Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3998 |
| ensemblid | ENSG00000074695.6 |
| hgncid | 6631 |
| symbol | LMAN1 |
| name | lectin, mannose binding 1 |
| refseq_nuc | NM_005570.4 |
| refseq_prot | NP_005561.1 |
| ensembl_nuc | ENST00000251047.6 |
| ensembl_prot | ENSP00000251047.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 59327823 |
| end | 59359265 |
| strand | - |
| ver | v1.2 |
| region | chr18:59327823-59359265 |
| region5000 | chr18:59322823-59364265 |
| regionname0 | LMAN1_chr18_59327823_59359265 |
| regionname5000 | LMAN1_chr18_59322823_59364265 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 510 | 312 | 60 | 61 | 155 | 8 | 26 | 124 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(505): Show |
chr18 | 59322823 | 59364265 |
| a0002 | 0/0 | 510 | 44 | 1 | 11 | 28 | 2 | 2 | 21 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(505): Show |
chr18 | 59322823 | 59364265 |
| a0003 | 0/0 | 510 | 24 | 16 | 3 | 0 | 3 | 2 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(505): Show |
chr18 | 59322823 | 59364265 |
| a0004 | 0/0 | 510 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(505): Show |
chr18 | 59322823 | 59364265 |
| a0005 | 0/0 | 510 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(505): Show |
chr18 | 59322823 | 59364265 |
| a0006 | 0/0 | 114 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(109): Show |
chr18 | 59322823 | 59364265 |
| a0007 | 0/0 | 510 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | MAGSR others(505): Show |
chr18 | 59322823 | 59364265 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1530 | 291 | 58 | 48 | 153 | 8 | 23 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0001c0003 | 0/1 | 1530 | 20 | 1 | 13 | 2 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0001c0010 | 0/0 | 1530 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0002c0002 | 0/0 | 1530 | 44 | 1 | 11 | 28 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0003c0004 | 0/0 | 1530 | 18 | 11 | 3 | 0 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0003c0005 | 0/0 | 1530 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0003c0007 | 0/0 | 1530 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0004c0006 | 0/0 | 1530 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0005c0009 | 0/0 | 1530 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 | ||
| a0006c0011 | 0/0 | 1513 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1508): Show |
chr18 | 59322823 | 59364265 | ||
| a0007c0008 | 0/0 | 1530 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | ATGGC others(1525): Show |
chr18 | 59322823 | 59364265 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4824 | 123 | 31 | 23 | 53 | 6 | 9 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0002 | 0/0 | 4824 | 134 | 16 | 23 | 80 | 2 | 13 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0003 | 0/0 | 4824 | 18 | 0 | 0 | 17 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0009 | 0/0 | 4805 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4800): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0010 | 0/0 | 4824 | 3 | 2 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0011 | 0/0 | 4824 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0012 | 0/0 | 4824 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0014 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0015 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0016 | 0/0 | 4824 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0017 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0018 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0001t0019 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0003t0001 | 0/1 | 4824 | 20 | 1 | 13 | 2 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0001c0010t0001 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0002c0002t0001 | 0/0 | 4824 | 30 | 1 | 4 | 21 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0002c0002t0006 | 0/0 | 4824 | 8 | 0 | 5 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0002c0002t0008 | 0/0 | 4824 | 4 | 0 | 1 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0002c0002t0013 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0002c0002t0020 | 0/0 | 4824 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0003c0004t0004 | 0/0 | 4824 | 9 | 2 | 3 | 0 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0003c0004t0005 | 0/0 | 4824 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0003c0005t0007 | 0/0 | 4824 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0003c0007t0004 | 0/0 | 4824 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0004c0006t0002 | 0/0 | 4824 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0005c0009t0002 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| a0006c0011t0001 | 0/0 | 4807 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4802): Show |
chr18 | 59322823 | 59364265 |
| a0007c0008t0002 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | CTCCG others(4819): Show |
chr18 | 59322823 | 59364265 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 26 | 2 | 5 | 15 | 2 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0006 | 0/0 | 7 | 4 | 3 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0002 | 0/0 | 16 | 1 | 1 | 12 | 1 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0003 | 0/0 | 14 | 1 | 2 | 8 | 0 | 3 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0005 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0009g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0009g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0012g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0015g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0016g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0017g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0018g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0001t0019g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0001c0010t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0004 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0006g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0006g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0008g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0008g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0013g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0002c0002t0020g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0004g0007 | 0/0 | 5 | 1 | 1 | 0 | 2 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0004t0005g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0005t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0005t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0005t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0005t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0005t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0003c0007t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0004c0006t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0004c0006t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0004c0006t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0005c0009t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0006c0011t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| a0007c0008t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0006 | t0002 | g0051 | EUR | GBR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00099 | hp2 | a0003 | c0004 | t0004 | g0007 | EUR | GBR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0227 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00639 | hp2 | a0002 | c0002 | t0006 | g0028 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG00741 | hp2 | a0003 | c0004 | t0004 | g0007 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0079 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01192 | hp1 | a0004 | c0006 | t0002 | g0049 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01255 | hp1 | a0003 | c0004 | t0004 | g0062 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01257 | hp1 | a0002 | c0002 | t0006 | g0046 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01258 | hp1 | a0002 | c0002 | t0006 | g0028 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01358 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0139 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01517 | hp2 | a0003 | c0004 | t0004 | g0007 | EUR | IBS | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0094 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0197 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01934 | hp1 | a0003 | c0004 | t0004 | g0061 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01943 | hp1 | a0002 | c0002 | t0006 | g0138 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01952 | hp1 | a0001 | c0001 | t0016 | g0164 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01952 | hp2 | a0002 | c0002 | t0020 | g0215 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0075 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01993 | hp2 | a0002 | c0002 | t0006 | g0028 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02055 | hp2 | a0003 | c0004 | t0005 | g0060 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02071 | hp2 | a0002 | c0002 | t0013 | g0217 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0070 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CDX | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02280 | hp1 | a0003 | c0004 | t0004 | g0058 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0127 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02451 | hp2 | a0003 | c0004 | t0005 | g0053 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0190 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02683 | hp1 | a0003 | c0004 | t0004 | g0007 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02698 | hp2 | a0004 | c0006 | t0002 | g0050 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02717 | hp1 | a0003 | c0004 | t0005 | g0030 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0033 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02809 | hp1 | a0003 | c0004 | t0005 | g0057 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02809 | hp2 | a0003 | c0004 | t0004 | g0007 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02818 | hp1 | a0003 | c0004 | t0005 | g0030 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02886 | hp1 | a0003 | c0004 | t0005 | g0056 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02895 | hp2 | a0003 | c0005 | t0007 | g0065 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02897 | hp1 | a0003 | c0005 | t0007 | g0064 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0033 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02922 | hp2 | a0003 | c0004 | t0005 | g0054 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02976 | hp2 | a0003 | c0005 | t0007 | g0063 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0071 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03486 | hp2 | a0003 | c0005 | t0007 | g0066 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03491 | hp1 | a0003 | c0004 | t0004 | g0059 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03516 | hp1 | a0001 | c0010 | t0001 | g0188 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03540 | hp1 | a0003 | c0004 | t0005 | g0052 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0196 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03704 | hp2 | a0006 | c0011 | t0001 | g0072 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0078 | SAS | PJL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0077 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0076 | SAS | BEB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18612 | hp1 | a0002 | c0002 | t0006 | g0046 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | CHB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18906 | hp1 | a0003 | c0005 | t0007 | g0067 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18906 | hp2 | a0003 | c0004 | t0005 | g0055 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18945 | hp2 | a0002 | c0002 | t0008 | g0223 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18951 | hp1 | a0001 | c0001 | t0019 | g0170 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18953 | hp2 | a0001 | c0001 | t0018 | g0168 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18975 | hp2 | a0002 | c0002 | t0006 | g0214 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18987 | hp1 | a0002 | c0002 | t0008 | g0141 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19003 | hp1 | a0002 | c0002 | t0006 | g0211 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | LWK | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0086 | AFR | LWK | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19062 | hp1 | a0001 | c0001 | t0015 | g0195 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19078 | hp1 | a0002 | c0002 | t0008 | g0222 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19085 | hp2 | a0007 | c0008 | t0002 | g0151 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ASW | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0004 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20805 | hp2 | a0003 | c0007 | t0004 | g0068 | EUR | TSI | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | GIH | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01123 | hp1 | a0002 | c0002 | t0008 | g0209 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02109 | hp2 | a0005 | c0009 | t0002 | g0132 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | USA | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | USA | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0074 | REF | REF | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0129 | REF | REF | LMAN1_chr18_59322823_59364265 | LMAN1 | chr18 | 59322823 | 59364265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:59333237 | T | A | 1 | a0002 | 44 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
missense_variant | MODERATE | c.1228A>T | p.Met410Leu | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/13 | 1249/4824 | 1228/1533 | 410/510 | chr18 | 59333237 | |||
| chr18:59338845 | A | G | 1 | a0007 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1064T>C | p.Ile355Thr | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 9/13 | 1085/4824 | 1064/1533 | 355/510 | chr18 | 59338845 | |||
| chr18:59347514 | G | A | 1 | a0005 | 1 | HG02109.hp2 | missense_variant&splice_region_variant | MODERATE | c.821C>T | p.Pro274Leu | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/13 | 842/4824 | 821/1533 | 274/510 | chr18 | 59347514 | |||
| chr18:59354565 | T | C | 1 | a0006 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.493A>G | p.Ile165Val | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/13 | 514/4824 | 493/1533 | 165/510 | chr18 | 59354565 | |||
| chr18:59355523 | CGACCTCT others(10): Show |
C | 1 | a0006 | 1 | HG03704.hp2 | frameshift_variant | HIGH | c.333_349delAGTGACTG others(9): Show |
p.Val112fs | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 2/13 | 370/4824 | 333/1533 | 111/510 | chr18 | 59355523 | |||
| chr18:59359129 | A | G | 1 | a0003 | 24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
missense_variant | MODERATE | c.116T>C | p.Val39Ala | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/13 | 137/4824 | 116/1533 | 39/510 | chr18 | 59359129 | |||
| chr18:59359204 | C | T | 1 | a0004 | 3 | HG00099.hp1 HG01192.hp1 HG02698.hp2 |
missense_variant | MODERATE | c.41G>A | p.Arg14Gln | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/13 | 62/4824 | 41/1533 | 14/510 | chr18 | 59359204 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:59338952 | C | T | 1 | a0003c0005 | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.957G>A | p.Ala319Ala | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 9/13 | 978/4824 | 957/1533 | 319/510 | chr18 | 59338952 | |||
| chr18:59349129 | T | G | 1 | a0001c0010 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.747A>C | p.Ala249Ala | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/13 | 768/4824 | 747/1533 | 249/510 | chr18 | 59349129 | |||
| chr18:59355522 | T | C | 4 | a0001c0003 a0003c0004 a0003c0005 others(1): Show |
43 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(40): Show |
synonymous_variant | LOW | c.351A>G | p.Arg117Arg | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 2/13 | 372/4824 | 351/1533 | 117/510 | chr18 | 59355522 | |||
| chr18:59359050 | G | A | 1 | a0003c0007 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.195C>T | p.Pro65Pro | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/13 | 216/4824 | 195/1533 | 65/510 | chr18 | 59359050 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:59327986 | A | T | 1 | a0001c0001t0003 | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3107T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 3107 | chr18 | 59327986 | ||||||
| chr18:59328164 | A | G | 9 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0016 others(6): Show |
146 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*2929T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2929 | chr18 | 59328164 | ||||||
| chr18:59328200 | C | T | 1 | a0001c0001t0015 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2893G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2893 | chr18 | 59328200 | ||||||
| chr18:59328347 | G | T | 1 | a0001c0001t0014 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2746C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2746 | chr18 | 59328347 | ||||||
| chr18:59328630 | G | A | 1 | a0001c0001t0016 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2463 | chr18 | 59328630 | ||||||
| chr18:59328688 | G | T | 2 | a0003c0004t0004 a0003c0007t0004 |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2405C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2405 | chr18 | 59328688 | ||||||
| chr18:59328706 | T | C | 4 | a0003c0004t0004 a0003c0004t0005 a0003c0005t0007 others(1): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2387A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2387 | chr18 | 59328706 | ||||||
| chr18:59328876 | C | T | 5 | a0001c0001t0009 a0003c0004t0004 a0003c0004t0005 others(2): Show |
27 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2217G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2217 | chr18 | 59328876 | ||||||
| chr18:59328897 | A | G | 1 | a0001c0001t0010 | 3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2196T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2196 | chr18 | 59328897 | ||||||
| chr18:59328909 | T | C | 1 | a0003c0005t0007 | 5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2184A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2184 | chr18 | 59328909 | ||||||
| chr18:59329030 | G | C | 4 | a0003c0004t0004 a0003c0004t0005 a0003c0005t0007 others(1): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2063C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 2063 | chr18 | 59329030 | ||||||
| chr18:59329122 | C | T | 1 | a0002c0002t0013 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1971G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1971 | chr18 | 59329122 | ||||||
| chr18:59329170 | T | G | 1 | a0001c0001t0017 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1923A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1923 | chr18 | 59329170 | ||||||
| chr18:59329271 | C | A | 2 | a0002c0002t0006 a0002c0002t0020 |
9 | HG00639.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1822 | chr18 | 59329271 | ||||||
| chr18:59329294 | T | G | 4 | a0003c0004t0004 a0003c0004t0005 a0003c0005t0007 others(1): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1799A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1799 | chr18 | 59329294 | ||||||
| chr18:59329822 | T | C | 1 | a0001c0001t0018 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 1271 | chr18 | 59329822 | ||||||
| chr18:59330233 | A | C | 1 | a0001c0001t0011 | 2 | HG02572.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*860T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 860 | chr18 | 59330233 | ||||||
| chr18:59330299 | T | C | 1 | a0001c0001t0019 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 794 | chr18 | 59330299 | ||||||
| chr18:59330421 | GAGGAATG others(12): Show |
