Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10960 |
| ensemblid | ENSG00000169223.16 |
| hgncid | 16986 |
| symbol | LMAN2 |
| name | lectin, mannose binding 2 |
| refseq_nuc | NM_006816.3 |
| refseq_prot | NP_006807.1 |
| ensembl_nuc | ENST00000303127.12 |
| ensembl_prot | ENSP00000303366.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 177331567 |
| end | 177351668 |
| strand | - |
| ver | v1.2 |
| region | chr5:177331567-177351668 |
| region5000 | chr5:177326567-177356668 |
| regionname0 | LMAN2_chr5_177331567_177351668 |
| regionname5000 | LMAN2_chr5_177326567_177356668 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 356 | 368 | 98 | 70 | 143 | 15 | 40 | 107 | LMAN2_chr5_177326567_177356668 | LMAN2 | MAAEG others(351): Show |
chr5 | 177326567 | 177356668 |
| a0002 | 0/0 | 356 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | LMAN2_chr5_177326567_177356668 | LMAN2 | MAAEG others(351): Show |
chr5 | 177326567 | 177356668 |
| a0003 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | MAAEG others(351): Show |
chr5 | 177326567 | 177356668 |
| a0004 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | MAAEG others(351): Show |
chr5 | 177326567 | 177356668 |
| a0005 | 0/0 | 356 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | MAAEG others(351): Show |
chr5 | 177326567 | 177356668 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1068 | 363 | 94 | 69 | 143 | 15 | 40 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0001c0005 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0001c0007 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0001c0008 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0001c0009 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0001c0010 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0002c0002 | 0/0 | 1068 | 5 | 0 | 0 | 5 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0003c0004 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0004c0003 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 | ||
| a0005c0006 | 0/0 | 1068 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | ATGGC others(1063): Show |
chr5 | 177326567 | 177356668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1611 | 302 | 45 | 63 | 139 | 13 | 40 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0002 | 0/0 | 1611 | 32 | 28 | 2 | 0 | 2 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0003 | 0/0 | 1611 | 21 | 21 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0004 | 0/0 | 1611 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0005 | 0/0 | 1611 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0007 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0008 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0009 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0001t0010 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0005t0003 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0007t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0008t0003 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0009t0006 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0001c0010t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0002c0002t0001 | 0/0 | 1611 | 5 | 0 | 0 | 5 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0003c0004t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0004c0003t0001 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| a0005c0006t0001 | 0/0 | 1611 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | AGTGG others(1606): Show |
chr5 | 177326567 | 177356668 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 18 | 0 | 2 | 15 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0002 | 1/0 | 14 | 0 | 0 | 10 | 1 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 6 | 3 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0005 | 0/0 | 8 | 1 | 2 | 0 | 2 | 3 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0064 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0004 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0005t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0007t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0008t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0009t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0001c0010t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0003c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0004c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| a0005c0006t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00733 | hp2 | a0001 | c0009 | t0006 | g0106 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0077 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0100 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0248 | EUR | IBS | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02970 | hp1 | a0001 | c0010 | t0001 | g0125 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03130 | hp1 | a0001 | c0005 | t0003 | g0042 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0243 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0041 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | ESN | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18522 | hp2 | a0004 | c0003 | t0001 | g0040 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0132 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | YRI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ASW | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20752 | hp1 | a0005 | c0006 | t0001 | g0158 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| NA21309 | hp2 | a0001 | c0008 | t0003 | g0240 | AFR | LWK | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0064 | REF | REF | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | LMAN2_chr5_177326567_177356668 | LMAN2 | chr5 | 177326567 | 177356668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177332169 | C | T | 1 | a0005 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.988G>A | p.Ala330Thr | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 1009/1611 | 988/1071 | 330/356 | chr5 | 177332169 | |||
| chr5:177334335 | T | C | 1 | a0002 | 5 | NA18945.hp1 NA18947.hp2 NA18977.hp1 others(2): Show |
missense_variant | MODERATE | c.859A>G | p.Ile287Val | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/8 | 880/1611 | 859/1071 | 287/356 | chr5 | 177334335 | |||
| chr5:177351454 | T | C | 1 | a0004 | 1 | NA18522.hp2 | missense_variant&splice_region_variant | MODERATE | c.194A>G | p.Gln65Arg | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 215/1611 | 194/1071 | 65/356 | chr5 | 177351454 | |||
| chr5:177351532 | A | G | 1 | a0003 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.116T>C | p.Leu39Ser | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 137/1611 | 116/1071 | 39/356 | chr5 | 177351532 | |||
| chr5:177351599 | G | T | 1 | a0004 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.49C>A | p.Leu17Met | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 70/1611 | 49/1071 | 17/356 | chr5 | 177351599 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177332212 | G | A | 1 | a0001c0007 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.945C>T | p.Ser315Ser | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 966/1611 | 945/1071 | 315/356 | chr5 | 177332212 | |||
