | ||||||
| chr2:47446826
|
G | C | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1386+1169G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446826 | ||||||
| chr2:47446842
|
C | T | 5 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(2): Show | 5 | HG00733.hp2 HG01099.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+1185C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446842 | ||||||
| chr2:47446879
|
A | T | 1 | a0001c0001t0001g0314 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1386+1222A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446879 | ||||||
| chr2:47446921
|
G | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1386+1264G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47446921 | ||||||
| chr2:47447145
|
T | G | 85 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1386+1488T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447145 | ||||||
| chr2:47447162
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+1505T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447162 | ||||||
| chr2:47447165
|
C | CT | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0012others(94): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1386+1537dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
C | CTT | 62 | a0001c0001t0001g0008a0001c0001t0001g0095a0001c0001t0001g0134others(59): Show | 62 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1386+1536_1386+153 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
C | CTTT | 20 | a0001c0001t0001g0011a0001c0001t0001g0105a0001c0001t0001g0131others(17): Show | 20 | HG00423.hp1 HG02080.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1386+1535_1386+153 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
C | CTTTT | 13 | a0001c0001t0001g0133a0001c0001t0001g0139a0001c0001t0001g0140others(10): Show | 13 | HG02486.hp1 HG02630.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1386+1534_1386+153 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
C | CTTTTT | 6 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0142others(3): Show | 6 | HG02622.hp2 HG02723.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1386+1533_1386+153 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CT | C | 14 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(11): Show | 14 | HG00642.hp1 HG01167.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1386+1537delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CTT | C | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+1536_1386+153 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CTTTTTTT others(1): Show |
C | 17 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 17 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1386+1530_1386+153 others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CTTTTTTT others(3): Show |
C | 12 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0265others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1386+1528_1386+153 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0277 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1386+1527_1386+153 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1386+1525_1386+153 others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447165
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0295 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1386+1522_1386+153 others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447165 | |||||
| chr2:47447196
|
A | G | 14 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1386+1539A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447196 | ||||||
| chr2:47447234
|
A | G | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1386+1577A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447234 | ||||||
| chr2:47447392
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1386+1735G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447392 | ||||||
| chr2:47447496
|
A | G | 3 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0358 | 3 | HG03516.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1386+1839A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447496 | ||||||
| chr2:47447651
|
T | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127 | 3 | HG02145.hp2 HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1386+1994T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447651 | ||||||
| chr2:47447692
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1386+2035G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447692 | ||||||
| chr2:47447696
|
C | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1386+2039C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447696 | ||||||
| chr2:47447735
|
G | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1386+2078G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447735 | ||||||
| chr2:47447785
|
C | CT | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1386+2147dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447785 | |||||
| chr2:47447785
|
CT | C | 14 | a0001c0001t0001g0057a0001c0001t0001g0064a0001c0001t0001g0085others(11): Show | 14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1386+2147delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47447785 | |||||
| chr2:47447809
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1386+2152C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447809 | ||||||
| chr2:47447837
|
G | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0084 | 2 | NA18982.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1386+2180G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447837 | ||||||
| chr2:47447847
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(22): Show | 25 | HG00099.hp2 HG00738.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1386+2190G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447847 | ||||||
| chr2:47447988
|
A | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1386+2331A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47447988 | ||||||
| chr2:47448027
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+2370A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448027 | ||||||
| chr2:47448192
|
G | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1386+2535G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448192 | ||||||
| chr2:47448265
|
T | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+2608T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448265 | ||||||
| chr2:47448316
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1386+2659A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448316 | ||||||
| chr2:47448372
|
A | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+2715A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448372 | ||||||
| chr2:47448382
|
T | C | 2 | a0001c0001t0001g0139a0001c0001t0001g0140 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1386+2725T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448382 | ||||||
| chr2:47448385
|
C | G | 3 | a0001c0001t0001g0313a0001c0001t0001g0344a0001c0001t0001g0352 | 3 | HG01175.hp2 NA18984.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1386+2728C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448385 | ||||||
| chr2:47448515
|
T | A | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1386+2858T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448515 | ||||||
| chr2:47448689
|
C | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+3032C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448689 | ||||||
| chr2:47448784
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1386+3127A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448784 | ||||||
| chr2:47448948
|
C | CGGAG | 3 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124 | 3 | HG02486.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1386+3293_1386+329 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47448948 | |||||
| chr2:47448948
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1386+3291C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448948 | ||||||
| chr2:47448989
|
G | C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1386+3332G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47448989 | ||||||
| chr2:47449014
|
T | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+3357T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449014 | ||||||
| chr2:47449014
|
TCAAAAAA others(9): Show |
T | 26 | a0001c0001t0001g0040a0001c0001t0001g0112a0001c0001t0001g0126others(23): Show | 26 | HG00408.hp1 HG00621.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449014 | |||||
| chr2:47449015
|
C | CA | 8 | a0001c0001t0001g0002a0001c0002t0001g0114a0001c0002t0001g0116others(5): Show | 8 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+3369dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAA | 7 | a0001c0001t0001g0141a0001c0001t0001g0174a0001c0001t0001g0215others(4): Show | 7 | HG02698.hp1 HG02896.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+3365_1386+336 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAA | 11 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0217others(8): Show | 11 | HG00423.hp1 HG01168.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1386+3364_1386+336 others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA | 8 | a0001c0001t0001g0105a0001c0001t0001g0189a0001c0001t0001g0237others(5): Show | 8 | HG00438.hp1 HG00544.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+3363_1386+336 others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0261a0001c0001t0003g0262 | 2 | NA18966.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1386+3359_1386+336 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0218a0001c0001t0001g0240a0001c0001t0001g0260 | 3 | HG02015.hp2 NA18994.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1386+3369_1386+337 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1386+3369_1386+337 others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0267a0001c0001t0001g0287 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1386+3369_1386+337 others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1386+3369_1386+337 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1386+3369_1386+337 others(22): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0255 | 2 | HG00621.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1386+3369_1386+337 others(23): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0250 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1386+3369_1386+337 others(25): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0306 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1386+3369_1386+337 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1386+3369_1386+337 others(43): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
CAAAAAAA others(10): Show |
C | 72 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0129others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(21): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
CAAAAAAA others(11): Show |
C | 13 | a0001c0001t0001g0148a0001c0001t0001g0163a0001c0001t0001g0167others(10): Show | 13 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(22): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
CAAAAAAA others(12): Show |
C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(23): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449015
|
CAAAAAAA others(13): Show |
C | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449015 | |||||
| chr2:47449016
|
AAAAAAAA others(8): Show |
A | 3 | a0001c0001t0001g0282a0001c0001t0001g0302a0002c0019t0001g0253 | 3 | HG02622.hp1 HG03669.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449016 | |||||
| chr2:47449017
|
AAAAAAAA others(7): Show |
A | 6 | a0001c0001t0001g0011a0002c0003t0001g0233a0002c0003t0001g0234others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449017 | |||||
| chr2:47449018
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1386+3370_1386+338 others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449018 | |||||
| chr2:47449020
|
AAAAAAAC others(4): Show |
A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG01261.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1386+3370_1386+338 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449020 | |||||
| chr2:47449021
|
AAAAAACA others(3): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1386+3370_1386+337 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449021 | |||||
| chr2:47449024
|
AAACAAAC | A | 12 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(9): Show | 12 | HG00099.hp2 HG01074.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1386+3370_1386+337 others(11): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449024 | |||||
| chr2:47449025
|
AACAAAC | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0087others(7): Show | 10 | HG00738.hp2 HG01175.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1386+3370_1386+337 others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449025 | |||||
| chr2:47449026
|
ACAAAC | A | 3 | a0001c0002t0001g0005a0001c0007t0001g0102a0002c0003t0002g0171 | 3 | HG02717.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1386+3370_1386+337 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449026 | ||||||
| chr2:47449027
|
C | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0105others(63): Show | 66 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.1386+3370C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449027 | ||||||
| chr2:47449030
|
AC | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0314a0010c0018t0001g0339 | 3 | HG02523.hp2 HG04184.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1386+3374delC | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449030 | ||||||
| chr2:47449031
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(70): Show | 73 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1386+3374C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449031 | ||||||
| chr2:47449031
|
C | CA | 18 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0027others(15): Show | 18 | HG00423.hp2 HG01099.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+3395dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47449031 | |||||
| chr2:47449043
|
A | C | 4 | a0001c0001t0001g0125a0001c0007t0001g0101a0001c0007t0001g0102others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+3386A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449043 | ||||||
| chr2:47449078
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0039 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1386+3421T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449078 | ||||||
| chr2:47449219
|
C | G | 2 | a0001c0009t0001g0274a0001c0009t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1386+3562C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449219 | ||||||
| chr2:47449288
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1386+3631G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449288 | ||||||
| chr2:47449449
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1386+3792C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449449 | ||||||
| chr2:47449450
|
C | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1386+3793C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449450 | ||||||
| chr2:47449482
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1386+3825C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449482 | ||||||
| chr2:47449507
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1386+3850T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449507 | ||||||
| chr2:47449522
|
G | T | 1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1386+3865G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449522 | ||||||
| chr2:47449556
|
