Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4439 |
| ensemblid | ENSG00000204410.16 |
| hgncid | 7328 |
| symbol | MSH5 |
| name | mutS homolog 5 |
| refseq_nuc | NM_172166.4 |
| refseq_prot | NP_751898.1 |
| ensembl_nuc | ENST00000375750.9 |
| ensembl_prot | ENSP00000364903.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 31740005 |
| end | 31762676 |
| strand | + |
| ver | v1.2 |
| region | chr6:31740005-31762676 |
| region5000 | chr6:31735005-31767676 |
| regionname0 | MSH5_chr6_31740005_31762676 |
| regionname5000 | MSH5_chr6_31735005_31767676 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 834 | 325 | 79 | 57 | 131 | 18 | 39 | 92 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0002 | 0/0 | 834 | 54 | 2 | 16 | 33 | 0 | 3 | 28 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0003 | 0/0 | 834 | 5 | 2 | 2 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0004 | 0/0 | 834 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0005 | 0/0 | 834 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0006 | 0/0 | 834 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0007 | 0/0 | 834 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0008 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0009 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| a0010 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | MASLG others(829): Show |
chr6 | 31735005 | 31767676 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2502 | 202 | 27 | 40 | 95 | 14 | 25 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0001c0002 | 0/0 | 2502 | 114 | 49 | 14 | 35 | 2 | 14 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0001c0004 | 0/0 | 2502 | 7 | 2 | 3 | 0 | 2 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0001c0008 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0001c0009 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0002c0003 | 0/0 | 2502 | 54 | 2 | 16 | 33 | 0 | 3 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0003c0006 | 0/0 | 2502 | 5 | 2 | 2 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0004c0005 | 0/0 | 2502 | 5 | 5 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0005c0007 | 0/0 | 2502 | 3 | 3 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0006c0013 | 0/0 | 2502 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0007c0014 | 0/0 | 2502 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0008c0010 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0009c0012 | 0/0 | 2502 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 | ||
| a0010c0011 | 0/0 | 2502 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | ATGGC others(2497): Show |
chr6 | 31735005 | 31767676 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2721 | 202 | 27 | 40 | 95 | 14 | 25 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0001c0002t0001 | 0/0 | 2721 | 113 | 48 | 14 | 35 | 2 | 14 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0001c0002t0003 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0001c0004t0001 | 0/0 | 2721 | 7 | 2 | 3 | 0 | 2 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0001c0008t0001 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0001c0009t0001 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0002c0003t0001 | 0/0 | 2721 | 54 | 2 | 16 | 33 | 0 | 3 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0003c0006t0001 | 0/0 | 2721 | 5 | 2 | 2 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0004c0005t0001 | 0/0 | 2721 | 5 | 5 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0005c0007t0002 | 0/0 | 2721 | 3 | 3 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0006c0013t0001 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0007c0014t0001 | 0/0 | 2721 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0008c0010t0001 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0009c0012t0001 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| a0010c0011t0001 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | CTTTT others(2716): Show |
chr6 | 31735005 | 31767676 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0002t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0004t0001g0003 | 0/0 | 6 | 2 | 2 | 0 | 2 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0008t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0001c0009t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0003c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0003c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0003c0006t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0003c0006t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0003c0006t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0004c0005t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0004c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0004c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0004c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0005c0007t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0005c0007t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0005c0007t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0006c0013t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0007c0014t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0008c0010t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0009c0012t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| a0010c0011t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0003 | EUR | GBR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00280 | hp2 | a0001 | c0004 | t0001 | g0003 | EUR | FIN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0209 | EUR | FIN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0071 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG00741 | hp2 | a0006 | c0013 | t0001 | g0110 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0111 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01106 | hp1 | a0003 | c0006 | t0001 | g0070 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | PUR | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0108 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0104 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0107 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0085 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01361 | hp1 | a0003 | c0006 | t0001 | g0050 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01496 | hp2 | a0002 | c0003 | t0001 | g0082 | AMR | CLM | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0270 | EUR | IBS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | IBS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01884 | hp1 | a0005 | c0007 | t0002 | g0095 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0308 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0081 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01981 | hp1 | a0002 | c0003 | t0001 | g0009 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02129 | hp2 | a0001 | c0008 | t0001 | g0233 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0253 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02273 | hp2 | a0002 | c0003 | t0001 | g0011 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02280 | hp2 | a0004 | c0005 | t0001 | g0025 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02293 | hp2 | a0002 | c0003 | t0001 | g0077 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PEL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0210 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0272 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0302 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02698 | hp2 | a0003 | c0006 | t0001 | g0051 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02723 | hp1 | a0005 | c0007 | t0002 | g0096 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0166 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02809 | hp1 | a0005 | c0007 | t0002 | g0097 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02809 | hp2 | a0003 | c0006 | t0001 | g0045 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02970 | hp2 | a0004 | c0005 | t0001 | g0053 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02976 | hp2 | a0003 | c0006 | t0001 | g0049 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03017 | hp1 | a0002 | c0003 | t0001 | g0106 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0313 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03098 | hp2 | a0001 | c0009 | t0001 | g0039 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0178 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0279 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03209 | hp2 | a0004 | c0005 | t0001 | g0093 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0065 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0303 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0278 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03654 | hp2 | a0007 | c0014 | t0001 | g0109 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0008 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0271 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0021 | SAS | STU | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | YRI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | YRI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18612 | hp2 | a0002 | c0003 | t0001 | g0008 | EAS | CHB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0008 | EAS | CHB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18906 | hp1 | a0004 | c0005 | t0001 | g0025 | AFR | YRI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18956 | hp1 | a0002 | c0003 | t0001 | g0102 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0092 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18984 | hp1 | a0008 | c0010 | t0001 | g0139 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18987 | hp2 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18994 | hp2 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19000 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19005 | hp2 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | LWK | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19074 | hp1 | a0009 | c0012 | t0001 | g0007 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0054 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | YRI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | YRI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20129 | hp1 | a0004 | c0005 | t0001 | g0105 | AFR | ASW | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0277 | AFR | ASW | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | TSI | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | GIH | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | MSL | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | USA | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | USA | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20300 | hp1 | a0010 | c0011 | t0001 | g0052 | AFR | USA | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0091 | AFR | USA | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | MSH5_chr6_31735005_31767676 | MSH5 | chr6 | 31735005 | 31767676 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31740551 | C | T | 4 | a0002 a0006 a0007 others(1): Show |
57 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(54): Show |
missense_variant | MODERATE | c.85C>T | p.Pro29Ser | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 2/25 | 156/2721 | 85/2505 | 29/834 | chr6 | 31740551 | |||
| chr6:31741268 | C | T | 2 | a0003 a0010 |
6 | HG01106.hp1 HG01361.hp1 HG02698.hp2 others(3): Show |
missense_variant | MODERATE | c.253C>T | p.Leu85Phe | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/25 | 324/2721 | 253/2505 | 85/834 | chr6 | 31741268 | |||
| chr6:31744227 | G | A | 1 | a0009 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.575G>A | p.Arg192Gln | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 7/25 | 646/2721 | 575/2505 | 192/834 | chr6 | 31744227 | |||
| chr6:31758201 | C | G | 2 | a0006 a0007 |
2 | HG00741.hp2 HG03654.hp2 |
missense_variant | MODERATE | c.1051C>G | p.Arg351Gly | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 13/25 | 1122/2721 | 1051/2505 | 351/834 | chr6 | 31758201 | |||
| chr6:31758279 | C | T | 1 | a0005 | 3 | HG01884.hp1 HG02723.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.1129C>T | p.Leu377Phe | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 13/25 | 1200/2721 | 1129/2505 | 377/834 | chr6 | 31758279 | |||
| chr6:31760104 | A | T | 1 | a0008 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.1700A>T | p.Glu567Val | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/25 | 1771/2721 | 1700/2505 | 567/834 | chr6 | 31760104 | |||
| chr6:31760142 | T | G | 1 | a0006 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.1738T>G | p.Cys580Gly | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/25 | 1809/2721 | 1738/2505 | 580/834 | chr6 | 31760142 | |||
| chr6:31760693 | G | A | 1 | a0008 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.1816G>A | p.Gly606Ser | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 20/25 | 1887/2721 | 1816/2505 | 606/834 | chr6 | 31760693 | |||
| chr6:31762148 | C | T | 2 | a0003 a0004 |
10 | HG01106.hp1 HG01361.hp1 HG02280.hp2 others(7): Show |
missense_variant | MODERATE | c.2356C>T | p.Pro786Ser | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 24/25 | 2427/2721 | 2356/2505 | 786/834 | chr6 | 31762148 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31760120 | C | T | 1 | a0001c0004 | 7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
synonymous_variant | LOW | c.1716C>T | p.Thr572Thr | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/25 | 1787/2721 | 1716/2505 | 572/834 | chr6 | 31760120 | |||
| chr6:31760692 | A | T | 1 | a0008c0010 | 1 | NA18984.hp1 | splice_region_variant&synonymous_variant | LOW | c.1815A>T | p.Val605Val | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 20/25 | 1886/2721 | 1815/2505 | 605/834 | chr6 | 31760692 | |||
| chr6:31761193 | G | A | 1 | a0001c0008 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1968G>A | p.Ala656Ala | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 21/25 | 2039/2721 | 1968/2505 | 656/834 | chr6 | 31761193 | |||
| chr6:31761495 | C | T | 1 | a0001c0009 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.2061C>T | p.Ala687Ala | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 22/25 | 2132/2721 | 2061/2505 | 687/834 | chr6 | 31761495 | |||
| chr6:31761582 | A | G | 11 | a0001c0002 a0001c0004 a0001c0009 others(8): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
synonymous_variant | LOW | c.2148A>G | p.Gln716Gln | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 22/25 | 2219/2721 | 2148/2505 | 716/834 | chr6 | 31761582 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31740052 | T | C | 1 | a0005c0007t0002 | 3 | HG01884.hp1 HG02723.hp1 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-24T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 1/25 | 415 | chr6 | 31740052 | ||||||
| chr6:31762612 | C | T | 1 | a0001c0002t0003 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 25/25 | 81 | chr6 | 31762612 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31740306 | C | T | 1 | a0001c0002t0001g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-13-148C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 1/24 | chr6 | 31740306 | |||||||
| chr6:31740370 | T | C | 80 | a0001c0002t0001g0002 a0001c0002t0001g0024 a0001c0002t0001g0026 others(77): Show |
100 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.-13-84T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 1/24 | chr6 | 31740370 | |||||||
| chr6:31740377 | C | T | 1 | a0001c0001t0001g0043 | 2 | NA18953.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-13-77C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 1/24 | chr6 | 31740377 | |||||||
| chr6:31740686 | C | A | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.147+73C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 2/24 | chr6 | 31740686 | |||||||
| chr6:31741055 | G | A | 1 | a0002c0003t0001g0044 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.148-108G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 2/24 | chr6 | 31741055 | |||||||
| chr6:31741133 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.148-30T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 2/24 | chr6 | 31741133 | |||||||
| chr6:31741336 | T | TAC | 16 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(13): Show |
19 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.271+96_271+97dupCA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | T | TACAC | 6 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
8 | HG00140.hp1 HG00408.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+94_271+97dupCA others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | T | TACACAC | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0002t0001g0115 others(3): Show |
6 | HG00280.hp1 HG00621.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+92_271+97dupCA others(4): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TAC | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0033 others(35): Show |
52 | HG00323.hp2 HG00423.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.271+96_271+97delCA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACAC | T | 55 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0112 others(52): Show |
62 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.271+94_271+97delCA others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACAC | T | 23 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0261 others(20): Show |
28 | HG00558.hp1 HG00741.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.271+92_271+97delCA others(4): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACACA others(1): Show |
T | 48 | a0001c0001t0001g0040 a0001c0001t0001g0267 a0001c0001t0001g0268 others(45): Show |
62 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.271+90_271+97delCA others(6): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACACA others(3): Show |
T | 18 | a0001c0002t0001g0022 a0001c0002t0001g0094 a0001c0002t0001g0098 others(15): Show |
20 | HG00642.hp2 HG01081.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.271+88_271+97delCA others(8): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACACA others(5): Show |
T | 11 | a0001c0002t0001g0280 a0002c0003t0001g0007 a0002c0003t0001g0028 others(8): Show |
14 | HG00735.hp2 HG00741.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.271+86_271+97delCA others(10): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACACA others(7): Show |