G | 1 | a0001c0001t0009 | 3 | HG01884.hp1 HG02717.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*653_*671delTGTGGG others(13): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 653 | chr18 | 59330421 | ||||||
| chr18:59330441 | A | G | 1 | a0002c0002t0008 | 4 | HG01123.hp1 NA18945.hp2 NA18987.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*652T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 652 | chr18 | 59330441 | ||||||
| chr18:59330444 | T | C | 1 | a0002c0002t0020 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*649A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 649 | chr18 | 59330444 | ||||||
| chr18:59330603 | G | A | 1 | a0001c0001t0003 | 18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*490C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 490 | chr18 | 59330603 | ||||||
| chr18:59330929 | T | C | 1 | a0001c0001t0012 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*164A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 13/13 | 164 | chr18 | 59330929 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:59331236 | C | T | 1 | a0001c0001t0002g0172 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1497-107G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 12/12 | chr18 | 59331236 | |||||||
| chr18:59331310 | A | G | 3 | a0001c0001t0001g0194 a0001c0001t0009g0033 a0001c0001t0009g0094 |
4 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1496+108T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 12/12 | chr18 | 59331310 | |||||||
| chr18:59331669 | C | T | 13 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(10): Show |
17 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1375-130G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59331669 | |||||||
| chr18:59331840 | A | G | 1 | a0004c0006t0002g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1375-301T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59331840 | |||||||
| chr18:59332076 | C | A | 3 | a0001c0001t0010g0196 a0001c0001t0010g0197 a0001c0001t0010g0228 |
3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1375-537G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332076 | |||||||
| chr18:59332104 | C | T | 2 | a0001c0001t0011g0189 a0001c0001t0011g0190 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1375-565G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332104 | |||||||
| chr18:59332170 | A | C | 1 | a0001c0001t0003g0204 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1375-631T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332170 | |||||||
| chr18:59332245 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(49): Show |
99 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1375-706A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332245 | |||||||
| chr18:59332379 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1374+712A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332379 | |||||||
| chr18:59332567 | G | A | 1 | a0002c0002t0001g0216 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1374+524C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332567 | |||||||
| chr18:59332739 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(15): Show |
29 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.1374+352A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332739 | |||||||
| chr18:59332796 | T | TTAAGCAA others(2): Show |
5 | a0003c0005t0007g0063 a0003c0005t0007g0064 a0003c0005t0007g0065 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1374+286_1374+294d others(11): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332796 | |||||||
| chr18:59332809 | G | A | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1374+282C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332809 | |||||||
| chr18:59332979 | A | T | 1 | a0005c0009t0002g0132 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1374+112T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59332979 | |||||||
| chr18:59333042 | T | C | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1374+49A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59333042 | |||||||
| chr18:59333071 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(65): Show |
126 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1374+20C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 11/12 | chr18 | 59333071 | |||||||
| chr18:59333286 | GT | G | 21 | a0001c0001t0001g0124 a0001c0001t0002g0154 a0003c0004t0004g0007 others(18): Show |
26 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.1221-43delA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333286 | |||||||
| chr18:59333298 | C | A | 1 | a0001c0001t0002g0174 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1221-54G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333298 | |||||||
| chr18:59333386 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1221-142C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333386 | |||||||
| chr18:59333690 | A | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0181 |
5 | HG00738.hp2 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-446T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333690 | |||||||
| chr18:59333851 | G | GA | 20 | a0002c0002t0001g0218 a0003c0004t0004g0007 a0003c0004t0004g0058 others(17): Show |
25 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.1221-608dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333851 | |||||||
| chr18:59333859 | A | G | 13 | a0001c0001t0003g0021 a0001c0001t0003g0042 a0001c0001t0003g0043 others(10): Show |
18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.1221-615T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333859 | |||||||
| chr18:59333945 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0085 |
3 | HG00323.hp1 HG01069.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.1221-701T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59333945 | |||||||
| chr18:59334007 | G | A | 1 | a0002c0002t0013g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1221-763C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334007 | |||||||
| chr18:59334083 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1221-839G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334083 | |||||||
| chr18:59334106 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(9): Show |
23 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1221-862T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334106 | |||||||
| chr18:59334328 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1221-1084T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334328 | |||||||
| chr18:59334478 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0095 |
4 | HG02300.hp1 NA18957.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1221-1234A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334478 | |||||||
| chr18:59334581 | C | T | 1 | a0004c0006t0002g0049 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1221-1337G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334581 | |||||||
| chr18:59334602 | A | G | 1 | a0002c0002t0001g0219 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1221-1358T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334602 | |||||||
| chr18:59334633 | T | C | 1 | a0001c0003t0001g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1221-1389A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334633 | |||||||
| chr18:59334842 | A | AT | 23 | a0001c0001t0001g0100 a0001c0001t0001g0113 a0001c0001t0002g0016 others(20): Show |
26 | HG00408.hp1 HG00609.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1221-1599dupA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59334842 | |||||||
| chr18:59335124 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1221-1880T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335124 | |||||||
| chr18:59335160 | G | A | 1 | a0001c0003t0001g0077 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1221-1916C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335160 | |||||||
| chr18:59335173 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(9): Show |
23 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1221-1929G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335173 | |||||||
| chr18:59335206 | C | G | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1221-1962G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335206 | |||||||
| chr18:59335229 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1221-1985A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335229 | |||||||
| chr18:59335231 | C | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1221-1987G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335231 | |||||||
| chr18:59335237 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1221-1993G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335237 | |||||||
| chr18:59335373 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1221-2129G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335373 | |||||||
| chr18:59335491 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0184 |
3 | HG02145.hp1 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1221-2247A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335491 | |||||||
| chr18:59335708 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1221-2464A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335708 | |||||||
| chr18:59335896 | C | T | 5 | a0003c0005t0007g0063 a0003c0005t0007g0064 a0003c0005t0007g0065 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-2652G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335896 | |||||||
| chr18:59335911 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1220+2646A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335911 | |||||||
| chr18:59335933 | A | G | 3 | a0001c0001t0002g0169 a0001c0001t0002g0171 a0001c0001t0002g0173 |
3 | HG00597.hp2 NA19072.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.1220+2624T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59335933 | |||||||
| chr18:59336202 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1220+2355G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336202 | |||||||