G | C | 17 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(14): Show | 17 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.1386+3899G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449556 | ||||||
| chr2:47449587
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0292 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1386+3930C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449587 | ||||||
| chr2:47449626
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1386+3969C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449626 | ||||||
| chr2:47449649
|
A | G | 1 | a0003c0005t0001g0247 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1386+3992A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449649 | ||||||
| chr2:47449694
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1386+4037A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449694 | ||||||
| chr2:47449767
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1386+4110A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449767 | ||||||
| chr2:47449837
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1386+4180C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449837 | ||||||
| chr2:47449890
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1386+4233C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449890 | ||||||
| chr2:47449997
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1386+4340C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47449997 | ||||||
| chr2:47450100
|
C | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1386+4443C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450100 | ||||||
| chr2:47450169
|
G | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0090 | 2 | NA18943.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1386+4512G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450169 | ||||||
| chr2:47450225
|
T | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+4568T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450225 | ||||||
| chr2:47450237
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+4580C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450237 | ||||||
| chr2:47450430
|
A | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1386+4773A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450430 | ||||||
| chr2:47450480
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1386+4823A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450480 | ||||||
| chr2:47450480
|
A | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1386+4823A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450480 | ||||||
| chr2:47450508
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1386+4851C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450508 | ||||||
| chr2:47450529
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1386+4872A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450529 | ||||||
| chr2:47450541
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1386+4884A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450541 | ||||||
| chr2:47450545
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(8): Show | 11 | HG00642.hp1 HG01167.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1386+4888G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450545 | ||||||
| chr2:47450575
|
C | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0236 | 3 | HG00423.hp1 HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1386+4918C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450575 | ||||||
| chr2:47450631
|
G | T | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1386+4974G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450631 | ||||||
| chr2:47450674
|
TA | T | 14 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1386+5024delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47450674 | |||||
| chr2:47450688
|
AG | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(15): Show | 18 | HG01074.hp1 HG02257.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1386+5033delG | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47450688 | |||||
| chr2:47450734
|
G | A | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1386+5077G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450734 | ||||||
| chr2:47450770
|
G | A | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1386+5113G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450770 | ||||||
| chr2:47450830
|
C | CA | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(198): Show | 201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1386+5185dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47450830 | |||||
| chr2:47450887
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+5230G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450887 | ||||||
| chr2:47450899
|
G | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+5242G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47450899 | ||||||
| chr2:47451012
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0176 | 2 | HG02074.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.1386+5355C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451012 | ||||||
| chr2:47451278
|
TTACATGG others(6): Show |
T | 38 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(35): Show | 38 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1386+5622_1386+563 others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451278 | ||||||
| chr2:47451391
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1386+5734G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451391 | ||||||
| chr2:47451411
|
C | T | 14 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(11): Show | 14 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1386+5754C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451411 | ||||||
| chr2:47451422
|
C | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1386+5765C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451422 | ||||||
| chr2:47451440
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1386+5783T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451440 | ||||||
| chr2:47451595
|
A | G | 1 | a0001c0006t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1386+5938A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451595 | ||||||
| chr2:47451632
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1386+5975C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451632 | ||||||
| chr2:47451686
|
T | TCTC | 304 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1386+6030_1386+603 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47451686 | |||||
| chr2:47451686
|
T | TTTC | 12 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(9): Show | 12 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.1386+6029_1386+603 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451686 | ||||||
| chr2:47451846
|
G | A | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1386+6189G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451846 | ||||||
| chr2:47451953
|
T | A | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1386+6296T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47451953 | ||||||
| chr2:47452213
|
C | CTTTTTTT others(4): Show |
98 | a0001c0001t0001g0105a0001c0001t0001g0129a0001c0001t0001g0130others(95): Show | 98 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.1386+6564_1386+656 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452213 | |||||
| chr2:47452213
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0119a0001c0001t0001g0160a0001c0001t0001g0229others(1): Show | 4 | HG01433.hp1 HG01981.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1386+6564_1386+656 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452213 | |||||
| chr2:47452214
|
T | TTTTC | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+6560_1386+656 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452214 | |||||
| chr2:47452217
|
T | TTTTTTCT others(4): Show |
2 | a0001c0001t0001g0187a0001c0001t0001g0197 | 2 | NA18980.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1386+6564_1386+656 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452217 | |||||
| chr2:47452222
|
C | CTTTTCTT others(3): Show |
79 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0112others(76): Show | 79 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1386+6569_1386+657 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452222 | |||||
| chr2:47452222
|
C | CTTTTTTT others(3): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(29): Show | 32 | HG00099.hp2 HG00738.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1386+6567_1386+657 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452222 | |||||
| chr2:47452222
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0098others(1): Show | 4 | HG01074.hp1 HG01358.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1386+6566_1386+657 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452222 | |||||
| chr2:47452222
|
C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+6576_1386+657 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452222 | |||||
| chr2:47452222
|
C | T | 115 | a0001c0001t0001g0105a0001c0001t0001g0119a0001c0001t0001g0129others(112): Show | 115 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.1386+6565C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452222 | ||||||
| chr2:47452233
|
T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0248 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1386+6576_1386+657 others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452233 | ||||||
| chr2:47452238
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1386+6581C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452238 | ||||||
| chr2:47452255
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1386+6598G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452255 | ||||||
| chr2:47452308
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+6651C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452308 | ||||||
| chr2:47452460
|
C | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+6803C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452460 | ||||||
| chr2:47452467
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1386+6810G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452467 | ||||||
| chr2:47452470
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1386+6813C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452470 | ||||||
| chr2:47452507
|
A | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(41): Show | 44 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1386+6850A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452507 | ||||||
| chr2:47452588
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1386+6931A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452588 | ||||||
| chr2:47452839
|
G | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1386+7182G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452839 | ||||||
| chr2:47452897
|
T | C | 12 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(9): Show | 12 | HG00738.hp2 HG01109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1386+7240T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47452897 | ||||||
| chr2:47452946
|
G | GCA | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1386+7305_1386+730 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452946 | |||||
| chr2:47452946
|
GCA | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1386+7305_1386+730 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47452946 | |||||
| chr2:47453034
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1386+7377G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453034 | ||||||
| chr2:47453257
|
G | C | 1 | a0001c0001t0001g0317 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1386+7600G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453257 | ||||||
| chr2:47453278
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1386+7621A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453278 | ||||||
| chr2:47453399
|
A | AG | 12 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(9): Show | 12 | HG00738.hp2 HG01109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1386+7747dupG | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47453399 | |||||
| chr2:47453445
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0312 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1386+7788A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453445 | ||||||
| chr2:47453551
|
G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1386+7894G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453551 | ||||||
| chr2:47453742
|
C | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(5): Show | 8 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+8085C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453742 | ||||||
| chr2:47453765
|
C | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1386+8108C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453765 | ||||||
| chr2:47453773
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1386+8116A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453773 | ||||||
| chr2:47453947
|
T | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(5): Show | 8 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+8290T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453947 | ||||||
| chr2:47453994
|
C | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(18): Show | 21 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1386+8337C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47453994 | ||||||
| chr2:47454041
|
C | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1386+8384C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454041 | ||||||
| chr2:47454171
|
GTAA | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 18 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1386+8516_1386+851 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47454171 | |||||
| chr2:47454351
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1387-8680T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454351 | ||||||
| chr2:47454370
|
A | T | 1 | a0001c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1387-8661A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454370 | ||||||
| chr2:47454384
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0294 | 2 | NA18949.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1387-8647G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454384 | ||||||
| chr2:47454428
|
C | CA | 10 | a0001c0001t0001g0038a0001c0001t0001g0188a0001c0001t0001g0244others(7): Show | 10 | HG00738.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-8586dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47454428 | |||||
| chr2:47454428
|
CA | C | 7 | a0001c0001t0001g0055a0001c0001t0001g0251a0001c0001t0001g0282others(4): Show | 7 | HG01074.hp1 HG02145.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-8586delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47454428 | |||||
| chr2:47454522
|
A | G | 5 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-8509A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454522 | ||||||
| chr2:47454644
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1387-8387C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454644 | ||||||
| chr2:47454832
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1387-8199C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454832 | ||||||
| chr2:47454950
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1387-8081C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454950 | ||||||
| chr2:47454964
|
G | A | 9 | a0001c0001t0001g0002a0001c0002t0001g0005a0001c0002t0001g0113others(6): Show | 9 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1387-8067G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47454964 | ||||||
