Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2956 |
| ensemblid | ENSG00000116062.19 |
| hgncid | 7329 |
| symbol | MSH6 |
| name | mutS homolog 6 |
| refseq_nuc | NM_000179.3 |
| refseq_prot | NP_000170.1 |
| ensembl_nuc | ENST00000234420.11 |
| ensembl_prot | ENSP00000234420.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 47783145 |
| end | 47806953 |
| strand | + |
| ver | v1.2 |
| region | chr2:47783145-47806953 |
| region5000 | chr2:47778145-47811953 |
| regionname0 | MSH6_chr2_47783145_47806953 |
| regionname5000 | MSH6_chr2_47778145_47811953 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1360 | 287 | 65 | 65 | 111 | 10 | 34 | 88 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0002 | 0/0 | 1360 | 90 | 19 | 12 | 49 | 6 | 4 | 37 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0003 | 0/0 | 1360 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0004 | 0/0 | 1360 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0005 | 0/0 | 1360 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0006 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0007 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0008 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0009 | 0/0 | 1360 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0010 | 0/0 | 1360 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0011 | 0/0 | 1360 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0012 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| a0013 | 0/0 | 1360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | MSRQS others(1355): Show |
chr2 | 47778145 | 47811953 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4080 | 234 | 41 | 48 | 108 | 6 | 29 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0004 | 0/0 | 4080 | 21 | 6 | 10 | 0 | 2 | 3 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0005 | 0/0 | 4080 | 10 | 10 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0006 | 0/0 | 4080 | 7 | 0 | 4 | 0 | 2 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0007 | 0/0 | 4080 | 5 | 3 | 2 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0008 | 0/0 | 4080 | 3 | 2 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0014 | 0/0 | 4080 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0015 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0016 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0018 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0021 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0025 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0001c0027 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0002c0002 | 0/0 | 4080 | 49 | 18 | 11 | 11 | 6 | 3 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0002c0003 | 0/0 | 4080 | 40 | 1 | 1 | 37 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0002c0010 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0003c0009 | 0/0 | 4080 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0004c0011 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0004c0012 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0005c0026 | 0/0 | 4080 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0006c0022 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0007c0028 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0008c0023 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0009c0024 | 0/0 | 4080 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0010c0013 | 0/0 | 4080 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0011c0017 | 0/0 | 4080 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0012c0020 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 | ||
| a0013c0019 | 0/0 | 4080 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | ATGTC others(4075): Show |
chr2 | 47778145 | 47811953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4265 | 232 | 40 | 48 | 107 | 6 | 29 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0001t0002 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0001t0003 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0004t0001 | 0/0 | 4265 | 21 | 6 | 10 | 0 | 2 | 3 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0005t0001 | 0/0 | 4265 | 10 | 10 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0006t0001 | 0/0 | 4265 | 7 | 0 | 4 | 0 | 2 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0007t0001 | 0/0 | 4265 | 5 | 3 | 2 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0008t0001 | 0/0 | 4265 | 3 | 2 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0014t0001 | 0/0 | 4265 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0015t0001 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0016t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0018t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0021t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0025t0001 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0001c0027t0001 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0002c0002t0001 | 0/0 | 4265 | 49 | 18 | 11 | 11 | 6 | 3 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0002c0003t0001 | 0/0 | 4265 | 40 | 1 | 1 | 37 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0002c0010t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0003c0009t0001 | 0/0 | 4265 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0004c0011t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0004c0012t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0005c0026t0001 | 0/0 | 4265 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0006c0022t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0007c0028t0001 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0008c0023t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0009c0024t0001 | 0/0 | 4265 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0010c0013t0001 | 0/0 | 4265 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0011c0017t0001 | 0/0 | 4265 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0012c0020t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| a0013c0019t0001 | 0/0 | 4265 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | AGATT others(4260): Show |
chr2 | 47778145 | 47811953 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0004t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0005t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0006t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0007t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0007t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0007t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0007t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0008t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0008t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0008t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0014t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0015t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0016t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0018t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0021t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0025t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0001c0027t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0002c0010t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0003c0009t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0003c0009t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0004c0011t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0004c0012t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0005c0026t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0006c0022t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0007c0028t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0008c0023t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0009c0024t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0010c0013t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0011c0017t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0012c0020t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| a0013c0019t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0254 | EUR | GBR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0336 | EUR | GBR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00280 | hp1 | a0001 | c0006 | t0001 | g0317 | EUR | FIN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | FIN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0196 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00438 | hp1 | a0003 | c0009 | t0001 | g0144 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00438 | hp2 | a0002 | c0010 | t0001 | g0006 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00544 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00609 | hp2 | a0002 | c0003 | t0001 | g0299 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00621 | hp2 | a0002 | c0003 | t0001 | g0233 | EAS | CHS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0325 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0331 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00733 | hp1 | a0005 | c0026 | t0001 | g0130 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0334 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0329 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00738 | hp1 | a0001 | c0007 | t0001 | g0193 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01070 | hp2 | a0001 | c0006 | t0001 | g0318 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01081 | hp1 | a0001 | c0006 | t0001 | g0321 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0022 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01109 | hp1 | a0001 | c0007 | t0001 | g0189 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0333 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0328 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01243 | hp2 | a0001 | c0008 | t0001 | g0200 | AMR | PUR | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01255 | hp1 | a0001 | c0006 | t0001 | g0316 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01257 | hp2 | a0001 | c0006 | t0001 | g0315 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0029 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01361 | hp2 | a0001 | c0004 | t0001 | g0335 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0027 | EUR | IBS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01516 | hp2 | a0001 | c0006 | t0001 | g0319 | EUR | IBS | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0030 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0235 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0241 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0253 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0298 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02129 | hp1 | a0001 | c0016 | t0001 | g0178 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02135 | hp1 | a0001 | c0021 | t0001 | g0001 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0340 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02155 | hp1 | a0006 | c0022 | t0001 | g0007 | EAS | CDX | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02155 | hp2 | a0002 | c0003 | t0001 | g0224 | EAS | CDX | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02165 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | CDX | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02257 | hp2 | a0007 | c0028 | t0001 | g0263 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02280 | hp1 | a0001 | c0004 | t0001 | g0327 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0076 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02300 | hp2 | a0001 | c0004 | t0001 | g0330 | AMR | PEL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02451 | hp2 | a0001 | c0025 | t0001 | g0078 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02523 | hp1 | a0008 | c0023 | t0001 | g0045 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0337 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0326 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0339 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0276 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0192 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02735 | hp1 | a0001 | c0006 | t0001 | g0320 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02886 | hp1 | a0001 | c0008 | t0001 | g0199 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0073 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02895 | hp1 | a0009 | c0024 | t0001 | g0303 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0190 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0212 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02970 | hp2 | a0001 | c0027 | t0001 | g0201 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0280 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02976 | hp2 | a0001 | c0008 | t0001 | g0202 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0215 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0281 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03195 | hp2 | a0001 | c0005 | t0001 | g0304 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0338 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03239 | hp2 | a0010 | c0013 | t0001 | g0322 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03453 | hp2 | a0001 | c0015 | t0001 | g0292 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0031 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | GWD | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0341 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0323 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0198 