T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
10 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.271+84_271+97delCA others(12): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACACA others(9): Show |
T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
24 | HG00735.hp1 HG01074.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.271+82_271+97delCA others(14): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741336 | TACACACA others(11): Show |
T | 9 | a0001c0002t0001g0006 a0001c0002t0001g0301 a0001c0002t0001g0302 others(6): Show |
13 | HG01891.hp1 HG02071.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.271+80_271+97delCA others(16): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741336 | ||||||
| chr6:31741362 | CACACACA others(15): Show |
C | 4 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG00558.hp2 HG04115.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+78_271+99delCA others(20): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741362 | ||||||
| chr6:31741369 | AC | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0171 |
3 | HG02165.hp2 HG02523.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.271+84delC | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741369 | |||||||
| chr6:31741370 | C | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0035 others(4): Show |
11 | HG00423.hp2 HG02040.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+84C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741370 | |||||||
| chr6:31741372 | CACACACA others(5): Show |
C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0149 a0001c0001t0001g0156 others(2): Show |
7 | HG00099.hp1 HG00738.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.271+88_271+99delCA others(10): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741372 | ||||||
| chr6:31741380 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.271+94C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741380 | |||||||
| chr6:31741380 | CACAT | C | 5 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(2): Show |
5 | HG00423.hp1 HG02738.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.271+96_271+99delCA others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741380 | ||||||
| chr6:31741541 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0213 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.271+255G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741541 | |||||||
| chr6:31741566 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0258 |
3 | HG02027.hp1 NA18953.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.271+280C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741566 | |||||||
| chr6:31741572 | C | T | 153 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(150): Show |
192 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(189): Show |
intron_variant | MODIFIER | c.271+286C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741572 | |||||||
| chr6:31741625 | G | A | 2 | a0002c0003t0001g0063 a0002c0003t0001g0064 |
2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.271+339G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741625 | |||||||
| chr6:31741753 | G | C | 4 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG00558.hp2 HG04115.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+467G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741753 | |||||||
| chr6:31741764 | TA | T | 107 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0032 others(104): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.271+493delA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741764 | ||||||
| chr6:31741764 | TAA | T | 64 | a0001c0001t0001g0037 a0001c0001t0001g0183 a0001c0001t0001g0211 others(61): Show |
84 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.271+492_271+493del others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr6 | 31741764 | ||||||
| chr6:31741803 | G | C | 10 | a0003c0006t0001g0045 a0003c0006t0001g0049 a0003c0006t0001g0050 others(7): Show |
11 | HG01106.hp1 HG01361.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.271+517G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741803 | |||||||
| chr6:31741920 | G | T | 1 | a0001c0002t0001g0304 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.271+634G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31741920 | |||||||
| chr6:31742001 | A | G | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+715A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742001 | |||||||
| chr6:31742037 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.271+751G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742037 | |||||||
| chr6:31742037 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.271+751G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742037 | |||||||
| chr6:31742112 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.272-765A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742112 | |||||||
| chr6:31742192 | C | A | 1 | a0001c0002t0001g0094 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.272-685C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742192 | |||||||
| chr6:31742243 | C | T | 159 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(156): Show |
203 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.272-634C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742243 | |||||||
| chr6:31742252 | G | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.272-625G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742252 | |||||||
| chr6:31742327 | G | A | 14 | a0001c0002t0001g0029 a0001c0002t0001g0115 a0001c0002t0001g0116 others(11): Show |
15 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.272-550G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742327 | |||||||
| chr6:31742335 | G | A | 1 | a0002c0003t0001g0071 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.272-542G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742335 | |||||||
| chr6:31742343 | C | T | 6 | a0001c0002t0001g0016 a0001c0002t0001g0165 a0001c0002t0001g0166 others(3): Show |
8 | HG00423.hp1 HG02738.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.272-534C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742343 | |||||||
| chr6:31742468 | G | A | 9 | a0001c0002t0001g0024 a0001c0002t0001g0026 a0001c0002t0001g0072 others(6): Show |
11 | HG00642.hp2 HG01081.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.272-409G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742468 | |||||||
| chr6:31742492 | C | T | 1 | a0001c0002t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.272-385C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 3/24 | chr6 | 31742492 | |||||||
| chr6:31743005 | A | G | 1 | a0001c0002t0001g0266 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.352+48A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 4/24 | chr6 | 31743005 | |||||||
| chr6:31743191 | T | A | 34 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(31): Show |
42 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.415+21T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743191 | |||||||
| chr6:31743301 | A | G | 9 | a0001c0002t0001g0024 a0001c0002t0001g0026 a0001c0002t0001g0072 others(6): Show |
11 | HG00642.hp2 HG01081.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.415+131A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743301 | |||||||
| chr6:31743347 | C | T | 79 | a0001c0002t0001g0002 a0001c0002t0001g0024 a0001c0002t0001g0026 others(76): Show |
99 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.415+177C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743347 | |||||||
| chr6:31743359 | T | C | 5 | a0001c0002t0001g0022 a0001c0002t0001g0274 a0001c0002t0001g0275 others(2): Show |
7 | HG01952.hp2 NA18945.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.415+189T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743359 | |||||||
| chr6:31743795 | G | A | 1 | a0003c0006t0001g0070 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.416-109G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743795 | |||||||
| chr6:31743803 | G | A | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.416-101G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743803 | |||||||
| chr6:31743805 | A | G | 1 | a0001c0002t0001g0308 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.416-99A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743805 | |||||||
| chr6:31743847 | A | C | 12 | a0001c0002t0001g0006 a0001c0002t0001g0022 a0001c0002t0001g0274 others(9): Show |
18 | HG01891.hp1 HG01952.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.416-57A>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 5/24 | chr6 | 31743847 | |||||||
| chr6:31744404 | T | G | 80 | a0001c0002t0001g0002 a0001c0002t0001g0024 a0001c0002t0001g0026 others(77): Show |
100 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.647+105T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 7/24 | chr6 | 31744404 | |||||||
| chr6:31744419 | G | A | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.647+120G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 7/24 | chr6 | 31744419 | |||||||
| chr6:31744788 | G | A | 1 | a0001c0002t0001g0274 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.683+207G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | chr6 | 31744788 | |||||||