| chr2:47455072
|
A | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(13): Show | 16 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1387-7959A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455072 | ||||||
| chr2:47455106
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1387-7925A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455106 | ||||||
| chr2:47455322
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1387-7709C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455322 | ||||||
| chr2:47455446
|
G | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-7585G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455446 | ||||||
| chr2:47455478
|
G | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1387-7553G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455478 | ||||||
| chr2:47455495
|
A | C | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-7536A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455495 | ||||||
| chr2:47455560
|
A | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-7471A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455560 | ||||||
| chr2:47455779
|
T | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-7252T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455779 | ||||||
| chr2:47455791
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1387-7240C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455791 | ||||||
| chr2:47455972
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1387-7059A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455972 | ||||||
| chr2:47455984
|
G | C | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1387-7047G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47455984 | ||||||
| chr2:47456031
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1387-7000A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456031 | ||||||
| chr2:47456082
|
G | C | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1387-6949G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456082 | ||||||
| chr2:47456099
|
T | C | 1 | a0002c0019t0001g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1387-6932T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456099 | ||||||
| chr2:47456115
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1387-6916A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456115 | ||||||
| chr2:47456121
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-6910T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456121 | ||||||
| chr2:47456122
|
G | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-6909G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456122 | ||||||
| chr2:47456292
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1387-6739G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456292 | ||||||
| chr2:47456474
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1387-6557C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456474 | ||||||
| chr2:47456501
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1387-6530C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456501 | ||||||
| chr2:47456579
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1387-6452C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456579 | ||||||
| chr2:47456636
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1387-6395A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456636 | ||||||
| chr2:47456675
|
C | T | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0236 | 3 | HG00423.hp1 HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1387-6356C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456675 | ||||||
| chr2:47456719
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1387-6312C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456719 | ||||||
| chr2:47456721
|
C | A | 6 | a0001c0001t0001g0265a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1387-6310C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456721 | ||||||
| chr2:47456791
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1387-6240A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456791 | ||||||
| chr2:47456798
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1387-6233C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456798 | ||||||
| chr2:47456817
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1387-6214G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456817 | ||||||
| chr2:47456844
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-6187G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456844 | ||||||
| chr2:47456844
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1387-6187G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456844 | ||||||
| chr2:47456904
|
A | G | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-6127A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47456904 | ||||||
| chr2:47457266
|
C | A | 1 | a0001c0001t0001g0354 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1387-5765C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457266 | ||||||
| chr2:47457453
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1387-5578G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457453 | ||||||
| chr2:47457464
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1387-5567T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457464 | ||||||
| chr2:47457471
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1387-5560G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457471 | ||||||
| chr2:47457491
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1387-5540G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457491 | ||||||
| chr2:47457561
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1387-5470C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457561 | ||||||
| chr2:47457650
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1387-5381G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457650 | ||||||
| chr2:47457715
|
T | C | 4 | a0001c0001t0001g0297a0001c0001t0001g0317a0001c0001t0001g0321others(1): Show | 4 | HG00408.hp2 NA18980.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-5316T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457715 | ||||||
| chr2:47457809
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-5222C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457809 | ||||||
| chr2:47457847
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1387-5184C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457847 | ||||||
| chr2:47457896
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1387-5135T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457896 | ||||||
| chr2:47457936
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-5095T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457936 | ||||||
| chr2:47457990
|
C | G | 19 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 19 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1387-5041C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47457990 | ||||||
| chr2:47458037
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1387-4994A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458037 | ||||||
| chr2:47458075
|
G | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.1387-4956G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458075 | ||||||
| chr2:47458268
|
A | C | 7 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0115others(4): Show | 7 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-4763A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458268 | ||||||
| chr2:47458297
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1387-4734C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458297 | ||||||
| chr2:47458320
|
G | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-4711G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458320 | ||||||
| chr2:47458329
|
C | G | 1 | a0001c0001t0001g0040 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1387-4702C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458329 | ||||||
| chr2:47458444
|
TA | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1387-4586delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458444 | ||||||
| chr2:47458520
|
G | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1387-4511G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458520 | ||||||
| chr2:47458537
|
A | AT | 138 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 138 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.1387-4481dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47458537 | |||||
| chr2:47458537
|
AT | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1387-4481delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47458537 | |||||
| chr2:47458543
|
T | G | 64 | a0001c0001t0001g0040a0001c0001t0001g0112a0001c0001t0001g0121others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.1387-4488T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458543 | ||||||
| chr2:47458571
|
C | T | 52 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(49): Show | 52 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1387-4460C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458571 | ||||||
| chr2:47458656
|
C | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1387-4375C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458656 | ||||||
| chr2:47458749
|
T | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1387-4282T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458749 | ||||||
| chr2:47458756
|
C | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(208): Show | 211 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1387-4275C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458756 | ||||||
| chr2:47458777
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1387-4254C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47458777 | ||||||
| chr2:47458958
|
T | TA | 85 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0056others(82): Show | 85 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.1387-4062dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47458958 | |||||
| chr2:47459063
|
C | G | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1387-3968C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459063 | ||||||
| chr2:47459125
|
C | CT | 29 | a0001c0001t0001g0003a0001c0001t0001g0112a0001c0001t0001g0126others(26): Show | 29 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.1387-3902dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47459125 | |||||
| chr2:47459187
|
C | A | 1 | a0001c0001t0001g0312 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1387-3844C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459187 | ||||||
| chr2:47459237
|
A | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0105others(189): Show | 192 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1387-3794A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459237 | ||||||
| chr2:47459243
|
T | TTA | 4 | a0001c0001t0001g0125a0001c0001t0002g0170a0001c0001t0002g0258others(1): Show | 4 | HG00738.hp2 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-3787_1387-378 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47459243 | |||||
| chr2:47459262
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1387-3769C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459262 | ||||||
| chr2:47459381
|
C | G | 3 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0236 | 3 | HG00423.hp1 HG02074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1387-3650C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459381 | ||||||
| chr2:47459409
|
A | G | 1 | a0001c0006t0001g0222 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1387-3622A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459409 | ||||||
| chr2:47459434
|
G | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1387-3597G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459434 | ||||||
| chr2:47459501
|
TTTTA | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0105others(183): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1387-3526_1387-352 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47459501 | |||||
| chr2:47459547
|
A | G | 87 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1387-3484A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459547 | ||||||
| chr2:47459630
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1387-3401C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459630 | ||||||
| chr2:47459718
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1387-3313C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459718 | ||||||
| chr2:47459763
|
C | T | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1387-3268C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459763 | ||||||
| chr2:47459812
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1387-3219C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47459812 | ||||||
| chr2:47460126
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1387-2905G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460126 | ||||||
| chr2:47460137
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1387-2894A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460137 | ||||||
| chr2:47460276
|
G | C | 1 | a0001c0001t0001g0307 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1387-2755G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460276 | ||||||
| chr2:47460337
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1387-2694T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460337 | ||||||
| chr2:47460510
|
A | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1387-2521A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460510 | ||||||
| chr2:47460520
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1387-2511G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460520 | ||||||
| chr2:47460591
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0161 | 2 | NA18973.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1387-2440A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460591 | ||||||
| chr2:47460671
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1387-2360T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460671 | ||||||
| chr2:47460755
|
A | G | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02015.hp2 HG02129.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-2276A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460755 | ||||||
| chr2:47460820
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1387-2211C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460820 | ||||||
| chr2:47460849
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1387-2182T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460849 | ||||||
| chr2:47460849
|
T | TA | 3 | a0001c0001t0001g0012a0001c0001t0001g0206a0002c0003t0001g0108 | 3 | HG00140.hp2 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1387-2182_1387-218 others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460849 | ||||||
| chr2:47460850
|
T | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0065others(12): Show | 15 | HG00140.hp2 HG00733.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-2181T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460850 | ||||||
| chr2:47460850
|
T | TA | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1387-2181_1387-218 others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460850 | ||||||
| chr2:47460850
|
T | TC | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(13): Show | 16 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1387-2181_1387-218 others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460850 | ||||||
| chr2:47460851
|
T | A | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(339): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1387-2180T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460851 | ||||||