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0024 | SAS | BEB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0229 | SAS | BEB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04115 | hp2 | a0001 | c0014 | t0001 | g0151 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04184 | hp1 | a0011 | c0017 | t0001 | g0084 | SAS | BEB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0252 | AFR | YRI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | YRI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | YRI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0243 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0244 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0213 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18957 | hp2 | a0012 | c0020 | t0001 | g0133 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18961 | hp1 | a0003 | c0009 | t0001 | g0143 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0257 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18965 | hp2 | a0001 | c0018 | t0001 | g0034 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0264 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18979 | hp2 | a0004 | c0011 | t0001 | g0297 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18998 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | LWK | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19055 | hp2 | a0002 | c0003 | t0001 | g0295 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19056 | hp2 | a0013 | c0019 | t0001 | g0117 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0236 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0234 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0300 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19084 | hp2 | a0004 | c0012 | t0001 | g0194 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19087 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19089 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ASW | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ASW | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0274 | EUR | TSI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0332 | EUR | TSI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0022 | EUR | TSI | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0324 | SAS | GIH | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0029 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02109 | hp1 | a0001 | c0005 | t0001 | g0306 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0008 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0191 | AFR | ACB | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0305 | AFR | MSL | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | USA | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | LWK | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0171 | REF | REF | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0060 | REF | REF | MSH6_chr2_47778145_47811953 | MSH6 | chr2 | 47778145 | 47811953 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47783349 | G | A | 2 | a0002 a0004 |
92 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(89): Show |
missense_variant | MODERATE | c.116G>A | p.Gly39Glu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/10 | 205/4265 | 116/4083 | 39/1360 | chr2 | 47783349 | |||
| chr2:47783357 | C | T | 1 | a0007 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.124C>T | p.Pro42Ser | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/10 | 213/4265 | 124/4083 | 42/1360 | chr2 | 47783357 | |||
| chr2:47791097 | G | T | 1 | a0005 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.431G>T | p.Ser144Ile | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/10 | 520/4265 | 431/4083 | 144/1360 | chr2 | 47791097 | |||
| chr2:47799011 | C | T | 1 | a0009 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1028C>T | p.Pro343Leu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1117/4265 | 1028/4083 | 343/1360 | chr2 | 47799011 | |||
| chr2:47799113 | A | C | 1 | a0008 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1130A>C | p.Lys377Thr | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1219/4265 | 1130/4083 | 377/1360 | chr2 | 47799113 | |||
| chr2:47799173 | A | G | 1 | a0006 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.1190A>G | p.Tyr397Cys | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1279/4265 | 1190/4083 | 397/1360 | chr2 | 47799173 | |||
| chr2:47800391 | A | G | 1 | a0010 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.2408A>G | p.Asp803Gly | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 2497/4265 | 2408/4083 | 803/1360 | chr2 | 47800391 | |||
| chr2:47800930 | G | A | 1 | a0011 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.2947G>A | p.Glu983Lys | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 3036/4265 | 2947/4083 | 983/1360 | chr2 | 47800930 | |||
| chr2:47803491 | C | T | 1 | a0004 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.3244C>T | p.Pro1082Ser | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/10 | 3333/4265 | 3244/4083 | 1082/1360 | chr2 | 47803491 | |||
| chr2:47803492 | C | T | 1 | a0004 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.3245C>T | p.Pro1082Leu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/10 | 3334/4265 | 3245/4083 | 1082/1360 | chr2 | 47803492 | |||
| chr2:47804959 | A | T | 1 | a0003 | 2 | HG00438.hp1 NA18961.hp1 |
missense_variant | MODERATE | c.3488A>T | p.Glu1163Val | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/10 | 3577/4265 | 3488/4083 | 1163/1360 | chr2 | 47804959 | |||
| chr2:47806314 | G | C | 1 | a0013 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.3757G>C | p.Val1253Leu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 8/10 | 3846/4265 | 3757/4083 | 1253/1360 | chr2 | 47806314 | |||
| chr2:47806329 | C | G | 1 | a0012 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.3772C>G | p.Gln1258Glu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 8/10 | 3861/4265 | 3772/4083 | 1258/1360 | chr2 | 47806329 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47783335 | C | A | 1 | a0002c0010 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.102C>A | p.Ala34Ala | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/10 | 191/4265 | 102/4083 | 34/1360 | chr2 | 47783335 | |||
| chr2:47783419 | C | A | 2 | a0001c0004 a0010c0013 |
22 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
synonymous_variant | LOW | c.186C>A | p.Arg62Arg | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/10 | 275/4265 | 186/4083 | 62/1360 | chr2 | 47783419 | |||
| chr2:47790942 | A | G | 4 | a0001c0004 a0001c0008 a0001c0027 others(1): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
synonymous_variant | LOW | c.276A>G | p.Pro92Pro | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/10 | 365/4265 | 276/4083 | 92/1360 | chr2 | 47790942 | |||
| chr2:47795976 | T | C | 8 | a0001c0004 a0001c0006 a0001c0007 others(5): Show |
40 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(37): Show |
synonymous_variant | LOW | c.540T>C | p.Asp180Asp | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/10 | 629/4265 | 540/4083 | 180/1360 | chr2 | 47795976 | |||
| chr2:47798625 | C | T | 1 | a0001c0006 | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
synonymous_variant | LOW | c.642C>T | p.Tyr214Tyr | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 731/4265 | 642/4083 | 214/1360 | chr2 | 47798625 | |||
| chr2:47798967 | C | T | 1 | a0001c0025 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.984C>T | p.Ser328Ser | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1073/4265 | 984/4083 | 328/1360 | chr2 | 47798967 | |||
| chr2:47799147 | C | T | 2 | a0001c0007 a0001c0015 |
6 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(3): Show |
synonymous_variant | LOW | c.1164C>T | p.His388His | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1253/4265 | 1164/4083 | 388/1360 | chr2 | 47799147 | |||
| chr2:47799648 | A | G | 1 | a0001c0025 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1665A>G | p.Ala555Ala | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1754/4265 | 1665/4083 | 555/1360 | chr2 | 47799648 | |||
| chr2:47799759 | A | T | 1 | a0001c0021 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.1776A>T | p.Val592Val | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 1865/4265 | 1776/4083 | 592/1360 | chr2 | 47799759 | |||
| chr2:47800236 | T | C | 3 | a0001c0005 a0001c0027 a0009c0024 |
12 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.2253T>C | p.Asn751Asn | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 2342/4265 | 2253/4083 | 751/1360 | chr2 | 47800236 | |||
| chr2:47800255 | C | T | 1 | a0001c0007 | 5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.2272C>T | p.Leu758Leu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 2361/4265 | 2272/4083 | 758/1360 | chr2 | 47800255 | |||
| chr2:47800356 | T | C | 1 | a0001c0016 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.2373T>C | p.Arg791Arg | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/10 | 2462/4265 | 2373/4083 | 791/1360 | chr2 | 47800356 | |||
| chr2:47803512 | T | C | 1 | a0007c0028 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.3265T>C | p.Leu1089Leu | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/10 | 3354/4265 | 3265/4083 | 1089/1360 | chr2 | 47803512 | |||
| chr2:47803553 | T | A | 5 | a0001c0018 a0002c0003 a0002c0010 others(2): Show |
44 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(41): Show |
synonymous_variant | LOW | c.3306T>A | p.Thr1102Thr | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/10 | 3395/4265 | 3306/4083 | 1102/1360 | chr2 | 47803553 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47806894 | G | C | 1 | a0001c0001t0002 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 10/10 | 34 | chr2 | 47806894 | ||||||
| chr2:47806922 | A | G | 1 | a0001c0001t0003 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 10/10 | 62 | chr2 | 47806922 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47783515 | C | G | 21 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(18): Show |
22 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.260+22C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783515 | |||||||
| chr2:47783584 | G | A | 1 | a0010c0013t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.260+91G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783584 | |||||||
| chr2:47783673 | T | A | 2 | a0001c0005t0001g0030 a0001c0005t0001g0031 |
2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.260+180T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783673 | |||||||
| chr2:47783733 | C | T | 11 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(8): Show |
11 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.260+240C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783733 | |||||||
| chr2:47783768 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.260+275C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783768 | |||||||
| chr2:47783823 | G | T | 1 | a0001c0001t0002g0313 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.260+330G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783823 | |||||||
| chr2:47783850 | C | G | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 |
3 | HG01358.hp2 HG02683.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.260+357C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783850 | |||||||
| chr2:47783882 | C | G | 163 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(160): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.260+389C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783882 | |||||||
| chr2:47783885 | C | G | 1 | a0002c0003t0001g0188 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.260+392C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783885 | |||||||
| chr2:47783898 | CGGGGCGG | C | 10 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0001g0308 others(7): Show |
10 | HG01074.hp1 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.260+415_260+421del others(7): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47783898 | ||||||
| chr2:47783903 | C | CG | 10 | a0001c0001t0001g0028 a0001c0001t0001g0147 a0001c0001t0001g0172 others(7): Show |
11 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.260+416dupG | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47783903 | ||||||
| chr2:47783910 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.260+417C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783910 | |||||||
| chr2:47783919 | G | A | 21 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(18): Show |
22 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.260+426G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783919 | |||||||
| chr2:47783921 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.260+428G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783921 | |||||||
| chr2:47783952 | G | C | 33 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(30): Show |
34 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.260+459G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783952 | |||||||
| chr2:47783971 | G | C | 5 | a0002c0003t0001g0188 a0002c0003t0001g0195 a0002c0003t0001g0196 others(2): Show |
5 | HG00423.hp2 NA18977.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.260+478G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47783971 | |||||||
| chr2:47784153 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0301 |
3 | HG01884.hp2 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.260+660G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784153 | |||||||