| chr6:31744832 | G | A | 1 | a0002c0003t0001g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.683+251G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | chr6 | 31744832 | |||||||
| chr6:31745040 | G | T | 24 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0029 others(21): Show |
29 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.684-197G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | chr6 | 31745040 | |||||||
| chr6:31745051 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.684-186C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | chr6 | 31745051 | |||||||
| chr6:31745103 | C | CA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0035 others(27): Show |
38 | HG01175.hp2 HG02056.hp1 HG02056.hp2 others(35): Show |
intron_variant | MODIFIER | c.684-111dupA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr6 | 31745103 | ||||||
| chr6:31745103 | CA | C | 7 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0201 others(4): Show |
7 | HG00099.hp1 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.684-111delA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr6 | 31745103 | ||||||
| chr6:31745103 | CAA | C | 12 | a0001c0002t0001g0024 a0001c0002t0001g0029 a0001c0002t0001g0072 others(9): Show |
15 | HG00673.hp1 HG01074.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.684-112_684-111del others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr6 | 31745103 | ||||||
| chr6:31745103 | CAAA | C | 146 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0127 others(143): Show |
187 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.684-113_684-111del others(3): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr6 | 31745103 | ||||||
| chr6:31745347 | A | G | 53 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0001g0068 others(50): Show |
65 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+28A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745347 | |||||||
| chr6:31745552 | G | T | 1 | a0001c0002t0003g0279 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.766+233G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745552 | |||||||
| chr6:31745616 | G | A | 14 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0214 others(11): Show |
14 | HG00408.hp1 HG02135.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.766+297G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745616 | |||||||
| chr6:31745677 | C | T | 79 | a0001c0002t0001g0002 a0001c0002t0001g0024 a0001c0002t0001g0026 others(76): Show |
99 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.766+358C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745677 | |||||||
| chr6:31745765 | G | GT | 28 | a0001c0001t0001g0036 a0001c0001t0001g0146 a0001c0001t0001g0147 others(25): Show |
29 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.766+466dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31745765 | ||||||
| chr6:31745765 | GT | G | 92 | a0001c0001t0001g0135 a0001c0001t0001g0177 a0001c0001t0001g0260 others(89): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.766+466delT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31745765 | ||||||
| chr6:31745765 | GTT | G | 31 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(28): Show |
39 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.766+465_766+466del others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31745765 | ||||||
| chr6:31745788 | T | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(284): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.766+469T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745788 | |||||||
| chr6:31745789 | A | G | 34 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(31): Show |
42 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+470A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745789 | |||||||
| chr6:31745807 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.766+488G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745807 | |||||||
| chr6:31745899 | C | T | 1 | a0001c0002t0001g0304 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.766+580C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745899 | |||||||
| chr6:31745971 | T | G | 2 | a0001c0002t0001g0252 a0001c0002t0001g0270 |
2 | HG01515.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.766+652T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31745971 | |||||||
| chr6:31746008 | C | T | 12 | a0001c0002t0001g0006 a0001c0002t0001g0022 a0001c0002t0001g0274 others(9): Show |
18 | HG01891.hp1 HG01952.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.766+689C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746008 | |||||||
| chr6:31746046 | G | A | 23 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0029 others(20): Show |
28 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.766+727G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746046 | |||||||
| chr6:31746056 | G | A | 5 | a0001c0002t0001g0275 a0001c0002t0001g0301 a0001c0002t0001g0302 others(2): Show |
5 | HG01952.hp2 HG02071.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+737G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746056 | |||||||
| chr6:31746058 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0114 a0001c0001t0001g0119 others(3): Show |
8 | HG00140.hp1 HG02080.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+739G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746058 | |||||||
| chr6:31746078 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0287 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.766+759_766+760ins others(11): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746078 | |||||||
| chr6:31746078 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0284 a0001c0001t0001g0288 |
4 | HG00735.hp1 HG02109.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+760_766+761ins others(10): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746078 | ||||||
| chr6:31746078 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0001g0289 a0001c0001t0001g0297 |
2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.766+760_766+761ins others(12): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746078 | ||||||
| chr6:31746080 | T | G | 6 | a0001c0001t0001g0041 a0001c0001t0001g0284 a0001c0001t0001g0287 others(3): Show |
7 | HG00735.hp1 HG01516.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+761T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(2): Show |
3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0002t0001g0206 |
3 | HG01516.hp1 HG02602.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.766+761_766+762ins others(9): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG02148.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.766+761_766+762ins others(11): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(8): Show |
2 | a0001c0001t0001g0149 a0002c0003t0001g0054 |
2 | HG00738.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.766+761_766+762ins others(15): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(12): Show |
2 | a0001c0002t0001g0067 a0001c0002t0001g0276 |
2 | HG02647.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.766+761_766+762ins others(19): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(14): Show |
1 | a0002c0003t0001g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.766+761_766+762ins others(21): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(16): Show |
1 | a0001c0002t0001g0305 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.766+761_766+762ins others(23): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(18): Show |
1 | a0001c0002t0001g0180 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.766+761_766+762ins others(25): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TGTGTGTG others(20): Show |
1 | a0001c0002t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.766+761_766+762ins others(27): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746080 | |||||||
| chr6:31746080 | T | TTG | 4 | a0001c0001t0001g0126 a0001c0001t0001g0204 a0001c0004t0001g0003 others(1): Show |
9 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.766+794_766+795dup others(2): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTG | 5 | a0001c0001t0001g0231 a0001c0001t0001g0261 a0001c0001t0001g0283 others(2): Show |
5 | HG01109.hp2 HG02132.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+792_766+795dup others(4): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(1): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
51 | HG00280.hp1 HG00597.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+788_766+795dup others(8): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(3): Show |
71 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(68): Show |
78 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+786_766+795dup others(10): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(5): Show |
24 | a0001c0001t0001g0034 a0001c0001t0001g0131 a0001c0001t0001g0132 others(21): Show |
29 | HG00323.hp1 HG01106.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.766+784_766+795dup others(12): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(7): Show |
37 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0112 others(34): Show |