| chr18:59336238 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1220+2319A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336238 | |||||||
| chr18:59336387 | T | C | 6 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(3): Show |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1220+2170A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336387 | |||||||
| chr18:59336472 | G | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0184 |
3 | HG02145.hp1 HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1220+2085C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336472 | |||||||
| chr18:59336482 | G | C | 8 | a0003c0004t0005g0030 a0003c0004t0005g0052 a0003c0004t0005g0053 others(5): Show |
9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1220+2075C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336482 | |||||||
| chr18:59336600 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1220+1957C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336600 | |||||||
| chr18:59336657 | G | A | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220+1900C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336657 | |||||||
| chr18:59336767 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1220+1790G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336767 | |||||||
| chr18:59336920 | T | TA | 33 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(30): Show |
50 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1220+1636dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59336920 | |||||||
| chr18:59337041 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1220+1516A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337041 | |||||||
| chr18:59337123 | A | G | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220+1434T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337123 | |||||||
| chr18:59337167 | T | C | 5 | a0003c0004t0005g0052 a0003c0004t0005g0054 a0003c0004t0005g0056 others(2): Show |
5 | HG02055.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+1390A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337167 | |||||||
| chr18:59337198 | A | G | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.1220+1359T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337198 | |||||||
| chr18:59337367 | C | T | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220+1190G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337367 | |||||||
| chr18:59337500 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(120): Show |
204 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1220+1057T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337500 | |||||||
| chr18:59337531 | T | C | 22 | a0001c0001t0010g0196 a0001c0001t0010g0197 a0001c0001t0010g0228 others(19): Show |
27 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1220+1026A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337531 | |||||||
| chr18:59337915 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0109 |
5 | HG00733.hp1 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220+642T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59337915 | |||||||
| chr18:59338296 | C | A | 1 | a0001c0001t0002g0158 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1220+261G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338296 | |||||||
| chr18:59338423 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(52): Show |
102 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1220+134A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338423 | |||||||
| chr18:59338507 | T | A | 6 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(3): Show |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1220+50A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338507 | |||||||
| chr18:59338538 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1220+19C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 10/12 | chr18 | 59338538 | |||||||
| chr18:59338690 | T | C | 1 | a0001c0001t0002g0038 | 2 | NA18942.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1150-63A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 9/12 | chr18 | 59338690 | |||||||
| chr18:59339266 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.956-313G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339266 | |||||||
| chr18:59339341 | A | G | 1 | a0004c0006t0002g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.956-388T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339341 | |||||||
| chr18:59339650 | T | A | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.956-697A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339650 | |||||||
| chr18:59339713 | G | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0118 |
3 | NA18967.hp1 NA18984.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.956-760C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339713 | |||||||
| chr18:59339879 | C | T | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.956-926G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59339879 | |||||||
| chr18:59340025 | T | C | 1 | a0001c0001t0011g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.956-1072A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340025 | |||||||
| chr18:59340222 | G | A | 3 | a0002c0002t0001g0140 a0002c0002t0001g0219 a0002c0002t0001g0220 |
3 | HG02083.hp2 NA18986.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.956-1269C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340222 | |||||||
| chr18:59340337 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(221): Show |
374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.956-1384C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340337 | |||||||
| chr18:59340421 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(15): Show |
29 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.956-1468A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340421 | |||||||
| chr18:59340641 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.956-1688C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340641 | |||||||
| chr18:59340696 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
7 | NA18940.hp1 NA18946.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.956-1743T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340696 | |||||||
| chr18:59340702 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.956-1749T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340702 | |||||||
| chr18:59340759 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0142 |
3 | HG02559.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.956-1806A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340759 | |||||||
| chr18:59340848 | T | C | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-1895A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340848 | |||||||
| chr18:59340903 | T | C | 8 | a0003c0004t0005g0030 a0003c0004t0005g0052 a0003c0004t0005g0053 others(5): Show |
9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-1950A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59340903 | |||||||
| chr18:59341020 | T | C | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-2067A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341020 | |||||||
| chr18:59341097 | AAAAAG | A | 8 | a0003c0004t0005g0030 a0003c0004t0005g0052 a0003c0004t0005g0053 others(5): Show |
9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.956-2149_956-2145d others(7): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341097 | |||||||
| chr18:59341604 | T | C | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.956-2651A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341604 | |||||||
| chr18:59341768 | T | C | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.956-2815A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341768 | |||||||
| chr18:59341852 | T | C | 3 | a0001c0001t0010g0196 a0001c0001t0010g0197 a0001c0001t0010g0228 |
3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.956-2899A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59341852 | |||||||
| chr18:59342075 | T | C | 4 | a0003c0005t0007g0064 a0003c0005t0007g0065 a0003c0005t0007g0066 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-3122A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342075 | |||||||
| chr18:59342224 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(141): Show |
238 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.956-3271G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342224 | |||||||
| chr18:59342250 | T | C | 1 | a0001c0001t0001g0015 | 4 | NA18947.hp2 NA18998.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-3297A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342250 | |||||||
| chr18:59342329 | A | G | 1 | a0002c0002t0001g0221 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.956-3376T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342329 | |||||||
| chr18:59342537 | T | C | 29 | a0001c0001t0009g0033 a0001c0001t0009g0094 a0002c0002t0001g0004 others(26): Show |
47 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.955+3382A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342537 | |||||||
| chr18:59342738 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0122 |
3 | HG01081.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.955+3181T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342738 | |||||||
| chr18:59342750 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.955+3169G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342750 | |||||||
| chr18:59342889 | A | G | 25 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(22): Show |
38 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.955+3030T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342889 | |||||||
| chr18:59342985 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(142): Show |
239 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.955+2934C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59342985 | |||||||
| chr18:59343054 | T | TA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(75): Show |
140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.955+2864dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343054 | |||||||