| chr2:47784288 | T | A | 2 | a0001c0004t0001g0338 a0001c0004t0001g0339 |
2 | HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.260+795T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784288 | |||||||
| chr2:47784402 | CGTGA | C | 16 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(13): Show |
16 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.260+914_260+917del others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47784402 | ||||||
| chr2:47784461 | C | CT | 23 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(20): Show |
23 | HG00609.hp2 HG01074.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.260+982dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47784461 | ||||||
| chr2:47784506 | A | G | 3 | a0002c0002t0001g0027 a0002c0002t0001g0293 a0002c0002t0001g0294 |
4 | HG01069.hp1 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+1013A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784506 | |||||||
| chr2:47784710 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.260+1217G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784710 | |||||||
| chr2:47784794 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(29): Show |
39 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.260+1301A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784794 | |||||||
| chr2:47784816 | T | G | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+1323T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784816 | |||||||
| chr2:47784850 | A | G | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+1357A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784850 | |||||||
| chr2:47784861 | C | G | 2 | a0003c0009t0001g0143 a0003c0009t0001g0144 |
2 | HG00438.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.260+1368C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784861 | |||||||
| chr2:47784888 | G | C | 1 | a0002c0002t0001g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.260+1395G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784888 | |||||||
| chr2:47784947 | C | T | 21 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(18): Show |
22 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.260+1454C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47784947 | |||||||
| chr2:47785013 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.260+1520C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785013 | |||||||
| chr2:47785041 | A | C | 6 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(3): Show |
6 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.260+1548A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785041 | |||||||
| chr2:47785159 | A | T | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.260+1666A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785159 | |||||||
| chr2:47785236 | G | C | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.260+1743G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785236 | |||||||
| chr2:47785267 | G | T | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+1774G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785267 | |||||||
| chr2:47785381 | C | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(5): Show |
10 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.260+1888C>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785381 | |||||||
| chr2:47785517 | C | T | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+2024C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785517 | |||||||
| chr2:47785707 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.260+2214C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785707 | |||||||
| chr2:47785745 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.260+2252T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785745 | |||||||
| chr2:47785842 | T | G | 1 | a0002c0002t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.260+2349T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785842 | |||||||
| chr2:47785960 | A | G | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.260+2467A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47785960 | |||||||
| chr2:47786063 | T | TC | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+2572dupC | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47786063 | ||||||
| chr2:47786099 | G | C | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.260+2606G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786099 | |||||||
| chr2:47786299 | C | T | 6 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG01261.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.260+2806C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786299 | |||||||
| chr2:47786337 | A | AT | 16 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0085 others(13): Show |
19 | HG00280.hp2 HG00738.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.260+2858dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47786337 | ||||||
| chr2:47786466 | C | G | 1 | a0001c0008t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.260+2973C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786466 | |||||||
| chr2:47786509 | G | A | 37 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(34): Show |
38 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.260+3016G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786509 | |||||||
| chr2:47786532 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(5): Show |
10 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.260+3039C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786532 | |||||||
| chr2:47786613 | C | T | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.260+3120C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786613 | |||||||
| chr2:47786653 | C | T | 1 | a0002c0003t0001g0283 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.260+3160C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786653 | |||||||
| chr2:47786710 | T | C | 3 | a0002c0002t0001g0210 a0002c0002t0001g0211 a0002c0002t0001g0212 |
3 | HG02922.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.260+3217T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786710 | |||||||
| chr2:47786719 | C | CT | 23 | a0001c0001t0001g0139 a0001c0004t0001g0029 a0001c0004t0001g0323 others(20): Show |
24 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.260+3236dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47786719 | ||||||
| chr2:47786801 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.260+3308C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47786801 | |||||||
| chr2:47787083 | T | G | 1 | a0001c0004t0001g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.260+3590T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47787083 | |||||||
| chr2:47787157 | C | T | 1 | a0002c0002t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.260+3664C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47787157 | |||||||
| chr2:47787260 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.261-3667A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47787260 | |||||||
| chr2:47787282 | CCT | C | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-3644_261-3643d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47787282 | |||||||
| chr2:47787408 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.261-3519A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47787408 | |||||||
| chr2:47787561 | T | C | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-3366T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47787561 | |||||||
| chr2:47788030 | G | C | 3 | a0001c0001t0001g0095 a0003c0009t0001g0143 a0003c0009t0001g0144 |
3 | HG00438.hp1 HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.261-2897G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788030 | |||||||
| chr2:47788060 | CACAAT | C | 2 | a0002c0002t0001g0026 a0002c0002t0001g0280 |
3 | HG01243.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.261-2863_261-2859d others(7): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788060 | ||||||
| chr2:47788145 | T | C | 3 | a0002c0002t0001g0027 a0002c0002t0001g0293 a0002c0002t0001g0294 |
4 | HG01069.hp1 HG01261.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-2782T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788145 | |||||||
| chr2:47788188 | A | G | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-2739A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788188 | |||||||
| chr2:47788216 | C | A | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-2711C>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788216 | |||||||
| chr2:47788246 | C | CT | 29 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(26): Show |
29 | HG00140.hp1 HG00735.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.261-2655dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788246 | ||||||
| chr2:47788246 | C | CTT | 9 | a0001c0001t0001g0168 a0001c0001t0001g0279 a0001c0001t0001g0307 others(6): Show |
9 | HG00738.hp1 HG01074.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-2656_261-2655d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788246 | ||||||
| chr2:47788246 | CT | C | 35 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(32): Show |
35 | HG00408.hp2 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.261-2655delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788246 | ||||||
| chr2:47788246 | CTT | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(11): Show |
16 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.261-2656_261-2655d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788246 | ||||||
| chr2:47788246 | CTTTTTTT others(1): Show |
C | 82 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(79): Show |
93 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.261-2662_261-2655d others(10): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788246 | ||||||
| chr2:47788252 | T | C | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-2675T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788252 | |||||||
| chr2:47788382 | G | A | 4 | a0001c0001t0001g0291 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG01358.hp2 HG02683.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-2545G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788382 | |||||||
| chr2:47788414 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.261-2513C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788414 | |||||||
| chr2:47788488 | C | T | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-2439C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788488 | |||||||
| chr2:47788551 | C | G | 1 | a0002c0002t0001g0259 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.261-2376C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788551 | |||||||
| chr2:47788559 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.261-2368T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788559 | |||||||
| chr2:47788570 | C | CT | 13 | a0001c0001t0001g0028 a0001c0001t0001g0166 a0001c0001t0001g0256 others(10): Show |
15 | HG01261.hp2 HG01884.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.261-2340dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788570 | ||||||
| chr2:47788570 | CT | C | 41 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0102 others(38): Show |
42 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.261-2340delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788570 | ||||||
| chr2:47788574 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG01346.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.261-2353T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788574 | |||||||
| chr2:47788575 | T | TC | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-2352_261-2351i others(3): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788575 | |||||||
| chr2:47788624 | T | C | 39 | a0001c0001t0001g0279 a0001c0004t0001g0029 a0001c0004t0001g0323 others(36): Show |
40 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.261-2303T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788624 | |||||||
| chr2:47788900 | CTTCTTCC others(4): Show |
C | 1 | a0001c0004t0001g0341 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.261-2024_261-2014d others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(5): Show |
C | 1 | a0001c0004t0001g0331 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.261-2024_261-2013d others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(6): Show |
C | 2 | a0001c0004t0001g0330 a0001c0008t0001g0202 |
2 | HG02300.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.261-2024_261-2012d others(15): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(7): Show |
C | 10 | a0001c0004t0001g0029 a0001c0004t0001g0327 a0001c0004t0001g0328 others(7): Show |
11 | HG00733.hp2 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.261-2024_261-2011d others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(8): Show |
C | 9 | a0001c0004t0001g0324 a0001c0004t0001g0325 a0001c0004t0001g0326 others(6): Show |
9 | HG00140.hp1 HG00639.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-2024_261-2010d others(17): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(17): Show |
C | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.261-2024_261-2001d others(26): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(19): Show |
C | 4 | a0001c0004t0001g0323 a0001c0007t0001g0190 a0001c0007t0001g0192 others(1): Show |
4 | HG00738.hp1 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-2024_261-1999d others(28): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(20): Show |