50 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.766+782_766+795dup others(14): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(9): Show |
19 | a0001c0001t0001g0309 a0001c0002t0001g0059 a0001c0002t0001g0062 others(16): Show |
23 | HG01496.hp2 HG01934.hp2 HG01981.hp1 others(20): Show |
intron_variant | MODIFIER | c.766+780_766+795dup others(16): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(11): Show |
17 | a0001c0001t0001g0311 a0001c0002t0001g0026 a0001c0002t0001g0029 others(14): Show |
22 | HG00621.hp1 HG00741.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+778_766+795dup others(18): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(13): Show |
17 | a0001c0002t0001g0006 a0001c0002t0001g0013 a0001c0002t0001g0024 others(14): Show |
26 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.766+776_766+795dup others(20): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(15): Show |
11 | a0001c0002t0001g0099 a0001c0002t0001g0123 a0001c0002t0001g0130 others(8): Show |
12 | HG00642.hp2 HG00735.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.766+774_766+795dup others(22): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(17): Show |
13 | a0001c0002t0001g0018 a0001c0002t0001g0069 a0001c0002t0001g0118 others(10): Show |
15 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+772_766+795dup others(24): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(19): Show |
6 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0129 others(3): Show |
6 | HG00621.hp2 HG01361.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+770_766+795dup others(26): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(21): Show |
1 | a0001c0002t0001g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.766+768_766+795dup others(28): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(23): Show |
1 | a0003c0006t0001g0070 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.766+766_766+795dup others(30): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746080 | T | TTGTGTGT others(25): Show |
1 | a0001c0002t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.766+764_766+795dup others(32): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746080 | ||||||
| chr6:31746113 | T | TGTGTGTG others(3): Show |
1 | a0001c0008t0001g0233 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766+795_766+796ins others(10): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746113 | ||||||
| chr6:31746113 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766+795_766+796ins others(18): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746113 | ||||||
| chr6:31746113 | T | TGTGTGTG others(17): Show |
3 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0304 |
3 | HG02071.hp1 HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.766+795_766+796ins others(24): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746113 | ||||||
| chr6:31746113 | T | TGTGTGTG others(19): Show |
1 | a0001c0002t0001g0303 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.766+795_766+796ins others(26): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr6 | 31746113 | ||||||
| chr6:31746115 | A | T | 45 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0120 others(42): Show |
53 | HG00323.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.766+796A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746115 | |||||||
| chr6:31746127 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.766+808G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746127 | |||||||
| chr6:31746165 | C | T | 1 | a0004c0005t0001g0093 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.766+846C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746165 | |||||||
| chr6:31746254 | G | A | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+935G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746254 | |||||||
| chr6:31746393 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.767-994G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746393 | |||||||
| chr6:31746409 | A | G | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0001t0001g0299 |
3 | HG01167.hp2 HG01169.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.767-978A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746409 | |||||||
| chr6:31746443 | G | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0211 a0001c0001t0001g0212 |
4 | HG03834.hp1 NA18948.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.767-944G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746443 | |||||||
| chr6:31746525 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.767-862G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746525 | |||||||
| chr6:31746605 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.767-782T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31746605 | |||||||
| chr6:31747033 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.767-354A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 9/24 | chr6 | 31747033 | |||||||
| chr6:31747592 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0127 |
3 | HG01346.hp1 HG01358.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.812+160C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31747592 | |||||||
| chr6:31747766 | G | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0072 a0001c0002t0001g0073 others(1): Show |
5 | HG02040.hp1 HG02523.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.812+334G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31747766 | |||||||
| chr6:31747792 | G | T | 1 | a0001c0002t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.812+360G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31747792 | |||||||
| chr6:31747793 | G | A | 1 | a0003c0006t0001g0070 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.812+361G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31747793 | |||||||
| chr6:31747813 | T | C | 1 | a0001c0002t0001g0303 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.812+381T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31747813 | |||||||
| chr6:31747865 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0173 a0001c0001t0001g0183 |
4 | HG00642.hp1 HG00733.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.812+433G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31747865 | |||||||
| chr6:31748002 | CA | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(280): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.812+585delA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31748002 | ||||||
| chr6:31748105 | T | C | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.812+673T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31748105 | |||||||
| chr6:31748125 | G | A | 1 | a0004c0005t0001g0105 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.812+693G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31748125 | |||||||
| chr6:31748344 | C | CT | 51 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(48): Show |
68 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.812+933dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31748344 | ||||||
| chr6:31748344 | CT | C | 9 | a0001c0002t0001g0022 a0001c0002t0001g0066 a0001c0002t0001g0167 others(6): Show |
11 | HG01952.hp2 HG02896.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.812+933delT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31748344 | ||||||
| chr6:31748480 | C | G | 1 | a0001c0002t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.812+1048C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31748480 | |||||||
| chr6:31748522 | T | A | 1 | a0001c0002t0001g0253 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.812+1090T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31748522 | |||||||
| chr6:31748659 | A | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG00140.hp2 HG01192.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.812+1227A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31748659 | |||||||
| chr6:31748807 | C | G | 1 | a0001c0002t0001g0305 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.812+1375C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31748807 | |||||||
| chr6:31748916 | CT | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(273): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.812+1501delT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31748916 | ||||||
| chr6:31749063 | C | G | 12 | a0001c0002t0001g0006 a0001c0002t0001g0022 a0001c0002t0001g0274 others(9): Show |
18 | HG01891.hp1 HG01952.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.812+1631C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749063 | |||||||
| chr6:31749127 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.812+1695G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749127 | |||||||
| chr6:31749152 | G | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.812+1720G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749152 | |||||||
| chr6:31749280 | G | A | 8 | a0001c0001t0001g0152 a0001c0001t0001g0163 a0001c0001t0001g0188 others(5): Show |
8 | HG01167.hp1 HG01192.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.812+1848G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749280 | |||||||
| chr6:31749289 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0149 a0001c0001t0001g0156 others(12): Show |