| chr2:47460851
|
T | TA | 7 | a0001c0001t0001g0157a0001c0001t0001g0165a0001c0001t0001g0166others(4): Show | 7 | HG01433.hp1 HG02698.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-2167dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47460851 | |||||
| chr2:47460851
|
T | TAA | 10 | a0001c0001t0001g0105a0001c0001t0001g0189a0001c0001t0001g0239others(7): Show | 10 | HG00438.hp1 HG00544.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.1387-2168_1387-216 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47460851 | |||||
| chr2:47460962
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1387-2069T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47460962 | ||||||
| chr2:47461269
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-1762G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461269 | ||||||
| chr2:47461276
|
C | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1387-1755C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461276 | ||||||
| chr2:47461430
|
T | C | 4 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-1601T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461430 | ||||||
| chr2:47461499
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1387-1532G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461499 | ||||||
| chr2:47461572
|
C | CT | 11 | a0001c0001t0001g0006a0001c0001t0001g0072a0001c0001t0001g0126others(8): Show | 11 | HG01109.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1387-1443dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461572 | |||||
| chr2:47461670
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0276 | 3 | HG00642.hp2 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1387-1361G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461670 | ||||||
| chr2:47461690
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1387-1341C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461690 | ||||||
| chr2:47461694
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1387-1337C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461694 | ||||||
| chr2:47461698
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1387-1333C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461698 | ||||||
| chr2:47461715
|
T | C | 2 | a0001c0001t0001g0288a0001c0001t0001g0292 | 2 | HG00639.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1387-1316T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461715 | ||||||
| chr2:47461736
|
AATTTTTT others(7): Show |
A | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-1294_1387-128 others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461736 | ||||||
| chr2:47461737
|
A | AT | 60 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 60 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1387-1263dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATT | 18 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0031others(15): Show | 18 | HG00609.hp1 HG00738.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1387-1264_1387-126 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTT | 39 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(36): Show | 39 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1387-1265_1387-126 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTT | 43 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0112others(40): Show | 43 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1387-1266_1387-126 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTT | 24 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0126others(21): Show | 24 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1387-1267_1387-126 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTTT | 7 | a0001c0001t0001g0013a0001c0001t0001g0127a0001c0001t0001g0177others(4): Show | 7 | HG02145.hp2 HG03516.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-1268_1387-126 others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTTTT others(3): Show |
2 | a0001c0002t0001g0114a0001c0002t0001g0116 | 2 | HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1387-1272_1387-126 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0117 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1387-1275_1387-126 others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1387-1276_1387-126 others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0223 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1387-1277_1387-126 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1387-1278_1387-126 others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
AT | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(11): Show | 14 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1387-1263delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTT | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0017others(12): Show | 15 | HG00099.hp2 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-1265_1387-126 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTTTT | A | 7 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0282others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-1267_1387-126 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1387-1272_1387-126 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTTTTTT others(5): Show |
A | 10 | a0001c0001t0001g0286a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 10 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-1274_1387-126 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0200a0002c0003t0001g0106 | 2 | HG02895.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1387-1275_1387-126 others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0001g0242a0010c0018t0001g0339 | 2 | HG00438.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1387-1276_1387-126 others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461737
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1387-1279_1387-126 others(21): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461737 | |||||
| chr2:47461837
|
C | T | 4 | a0001c0001t0001g0309a0001c0007t0001g0101a0001c0007t0001g0102others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-1194C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461837 | ||||||
| chr2:47461846
|
C | T | 1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1387-1185C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461846 | ||||||
| chr2:47461871
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1387-1160G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461871 | ||||||
| chr2:47461875
|
G | A | 2 | a0001c0001t0001g0365a0001c0001t0001g0366 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1387-1156G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461875 | ||||||
| chr2:47461880
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 208 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1387-1151C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461880 | ||||||
| chr2:47461912
|
T | TTTTTC | 13 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0169others(10): Show | 13 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1387-1065_1387-106 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
T | TTTTTCTT others(3): Show |
3 | a0001c0001t0001g0078a0001c0001t0001g0104a0002c0003t0001g0233 | 3 | HG02735.hp2 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1387-1070_1387-106 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
T | TTTTTCTT others(8): Show |
7 | a0001c0001t0001g0050a0001c0001t0001g0058a0001c0001t0001g0082others(4): Show | 7 | HG00639.hp2 HG01069.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-1075_1387-106 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
T | TTTTTCTT others(13): Show |
1 | a0001c0001t0001g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1387-1080_1387-106 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
T | TTTTTCTT others(14): Show |
1 | a0001c0001t0001g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1387-1110_1387-110 others(25): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
TTTTTC | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(22): Show | 25 | HG00609.hp1 HG00642.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1387-1065_1387-106 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
TTTTTCTT others(3): Show |
T | 7 | a0001c0001t0001g0075a0001c0001t0001g0296a0001c0001t0001g0314others(4): Show | 7 | HG04184.hp1 NA18612.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1387-1070_1387-106 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461912
|
TTTTTCTT others(13): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1387-1080_1387-106 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461912 | |||||
| chr2:47461931
|
T | TCTTTTCT others(8): Show |
1 | a0001c0006t0001g0144 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1387-1086_1387-108 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461931 | |||||
| chr2:47461936
|
T | TCTTTTCT others(3): Show |
12 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0019others(9): Show | 12 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.1387-1086_1387-108 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461936 | |||||
| chr2:47461941
|
TCTTTTCT others(28): Show |
T | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1387-1085_1387-105 others(39): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461941 | |||||
| chr2:47461946
|
TCTTTTCT others(18): Show |
T | 1 | a0001c0001t0001g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1387-1080_1387-105 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461946 | |||||
| chr2:47461946
|
TCTTTTCT others(23): Show |
T | 4 | a0001c0001t0001g0002a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-1080_1387-105 others(34): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461946 | |||||
| chr2:47461946
|
TCTTTTCT others(28): Show |
T | 1 | a0001c0001t0001g0136 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1387-1080_1387-104 others(39): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461946 | |||||
| chr2:47461946
|
TCTTTTCT others(33): Show |
T | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1387-1080_1387-104 others(44): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461946 | |||||
| chr2:47461951
|
TCTTTTCT others(18): Show |
T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0223others(1): Show | 4 | HG02896.hp1 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1387-1075_1387-105 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461951 | |||||
| chr2:47461951
|
TCTTTTCT others(28): Show |
T | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG02257.hp2 HG02615.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-1075_1387-104 others(39): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461951 | |||||
| chr2:47461956
|
T | C | 5 | a0001c0001t0001g0135a0001c0001t0001g0286a0001c0001t0001g0323others(2): Show | 5 | HG02074.hp2 HG02083.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1387-1075T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461956 | ||||||
| chr2:47461956
|
TCTTTTCT others(8): Show |
T | 2 | a0001c0001t0001g0232a0001c0007t0001g0103 | 2 | HG01361.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1387-1070_1387-105 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461956 | |||||
| chr2:47461956
|
TCTTTTCT others(13): Show |
T | 11 | a0001c0001t0001g0160a0001c0001t0001g0264a0001c0001t0001g0280others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1387-1070_1387-105 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461956 | |||||
| chr2:47461956
|
TCTTTTCT others(18): Show |
T | 15 | a0001c0001t0001g0040a0001c0001t0001g0176a0001c0001t0001g0177others(12): Show | 15 | HG00099.hp1 HG00423.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-1070_1387-104 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461956 | |||||
| chr2:47461961
|
T | C | 24 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0075others(21): Show | 24 | HG00609.hp1 HG01175.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.1387-1070T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461961 | ||||||
| chr2:47461961
|
TCTTTTCT others(3): Show |
T | 9 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(6): Show | 9 | HG01099.hp1 HG01192.hp1 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-1065_1387-105 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461961 | |||||
| chr2:47461961
|
TCTTTTCT others(8): Show |
T | 11 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0137others(8): Show | 11 | HG00558.hp1 HG01071.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.1387-1065_1387-105 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461961 | |||||
| chr2:47461961
|
TCTTTTCT others(13): Show |
T | 9 | a0001c0001t0001g0121a0001c0001t0001g0190a0001c0001t0001g0201others(6): Show | 9 | HG00408.hp1 HG00597.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-1065_1387-104 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461961 | |||||
| chr2:47461961
|
TCTTTTCT others(18): Show |
T | 2 | a0001c0001t0001g0006a0001c0001t0001g0013 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1387-1065_1387-104 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461961 | |||||
| chr2:47461966
|
T | C | 40 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 40 | HG00423.hp2 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1387-1065T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461966 | ||||||
| chr2:47461966
|
T | TCTTTC | 22 | a0001c0001t0001g0001a0001c0001t0001g0028a0001c0001t0001g0032others(19): Show | 22 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1387-1025_1387-102 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTCCT others(3): Show |
2 | a0001c0001t0001g0356a0001c0001t0001g0357 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1387-1030_1387-102 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTCCT others(8): Show |
4 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0063others(1): Show | 4 | HG00741.hp2 HG02809.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-1035_1387-102 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(3): Show |
16 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0038others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(8): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0319 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(13): Show |
3 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0073 | 3 | HG00642.hp2 HG01109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(8): Show |
8 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0055others(5): Show | 8 | NA18940.hp1 NA18941.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(13): Show |
1 | a0001c0001t0001g0288 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1387-1061_1387-106 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(23): Show |
1 | a0001c0001t0001g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1387-1061_1387-106 others(34): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(12): Show |
1 | a0001c0004t0001g0047 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1387-1061_1387-106 others(23): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(13): Show |
9 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0072others(6): Show | 9 | HG00544.hp1 HG01258.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(24): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(18): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0346 | 2 | HG02273.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
T | TCTTTTCT others(18): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0345 | 2 | HG00738.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1387-1061_1387-106 others(29): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