C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(7): Show |
12 | HG01109.hp1 HG01346.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.261-2024_261-1998d others(29): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(21): Show |
C | 1 | a0001c0004t0001g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.261-2024_261-1997d others(30): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788900 | CTTCTTCC others(24): Show |
C | 1 | a0001c0001t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.261-2024_261-1994d others(33): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788900 | ||||||
| chr2:47788902 | TCTTCCTT others(13): Show |
T | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-2024_261-2005d others(22): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788902 | |||||||
| chr2:47788903 | CTTCCTTT others(3): Show |
C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0125 |
2 | HG02135.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2012d others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788903 | ||||||
| chr2:47788905 | TC | T | 58 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(55): Show |
65 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(62): Show |
intron_variant | MODIFIER | c.261-2020delC | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788905 | ||||||
| chr2:47788906 | C | CT | 9 | a0001c0001t0001g0019 a0001c0001t0001g0137 a0001c0001t0001g0147 others(6): Show |
10 | HG00099.hp2 HG00621.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.261-2021_261-2020i others(3): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTT | 4 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0159 others(1): Show |
4 | NA19012.hp1 NA19064.hp2 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-2021_261-2020i others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTT | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
3 | HG00408.hp1 NA18964.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(7): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT | 4 | a0001c0001t0001g0004 a0001c0001t0001g0153 a0001c0001t0001g0170 others(1): Show |
4 | HG02074.hp1 HG03669.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-2021_261-2020i others(9): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.261-2021_261-2020i others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0127 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0145 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.261-2021_261-2020i others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0164 a0001c0014t0001g0151 |
2 | HG02015.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(15): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(41): Show |
1 | a0002c0003t0001g0025 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(50): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(44): Show |
1 | a0002c0003t0001g0025 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(53): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(7): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0167 a0002c0002t0001g0251 others(10): Show |
14 | HG01993.hp1 HG02155.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.261-2021_261-2020i others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(8): Show |
6 | a0002c0003t0001g0024 a0002c0003t0001g0239 a0002c0003t0001g0242 others(3): Show |
6 | HG00544.hp1 HG00609.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-2021_261-2020i others(17): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(10): Show |
1 | a0002c0002t0001g0022 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(19): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(11): Show |
1 | a0002c0002t0001g0022 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(20): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(12): Show |
2 | a0002c0003t0001g0024 a0002c0003t0001g0241 |
2 | HG02040.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(21): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(13): Show |
2 | a0002c0003t0001g0195 a0002c0003t0001g0197 |
2 | NA18977.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(22): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(14): Show |
2 | a0002c0003t0001g0188 a0002c0003t0001g0247 |
2 | NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(23): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(16): Show |
1 | a0002c0002t0001g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.261-2021_261-2020i others(25): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(17): Show |
1 | a0002c0003t0001g0233 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(26): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(20): Show |
2 | a0002c0002t0001g0250 a0002c0003t0001g0196 |
2 | HG00423.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(29): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(24): Show |
1 | a0002c0003t0001g0283 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(33): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0001g0004 a0002c0003t0001g0213 a0002c0003t0001g0295 |
3 | NA18957.hp1 NA19055.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(17): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(10): Show |
1 | a0002c0003t0001g0234 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(19): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(11): Show |
1 | a0002c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.261-2021_261-2020i others(20): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0186 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.261-2021_261-2020i others(21): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(13): Show |
1 | a0002c0003t0001g0300 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.261-2021_261-2020i others(22): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0217 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.261-2021_261-2020i others(26): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTT | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0121 a0001c0001t0001g0289 |
3 | HG02055.hp2 NA19066.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.261-2020_261-2018d others(5): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTT | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0017 others(6): Show |
11 | HG04204.hp1 NA18971.hp1 NA19030.hp1 others(8): Show |
intron_variant | MODIFIER | c.261-2020_261-2017d others(6): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTT | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0107 others(9): Show |
13 | HG02015.hp1 HG02071.hp1 HG03516.hp2 others(10): Show |
intron_variant | MODIFIER | c.261-2020_261-2016d others(7): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTT | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0118 others(9): Show |
13 | HG00140.hp2 HG01884.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.261-2020_261-2015d others(8): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(30): Show |
39 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.261-2020_261-2014d others(9): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(1): Show |
C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0096 others(17): Show |
20 | HG00558.hp2 HG01099.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.261-2020_261-2013d others(10): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0284 a0001c0001t0003g0055 others(1): Show |
4 | HG02258.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-2020_261-2010d others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.261-2020_261-2009d others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.261-2020_261-2008d others(15): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0002c0003t0001g0023 |
3 | HG00323.hp1 HG02071.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.261-2020_261-2007d others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0007c0028t0001g0263 |
3 | HG02257.hp2 NA18952.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.261-2020_261-2005d others(18): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0175 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.261-2020_261-2004d others(19): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(11): Show |
C | 4 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG01074.hp2 HG02129.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-2020_261-2003d others(20): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(12): Show |
C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0039 |
2 | HG01993.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.261-2020_261-2002d others(21): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(13): Show |
C | 2 | a0001c0025t0001g0078 a0004c0012t0001g0194 |
2 | HG02451.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.261-2020_261-2001d others(22): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788906 | CCTTTTTT others(16): Show |
C | 1 | a0001c0001t0001g0111 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.261-2020_261-1998d others(25): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788906 | |||||||
| chr2:47788907 | C | G | 11 | a0002c0002t0001g0251 a0002c0002t0001g0252 a0002c0003t0001g0006 others(8): Show |
12 | HG01993.hp1 HG02155.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.261-2020C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788907 | |||||||
| chr2:47788907 | C | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(114): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.261-2020C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788907 | |||||||
| chr2:47788908 | T | TTTTTTTT others(6): Show |
3 | a0001c0018t0001g0034 a0002c0003t0001g0006 a0002c0003t0001g0244 |
3 | NA18954.hp2 NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.261-2007_261-2006i others(15): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788908 | ||||||
| chr2:47788909 | T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0032 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.261-2007_261-2006i others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788909 | ||||||
| chr2:47788910 | T | TTTTTTTT others(4): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0273 |
2 | HG02647.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.261-2007_261-2006i others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788910 | ||||||
| chr2:47788911 | T | TTTTTTTT others(3): Show |
3 | a0001c0001t0001g0142 a0002c0002t0001g0210 a0002c0002t0001g0212 |
3 | HG02257.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.261-2007_261-2006i others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788911 | ||||||
| chr2:47788911 | T | TTTTTTTT others(26): Show |
2 | a0001c0001t0001g0267 a0001c0001t0001g0272 |
2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.261-2007_261-2006i others(35): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788911 | ||||||
| chr2:47788912 | T | TTTTTTTT others(25): Show |
2 | a0001c0001t0001g0270 a0001c0001t0001g0278 |
2 | HG01433.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.261-2007_261-2006i others(34): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788912 | ||||||
| chr2:47788913 | T | TTTTTTTT others(16): Show |
1 | a0002c0002t0001g0231 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.261-2007_261-2006i others(25): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788913 | ||||||
| chr2:47788913 | T | TTTTTTTT others(24): Show |
1 | a0001c0001t0001g0268 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.261-2007_261-2006i others(33): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788913 | ||||||
| chr2:47788914 | T | TTTTTTTG others(23): Show |
1 | a0001c0001t0001g0269 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.261-2007_261-2006i others(32): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788914 | ||||||
| chr2:47788914 | T | TTTTTTTT others(23): Show |
1 | a0001c0001t0001g0277 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.261-2006_261-2005i others(32): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788914 | ||||||
| chr2:47788915 | T | TTTTTTGT others(22): Show |
3 | a0001c0001t0001g0260 a0001c0001t0001g0262 a0001c0001t0001g0266 |
3 | HG02559.hp1 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.261-2007_261-2006i others(31): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788915 | ||||||
| chr2:47788916 | T | TTTTTGTT others(11): Show |
1 | a0002c0003t0001g0245 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.261-2007_261-2006i others(20): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788916 | ||||||
| chr2:47788917 | T | TTTTGTTT others(15): Show |
1 | a0002c0002t0001g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.261-2007_261-2006i others(24): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788917 | ||||||
| chr2:47788918 | T | TTTGTTTT others(14): Show |
1 | a0001c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.261-2007_261-2006i others(23): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788918 | ||||||
| chr2:47788920 | T | TG | 6 | a0001c0001t0001g0009 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
7 | HG00280.hp2 HG00738.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-2007_261-2006i others(3): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788920 | |||||||
| chr2:47788920 | T | TGTTTTTT others(4): Show |
1 | a0002c0002t0001g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.261-2007_261-2006i others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788920 | |||||||
| chr2:47788921 | T | G | 18 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(15): Show |