| chr18:59343054 | T | TAA | 5 | a0001c0001t0001g0107 a0001c0001t0001g0112 a0001c0001t0001g0118 others(2): Show |
6 | HG02257.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.955+2863_955+2864d others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343054 | |||||||
| chr18:59343143 | T | G | 1 | a0001c0001t0002g0155 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.955+2776A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343143 | |||||||
| chr18:59343221 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(129): Show |
221 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.955+2698A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343221 | |||||||
| chr18:59343274 | T | A | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+2645A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343274 | |||||||
| chr18:59343289 | G | GA | 13 | a0001c0001t0001g0108 a0001c0001t0003g0021 a0001c0001t0003g0042 others(10): Show |
18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.955+2629dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343289 | |||||||
| chr18:59343345 | C | T | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+2574G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343345 | |||||||
| chr18:59343484 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(142): Show |
239 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.955+2435C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343484 | |||||||
| chr18:59343563 | T | C | 27 | a0002c0002t0001g0004 a0002c0002t0001g0011 a0002c0002t0001g0044 others(24): Show |
44 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.955+2356A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343563 | |||||||
| chr18:59343578 | A | T | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+2341T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343578 | |||||||
| chr18:59343646 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.955+2273A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343646 | |||||||
| chr18:59343732 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.955+2187A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343732 | |||||||
| chr18:59343817 | G | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+2102C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343817 | |||||||
| chr18:59343960 | C | T | 1 | a0003c0004t0005g0030 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.955+1959G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343960 | |||||||
| chr18:59343988 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.955+1931T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59343988 | |||||||
| chr18:59344069 | T | C | 3 | a0002c0002t0001g0140 a0002c0002t0001g0219 a0002c0002t0001g0220 |
3 | HG02083.hp2 NA18986.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.955+1850A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344069 | |||||||
| chr18:59344072 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.955+1847T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344072 | |||||||
| chr18:59344147 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.955+1772C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344147 | |||||||
| chr18:59344489 | G | C | 3 | a0002c0002t0001g0136 a0002c0002t0001g0139 a0002c0002t0001g0221 |
3 | HG00642.hp1 HG00735.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.955+1430C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344489 | |||||||
| chr18:59344617 | G | GACAAATG others(26): Show |
1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.955+1269_955+1301d others(35): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344617 | |||||||
| chr18:59344654 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0041 others(5): Show |
18 | HG00738.hp2 HG01109.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.955+1265T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344654 | |||||||
| chr18:59344666 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.955+1253C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344666 | |||||||
| chr18:59344700 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(141): Show |
238 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.955+1219C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344700 | |||||||
| chr18:59344798 | A | C | 29 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0002c0002t0001g0004 others(26): Show |
46 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.955+1121T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344798 | |||||||
| chr18:59344828 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.955+1091A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344828 | |||||||
| chr18:59344989 | C | A | 8 | a0003c0004t0005g0030 a0003c0004t0005g0052 a0003c0004t0005g0053 others(5): Show |
9 | HG02055.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.955+930G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59344989 | |||||||
| chr18:59345013 | C | T | 5 | a0003c0005t0007g0063 a0003c0005t0007g0064 a0003c0005t0007g0065 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+906G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345013 | |||||||
| chr18:59345096 | G | GT | 3 | a0001c0001t0010g0196 a0001c0001t0010g0197 a0001c0001t0010g0228 |
3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.955+822dupA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345096 | |||||||
| chr18:59345118 | G | C | 1 | a0001c0001t0012g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.955+801C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345118 | |||||||
| chr18:59345129 | A | G | 1 | a0001c0003t0001g0076 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.955+790T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345129 | |||||||
| chr18:59345344 | C | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(141): Show |
238 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.955+575G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345344 | |||||||
| chr18:59345657 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.955+262A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345657 | |||||||
| chr18:59345747 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.955+172T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 8/12 | chr18 | 59345747 | |||||||
| chr18:59346209 | C | CT | 31 | a0001c0001t0001g0124 a0001c0001t0002g0025 a0001c0001t0002g0027 others(28): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.823-159dupA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346209 | C | CTT | 12 | a0001c0001t0002g0150 a0001c0001t0002g0157 a0001c0001t0002g0161 others(9): Show |
16 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.823-160_823-159dup others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346209 | CT | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(64): Show |
126 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.823-159delA | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346209 | CTT | C | 10 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0120 others(7): Show |
12 | HG01167.hp1 HG01257.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.823-160_823-159del others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346209 | CTTT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(9): Show |
23 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.823-161_823-159del others(3): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346209 | CTTTTTTT | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0119 others(5): Show |
12 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.823-165_823-159del others(7): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346209 | CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0001g0047 | 2 | NA18981.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.823-171_823-159del others(13): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346209 | |||||||
| chr18:59346236 | T | A | 1 | a0001c0001t0002g0156 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.823-185A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346236 | |||||||
| chr18:59346236 | T | TA | 4 | a0001c0001t0002g0026 a0001c0001t0002g0039 a0001c0001t0002g0091 others(1): Show |
7 | HG00280.hp2 HG01074.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.823-186dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346236 | |||||||
| chr18:59346250 | G | A | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-199C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346250 | |||||||
| chr18:59346377 | T | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0041 others(33): Show |
51 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.823-326A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346377 | |||||||
| chr18:59346466 | G | C | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.823-415C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346466 | |||||||
| chr18:59346542 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.823-491T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346542 | |||||||
| chr18:59346547 | C | G | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.823-496G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346547 | |||||||
| chr18:59346675 | C | G | 1 | a0001c0001t0002g0212 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.823-624G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346675 | |||||||
| chr18:59346787 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+726A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346787 | |||||||
| chr18:59346815 | C | T | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.822+698G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346815 | |||||||
| chr18:59346946 | C | G | 1 | a0002c0002t0001g0044 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.822+567G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346946 | |||||||
| chr18:59346953 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18944.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.822+560C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59346953 | |||||||