TCTTTC | T | 52 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0132others(49): Show | 52 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1387-1025_1387-102 others(9): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
TCTTTCCT others(3): Show |
T | 50 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(47): Show | 50 | HG00597.hp2 HG00621.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.1387-1030_1387-102 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461966
|
TCTTTCCT others(8): Show |
T | 13 | a0001c0001t0001g0143a0001c0001t0001g0187a0001c0001t0001g0196others(10): Show | 13 | HG00140.hp2 HG00609.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1387-1035_1387-102 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47461966 | |||||
| chr2:47461971
|
C | T | 35 | a0001c0001t0001g0018a0001c0001t0001g0080a0001c0001t0001g0081others(32): Show | 35 | HG00438.hp2 HG00738.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1387-1060C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461971 | ||||||
| chr2:47461976
|
C | T | 60 | a0001c0001t0001g0105a0001c0001t0001g0119a0001c0001t0001g0131others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1387-1055C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461976 | ||||||
| chr2:47461981
|
C | T | 26 | a0001c0001t0001g0126a0001c0001t0001g0133a0001c0001t0001g0150others(23): Show | 26 | HG00738.hp2 HG01261.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1387-1050C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461981 | ||||||
| chr2:47461986
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0358 | 2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1387-1045C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47461986 | ||||||
| chr2:47462034
|
C | CTCTCT | 44 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(41): Show | 44 | HG00735.hp1 HG00735.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1387-971_1387-967d others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47462034 | |||||
| chr2:47462034
|
C | CTCTCTTC others(3): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0040 | 2 | HG03041.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1387-976_1387-967d others(12): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47462034 | |||||
| chr2:47462034
|
C | CTCTCTTC others(8): Show |
1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1387-981_1387-967d others(17): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47462034 | |||||
| chr2:47462034
|
CTCTCT | C | 10 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(7): Show | 10 | HG01258.hp2 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1387-971_1387-967d others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 47462034 | |||||
| chr2:47462053
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1387-978C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462053 | ||||||
| chr2:47462061
|
C | T | 17 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(14): Show | 17 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1387-970C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462061 | ||||||
| chr2:47462078
|
G | T | 49 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0130others(46): Show | 49 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1387-953G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462078 | ||||||
| chr2:47462117
|
A | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1387-914A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462117 | ||||||
| chr2:47462323
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-708G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462323 | ||||||
| chr2:47462410
|
C | A | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1387-621C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462410 | ||||||
| chr2:47462620
|
T | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-411T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462620 | ||||||
| chr2:47462643
|
A | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1387-388A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462643 | ||||||
| chr2:47462724
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1387-307A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462724 | ||||||
| chr2:47462781
|
G | A | 15 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(12): Show | 15 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1387-250G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462781 | ||||||
| chr2:47462887
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1387-144C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 8/15 | chr2 | 47462887 | ||||||
| chr2:47463265
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(221): Show | 224 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1510+111T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463265 | ||||||
| chr2:47463269
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1510+115A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463269 | ||||||
| chr2:47463272
|
T | C | 224 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(221): Show | 224 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.1510+118T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463272 | ||||||
| chr2:47463437
|
A | C | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510+283A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463437 | ||||||
| chr2:47463464
|
T | A | 1 | a0001c0001t0001g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1510+310T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463464 | ||||||
| chr2:47463505
|
T | G | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510+351T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463505 | ||||||
| chr2:47463765
|
T | C | 1 | a0005c0008t0001g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1510+611T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463765 | ||||||
| chr2:47463825
|
A | G | 2 | a0002c0003t0001g0235a0002c0019t0001g0253 | 2 | HG02055.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1510+671A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463825 | ||||||
| chr2:47463978
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1510+824G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463978 | ||||||
| chr2:47463981
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(199): Show | 202 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1510+827G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47463981 | ||||||
| chr2:47464033
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1510+879G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464033 | ||||||
| chr2:47464089
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1510+935G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464089 | ||||||
| chr2:47464178
|
C | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1510+1024C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464178 | ||||||
| chr2:47464240
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1510+1086C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464240 | ||||||
| chr2:47464484
|
G | C | 1 | a0001c0001t0002g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1510+1330G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464484 | ||||||
| chr2:47464519
|
T | TA | 91 | a0001c0001t0001g0040a0001c0001t0001g0072a0001c0001t0001g0119others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1510+1376dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 47464519 | |||||
| chr2:47464576
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1510+1422T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464576 | ||||||
| chr2:47464634
|
A | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1510+1480A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464634 | ||||||
| chr2:47464653
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241 | 3 | NA18941.hp1 NA19012.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1510+1499A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464653 | ||||||
| chr2:47464695
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1510+1541A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464695 | ||||||
| chr2:47464720
|
T | G | 1 | a0001c0007t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1510+1566T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464720 | ||||||
| chr2:47464752
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1510+1598C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464752 | ||||||
| chr2:47464959
|
T | C | 10 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0296others(7): Show | 10 | HG00609.hp1 NA18612.hp1 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1511-1699T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47464959 | ||||||
| chr2:47465047
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1511-1611G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465047 | ||||||
| chr2:47465100
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1511-1558T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465100 | ||||||
| chr2:47465142
|
C | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1511-1516C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465142 | ||||||
| chr2:47465204
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1511-1454G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465204 | ||||||
| chr2:47465216
|
T | A | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1511-1442T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465216 | ||||||
| chr2:47465288
|
A | G | 1 | a0001c0001t0001g0012 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1511-1370A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465288 | ||||||
| chr2:47465330
|
TTCTC | T | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1511-1320_1511-131 others(8): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 47465330 | |||||
| chr2:47465352
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1511-1306A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465352 | ||||||
| chr2:47465453
|
C | T | 1 | a0008c0015t0001g0092 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1511-1205C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465453 | ||||||
| chr2:47465493
|
T | C | 181 | a0001c0001t0001g0040a0001c0001t0001g0105a0001c0001t0001g0112others(178): Show | 181 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1511-1165T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465493 | ||||||
| chr2:47465595
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1511-1063G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465595 | ||||||
| chr2:47465636
|
G | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1511-1022G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465636 | ||||||
| chr2:47465701
|
CA | C | 4 | a0001c0002t0001g0114a0001c0002t0001g0116a0001c0002t0001g0118others(1): Show | 4 | HG01109.hp1 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1511-953delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 47465701 | |||||
| chr2:47465709
|
T | G | 1 | a0001c0002t0001g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1511-949T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465709 | ||||||
| chr2:47465735
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0333 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1511-923C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465735 | ||||||
| chr2:47465912
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1511-746T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47465912 | ||||||
| chr2:47466012
|
T | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1511-646T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466012 | ||||||
| chr2:47466090
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1511-568C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466090 | ||||||
| chr2:47466224
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1511-434A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466224 | ||||||
| chr2:47466323
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1511-335A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466323 | ||||||
| chr2:47466392
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1511-266A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466392 | ||||||
| chr2:47466567
|
G | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1511-91G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466567 | ||||||
| chr2:47466600
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1511-58T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466600 | ||||||
| chr2:47466649
|
A | T | 8 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(5): Show | 8 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1511-9A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 9/15 | chr2 | 47466649 | ||||||
| chr2:47466820
|
G | A | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1661+12G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47466820 | ||||||
| chr2:47466898
|
T | C | 5 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0063others(2): Show | 5 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661+90T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47466898 | ||||||
| chr2:47467042
|
C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0266 | 2 | NA18984.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1661+234C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467042 | ||||||
| chr2:47467057
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1661+249A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467057 | ||||||
| chr2:47467106
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1661+298A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467106 | ||||||
| chr2:47467113
|
C | G | 53 | a0001c0001t0001g0094a0001c0001t0001g0119a0001c0001t0001g0129others(50): Show | 53 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1661+305C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467113 | ||||||
| chr2:47467155
|
C | CT | 7 | a0001c0001t0001g0017a0001c0001t0001g0184a0001c0001t0001g0210others(4): Show | 7 | HG00597.hp1 HG00738.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1661+359dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47467155 | |||||
| chr2:47467155
|
C | CTT | 24 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(21): Show | 24 | HG00099.hp2 HG01109.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1661+358_1661+359d others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47467155 | |||||
| chr2:47467168
|
G | T | 1 | a0005c0008t0001g0212 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1661+360G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467168 | ||||||
| chr2:47467173
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.1661+365T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467173 | ||||||
| chr2:47467184
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1661+376T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467184 | ||||||
| chr2:47467256
|
T | C | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1661+448T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467256 | ||||||
| chr2:47467308
|
G | A | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0098 | 3 | HG01256.hp1 HG01258.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1661+500G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467308 | ||||||
| chr2:47467442
|
C | CT | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(208): Show | 211 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1661+646dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47467442 | |||||
| chr2:47467442
|