19 | HG01123.hp2 HG01175.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.261-2006T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788921 | |||||||
| chr2:47788922 | G | GTTTTTTT others(7): Show |
1 | a0002c0003t0001g0246 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.261-1993_261-1980d others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788922 | ||||||
| chr2:47788922 | G | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.261-2005G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788922 | |||||||
| chr2:47788922 | GT | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0061 others(5): Show |
9 | HG01975.hp1 HG02027.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-1980delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788922 | ||||||
| chr2:47788922 | GTTTTTTT others(3): Show |
G | 5 | a0001c0001t0001g0074 a0001c0005t0001g0008 a0001c0005t0001g0073 others(2): Show |
6 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-1989_261-1980d others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788922 | ||||||
| chr2:47788922 | GTTTTTTT others(5): Show |
G | 1 | a0002c0002t0001g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.261-1991_261-1980d others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788922 | ||||||
| chr2:47788922 | GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0001g0302 a0001c0001t0001g0307 a0001c0001t0001g0308 others(1): Show |
4 | HG01074.hp1 NA19043.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-1993_261-1980d others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788922 | ||||||
| chr2:47788929 | T | TTTTTTTT others(7): Show |
2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.261-1985_261-1984i others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47788929 | ||||||
| chr2:47788930 | T | TGTTTTTG others(15): Show |
1 | a0002c0002t0001g0259 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.261-1997_261-1996i others(24): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788930 | |||||||
| chr2:47788934 | T | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0301 |
4 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-1993T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788934 | |||||||
| chr2:47788935 | T | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0260 a0001c0001t0001g0262 |
3 | HG02559.hp1 HG02965.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.261-1992T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788935 | |||||||
| chr2:47788941 | T | G | 1 | a0004c0012t0001g0194 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.261-1986T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788941 | |||||||
| chr2:47788955 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.261-1972G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788955 | |||||||
| chr2:47788985 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261-1942G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788985 | |||||||
| chr2:47788986 | C | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(6): Show |
9 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-1941C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788986 | |||||||
| chr2:47788987 | G | A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
8 | HG02976.hp1 NA18946.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.261-1940G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47788987 | |||||||
| chr2:47789018 | C | G | 95 | a0001c0001t0001g0028 a0001c0001t0001g0209 a0001c0001t0001g0256 others(92): Show |
107 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.261-1909C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789018 | |||||||
| chr2:47789085 | T | C | 6 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(3): Show |
6 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.261-1842T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789085 | |||||||
| chr2:47789169 | C | T | 2 | a0002c0002t0001g0255 a0002c0002t0001g0276 |
2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.261-1758C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789169 | |||||||
| chr2:47789175 | T | C | 47 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(44): Show |
50 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.261-1752T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789175 | |||||||
| chr2:47789214 | G | A | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.261-1713G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789214 | |||||||
| chr2:47789499 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.261-1428T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789499 | |||||||
| chr2:47789728 | T | C | 9 | a0001c0001t0001g0256 a0002c0002t0001g0216 a0002c0002t0001g0217 others(6): Show |
9 | HG03704.hp1 HG04199.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.261-1199T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789728 | |||||||
| chr2:47789741 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.261-1186T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789741 | |||||||
| chr2:47789757 | G | T | 47 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(44): Show |
50 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.261-1170G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789757 | |||||||
| chr2:47789762 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.261-1165A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789762 | |||||||
| chr2:47789788 | A | G | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-1139A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789788 | |||||||
| chr2:47789831 | C | CT | 21 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(18): Show |
22 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.261-1087dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47789831 | ||||||
| chr2:47789913 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(5): Show |
10 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.261-1014C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789913 | |||||||
| chr2:47789924 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.261-1003G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789924 | |||||||
| chr2:47789936 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.261-991C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47789936 | |||||||
| chr2:47790130 | T | C | 1 | a0002c0002t0001g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.261-797T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790130 | |||||||
| chr2:47790346 | C | T | 1 | a0001c0015t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.261-581C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790346 | |||||||
| chr2:47790390 | C | T | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.261-537C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790390 | |||||||
| chr2:47790407 | G | A | 1 | a0007c0028t0001g0263 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.261-520G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790407 | |||||||
| chr2:47790480 | G | A | 1 | a0001c0004t0001g0324 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.261-447G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790480 | |||||||
| chr2:47790499 | A | C | 1 | a0001c0001t0001g0309 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.261-428A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790499 | |||||||
| chr2:47790512 | G | A | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-415G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790512 | |||||||
| chr2:47790530 | A | G | 4 | a0001c0008t0001g0199 a0001c0008t0001g0200 a0001c0008t0001g0202 others(1): Show |
4 | HG01243.hp2 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.261-397A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790530 | |||||||
| chr2:47790629 | C | A | 20 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.261-298C>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790629 | |||||||
| chr2:47790678 | TTC | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0086 others(7): Show |
13 | HG00280.hp2 HG00738.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.261-247_261-246del others(2): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47790678 | ||||||
| chr2:47790700 | AATAAC | A | 6 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(3): Show |
6 | HG01261.hp1 HG02055.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.261-221_261-217del others(5): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 47790700 | ||||||
| chr2:47790706 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0083 |
5 | HG01069.hp2 HG01071.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.261-221A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790706 | |||||||
| chr2:47790841 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.261-86A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790841 | |||||||
| chr2:47790873 | T | A | 1 | a0002c0003t0001g0224 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.261-54T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790873 | |||||||
| chr2:47790891 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0077 a0001c0001t0001g0131 others(4): Show |
7 | HG00558.hp2 HG01074.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.261-36A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 1/9 | chr2 | 47790891 | |||||||
| chr2:47791136 | A | G | 1 | a0002c0002t0001g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.457+13A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791136 | |||||||
| chr2:47791154 | T | TTG | 19 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0075 others(16): Show |
21 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.457+52_457+53dupTG | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47791154 | ||||||
| chr2:47791154 | TTG | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0301 |
4 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+52_457+53delTG | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47791154 | ||||||
| chr2:47791175 | T | A | 48 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(45): Show |
51 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.457+52T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791175 | |||||||
| chr2:47791223 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.457+100A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791223 | |||||||
| chr2:47791340 | G | T | 20 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(17): Show |
21 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.457+217G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791340 | |||||||
| chr2:47791517 | T | C | 21 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(18): Show |
22 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.457+394T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791517 | |||||||
| chr2:47791675 | C | CT | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0071 others(18): Show |
23 | HG01346.hp2 HG01515.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.457+570dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47791675 | ||||||
| chr2:47791675 | CT | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0046 others(15): Show |
19 | HG01109.hp1 HG01257.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.457+570delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47791675 | ||||||
| chr2:47791679 | T | C | 1 | a0001c0025t0001g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.457+556T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791679 | |||||||
| chr2:47791680 | T | C | 1 | a0001c0014t0001g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.457+557T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791680 | |||||||
| chr2:47791699 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.457+576G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791699 | |||||||
| chr2:47791853 | A | T | 2 | a0001c0001t0001g0070 a0001c0005t0001g0076 |
2 | HG02280.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.457+730A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791853 | |||||||
| chr2:47791855 | T | A | 47 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0169 others(44): Show |
53 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.457+732T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791855 | |||||||
| chr2:47791857 | T | C | 4 | a0002c0003t0001g0023 a0002c0003t0001g0233 a0002c0003t0001g0234 others(1): Show |
5 | HG00621.hp2 HG01993.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+734T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791857 | |||||||
| chr2:47791908 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(5): Show |
10 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.457+785G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47791908 | |||||||
| chr2:47792045 | C | T | 1 | a0002c0002t0001g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.457+922C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792045 | |||||||
| chr2:47792091 | C | T | 1 | a0005c0026t0001g0130 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.457+968C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792091 | |||||||
| chr2:47792145 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.457+1022C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792145 | |||||||
| chr2:47792205 | T | C | 1 | a0001c0006t0001g0316 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.457+1082T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792205 | |||||||