| chr18:59347046 | T | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | HG02257.hp2 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.822+467A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347046 | |||||||
| chr18:59347076 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.822+437T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347076 | |||||||
| chr18:59347115 | C | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.822+398G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347115 | |||||||
| chr18:59347149 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.822+364C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347149 | |||||||
| chr18:59347264 | A | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(221): Show |
374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.822+249T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347264 | |||||||
| chr18:59347269 | A | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(221): Show |
374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.822+244T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347269 | |||||||
| chr18:59347302 | CAG | C | 3 | a0003c0005t0007g0064 a0003c0005t0007g0065 a0003c0005t0007g0067 |
3 | HG02895.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.822+209_822+210del others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347302 | |||||||
| chr18:59347304 | G | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0017 others(9): Show |
20 | HG00621.hp1 HG02056.hp2 HG03834.hp1 others(17): Show |
intron_variant | MODIFIER | c.822+209C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347304 | |||||||
| chr18:59347320 | CA | C | 9 | a0001c0001t0002g0018 a0001c0001t0002g0024 a0001c0001t0002g0083 others(6): Show |
14 | HG00642.hp2 HG02109.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.822+192delT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAA | C | 14 | a0001c0001t0002g0017 a0001c0001t0002g0032 a0001c0001t0002g0082 others(11): Show |
18 | HG00609.hp1 HG01099.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.822+191_822+192del others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAA | C | 11 | a0001c0001t0002g0003 a0001c0001t0002g0027 a0001c0001t0002g0039 others(8): Show |
27 | HG00544.hp2 HG00597.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.822+190_822+192del others(3): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAA | C | 21 | a0001c0001t0002g0002 a0001c0001t0002g0025 a0001c0001t0002g0026 others(18): Show |
42 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.822+189_822+192del others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAA | C | 10 | a0001c0001t0002g0010 a0001c0001t0002g0016 a0001c0001t0002g0073 others(7): Show |
17 | HG01168.hp2 HG02074.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.822+188_822+192del others(5): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0087 a0003c0004t0004g0058 a0003c0004t0004g0061 others(6): Show |
10 | HG01934.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.822+183_822+192del others(10): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(4): Show |
C | 4 | a0003c0004t0004g0007 a0003c0004t0004g0059 a0003c0004t0004g0062 others(1): Show |
8 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.822+182_822+192del others(11): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(5): Show |
C | 1 | a0003c0005t0007g0065 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.822+181_822+192del others(12): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0001g0194 a0003c0005t0007g0063 a0003c0005t0007g0064 others(2): Show |
5 | HG02723.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.822+180_822+192del others(13): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0122 |
3 | HG02486.hp1 HG03688.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.822+178_822+192del others(15): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(9): Show |
C | 13 | a0001c0001t0001g0097 a0001c0001t0001g0112 a0001c0001t0001g0113 others(10): Show |
13 | HG00621.hp2 HG00735.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.822+177_822+192del others(16): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(10): Show |
C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(59): Show |
121 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.822+176_822+192del others(17): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(11): Show |
C | 13 | a0001c0001t0001g0180 a0001c0001t0003g0021 a0001c0001t0003g0042 others(10): Show |
21 | HG01106.hp2 HG01123.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.822+175_822+192del others(18): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(12): Show |
C | 35 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0001c0001t0009g0033 others(32): Show |
57 | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.822+174_822+192del others(19): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(13): Show |
C | 2 | a0002c0002t0001g0210 a0002c0002t0006g0211 |
2 | HG02132.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.822+173_822+192del others(20): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(15): Show |
C | 1 | a0001c0001t0002g0146 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.822+171_822+192del others(22): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347320 | CAAAAAAA others(18): Show |
C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.822+168_822+192del others(25): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347320 | |||||||
| chr18:59347472 | A | AAACC | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.822+40_822+41insGG others(2): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347472 | |||||||
| chr18:59347481 | G | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(16): Show |
30 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.822+32C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 7/12 | chr18 | 59347481 | |||||||
| chr18:59347580 | T | TA | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.764-10dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347580 | |||||||
| chr18:59347657 | T | C | 25 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(22): Show |
38 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.764-86A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347657 | |||||||
| chr18:59347677 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0120 a0001c0001t0001g0121 |
5 | HG00408.hp2 NA18961.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-106A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347677 | |||||||
| chr18:59347681 | G | A | 5 | a0003c0005t0007g0063 a0003c0005t0007g0064 a0003c0005t0007g0065 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.764-110C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347681 | |||||||
| chr18:59347970 | G | T | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-399C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347970 | |||||||
| chr18:59347979 | T | A | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG00408.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.764-408A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59347979 | |||||||
| chr18:59348044 | C | T | 14 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(11): Show |
19 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.764-473G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348044 | |||||||
| chr18:59348116 | T | C | 1 | a0003c0005t0007g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.764-545A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348116 | |||||||
| chr18:59348276 | C | T | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-705G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348276 | |||||||
| chr18:59348291 | T | C | 6 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(3): Show |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.764-720A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348291 | |||||||
| chr18:59348453 | C | T | 13 | a0001c0001t0003g0021 a0001c0001t0003g0042 a0001c0001t0003g0043 others(10): Show |
18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.763+660G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348453 | |||||||
| chr18:59348530 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.763+583A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348530 | |||||||
| chr18:59348568 | T | A | 29 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0002c0002t0001g0004 others(26): Show |
46 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.763+545A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348568 | |||||||
| chr18:59348803 | C | T | 1 | a0003c0005t0007g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.763+310G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 6/12 | chr18 | 59348803 | |||||||
| chr18:59349378 | T | C | 25 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(22): Show |
38 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.640-142A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349378 | |||||||
| chr18:59349442 | G | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(11): Show |
25 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.640-206C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349442 | |||||||
| chr18:59349835 | T | C | 25 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(22): Show |
38 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.640-599A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349835 | |||||||
| chr18:59349840 | A | C | 1 | a0002c0002t0008g0209 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.640-604T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349840 | |||||||
| chr18:59349841 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.640-605A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59349841 | |||||||
| chr18:59350155 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.640-919A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350155 | |||||||
| chr18:59350222 | A | G | 13 | a0001c0001t0003g0021 a0001c0001t0003g0042 a0001c0001t0003g0043 others(10): Show |