C | CTT | 29 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(26): Show | 29 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1661+645_1661+646d others(4): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47467442 | |||||
| chr2:47467505
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1661+697C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467505 | ||||||
| chr2:47467506
|
G | T | 1 | a0001c0001t0001g0336 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1661+698G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467506 | ||||||
| chr2:47467675
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1661+867C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467675 | ||||||
| chr2:47467698
|
G | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1661+890G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467698 | ||||||
| chr2:47467734
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1661+926C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467734 | ||||||
| chr2:47467743
|
C | T | 1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1661+935C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467743 | ||||||
| chr2:47467765
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1661+957G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467765 | ||||||
| chr2:47467816
|
T | C | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661+1008T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467816 | ||||||
| chr2:47467965
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1661+1157A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467965 | ||||||
| chr2:47467967
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1661+1159A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467967 | ||||||
| chr2:47467993
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1661+1185T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47467993 | ||||||
| chr2:47468028
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1661+1220G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47468028 | ||||||
| chr2:47468175
|
T | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0083 | 2 | HG00544.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1661+1367T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47468175 | ||||||
| chr2:47468842
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1661+2034T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47468842 | ||||||
| chr2:47468953
|
C | CT | 18 | a0001c0001t0001g0026a0001c0001t0001g0075a0001c0001t0001g0076others(15): Show | 18 | HG00544.hp1 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1662-1993dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47468953 | |||||
| chr2:47468953
|
CT | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(123): Show | 126 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1662-1993delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47468953 | |||||
| chr2:47469019
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1662-1946A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469019 | ||||||
| chr2:47469066
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1662-1899C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469066 | ||||||
| chr2:47469255
|
A | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662-1710A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469255 | ||||||
| chr2:47469338
|
A | T | 1 | a0001c0001t0001g0264 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1662-1627A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469338 | ||||||
| chr2:47469448
|
T | C | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1662-1517T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469448 | ||||||
| chr2:47469512
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0242 | 2 | HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1662-1453C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469512 | ||||||
| chr2:47469542
|
G | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(227): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1662-1423G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469542 | ||||||
| chr2:47469547
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1662-1418C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469547 | ||||||
| chr2:47469564
|
G | A | 15 | a0001c0001t0001g0112a0001c0001t0001g0126a0001c0001t0001g0127others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1662-1401G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469564 | ||||||
| chr2:47469614
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1662-1351G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469614 | ||||||
| chr2:47469693
|
G | C | 2 | a0001c0001t0001g0254a0001c0001t0001g0256 | 2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1662-1272G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469693 | ||||||
| chr2:47469813
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 4 | HG03041.hp2 HG03516.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662-1152G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469813 | ||||||
| chr2:47469844
|
G | A | 1 | a0001c0001t0001g0359 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1662-1121G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469844 | ||||||
| chr2:47469868
|
C | G | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1662-1097C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469868 | ||||||
| chr2:47469878
|
C | T | 2 | a0001c0002t0001g0122a0001c0002t0001g0124 | 2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1662-1087C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47469878 | ||||||
| chr2:47469886
|
C | CA | 13 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG00639.hp1 HG00738.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1662-1069dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47469886 | |||||
| chr2:47469985
|
G | GT | 7 | a0001c0001t0001g0003a0001c0001t0001g0130a0001c0001t0001g0259others(4): Show | 7 | HG00597.hp2 HG02135.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662-969dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47469985 | |||||
| chr2:47470013
|
C | G | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662-952C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470013 | ||||||
| chr2:47470019
|
CT | C | 14 | a0001c0001t0001g0002a0001c0001t0001g0225a0001c0001t0001g0226others(11): Show | 14 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1662-932delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr2 | 47470019 | |||||
| chr2:47470021
|
T | C | 28 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0051others(25): Show | 28 | HG00408.hp2 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1662-944T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470021 | ||||||
| chr2:47470072
|
T | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662-893T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470072 | ||||||
| chr2:47470084
|
G | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662-881G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470084 | ||||||
| chr2:47470139
|
C | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662-826C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470139 | ||||||
| chr2:47470140
|
G | A | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1662-825G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470140 | ||||||
| chr2:47470199
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1662-766G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470199 | ||||||
| chr2:47470216
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1662-749G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470216 | ||||||
| chr2:47470319
|
G | T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662-646G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470319 | ||||||
| chr2:47470355
|
G | A | 1 | a0001c0001t0001g0318 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1662-610G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470355 | ||||||
| chr2:47470401
|
T | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662-564T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470401 | ||||||
| chr2:47470419
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1662-546A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470419 | ||||||
| chr2:47470532
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1662-433C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470532 | ||||||
| chr2:47470536
|
T | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 7 | HG02622.hp2 HG02896.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662-429T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470536 | ||||||
| chr2:47470579
|
G | A | 33 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(30): Show | 33 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1662-386G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470579 | ||||||
| chr2:47470922
|
C | T | 1 | a0001c0001t0001g0359 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1662-43C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470922 | ||||||
| chr2:47470942
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1662-23A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470942 | ||||||
| chr2:47470956
|
G | A | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1662-9G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 10/15 | chr2 | 47470956 | ||||||
| chr2:47471157
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1759+95G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471157 | ||||||
| chr2:47471168
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1759+106C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471168 | ||||||
| chr2:47471169
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1759+107A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471169 | ||||||
| chr2:47471245
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1759+183G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471245 | ||||||
| chr2:47471258
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1759+196A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471258 | ||||||
| chr2:47471526
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1759+464T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471526 | ||||||
| chr2:47471541
|
G | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1759+479G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471541 | ||||||
| chr2:47471563
|
A | G | 92 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1759+501A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471563 | ||||||
| chr2:47471590
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1759+528C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471590 | ||||||
| chr2:47471591
|
G | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1759+529G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471591 | ||||||
| chr2:47471642
|
T | C | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1759+580T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471642 | ||||||
| chr2:47471840
|
G | A | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02698.hp1 NA18992.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1759+778G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471840 | ||||||
| chr2:47471958
|
A | G | 2 | a0001c0001t0001g0309a0001c0001t0001g0340 | 2 | HG02257.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1759+896A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47471958 | ||||||
| chr2:47472005
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1759+943C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472005 | ||||||
| chr2:47472051
|
TTTC | T | 6 | a0001c0001t0001g0296a0001c0001t0001g0323a0001c0001t0001g0328others(3): Show | 6 | NA18952.hp1 NA18970.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1759+992_1759+994d others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47472051 | |||||
| chr2:47472134
|
A | G | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0307others(2): Show | 5 | NA18959.hp1 NA19058.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1759+1072A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472134 | ||||||
| chr2:47472150
|
A | G | 3 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | HG02698.hp1 NA18992.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1759+1088A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472150 | ||||||
| chr2:47472343
|
G | A | 5 | a0002c0003t0001g0107a0002c0003t0001g0108a0002c0003t0001g0109others(2): Show | 5 | HG02630.hp1 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1759+1281G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472343 | ||||||
| chr2:47472393
|
T | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1759+1331T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472393 | ||||||
| chr2:47472556
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1759+1494T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472556 | ||||||
| chr2:47472659
|
C | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1759+1597C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472659 | ||||||
| chr2:47472705
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1759+1643A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472705 | ||||||
| chr2:47472714
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1759+1652G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472714 | ||||||
| chr2:47472755
|
G | A | 9 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0265others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1759+1693G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472755 | ||||||
| chr2:47472876
|
C | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0266 | 2 | NA18984.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1759+1814C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47472876 | ||||||
| chr2:47473079
|
C | T | 6 | a0002c0003t0001g0106a0002c0003t0001g0107a0002c0003t0001g0108others(3): Show | 6 | HG02630.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1760-1946C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473079 | ||||||
| chr2:47473185
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1760-1840A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473185 | ||||||
| chr2:47473224
|
A | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1760-1801A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473224 | ||||||
| chr2:47473251
|
G | A | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1760-1774G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473251 | ||||||
| chr2:47473340
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(4): Show | 7 | HG02257.hp2 HG02615.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1760-1685C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473340 | ||||||
| chr2:47473491
|
G | A | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1760-1534G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473491 | ||||||
| chr2:47473703
|
C | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1760-1322C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473703 | ||||||
| chr2:47473725
|
C | CA | 10 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0038others(7): Show | 10 | HG01175.hp2 HG02055.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1760-1271dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CA | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1760-1271delA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAA | C | 116 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 116 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1760-1272_1760-127 others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAAA | C | 13 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0289others(10): Show | 13 | HG01515.hp1 HG02300.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1760-1273_1760-127 others(7): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAAAAAA | C | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1760-1276_1760-127 others(10): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1760-1280_1760-127 others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0236a0001c0001t0001g0318 | 2 | HG00423.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1760-1282_1760-127 others(16): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1760-1284_1760-127 others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473725