| chr2:47792233 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.457+1110C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792233 | |||||||
| chr2:47792237 | T | C | 7 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(4): Show |
7 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+1114T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792237 | |||||||
| chr2:47792257 | C | G | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.457+1134C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792257 | |||||||
| chr2:47792275 | G | A | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.457+1152G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792275 | |||||||
| chr2:47792346 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(63): Show |
81 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.457+1223T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792346 | |||||||
| chr2:47792457 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.457+1334C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792457 | |||||||
| chr2:47792550 | A | T | 1 | a0002c0002t0001g0254 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.457+1427A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792550 | |||||||
| chr2:47792555 | G | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0019 others(35): Show |
45 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.457+1432G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792555 | |||||||
| chr2:47792584 | G | C | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.457+1461G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792584 | |||||||
| chr2:47792802 | G | T | 1 | a0002c0002t0001g0281 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.457+1679G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792802 | |||||||
| chr2:47792846 | G | GT | 15 | a0001c0001t0001g0047 a0001c0001t0001g0070 a0001c0001t0001g0081 others(12): Show |
15 | HG00423.hp2 HG00735.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1747dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47792846 | ||||||
| chr2:47792846 | GT | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(142): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.457+1747delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47792846 | ||||||
| chr2:47792846 | GTTT | G | 9 | a0001c0001t0001g0279 a0001c0004t0001g0341 a0001c0006t0001g0315 others(6): Show |
9 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.457+1745_457+1747d others(5): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47792846 | ||||||
| chr2:47792846 | GTTTT | G | 10 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(7): Show |
10 | HG00738.hp1 HG01109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.457+1744_457+1747d others(6): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47792846 | ||||||
| chr2:47792846 | GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0301 |
4 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.457+1736_457+1747d others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47792846 | ||||||
| chr2:47792891 | A | G | 1 | a0002c0002t0001g0258 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.457+1768A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792891 | |||||||
| chr2:47792992 | A | G | 1 | a0010c0013t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.457+1869A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47792992 | |||||||
| chr2:47793243 | T | C | 40 | a0001c0001t0001g0279 a0001c0004t0001g0029 a0001c0004t0001g0323 others(37): Show |
41 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.457+2120T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793243 | |||||||
| chr2:47793280 | C | T | 1 | a0001c0014t0001g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.457+2157C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793280 | |||||||
| chr2:47793318 | C | CA | 73 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(70): Show |
83 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.457+2224dupA | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793318 | ||||||
| chr2:47793318 | C | CAA | 18 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0077 others(15): Show |
19 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.457+2223_457+2224d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793318 | ||||||
| chr2:47793318 | C | CTCAAAA | 4 | a0001c0004t0001g0324 a0001c0004t0001g0340 a0001c0008t0001g0202 others(1): Show |
4 | HG02145.hp1 HG02976.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.457+2195_457+2196i others(8): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793318 | |||||||
| chr2:47793318 | C | CTCAAAAA others(1): Show |
5 | a0001c0004t0001g0326 a0001c0004t0001g0329 a0001c0004t0001g0330 others(2): Show |
5 | HG00735.hp1 HG01243.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+2195_457+2196i others(10): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793318 | |||||||
| chr2:47793318 | C | CTCAAAAA others(2): Show |
5 | a0001c0004t0001g0327 a0001c0004t0001g0328 a0001c0004t0001g0332 others(2): Show |
5 | HG00140.hp1 HG00733.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.457+2195_457+2196i others(11): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793318 | |||||||
| chr2:47793318 | C | CTCAAAAA others(3): Show |
5 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0331 others(2): Show |
6 | HG00642.hp1 HG01109.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+2195_457+2196i others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793318 | |||||||
| chr2:47793318 | C | CTCAAAAA others(4): Show |
1 | a0001c0004t0001g0325 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.457+2195_457+2196i others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793318 | |||||||
| chr2:47793318 | CA | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(67): Show |
82 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.457+2224delA | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793318 | ||||||
| chr2:47793318 | CAA | C | 17 | a0001c0001t0001g0095 a0001c0001t0001g0124 a0001c0001t0001g0138 others(14): Show |
17 | HG00558.hp1 HG01070.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.457+2223_457+2224d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793318 | ||||||
| chr2:47793318 | CAAAAAAA | C | 7 | a0001c0001t0001g0279 a0001c0007t0001g0189 a0001c0007t0001g0190 others(4): Show |
7 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+2218_457+2224d others(9): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793318 | ||||||
| chr2:47793318 | CAAAAAAA others(6): Show |
C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(5): Show |
10 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.457+2212_457+2224d others(15): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793318 | ||||||
| chr2:47793343 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.457+2220A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793343 | |||||||
| chr2:47793627 | A | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0154 |
3 | HG00621.hp1 HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.458-2267A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793627 | |||||||
| chr2:47793641 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(6): Show |
13 | NA18944.hp1 NA18970.hp2 NA18971.hp1 others(10): Show |
intron_variant | MODIFIER | c.458-2253A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793641 | |||||||
| chr2:47793642 | TAATA | T | 7 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(4): Show |
7 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-2245_458-2242d others(6): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47793642 | ||||||
| chr2:47793726 | T | G | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-2168T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793726 | |||||||
| chr2:47793753 | C | T | 4 | a0001c0004t0001g0029 a0001c0004t0001g0325 a0001c0004t0001g0332 others(1): Show |
5 | HG00639.hp1 HG01109.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-2141C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793753 | |||||||
| chr2:47793754 | G | A | 1 | a0002c0003t0001g0243 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.458-2140G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793754 | |||||||
| chr2:47793778 | T | A | 1 | a0012c0020t0001g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.458-2116T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793778 | |||||||
| chr2:47793829 | C | T | 1 | a0001c0004t0001g0329 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.458-2065C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793829 | |||||||
| chr2:47793952 | A | G | 7 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(4): Show |
7 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-1942A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793952 | |||||||
| chr2:47793975 | G | A | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-1919G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47793975 | |||||||
| chr2:47794065 | CA | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.458-1828delA | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794065 | |||||||
| chr2:47794240 | G | C | 165 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0028 others(162): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.458-1654G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794240 | |||||||
| chr2:47794265 | G | T | 1 | a0001c0015t0001g0292 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.458-1629G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794265 | |||||||
| chr2:47794328 | A | G | 8 | a0001c0001t0001g0122 a0001c0006t0001g0315 a0001c0006t0001g0316 others(5): Show |
8 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.458-1566A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794328 | |||||||
| chr2:47794389 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.458-1505A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794389 | |||||||
| chr2:47794412 | C | T | 1 | a0002c0002t0001g0232 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.458-1482C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794412 | |||||||
| chr2:47794570 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.458-1324C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794570 | |||||||
| chr2:47794749 | A | C | 1 | a0001c0014t0001g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.458-1145A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794749 | |||||||
| chr2:47794761 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.458-1133C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794761 | |||||||
| chr2:47794832 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0161 a0001c0001t0001g0166 |
3 | NA18952.hp2 NA18962.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.458-1062T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794832 | |||||||
| chr2:47794869 | A | G | 1 | a0002c0003t0001g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.458-1025A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794869 | |||||||
| chr2:47794917 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.458-977C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794917 | |||||||
| chr2:47794949 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.458-945C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47794949 | |||||||
| chr2:47795040 | G | C | 3 | a0002c0002t0001g0210 a0002c0002t0001g0211 a0002c0002t0001g0212 |
3 | HG02922.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.458-854G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795040 | |||||||
| chr2:47795075 | G | A | 3 | a0001c0001t0001g0095 a0003c0009t0001g0143 a0003c0009t0001g0144 |
3 | HG00438.hp1 HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.458-819G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795075 | |||||||
| chr2:47795205 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0138 |
2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.458-689G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795205 | |||||||
| chr2:47795394 | GTCAAGTG others(1): Show |
G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(5): Show |
10 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-499_458-492del others(8): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795394 | |||||||
| chr2:47795401 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.458-493G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795401 | |||||||
| chr2:47795422 | A | ATG | 27 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0068 others(24): Show |
29 | HG01074.hp1 HG01884.hp1 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-446_458-445dup others(2): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795422 | ||||||
| chr2:47795422 | A | ATGTG | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
143 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.458-448_458-445dup others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795422 | ||||||
| chr2:47795422 | A | ATGTGTGT others(7): Show |
7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.458-458_458-445dup others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795422 | ||||||
| chr2:47795422 | ATG | A | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(13): Show |
18 | HG00738.hp1 HG01109.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.458-446_458-445del others(2): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795422 | ||||||
| chr2:47795422 | ATGTG | A | 18 | a0001c0001t0001g0277 a0001c0004t0001g0029 a0001c0004t0001g0323 others(15): Show |