18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.640-986T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350222 | |||||||
| chr18:59350466 | T | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.640-1230A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350466 | |||||||
| chr18:59350479 | G | T | 1 | a0001c0001t0003g0202 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.640-1243C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350479 | |||||||
| chr18:59350526 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.640-1290C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350526 | |||||||
| chr18:59350534 | G | A | 3 | a0002c0002t0008g0141 a0002c0002t0008g0222 a0002c0002t0008g0223 |
3 | NA18945.hp2 NA18987.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.640-1298C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350534 | |||||||
| chr18:59350686 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.640-1450C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350686 | |||||||
| chr18:59350759 | T | C | 1 | a0001c0003t0001g0227 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.640-1523A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350759 | |||||||
| chr18:59350790 | C | T | 6 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(3): Show |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.640-1554G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59350790 | |||||||
| chr18:59351001 | G | A | 25 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(22): Show |
38 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.640-1765C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351001 | |||||||
| chr18:59351006 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.640-1770C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351006 | |||||||
| chr18:59351023 | C | T | 3 | a0001c0001t0010g0196 a0001c0001t0010g0197 a0001c0001t0010g0228 |
3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.640-1787G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351023 | |||||||
| chr18:59351490 | G | C | 13 | a0001c0001t0003g0021 a0001c0001t0003g0042 a0001c0001t0003g0043 others(10): Show |
18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.639+1712C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351490 | |||||||
| chr18:59351513 | T | C | 1 | a0001c0003t0001g0080 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.639+1689A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351513 | |||||||
| chr18:59351665 | T | C | 1 | a0001c0001t0003g0208 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.639+1537A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351665 | |||||||
| chr18:59351690 | G | A | 25 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(22): Show |
38 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.639+1512C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351690 | |||||||
| chr18:59351807 | G | A | 1 | a0004c0006t0002g0051 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.639+1395C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351807 | |||||||
| chr18:59351889 | T | C | 4 | a0003c0005t0007g0064 a0003c0005t0007g0065 a0003c0005t0007g0066 others(1): Show |
4 | HG02895.hp2 HG02897.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+1313A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351889 | |||||||
| chr18:59351916 | C | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
5 | NA18940.hp1 NA18946.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+1286G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59351916 | |||||||
| chr18:59352042 | T | G | 6 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(3): Show |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.639+1160A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352042 | |||||||
| chr18:59352429 | C | T | 5 | a0003c0005t0007g0063 a0003c0005t0007g0064 a0003c0005t0007g0065 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+773G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352429 | |||||||
| chr18:59352442 | T | C | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.639+760A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352442 | |||||||
| chr18:59352475 | C | T | 1 | a0001c0001t0003g0201 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.639+727G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352475 | |||||||
| chr18:59352528 | A | G | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.639+674T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352528 | |||||||
| chr18:59352547 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.639+655G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352547 | |||||||
| chr18:59352586 | C | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.639+616G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352586 | |||||||
| chr18:59352593 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.639+609G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352593 | |||||||
| chr18:59352801 | T | C | 4 | a0001c0001t0002g0024 a0001c0001t0002g0130 a0001c0001t0002g0131 others(1): Show |
6 | HG00642.hp2 HG00733.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+401A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352801 | |||||||
| chr18:59352905 | GTCTA | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(45): Show |
95 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.639+293_639+296del others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59352905 | |||||||
| chr18:59353074 | T | C | 13 | a0001c0001t0003g0021 a0001c0001t0003g0042 a0001c0001t0003g0043 others(10): Show |
18 | HG02015.hp2 HG02083.hp1 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.639+128A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 5/12 | chr18 | 59353074 | |||||||
| chr18:59353545 | A | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0095 |
4 | HG02300.hp1 NA18957.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-244T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353545 | |||||||
| chr18:59353647 | C | T | 2 | a0001c0001t0009g0033 a0001c0001t0009g0094 |
3 | HG01884.hp1 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.540-346G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353647 | |||||||
| chr18:59353708 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.540-407G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353708 | |||||||
| chr18:59353924 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.539+595A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353924 | |||||||
| chr18:59353974 | T | C | 29 | a0001c0001t0002g0212 a0001c0001t0002g0213 a0002c0002t0001g0004 others(26): Show |
46 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.539+545A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59353974 | |||||||
| chr18:59354048 | C | T | 3 | a0003c0005t0007g0064 a0003c0005t0007g0065 a0003c0005t0007g0067 |
3 | HG02895.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.539+471G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354048 | |||||||
| chr18:59354093 | A | G | 30 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(27): Show |
43 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.539+426T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354093 | |||||||
| chr18:59354191 | A | C | 1 | a0003c0005t0007g0063 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.539+328T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354191 | |||||||
| chr18:59354246 | A | T | 6 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(3): Show |
10 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.539+273T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354246 | |||||||
| chr18:59354262 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.539+257G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354262 | |||||||
| chr18:59354317 | G | T | 30 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(27): Show |
43 | HG00099.hp2 HG00423.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.539+202C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354317 | |||||||
| chr18:59354341 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.539+178A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354341 | |||||||
| chr18:59354506 | AAC | A | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.539+11_539+12delGT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 4/12 | chr18 | 59354506 | |||||||
| chr18:59354595 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.478-15T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354595 | |||||||
| chr18:59354597 | C | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0092 |
3 | HG02257.hp2 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.478-17G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354597 | |||||||
| chr18:59354726 | A | G | 3 | a0001c0001t0010g0196 a0001c0001t0010g0197 a0001c0001t0010g0228 |
3 | HG00735.hp2 HG01884.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.478-146T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354726 | |||||||
| chr18:59354971 | G | C | 67 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0010 others(64): Show |
120 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.477+342C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354971 | |||||||
| chr18:59354975 | G | A | 2 | a0001c0001t0011g0189 a0001c0001t0011g0190 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.477+338C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59354975 | |||||||
| chr18:59355197 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.477+116A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355197 | |||||||
| chr18:59355205 | T | A | 2 | a0003c0004t0005g0057 a0003c0004t0005g0060 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.477+108A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355205 | |||||||
| chr18:59355266 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.477+47C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355266 | |||||||
| chr18:59355308 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.477+5A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 3/12 | chr18 | 59355308 | |||||||