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1760-1285_1760-127 others(19): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47473725 | |||||
| chr2:47473773
|
A | C | 3 | a0001c0007t0001g0101a0001c0007t0001g0102a0001c0007t0001g0103 | 3 | HG02559.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1760-1252A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473773 | ||||||
| chr2:47473818
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1760-1207C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473818 | ||||||
| chr2:47473823
|
C | T | 1 | a0002c0003t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1760-1202C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473823 | ||||||
| chr2:47473824
|
A | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1760-1201A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473824 | ||||||
| chr2:47473909
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1760-1116C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47473909 | ||||||
| chr2:47474010
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1760-1015C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474010 | ||||||
| chr2:47474098
|
T | A | 1 | a0001c0001t0001g0014 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1760-927T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474098 | ||||||
| chr2:47474118
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1760-907T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474118 | ||||||
| chr2:47474178
|
A | G | 2 | a0001c0001t0002g0170a0002c0003t0002g0171 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1760-847A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474178 | ||||||
| chr2:47474223
|
A | T | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01515.hp1 HG02300.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.1760-802A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474223 | ||||||
| chr2:47474296
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18953.hp1 NA18964.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1760-729C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474296 | ||||||
| chr2:47474342
|
G | T | 1 | a0001c0001t0001g0055 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1760-683G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474342 | ||||||
| chr2:47474355
|
T | C | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1760-670T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474355 | ||||||
| chr2:47474519
|
C | T | 7 | a0001c0001t0001g0298a0001c0001t0001g0331a0001c0001t0001g0334others(4): Show | 7 | HG02818.hp1 HG02886.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1760-506C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474519 | ||||||
| chr2:47474566
|
C | T | 88 | a0001c0001t0001g0105a0001c0001t0001g0119a0001c0001t0001g0129others(85): Show | 88 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1760-459C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474566 | ||||||
| chr2:47474569
|
G | A | 67 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0132others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1760-456G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474569 | ||||||
| chr2:47474899
|
A | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1760-126A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474899 | ||||||
| chr2:47474913
|
T | TAGG | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1760-110_1760-108d others(5): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 47474913 | |||||
| chr2:47474963
|
G | A | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1760-62G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 11/15 | chr2 | 47474963 | ||||||
| chr2:47475311
|
TG | T | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005+42delG | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475311 | ||||||
| chr2:47475312
|
G | GT | 28 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(25): Show | 28 | HG00099.hp2 HG00423.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.2005+61dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 47475312 | |||||
| chr2:47475312
|
G | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0188a0001c0001t0001g0271others(1): Show | 4 | HG01981.hp1 HG02451.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.2005+42G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475312 | ||||||
| chr2:47475312
|
GT | G | 14 | a0001c0001t0001g0029a0001c0001t0001g0048a0001c0001t0001g0096others(11): Show | 14 | HG00741.hp1 HG01074.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.2005+61delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 47475312 | |||||
| chr2:47475314
|
T | G | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2005+44T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475314 | ||||||
| chr2:47475321
|
T | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(20): Show | 23 | HG01109.hp1 HG02257.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.2005+51T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475321 | ||||||
| chr2:47475322
|
T | G | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2005+52T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475322 | ||||||
| chr2:47475512
|
G | T | 1 | a0001c0001t0001g0001 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2005+242G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475512 | ||||||
| chr2:47475587
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2005+317T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475587 | ||||||
| chr2:47475677
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2005+407C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475677 | ||||||
| chr2:47475785
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2005+515A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475785 | ||||||
| chr2:47475857
|
C | T | 2 | a0001c0009t0001g0274a0001c0009t0001g0275 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2006-510C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475857 | ||||||
| chr2:47475901
|
C | G | 1 | a0001c0001t0001g0347 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2006-466C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47475901 | ||||||
| chr2:47476102
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2006-265A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47476102 | ||||||
| chr2:47476151
|
G | A | 9 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0268others(6): Show | 9 | HG01071.hp2 HG01106.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.2006-216G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47476151 | ||||||
| chr2:47476240
|
C | T | 369 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(366): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.2006-127C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47476240 | ||||||
| chr2:47476270
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2006-97C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47476270 | ||||||
| chr2:47476361
|
T | C | 68 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0132others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.2006-6T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 12/15 | chr2 | 47476361 | ||||||
| chr2:47476576
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18984.hp2 | splice_region_variant&intron_variant | LOW | c.2210+5G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476576 | ||||||
| chr2:47476746
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.2210+175G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476746 | ||||||
| chr2:47476845
|
T | G | 65 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0131others(62): Show | 65 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2210+274T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476845 | ||||||
| chr2:47476856
|
T | G | 6 | a0001c0001t0001g0265a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG01884.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2210+285T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476856 | ||||||
| chr2:47476862
|
C | G | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2210+291C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476862 | ||||||
| chr2:47476888
|
G | C | 364 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(361): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2210+317G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476888 | ||||||
| chr2:47476906
|
T | C | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2210+335T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476906 | ||||||
| chr2:47476937
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(8): Show | 11 | HG01515.hp1 HG02257.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.2210+366A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476937 | ||||||
| chr2:47476946
|
G | A | 1 | a0002c0003t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2210+375G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476946 | ||||||
| chr2:47476969
|
G | C | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2210+398G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476969 | ||||||
| chr2:47476982
|
T | C | 1 | a0001c0001t0001g0342 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2210+411T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47476982 | ||||||
| chr2:47477094
|
A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG03041.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2210+523A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477094 | ||||||
| chr2:47477098
|
A | T | 2 | a0001c0001t0001g0001a0001c0001t0001g0069 | 2 | HG01099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.2210+527A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477098 | ||||||
| chr2:47477115
|
T | G | 1 | a0001c0001t0001g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2210+544T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477115 | ||||||
| chr2:47477165
|
T | G | 6 | a0001c0001t0001g0191a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | NA18959.hp1 NA19009.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.2210+594T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477165 | ||||||
| chr2:47477260
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2210+689G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477260 | ||||||
| chr2:47477304
|
T | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2210+733T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477304 | ||||||
| chr2:47477331
|
G | GA | 4 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2210+761dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 47477331 | |||||
| chr2:47477443
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2211-829T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477443 | ||||||
| chr2:47477443
|
T | G | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2211-829T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477443 | ||||||
| chr2:47477494
|
T | A | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2211-778T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477494 | ||||||
| chr2:47477570
|
A | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2211-702A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477570 | ||||||
| chr2:47477838
|
CT | C | 53 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(50): Show | 53 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.2211-421delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 47477838 | |||||
| chr2:47477840
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-432T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477840 | ||||||
| chr2:47477842
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-430T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477842 | ||||||
| chr2:47477843
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-429T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477843 | ||||||
| chr2:47477844
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-428T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477844 | ||||||
| chr2:47477846
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-426T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477846 | ||||||
| chr2:47477847
|
T | G | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-425T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477847 | ||||||
| chr2:47477849
|
T | G | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-423T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477849 | ||||||
| chr2:47477850
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-422T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477850 | ||||||
| chr2:47477852
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-420C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477852 | ||||||
| chr2:47477853
|
C | G | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2211-419C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477853 | ||||||
| chr2:47477853
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2211-419C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477853 | ||||||
| chr2:47477859
|
TCCTC | T | 204 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2211-389_2211-386d others(6): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 47477859 | |||||
| chr2:47477859
|
TCCTCCCT others(9): Show |
T | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2211-401_2211-386d others(18): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 47477859 | |||||
| chr2:47477883
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0287 | 2 | HG00408.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2211-389C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47477883 | ||||||
| chr2:47477965
|
A | AT | 76 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 76 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.2211-284dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 47477965 | |||||
| chr2:47477965
|
AT | A | 24 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0057others(21): Show | 24 | HG00738.hp1 HG01074.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.2211-284delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 47477965 | |||||
| chr2:47478046
|
C | G | 1 | a0001c0001t0001g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2211-226C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47478046 | ||||||
| chr2:47478052
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2211-220C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47478052 | ||||||
| chr2:47478111
|
T | C | 1 | a0002c0003t0001g0106 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2211-161T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47478111 | ||||||
| chr2:47478112
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2211-160A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 13/15 | chr2 | 47478112 | ||||||
| chr2:47478709
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2458+190C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47478709 | ||||||
| chr2:47478828
|
C | G | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2458+309C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47478828 | ||||||