19 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-448_458-445del others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795422 | ||||||
| chr2:47795462 | A | AT | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0047 others(15): Show |
20 | HG01243.hp2 HG01261.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.458-415dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795462 | ||||||
| chr2:47795462 | A | ATT | 26 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(23): Show |
27 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.458-416_458-415dup others(2): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 47795462 | ||||||
| chr2:47795492 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.458-402G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795492 | |||||||
| chr2:47795504 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.458-390C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795504 | |||||||
| chr2:47795549 | T | C | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.458-345T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795549 | |||||||
| chr2:47795621 | A | G | 25 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(22): Show |
26 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.458-273A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795621 | |||||||
| chr2:47795761 | A | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.458-133A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795761 | |||||||
| chr2:47795767 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.458-127G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795767 | |||||||
| chr2:47795842 | G | T | 86 | a0001c0001t0001g0028 a0001c0001t0001g0209 a0001c0001t0001g0256 others(83): Show |
98 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.458-52G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 2/9 | chr2 | 47795842 | |||||||
| chr2:47796220 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0074 a0001c0001t0001g0261 others(1): Show |
5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+157A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47796220 | |||||||
| chr2:47796734 | T | G | 37 | a0001c0004t0001g0029 a0001c0004t0001g0323 a0001c0004t0001g0324 others(34): Show |
38 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.627+671T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47796734 | |||||||
| chr2:47796758 | C | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG01346.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.627+695C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47796758 | |||||||
| chr2:47796904 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627+841G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47796904 | |||||||
| chr2:47796976 | C | G | 1 | a0007c0028t0001g0263 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.627+913C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47796976 | |||||||
| chr2:47797133 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.627+1070A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797133 | |||||||
| chr2:47797172 | G | T | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1109G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797172 | |||||||
| chr2:47797185 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.627+1122G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797185 | |||||||
| chr2:47797216 | C | T | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1153C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797216 | |||||||
| chr2:47797263 | T | C | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.627+1200T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797263 | |||||||
| chr2:47797276 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.627+1213A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797276 | |||||||
| chr2:47797364 | A | C | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1247A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797364 | |||||||
| chr2:47797398 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.628-1213T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797398 | |||||||
| chr2:47797426 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.628-1185T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797426 | |||||||
| chr2:47797520 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA18992.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.628-1091C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797520 | |||||||
| chr2:47797638 | C | G | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-973C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797638 | |||||||
| chr2:47797737 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.628-874C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797737 | |||||||
| chr2:47797851 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0176 |
2 | NA18994.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.628-760C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47797851 | |||||||
| chr2:47798033 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.628-578C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47798033 | |||||||
| chr2:47798195 | A | G | 1 | a0001c0004t0001g0332 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.628-416A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47798195 | |||||||
| chr2:47798423 | T | C | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.628-188T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47798423 | |||||||
| chr2:47798555 | C | T | 13 | a0001c0001t0001g0028 a0001c0004t0001g0329 a0001c0006t0001g0316 others(10): Show |
14 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.628-56C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 3/9 | chr2 | 47798555 | |||||||
| chr2:47801326 | C | T | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3172+171C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801326 | |||||||
| chr2:47801361 | G | GT | 6 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(3): Show |
6 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.3172+231dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0124 others(5): Show |
9 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3172+230_3172+231d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTT | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(148): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.3172+229_3172+231d others(5): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTT | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(78): Show |
92 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.3172+228_3172+231d others(6): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTT | 17 | a0001c0001t0001g0116 a0001c0001t0001g0123 a0001c0001t0001g0147 others(14): Show |
17 | HG00323.hp1 HG00423.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.3172+227_3172+231d others(7): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(3): Show |
17 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0042 others(14): Show |
18 | HG01106.hp2 HG01123.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.3172+222_3172+231d others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(4): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
23 | HG00738.hp2 HG01071.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.3172+221_3172+231d others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(5): Show |
15 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0046 others(12): Show |
16 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.3172+220_3172+231d others(14): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0062 |
3 | NA18953.hp1 NA18985.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3172+219_3172+231d others(15): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(7): Show |
1 | a0008c0023t0001g0045 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3172+218_3172+231d others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0287 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3172+217_3172+231d others(17): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(9): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0059 |
2 | HG01975.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3172+216_3172+231d others(18): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801361 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0053 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3172+214_3172+231d others(20): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801361 | ||||||
| chr2:47801386 | T | TTTTTTTT others(3): Show |
1 | a0001c0004t0001g0338 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3172+231_3172+232i others(12): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801386 | |||||||
| chr2:47801386 | T | TTTTTTTT others(4): Show |
1 | a0001c0004t0001g0339 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3172+231_3172+232i others(13): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801386 | |||||||
| chr2:47801386 | T | TTTTTTTT others(7): Show |
2 | a0001c0004t0001g0340 a0001c0004t0001g0341 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3172+231_3172+232i others(16): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801386 | |||||||
| chr2:47801418 | G | GA | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3172+265dupA | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47801418 | ||||||
| chr2:47801559 | G | A | 3 | a0001c0005t0001g0008 a0001c0005t0001g0073 a0001c0005t0001g0076 |
5 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3172+404G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801559 | |||||||
| chr2:47801727 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3172+572C>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801727 | |||||||
| chr2:47801856 | C | G | 1 | a0002c0002t0001g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3172+701C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801856 | |||||||
| chr2:47801931 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3172+776A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47801931 | |||||||
| chr2:47802011 | A | G | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3172+856A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802011 | |||||||
| chr2:47802030 | A | C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01099.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.3172+875A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802030 | |||||||
| chr2:47802036 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3172+881T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802036 | |||||||
| chr2:47802138 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(4): Show |
9 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3172+983C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802138 | |||||||
| chr2:47802334 | A | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG01261.hp1 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3173-1086A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802334 | |||||||
| chr2:47802335 | T | C | 1 | a0002c0002t0001g0225 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3173-1085T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802335 | |||||||
| chr2:47802611 | G | A | 4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3173-809G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802611 | |||||||
| chr2:47802635 | G | GT | 21 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0103 others(18): Show |
21 | HG00621.hp1 HG00639.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.3173-763dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47802635 | ||||||
| chr2:47802635 | GT | G | 23 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0047 others(20): Show |
24 | HG00738.hp1 HG01109.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.3173-763delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47802635 | ||||||
| chr2:47802635 | GTT | G | 11 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(8): Show |
11 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.3173-764_3173-763d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 47802635 | ||||||
| chr2:47802657 | T | A | 1 | a0001c0001t0001g0167 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3173-763T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802657 | |||||||
| chr2:47802718 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3173-702G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802718 | |||||||
| chr2:47802718 | G | T | 1 | a0002c0003t0001g0238 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3173-702G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802718 | |||||||
| chr2:47802755 | T | C | 1 | a0002c0003t0001g0283 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3173-665T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802755 | |||||||
| chr2:47802758 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3173-662T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802758 | |||||||
| chr2:47802790 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0086 a0001c0001t0001g0088 others(1): Show |
5 | NA18943.hp1 NA18966.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.3173-630T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802790 | |||||||
| chr2:47802854 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0301 |
4 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3173-566C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802854 | |||||||