| chr18:59355921 | ACTAT | A | 5 | a0003c0005t0007g0063 a0003c0005t0007g0064 a0003c0005t0007g0065 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.215-267_215-264del others(4): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59355921 | |||||||
| chr18:59356405 | G | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0040 others(15): Show |
29 | HG00323.hp1 HG00738.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.215-747C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356405 | |||||||
| chr18:59356469 | G | A | 1 | a0001c0001t0002g0191 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.215-811C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356469 | |||||||
| chr18:59356503 | G | T | 1 | a0001c0001t0002g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.215-845C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356503 | |||||||
| chr18:59356623 | T | G | 1 | a0001c0001t0002g0192 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.215-965A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356623 | |||||||
| chr18:59356639 | T | G | 1 | a0001c0001t0014g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.215-981A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356639 | |||||||
| chr18:59356670 | TG | T | 11 | a0001c0003t0001g0008 a0001c0003t0001g0012 a0001c0003t0001g0031 others(8): Show |
19 | HG00423.hp2 HG01106.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.215-1013delC | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356670 | |||||||
| chr18:59356864 | G | T | 1 | a0001c0001t0002g0073 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.215-1206C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356864 | |||||||
| chr18:59356990 | G | T | 1 | a0001c0001t0002g0089 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.215-1332C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59356990 | |||||||
| chr18:59357012 | G | T | 1 | a0001c0001t0002g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.215-1354C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357012 | |||||||
| chr18:59357019 | A | C | 1 | a0001c0001t0010g0196 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.215-1361T>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357019 | |||||||
| chr18:59357022 | T | C | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1364A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357022 | |||||||
| chr18:59357023 | T | A | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1365A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357023 | |||||||
| chr18:59357025 | T | G | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1367A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357025 | |||||||
| chr18:59357026 | C | A | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1368G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357026 | |||||||
| chr18:59357027 | T | C | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1369A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357027 | |||||||
| chr18:59357030 | T | G | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1372A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357030 | |||||||
| chr18:59357031 | T | A | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1373A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357031 | |||||||
| chr18:59357032 | T | C | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1374A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357032 | |||||||
| chr18:59357033 | T | G | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1375A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357033 | |||||||
| chr18:59357034 | T | A | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1376A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357034 | |||||||
| chr18:59357036 | T | G | 1 | a0003c0004t0004g0061 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.215-1378A>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357036 | |||||||
| chr18:59357037 | T | A | 18 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(15): Show |
23 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.215-1379A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357037 | |||||||
| chr18:59357086 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.215-1428A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357086 | |||||||
| chr18:59357129 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.215-1471C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357129 | |||||||
| chr18:59357386 | T | C | 1 | a0001c0001t0014g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.214+1645A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357386 | |||||||
| chr18:59357882 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.214+1149T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357882 | |||||||
| chr18:59357892 | C | A | 1 | a0001c0001t0015g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.214+1139G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357892 | |||||||
| chr18:59357917 | T | C | 4 | a0003c0004t0004g0058 a0003c0004t0004g0061 a0003c0004t0004g0062 others(1): Show |
4 | HG01255.hp1 HG01934.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.214+1114A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357917 | |||||||
| chr18:59357933 | C | A | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1098G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357933 | |||||||
| chr18:59357934 | G | C | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1097C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357934 | |||||||
| chr18:59357935 | T | TATAAAAC others(10): Show |
1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1095_214+1096i others(19): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357935 | |||||||
| chr18:59357937 | G | C | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1094C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357937 | |||||||
| chr18:59357939 | G | A | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1092C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357939 | |||||||
| chr18:59357940 | C | A | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1091G>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357940 | |||||||
| chr18:59357950 | C | G | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1081G>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357950 | |||||||
| chr18:59357958 | T | A | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1073A>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357958 | |||||||
| chr18:59357959 | A | G | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1072T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357959 | |||||||
| chr18:59357962 | G | C | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1069C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357962 | |||||||
| chr18:59357963 | T | TA | 39 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(36): Show |
61 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.214+1067dupT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357963 | |||||||
| chr18:59357963 | TA | T | 24 | a0001c0001t0001g0085 a0001c0001t0002g0073 a0001c0001t0002g0081 others(21): Show |
32 | HG00423.hp2 HG01123.hp2 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.214+1067delT | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357963 | |||||||
| chr18:59357963 | TAAA | T | 10 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0005g0030 others(7): Show |
15 | HG00099.hp2 HG00741.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.214+1065_214+1067d others(5): Show |
LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357963 | |||||||
| chr18:59357969 | A | T | 1 | a0006c0011t0001g0072 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.214+1062T>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59357969 | |||||||
| chr18:59358191 | A | G | 2 | a0001c0001t0012g0070 a0001c0001t0012g0071 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.214+840T>C | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358191 | |||||||
| chr18:59358204 | T | C | 3 | a0001c0001t0002g0048 a0001c0001t0002g0224 a0001c0001t0002g0225 |
4 | HG00423.hp1 HG02080.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+827A>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358204 | |||||||
| chr18:59358380 | C | T | 15 | a0001c0001t0010g0228 a0003c0004t0004g0007 a0003c0004t0004g0058 others(12): Show |
20 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.214+651G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358380 | |||||||
| chr18:59358730 | G | C | 1 | a0001c0001t0002g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.214+301C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358730 | |||||||
| chr18:59358846 | G | C | 1 | a0001c0003t0001g0227 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.214+185C>G | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358846 | |||||||
| chr18:59358863 | C | T | 19 | a0003c0004t0004g0007 a0003c0004t0004g0058 a0003c0004t0004g0059 others(16): Show |
24 | HG00099.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.214+168G>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358863 | |||||||
| chr18:59358866 | G | A | 1 | a0001c0001t0010g0228 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.214+165C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358866 | |||||||
| chr18:59358937 | G | A | 1 | a0003c0005t0007g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.214+94C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358937 | |||||||
| chr18:59358993 | G | T | 1 | a0001c0001t0002g0069 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.214+38C>A | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59358993 | |||||||
| chr18:59359024 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0229 |
4 | HG00544.hp1 NA19055.hp1 NA19076.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.214+7C>T | LMAN1 | ENSG00000074695.6 | transcript | ENST00000251047.6 | protein_coding | 1/12 | chr18 | 59359024 |