19 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.812+1857C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749289 | |||||||
| chr6:31749502 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.812+2070A>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749502 | |||||||
| chr6:31749768 | C | CT | 4 | a0001c0002t0001g0136 a0001c0002t0001g0178 a0001c0002t0001g0210 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.812+2337dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31749768 | ||||||
| chr6:31749820 | T | C | 5 | a0001c0002t0001g0165 a0001c0002t0001g0166 a0001c0002t0001g0167 others(2): Show |
5 | HG00423.hp1 HG02738.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.812+2388T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749820 | |||||||
| chr6:31749827 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.812+2395G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749827 | |||||||
| chr6:31749907 | G | A | 1 | a0001c0002t0001g0303 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.812+2475G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749907 | |||||||
| chr6:31749915 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(283): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(352): Show |
intron_variant | MODIFIER | c.812+2483A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749915 | |||||||
| chr6:31749919 | A | G | 34 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(31): Show |
42 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.812+2487A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31749919 | |||||||
| chr6:31750043 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.812+2611C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750043 | |||||||
| chr6:31750198 | A | T | 1 | a0001c0002t0001g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.812+2766A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750198 | |||||||
| chr6:31750258 | C | T | 12 | a0001c0002t0001g0029 a0001c0002t0001g0116 a0001c0002t0001g0117 others(9): Show |
13 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.812+2826C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750258 | |||||||
| chr6:31750272 | T | G | 4 | a0001c0002t0001g0136 a0001c0002t0001g0178 a0001c0002t0001g0210 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.812+2840T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750272 | |||||||
| chr6:31750451 | A | G | 1 | a0003c0006t0001g0050 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.813-2850A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750451 | |||||||
| chr6:31750582 | G | C | 1 | a0001c0001t0001g0038 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.813-2719G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750582 | |||||||
| chr6:31750593 | G | C | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.813-2708G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750593 | |||||||
| chr6:31750618 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.813-2683G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750618 | |||||||
| chr6:31750619 | C | G | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.813-2682C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750619 | |||||||
| chr6:31750636 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.813-2665G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750636 | |||||||
| chr6:31750825 | G | A | 43 | a0002c0003t0001g0007 a0002c0003t0001g0008 a0002c0003t0001g0009 others(40): Show |
55 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.813-2476G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750825 | |||||||
| chr6:31750886 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0134 |
3 | HG02080.hp1 HG02735.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.813-2415T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750886 | |||||||
| chr6:31750992 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.813-2309T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750992 | |||||||
| chr6:31750999 | A | T | 6 | a0001c0001t0001g0154 a0001c0001t0001g0219 a0001c0001t0001g0238 others(3): Show |
6 | NA18948.hp2 NA18949.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.813-2302A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31750999 | |||||||
| chr6:31751000 | T | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0219 a0001c0001t0001g0238 others(3): Show |
6 | NA18948.hp2 NA18949.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.813-2301T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31751000 | |||||||
| chr6:31751157 | G | A | 12 | a0001c0002t0001g0006 a0001c0002t0001g0022 a0001c0002t0001g0274 others(9): Show |
18 | HG01891.hp1 HG01952.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.813-2144G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31751157 | |||||||
| chr6:31751509 | C | G | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.813-1792C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31751509 | |||||||
| chr6:31751550 | C | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.813-1751C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31751550 | |||||||
| chr6:31751606 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.813-1695A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31751606 | |||||||
| chr6:31751637 | G | GA | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.813-1651dupA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31751637 | ||||||
| chr6:31752078 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.813-1223G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752078 | |||||||
| chr6:31752233 | G | A | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.813-1068G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752233 | |||||||
| chr6:31752460 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.813-841C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752460 | |||||||
| chr6:31752492 | C | T | 5 | a0001c0001t0001g0281 a0001c0002t0001g0021 a0001c0002t0001g0264 others(2): Show |
7 | HG02572.hp2 HG02735.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.813-809C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752492 | |||||||
| chr6:31752718 | C | CA | 17 | a0001c0001t0001g0188 a0001c0002t0001g0115 a0001c0002t0001g0116 others(14): Show |
17 | HG00408.hp2 HG00597.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.813-567dupA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31752718 | ||||||
| chr6:31752718 | CA | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(204): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.813-567delA | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr6 | 31752718 | ||||||
| chr6:31752728 | A | C | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.813-573A>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752728 | |||||||
| chr6:31752748 | C | CATT | 181 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0037 others(178): Show |
229 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.813-553_813-552ins others(3): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752748 | |||||||
| chr6:31752750 | T | C | 1 | a0001c0002t0001g0304 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.813-551T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752750 | |||||||
| chr6:31752860 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.813-441A>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31752860 | |||||||
| chr6:31753190 | G | A | 2 | a0001c0002t0001g0072 a0001c0002t0001g0073 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.813-111G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31753190 | |||||||
| chr6:31753256 | G | A | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.813-45G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31753256 | |||||||
| chr6:31753278 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.813-23C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 10/24 | chr6 | 31753278 | |||||||
| chr6:31753542 | C | A | 1 | a0004c0005t0001g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.952-25C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 11/24 | chr6 | 31753542 | |||||||
| chr6:31753733 | C | CT | 8 | a0001c0001t0001g0141 a0001c0001t0001g0204 a0001c0001t0001g0242 others(5): Show |
8 | HG01361.hp1 HG02698.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014+118dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31753733 | ||||||
| chr6:31753733 | CT | C | 25 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0029 others(22): Show |
30 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1014+118delT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31753733 | ||||||
| chr6:31753768 | G | A | 12 | a0001c0002t0001g0029 a0001c0002t0001g0116 a0001c0002t0001g0117 others(9): Show |
13 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1014+139G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31753768 | |||||||
| chr6:31753907 | G | A | 12 | a0001c0002t0001g0006 a0001c0002t0001g0022 a0001c0002t0001g0274 others(9): Show |
18 | HG01891.hp1 HG01952.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1014+278G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31753907 | |||||||
| chr6:31754122 | CTT | C | 3 | a0002c0003t0001g0079 a0002c0003t0001g0083 a0002c0003t0001g0088 |