| chr2:47478833
|
G | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG00099.hp2 HG01175.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.2458+314G>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47478833 | ||||||
| chr2:47478862
|
T | A | 1 | a0001c0001t0001g0190 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2458+343T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47478862 | ||||||
| chr2:47478916
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2458+397G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47478916 | ||||||
| chr2:47479004
|
A | C | 1 | a0001c0002t0001g0228 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2458+485A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479004 | ||||||
| chr2:47479008
|
G | A | 8 | a0001c0001t0001g0358a0001c0001t0001g0360a0001c0001t0001g0361others(5): Show | 8 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2458+489G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479008 | ||||||
| chr2:47479283
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2458+764T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479283 | ||||||
| chr2:47479289
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2458+770G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479289 | ||||||
| chr2:47479728
|
A | T | 1 | a0001c0001t0001g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2459-968A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479728 | ||||||
| chr2:47479781
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2459-915C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479781 | ||||||
| chr2:47479887
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2459-809A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479887 | ||||||
| chr2:47479936
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2459-760A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479936 | ||||||
| chr2:47479962
|
C | T | 61 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(58): Show | 61 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2459-734C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47479962 | ||||||
| chr2:47480003
|
G | A | 1 | a0001c0001t0001g0368 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2459-693G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480003 | ||||||
| chr2:47480124
|
T | TCTTCTCT others(5): Show |
229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2459-571_2459-560d others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 47480124 | |||||
| chr2:47480131
|
T | TTCCCCCT others(5): Show |
1 | a0001c0001t0001g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2459-560_2459-559i others(14): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 47480131 | |||||
| chr2:47480136
|
C | CCTTCTCT others(6): Show |
1 | a0001c0001t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2459-560_2459-559i others(15): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480136 | ||||||
| chr2:47480137
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2459-559T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480137 | ||||||
| chr2:47480146
|
C | T | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-550C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480146 | ||||||
| chr2:47480148
|
A | T | 2 | a0001c0001t0001g0267a0001c0006t0001g0128 | 2 | HG03225.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2459-548A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480148 | ||||||
| chr2:47480154
|
C | T | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-542C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480154 | ||||||
| chr2:47480155
|
A | C | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-541A>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480155 | ||||||
| chr2:47480156
|
T | C | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-540T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480156 | ||||||
| chr2:47480165
|
T | A | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-531T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480165 | ||||||
| chr2:47480179
|
T | C | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-517T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480179 | ||||||
| chr2:47480184
|
T | C | 1 | a0001c0006t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2459-512T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480184 | ||||||
| chr2:47480202
|
T | TCTTCCTC others(11): Show |
2 | a0001c0001t0002g0170a0002c0003t0002g0171 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2459-492_2459-475d others(20): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 47480202 | |||||
| chr2:47480202
|
T | TCTTCCTC others(12): Show |
7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2459-459_2459-441d others(21): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 47480202 | |||||
| chr2:47480217
|
TC | T | 15 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG00099.hp2 HG00738.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.2459-474delC | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 47480217 | |||||
| chr2:47480304
|
C | CCCCTTCC others(4): Show |
1 | a0001c0001t0001g0309 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2459-384_2459-383i others(13): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 47480304 | |||||
| chr2:47480326
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2459-370C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480326 | ||||||
| chr2:47480327
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2459-369T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480327 | ||||||
| chr2:47480371
|
A | T | 1 | a0001c0001t0001g0319 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2459-325A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480371 | ||||||
| chr2:47480384
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2459-312A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480384 | ||||||
| chr2:47480409
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2459-287T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480409 | ||||||
| chr2:47480419
|
C | T | 3 | a0001c0001t0002g0170a0001c0001t0002g0258a0002c0003t0002g0171 | 3 | HG00738.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2459-277C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480419 | ||||||
| chr2:47480435
|
A | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | HG01884.hp2 HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2459-261A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480435 | ||||||
| chr2:47480490
|
A | G | 1 | a0001c0001t0001g0369 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2459-206A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480490 | ||||||
| chr2:47480659
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2459-37C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 14/15 | chr2 | 47480659 | ||||||
| chr2:47480948
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2634+77T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47480948 | ||||||
| chr2:47481199
|
G | A | 88 | a0001c0001t0001g0040a0001c0001t0001g0119a0001c0001t0001g0121others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2634+328G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481199 | ||||||
| chr2:47481301
|
A | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 26 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2634+430A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481301 | ||||||
| chr2:47481316
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2634+445G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481316 | ||||||
| chr2:47481374
|
A | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(23): Show | 26 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2634+503A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481374 | ||||||
| chr2:47481376
|
G | A | 63 | a0001c0001t0001g0105a0001c0001t0001g0131a0001c0001t0001g0145others(60): Show | 63 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.2634+505G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481376 | ||||||
| chr2:47481450
|
A | G | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2634+579A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481450 | ||||||
| chr2:47481491
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2634+620A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481491 | ||||||
| chr2:47481567
|
T | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2634+696T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481567 | ||||||
| chr2:47481644
|
C | T | 1 | a0003c0005t0001g0173 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2634+773C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481644 | ||||||
| chr2:47481645
|
G | A | 7 | a0001c0001t0001g0360a0001c0001t0001g0361a0001c0001t0001g0362others(4): Show | 7 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2634+774G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481645 | ||||||
| chr2:47481700
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.2634+829A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481700 | ||||||
| chr2:47481717
|
G | T | 12 | a0001c0001t0001g0105a0001c0001t0001g0189a0001c0001t0001g0239others(9): Show | 12 | HG00438.hp1 HG00544.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.2634+846G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481717 | ||||||
| chr2:47481752
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+881T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481752 | ||||||
| chr2:47481753
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+882G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481753 | ||||||
| chr2:47481754
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+883G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481754 | ||||||
| chr2:47481756
|
C | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+885C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481756 | ||||||
| chr2:47481758
|
C | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+887C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481758 | ||||||
| chr2:47481759
|
C | G | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+888C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481759 | ||||||
| chr2:47481760
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+889C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481760 | ||||||
| chr2:47481761
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+890A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481761 | ||||||
| chr2:47481763
|
A | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+892A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481763 | ||||||
| chr2:47481766
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2634+895G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481766 | ||||||
| chr2:47481784
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(18): Show | 21 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2634+913G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481784 | ||||||
| chr2:47481801
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2634+930C>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481801 | ||||||
| chr2:47481801
|
C | CT | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(23): Show | 26 | HG02055.hp2 HG02132.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.2634+950dupT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 47481801 | |||||
| chr2:47481801
|
CT | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0143a0001c0001t0001g0155others(10): Show | 13 | HG01074.hp2 HG01256.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2634+950delT | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 47481801 | |||||
| chr2:47481802
|
T | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(19): Show | 22 | HG00099.hp2 HG01109.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2634+931T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481802 | ||||||
| chr2:47481803
|
T | C | 1 | a0001c0002t0001g0115 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2634+932T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481803 | ||||||
| chr2:47481959
|
G | T | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2635-820G>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481959 | ||||||
| chr2:47481978
|
C | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2635-801C>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47481978 | ||||||
| chr2:47482001
|
A | ATAATAAT others(37): Show |
1 | a0001c0001t0003g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2635-766_2635-765i others(46): Show |
MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 47482001 | |||||
| chr2:47482014
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2635-765G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482014 | ||||||
| chr2:47482079
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2635-700T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482079 | ||||||
| chr2:47482089
|
T | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0060others(3): Show | 6 | HG01099.hp2 HG01975.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2635-690T>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482089 | ||||||
| chr2:47482155
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2635-624G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482155 | ||||||
| chr2:47482180
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2635-599T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482180 | ||||||
| chr2:47482258
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2635-521T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482258 | ||||||
| chr2:47482329
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 7 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2635-450G>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482329 | ||||||
| chr2:47482454
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0368 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2635-325C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482454 | ||||||
| chr2:47482459
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2635-320A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482459 | ||||||
| chr2:47482565
|
T | C | 93 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0129others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2635-214T>C | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482565 | ||||||
| chr2:47482623
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01081.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2635-156A>G | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482623 | ||||||
| chr2:47482641
|
C | T | 1 | a0008c0015t0001g0092 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2635-138C>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482641 | ||||||
| chr2:47482657
|
T | TA | 9 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2635-112dupA | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 47482657 | |||||
| chr2:47482667
|
A | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0264a0001c0001t0001g0368others(1): Show | 4 | HG02109.hp2 NA19011.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2635-112A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482667 | ||||||
| chr2:47482668
|
T | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG00099.hp2 HG00741.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.2635-111T>A | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482668 | ||||||
| chr2:47482674
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2635-105A>T | MSH2 | ENSG00000095002.15 | transcript | ENST00000233146.7 | protein_coding | 15/15 | chr2 | 47482674 |