| chr5:177337146 | G | A | 1 | a0001c0008 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.780C>T | p.Gly260Gly | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/8 | 801/1611 | 780/1071 | 260/356 | chr5 | 177337146 | |||
| chr5:177337179 | G | A | 1 | a0001c0009 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.747C>T | p.Thr249Thr | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/8 | 768/1611 | 747/1071 | 249/356 | chr5 | 177337179 | |||
| chr5:177337435 | G | A | 1 | a0001c0009 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.603C>T | p.Gly201Gly | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 5/8 | 624/1611 | 603/1071 | 201/356 | chr5 | 177337435 | |||
| chr5:177337738 | G | A | 1 | a0001c0010 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.481C>T | p.Leu161Leu | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/8 | 502/1611 | 481/1071 | 161/356 | chr5 | 177337738 | |||
| chr5:177351215 | G | T | 1 | a0004c0003 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.273C>A | p.Thr91Thr | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/8 | 294/1611 | 273/1071 | 91/356 | chr5 | 177351215 | |||
| chr5:177351477 | C | T | 1 | a0001c0005 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.171G>A | p.Glu57Glu | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/8 | 192/1611 | 171/1071 | 57/356 | chr5 | 177351477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177331617 | C | T | 1 | a0001c0001t0004 | 2 | HG01496.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*469G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 469 | chr5 | 177331617 | ||||||
| chr5:177331640 | A | C | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 446 | chr5 | 177331640 | ||||||
| chr5:177331695 | G | A | 1 | a0001c0001t0005 | 2 | NA18943.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*391C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 391 | chr5 | 177331695 | ||||||
| chr5:177331708 | G | A | 1 | a0001c0001t0009 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 378 | chr5 | 177331708 | ||||||
| chr5:177331734 | A | C | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 352 | chr5 | 177331734 | ||||||
| chr5:177331778 | C | T | 3 | a0001c0001t0003 a0001c0005t0003 a0001c0008t0003 |
23 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*308G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 308 | chr5 | 177331778 | ||||||
| chr5:177331785 | C | T | 1 | a0001c0001t0002 | 32 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*301G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 301 | chr5 | 177331785 | ||||||
| chr5:177331800 | C | T | 1 | a0001c0001t0008 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 286 | chr5 | 177331800 | ||||||
| chr5:177331970 | A | C | 1 | a0001c0001t0007 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 116 | chr5 | 177331970 | ||||||
| chr5:177332071 | C | T | 1 | a0001c0009t0006 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 15 | chr5 | 177332071 | ||||||
| chr5:177332075 | G | A | 1 | a0001c0001t0010 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 8/8 | 11 | chr5 | 177332075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:177332303 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.911-57G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332303 | |||||||
| chr5:177332343 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0002g0215 a0001c0001t0002g0218 others(5): Show |
9 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.911-97G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332343 | |||||||
| chr5:177332422 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.911-176G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332422 | |||||||
| chr5:177332532 | T | G | 4 | a0001c0001t0003g0043 a0001c0001t0003g0211 a0001c0001t0003g0222 others(1): Show |
4 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-286A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332532 | |||||||
| chr5:177332552 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.911-306T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332552 | |||||||
| chr5:177332655 | C | T | 3 | a0001c0001t0002g0039 a0001c0001t0002g0250 a0001c0001t0002g0251 |
4 | HG02055.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-409G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332655 | |||||||
| chr5:177332690 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.911-444G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332690 | |||||||
| chr5:177332777 | C | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(37): Show |
52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.911-531G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177332777 | |||||||
| chr5:177333068 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0148 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-822G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333068 | |||||||
| chr5:177333114 | C | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0001g0148 |
3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-868G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333114 | |||||||
| chr5:177333123 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0001g0148 |
3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.911-877G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333123 | |||||||
| chr5:177333130 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.911-884A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333130 | |||||||
| chr5:177333221 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0124 |
2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.911-975G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333221 | |||||||
| chr5:177333226 | A | C | 106 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(103): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.911-980T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333226 | |||||||
| chr5:177333266 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0066 others(2): Show |
11 | HG01255.hp1 HG01258.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.910+1018C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333266 | |||||||
| chr5:177333271 | T | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+1013A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333271 | |||||||
| chr5:177333436 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.910+848A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333436 | |||||||
| chr5:177333570 | T | C | 1 | a0001c0008t0003g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.910+714A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333570 | |||||||
| chr5:177333615 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.910+669G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333615 | |||||||
| chr5:177333650 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.910+634C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333650 | |||||||