3 | NA18957.hp2 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1014+495_1014+496d others(4): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31754122 | ||||||
| chr6:31754132 | C | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+503C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754132 | |||||||
| chr6:31754137 | A | AT | 58 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(55): Show |
71 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1014+517dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31754137 | ||||||
| chr6:31754433 | A | G | 1 | a0002c0003t0001g0089 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1014+804A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754433 | |||||||
| chr6:31754485 | C | T | 24 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0029 others(21): Show |
29 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1014+856C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754485 | |||||||
| chr6:31754710 | T | C | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+1081T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754710 | |||||||
| chr6:31754735 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1106C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754735 | |||||||
| chr6:31754736 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1107A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754736 | |||||||
| chr6:31754746 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1117C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754746 | |||||||
| chr6:31754747 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1118T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754747 | |||||||
| chr6:31754751 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1122T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754751 | |||||||
| chr6:31754753 | C | CT | 28 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0042 others(25): Show |
32 | HG00735.hp1 HG01106.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.1014+1141dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31754753 | ||||||
| chr6:31754753 | CT | C | 23 | a0001c0001t0001g0156 a0001c0001t0001g0221 a0001c0001t0001g0309 others(20): Show |
29 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1014+1141delT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31754753 | ||||||
| chr6:31754912 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1283C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754912 | |||||||
| chr6:31754914 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1014+1285A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754914 | |||||||
| chr6:31754963 | A | G | 19 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(16): Show |
21 | HG00642.hp1 HG00733.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1014+1334A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31754963 | |||||||
| chr6:31755003 | C | T | 81 | a0001c0002t0001g0002 a0001c0002t0001g0024 a0001c0002t0001g0026 others(78): Show |
106 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1014+1374C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755003 | |||||||
| chr6:31755282 | G | T | 1 | a0001c0001t0001g0232 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1014+1653G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755282 | |||||||
| chr6:31755311 | C | T | 24 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0029 others(21): Show |
29 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1014+1682C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755311 | |||||||
| chr6:31755318 | AGTTT | A | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+1690_1014+169 others(8): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755318 | |||||||
| chr6:31755323 | T | A | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+1694T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755323 | |||||||
| chr6:31755337 | C | CATTT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0015 others(69): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1014+1745_1014+174 others(8): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31755337 | ||||||
| chr6:31755337 | C | CATTTATT others(1): Show |
87 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 others(84): Show |
109 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1014+1741_1014+174 others(12): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31755337 | ||||||
| chr6:31755337 | C | CATTTATT others(5): Show |
8 | a0001c0001t0001g0157 a0001c0001t0001g0191 a0001c0001t0001g0202 others(5): Show |
8 | HG00733.hp2 NA18943.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014+1737_1014+174 others(16): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31755337 | ||||||
| chr6:31755337 | CATTT | C | 61 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(58): Show |
74 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1014+1745_1014+174 others(8): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31755337 | ||||||
| chr6:31755337 | CATTTATT others(1): Show |
C | 3 | a0001c0002t0001g0075 a0001c0004t0001g0003 a0001c0004t0001g0111 |
8 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014+1741_1014+174 others(12): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31755337 | ||||||
| chr6:31755337 | CATTTATT others(5): Show |
C | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.1014+1737_1014+174 others(16): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31755337 | ||||||
| chr6:31755582 | G | A | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+1953G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755582 | |||||||
| chr6:31755612 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(309): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1014+1983C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755612 | |||||||
| chr6:31755785 | G | A | 1 | a0001c0002t0001g0305 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1014+2156G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755785 | |||||||
| chr6:31755883 | C | G | 1 | a0001c0002t0001g0075 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1014+2254C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755883 | |||||||
| chr6:31755958 | C | T | 7 | a0001c0002t0001g0002 a0001c0002t0001g0057 a0001c0002t0001g0058 others(4): Show |
12 | NA18945.hp1 NA18963.hp2 NA18984.hp2 others(9): Show |
intron_variant | MODIFIER | c.1015-2207C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31755958 | |||||||
| chr6:31756040 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1015-2125T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756040 | |||||||
| chr6:31756046 | GT | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(33): Show |
51 | HG00280.hp1 HG00597.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1015-2107delT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31756046 | ||||||
| chr6:31756103 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1015-2062G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756103 | |||||||
| chr6:31756361 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1015-1804G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756361 | |||||||
| chr6:31756442 | G | C | 153 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(150): Show |
192 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(189): Show |
intron_variant | MODIFIER | c.1015-1723G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756442 | |||||||
| chr6:31756638 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1015-1527C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756638 | |||||||
| chr6:31756640 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1015-1525A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756640 | |||||||
| chr6:31756727 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0207 |
3 | HG02486.hp2 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1015-1438C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756727 | |||||||
| chr6:31756890 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1015-1275C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756890 | |||||||
| chr6:31756976 | T | C | 1 | a0004c0005t0001g0025 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1015-1189T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31756976 | |||||||
| chr6:31757135 | T | TTTTG | 13 | a0001c0002t0001g0024 a0001c0002t0001g0026 a0001c0002t0001g0072 others(10): Show |
15 | HG00642.hp2 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1015-1005_1015-100 others(8): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31757135 | ||||||
| chr6:31757208 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0225 a0001c0001t0001g0228 |
3 | HG00408.hp1 NA19010.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1015-957G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757208 | |||||||
| chr6:31757214 | G | A | 1 | a0002c0003t0001g0065 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1015-951G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757214 | |||||||
| chr6:31757237 | C | T | 9 | a0001c0001t0001g0152 a0001c0001t0001g0163 a0001c0001t0001g0188 others(6): Show |
9 | HG01167.hp1 HG01192.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1015-928C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757237 | |||||||