| chr2:47802883 | T | A | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3173-537T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802883 | |||||||
| chr2:47802950 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3173-470C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47802950 | |||||||
| chr2:47803024 | G | C | 1 | a0002c0002t0001g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3173-396G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803024 | |||||||
| chr2:47803038 | C | T | 16 | a0001c0004t0001g0029 a0001c0004t0001g0324 a0001c0004t0001g0325 others(13): Show |
17 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.3173-382C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803038 | |||||||
| chr2:47803062 | C | G | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3173-358C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803062 | |||||||
| chr2:47803165 | G | A | 1 | a0002c0002t0001g0022 | 2 | HG01081.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3173-255G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803165 | |||||||
| chr2:47803208 | G | A | 1 | a0001c0014t0001g0151 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3173-212G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803208 | |||||||
| chr2:47803318 | T | G | 1 | a0001c0001t0002g0313 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3173-102T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803318 | |||||||
| chr2:47803319 | G | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.3173-101G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 4/9 | chr2 | 47803319 | |||||||
| chr2:47803699 | A | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.3438+14A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47803699 | |||||||
| chr2:47803775 | A | G | 1 | a0001c0025t0001g0078 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3438+90A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47803775 | |||||||
| chr2:47803791 | G | C | 1 | a0003c0009t0001g0143 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.3438+106G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47803791 | |||||||
| chr2:47803861 | C | T | 6 | a0002c0003t0001g0006 a0002c0003t0001g0224 a0002c0003t0001g0238 others(3): Show |
8 | HG00438.hp2 HG02155.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.3438+176C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47803861 | |||||||
| chr2:47804047 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3438+362G>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804047 | |||||||
| chr2:47804053 | C | G | 1 | a0001c0001t0002g0313 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3438+368C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804053 | |||||||
| chr2:47804082 | A | T | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3438+397A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804082 | |||||||
| chr2:47804133 | C | CT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0123 a0001c0005t0001g0030 others(6): Show |
9 | HG01884.hp1 HG02109.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.3438+458dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 47804133 | ||||||
| chr2:47804141 | T | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0036 others(27): Show |
31 | HG00280.hp1 HG00735.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.3438+456T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804141 | |||||||
| chr2:47804182 | C | T | 1 | a0007c0028t0001g0263 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3438+497C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804182 | |||||||
| chr2:47804196 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0291 a0001c0001t0001g0310 others(2): Show |
5 | HG01358.hp2 HG02683.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.3438+511G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804196 | |||||||
| chr2:47804233 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(247): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.3438+548C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804233 | |||||||
| chr2:47804282 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0137 |
2 | NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3438+597T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804282 | |||||||
| chr2:47804287 | A | T | 3 | a0001c0018t0001g0034 a0002c0003t0001g0237 a0002c0003t0001g0243 |
3 | NA18952.hp1 NA18965.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3438+602A>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804287 | |||||||
| chr2:47804481 | G | A | 1 | a0002c0003t0001g0283 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.3439-429G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804481 | |||||||
| chr2:47804535 | TA | T | 13 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(10): Show |
13 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.3439-360delA | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 47804535 | ||||||
| chr2:47804541 | A | G | 1 | a0001c0004t0001g0341 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3439-369A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804541 | |||||||
| chr2:47804549 | AAG | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.3439-360_3439-359d others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804549 | |||||||
| chr2:47804550 | AG | A | 18 | a0001c0001t0001g0038 a0001c0001t0001g0074 a0001c0001t0001g0093 others(15): Show |
20 | HG02056.hp2 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.3439-358delG | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 47804550 | ||||||
| chr2:47804556 | A | G | 5 | a0001c0006t0001g0317 a0001c0006t0001g0318 a0001c0006t0001g0319 others(2): Show |
5 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.3439-354A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804556 | |||||||
| chr2:47804759 | G | A | 3 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0341 |
3 | HG02717.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3439-151G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804759 | |||||||
| chr2:47804785 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3439-125C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 5/9 | chr2 | 47804785 | |||||||
| chr2:47805173 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(237): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.3556+146G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805173 | |||||||
| chr2:47805173 | GTCTC | G | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3556+154_3556+157d others(6): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 47805173 | ||||||
| chr2:47805187 | T | C | 5 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0175 others(2): Show |
5 | HG01074.hp2 HG01952.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.3556+160T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805187 | |||||||
| chr2:47805244 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3556+217G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805244 | |||||||
| chr2:47805353 | G | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0203 others(4): Show |
9 | HG01346.hp2 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3557-265G>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805353 | |||||||
| chr2:47805433 | C | T | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3557-185C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805433 | |||||||
| chr2:47805473 | C | T | 1 | a0001c0007t0001g0190 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3557-145C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805473 | |||||||
| chr2:47805474 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.3557-144G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805474 | |||||||
| chr2:47805578 | T | A | 1 | a0002c0002t0001g0022 | 2 | HG01081.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3557-40T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | chr2 | 47805578 | |||||||
| chr2:47805601 | A | AT | 29 | a0001c0001t0001g0105 a0001c0001t0001g0124 a0001c0001t0001g0142 others(26): Show |
35 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.3557-4dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 47805601 | ||||||
| chr2:47805601 | AT | A | 10 | a0001c0001t0001g0056 a0001c0001t0001g0308 a0001c0005t0001g0030 others(7): Show |
10 | HG01255.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.3557-4delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 47805601 | ||||||
| chr2:47805735 | ACTAT | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.3646+35_3646+38del others(4): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 47805735 | ||||||
| chr2:47805774 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3646+67T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47805774 | |||||||
| chr2:47805798 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.3646+91T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47805798 | |||||||
| chr2:47805798 | T | G | 3 | a0001c0001t0001g0275 a0002c0002t0001g0228 a0002c0002t0001g0232 |
3 | NA18962.hp1 NA18991.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.3646+91T>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47805798 | |||||||
| chr2:47805860 | GATAAAAG others(8): Show |
G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0261 a0001c0001t0001g0301 |
4 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3646+154_3646+168d others(17): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47805860 | |||||||
| chr2:47805865 | A | G | 2 | a0002c0002t0001g0214 a0002c0002t0001g0215 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3646+158A>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47805865 | |||||||
| chr2:47805873 | A | C | 6 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(3): Show |
6 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3646+166A>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47805873 | |||||||
| chr2:47806053 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3647-151C>T | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | chr2 | 47806053 | |||||||
| chr2:47806133 | ATTTTTGT others(10): Show |
A | 18 | a0001c0001t0001g0123 a0001c0004t0001g0338 a0001c0004t0001g0339 others(15): Show |
18 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.3647-51_3647-35del others(17): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 47806133 | ||||||
| chr2:47806379 | T | C | 2 | a0001c0004t0001g0340 a0002c0002t0001g0214 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.3801+21T>C | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 8/9 | chr2 | 47806379 | |||||||
| chr2:47806407 | C | CT | 7 | a0001c0006t0001g0315 a0001c0006t0001g0316 a0001c0006t0001g0317 others(4): Show |
7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.3802-43dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 47806407 | ||||||
| chr2:47806412 | C | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.3802-40C>G | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 8/9 | chr2 | 47806412 | |||||||
| chr2:47806430 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3802-22G>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 8/9 | chr2 | 47806430 | |||||||
| chr2:47806699 | C | CAA | 5 | a0001c0007t0001g0189 a0001c0007t0001g0190 a0001c0007t0001g0191 others(2): Show |
5 | HG00738.hp1 HG01109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4001+50_4001+51dup others(2): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806699 | ||||||
| chr2:47806699 | C | CCTAACTG others(14): Show |
4 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4001+48_4001+49ins others(21): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | chr2 | 47806699 | |||||||
| chr2:47806750 | A | ACTT | 6 | a0001c0001t0001g0095 a0001c0001t0001g0108 a0001c0001t0001g0177 others(3): Show |
6 | HG00438.hp1 HG00558.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.4002-28_4002-26dup others(3): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806750 | ||||||
| chr2:47806751 | C | CT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0039 others(13): Show |
18 | HG00558.hp2 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.4002-10dupT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806751 | ||||||
| chr2:47806751 | C | CTTT | 8 | a0001c0005t0001g0030 a0001c0005t0001g0031 a0001c0005t0001g0304 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4002-12_4002-10dup others(3): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806751 | ||||||
| chr2:47806751 | CT | C | 91 | a0001c0001t0001g0028 a0001c0001t0001g0054 a0001c0001t0001g0074 others(88): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.4002-10delT | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806751 | ||||||
| chr2:47806751 | CTT | C | 5 | a0001c0006t0001g0316 a0001c0006t0001g0318 a0001c0006t0001g0320 others(2): Show |
6 | HG01069.hp1 HG01070.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.4002-11_4002-10del others(2): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806751 | ||||||
| chr2:47806751 | CTTT | C | 7 | a0001c0004t0001g0338 a0001c0004t0001g0339 a0001c0004t0001g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4002-12_4002-10del others(3): Show |
MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 47806751 | ||||||
| chr2:47806769 | T | A | 2 | a0001c0001t0001g0180 a0002c0003t0001g0196 |
2 | HG00423.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.4002-10T>A | MSH6 | ENSG00000116062.19 | transcript | ENST00000234420.11 | protein_coding | 9/9 | chr2 | 47806769 |