| chr6:31757404 | A | G | 1 | a0005c0007t0002g0096 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1015-761A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757404 | |||||||
| chr6:31757453 | G | A | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1015-712G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757453 | |||||||
| chr6:31757491 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1015-674C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757491 | |||||||
| chr6:31757508 | A | G | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1015-657A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757508 | |||||||
| chr6:31757530 | C | T | 2 | a0001c0002t0001g0098 a0001c0002t0001g0099 |
2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1015-635C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757530 | |||||||
| chr6:31757634 | A | G | 4 | a0001c0002t0001g0066 a0001c0002t0001g0067 a0001c0002t0001g0068 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-531A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757634 | |||||||
| chr6:31757707 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1015-458C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757707 | |||||||
| chr6:31757764 | G | A | 1 | a0001c0002t0001g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1015-401G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757764 | |||||||
| chr6:31757820 | C | T | 1 | a0004c0005t0001g0025 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1015-345C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31757820 | |||||||
| chr6:31757836 | A | AT | 34 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0131 others(31): Show |
42 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1015-324dupT | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr6 | 31757836 | ||||||
| chr6:31758082 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1015-83C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31758082 | |||||||
| chr6:31758121 | C | A | 1 | a0001c0008t0001g0233 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1015-44C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 12/24 | chr6 | 31758121 | |||||||
| chr6:31758386 | A | G | 1 | a0006c0013t0001g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1143+93A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 13/24 | chr6 | 31758386 | |||||||
| chr6:31758476 | T | C | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-72T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 13/24 | chr6 | 31758476 | |||||||
| chr6:31758479 | G | A | 4 | a0001c0002t0001g0301 a0001c0002t0001g0302 a0001c0002t0001g0303 others(1): Show |
4 | HG02071.hp1 HG02683.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-69G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 13/24 | chr6 | 31758479 | |||||||
| chr6:31758911 | C | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(87): Show |
107 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1326+36C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 15/24 | chr6 | 31758911 | |||||||
| chr6:31759017 | T | C | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-80T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 15/24 | chr6 | 31759017 | |||||||
| chr6:31759073 | G | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
22 | HG00735.hp1 HG01074.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1327-24G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 15/24 | chr6 | 31759073 | |||||||
| chr6:31759192 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1407+15C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 16/24 | chr6 | 31759192 | |||||||
| chr6:31759697 | A | G | 2 | a0001c0004t0001g0003 a0001c0004t0001g0111 |
7 | HG00099.hp2 HG00280.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1496-89A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 17/24 | chr6 | 31759697 | |||||||
| chr6:31760015 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1685+40C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 18/24 | chr6 | 31760015 | |||||||
| chr6:31760019 | A | AGGGCCCA others(3): Show |
1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1685+46_1685+47ins others(10): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr6 | 31760019 | ||||||
| chr6:31760045 | A | C | 24 | a0001c0002t0001g0013 a0001c0002t0001g0018 a0001c0002t0001g0029 others(21): Show |
29 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1686-45A>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 18/24 | chr6 | 31760045 | |||||||
| chr6:31760071 | G | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1686-19G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 18/24 | chr6 | 31760071 | |||||||
| chr6:31760072 | C | G | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1686-18C>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 18/24 | chr6 | 31760072 | |||||||
| chr6:31760325 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1812+109G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760325 | |||||||
| chr6:31760346 | A | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1812+130A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760346 | |||||||
| chr6:31760367 | C | A | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1812+151C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760367 | |||||||
| chr6:31760369 | T | C | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1812+153T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760369 | |||||||
| chr6:31760370 | C | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1812+154C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760370 | |||||||
| chr6:31760413 | C | A | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1812+197C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760413 | |||||||
| chr6:31760414 | T | C | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1812+198T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760414 | |||||||
| chr6:31760490 | G | A | 81 | a0001c0002t0001g0002 a0001c0002t0001g0024 a0001c0002t0001g0026 others(78): Show |
101 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1813-200G>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760490 | |||||||
| chr6:31760552 | CAG | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0179 a0001c0002t0001g0181 |
5 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1813-135_1813-134d others(4): Show |
MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr6 | 31760552 | ||||||
| chr6:31760597 | C | A | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-93C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760597 | |||||||
| chr6:31760598 | A | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-92A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760598 | |||||||
| chr6:31760601 | T | G | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-89T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760601 | |||||||
| chr6:31760606 | T | G | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-84T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760606 | |||||||
| chr6:31760611 | G | C | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-79G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760611 | |||||||
| chr6:31760612 | T | A | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-78T>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760612 | |||||||
| chr6:31760614 | C | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-76C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760614 | |||||||
| chr6:31760615 | C | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-75C>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760615 | |||||||
| chr6:31760616 | A | G | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-74A>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760616 | |||||||
| chr6:31760617 | T | C | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-73T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760617 | |||||||
| chr6:31760618 | T | G | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-72T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760618 | |||||||
| chr6:31760622 | G | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-68G>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760622 | |||||||
| chr6:31760636 | T | G | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-54T>G | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760636 | |||||||
| chr6:31760638 | T | C | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-52T>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760638 | |||||||
| chr6:31760651 | C | A | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-39C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760651 | |||||||
| chr6:31760653 | G | C | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-37G>C | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760653 | |||||||
| chr6:31760665 | A | T | 1 | a0008c0010t0001g0139 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1813-25A>T | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 19/24 | chr6 | 31760665 | |||||||
| chr6:31760991 | C | A | 1 | a0001c0002t0001g0182 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1962+152C>A | MSH5 | ENSG00000204410.16 | transcript | ENST00000375750.9 | protein_coding | 20/24 | chr6 | 31760991 |