| chr5:177333851 | CACG | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.910+430_910+432del others(3): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333851 | |||||||
| chr5:177333904 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0119 |
2 | HG00558.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.910+380G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177333904 | |||||||
| chr5:177334042 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.910+242G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177334042 | |||||||
| chr5:177334094 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.910+190G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177334094 | |||||||
| chr5:177334231 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.910+53G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 7/7 | chr5 | 177334231 | |||||||
| chr5:177334455 | C | T | 3 | a0001c0001t0003g0236 a0001c0001t0003g0241 a0001c0001t0003g0244 |
3 | HG02572.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.791-52G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334455 | |||||||
| chr5:177334534 | A | G | 112 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(109): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.791-131T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334534 | |||||||
| chr5:177334535 | G | T | 1 | a0001c0001t0002g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-132C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334535 | |||||||
| chr5:177334538 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.791-135C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334538 | |||||||
| chr5:177334620 | G | C | 2 | a0001c0001t0003g0004 a0001c0001t0003g0210 |
10 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.791-217C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334620 | |||||||
| chr5:177334621 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.791-218C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334621 | |||||||
| chr5:177334924 | A | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.791-521T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177334924 | |||||||
| chr5:177335044 | T | A | 1 | a0001c0005t0003g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.791-641A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335044 | |||||||
| chr5:177335051 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.791-648C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335051 | |||||||
| chr5:177335232 | G | A | 14 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 others(11): Show |
22 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.791-829C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335232 | |||||||
| chr5:177335258 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.791-855G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335258 | |||||||
| chr5:177335326 | C | T | 2 | a0001c0001t0003g0004 a0001c0001t0003g0210 |
10 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.791-923G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335326 | |||||||
| chr5:177335449 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.791-1046G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177335449 | |||||||
| chr5:177336265 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01109.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.790+871C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336265 | |||||||
| chr5:177336432 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.790+704A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336432 | |||||||
| chr5:177336444 | G | A | 6 | a0001c0001t0003g0004 a0001c0001t0003g0210 a0001c0001t0003g0232 others(3): Show |
14 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.790+692C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336444 | |||||||
| chr5:177336487 | A | C | 21 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 others(18): Show |
29 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.790+649T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336487 | |||||||
| chr5:177336642 | T | C | 2 | a0001c0001t0003g0004 a0001c0001t0003g0210 |
10 | HG02145.hp2 HG02559.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.790+494A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336642 | |||||||
| chr5:177336655 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.790+481C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336655 | |||||||
| chr5:177336662 | T | C | 16 | a0001c0001t0001g0242 a0001c0001t0003g0004 a0001c0001t0003g0043 others(13): Show |
24 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.790+474A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336662 | |||||||
| chr5:177336794 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.790+342A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336794 | |||||||
| chr5:177336834 | G | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0101 others(2): Show |
5 | HG01928.hp1 HG01975.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.790+302C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336834 | |||||||
| chr5:177336855 | AAGG | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.790+278_790+280del others(3): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336855 | |||||||
| chr5:177336951 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.790+185G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336951 | |||||||
| chr5:177336986 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.790+150C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177336986 | |||||||
| chr5:177337107 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0065 others(11): Show |
16 | HG00408.hp1 HG01099.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.790+29C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 6/7 | chr5 | 177337107 | |||||||
| chr5:177337339 | A | AC | 8 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0087 others(5): Show |
8 | HG00597.hp2 HG01517.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+23dupG | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 5/7 | chr5 | 177337339 | |||||||
| chr5:177337584 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.514-60G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/7 | chr5 | 177337584 | |||||||
| chr5:177337655 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.513+51G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/7 | chr5 | 177337655 | |||||||
| chr5:177337684 | G | A | 1 | a0001c0001t0001g0030 | 2 | NA18991.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.513+22C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 4/7 | chr5 | 177337684 | |||||||
| chr5:177338043 | G | T | 1 | a0001c0001t0001g0075 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.434-258C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338043 | |||||||
| chr5:177338332 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.433+156G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338332 | |||||||
| chr5:177338366 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.433+122A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338366 | |||||||
| chr5:177338394 | G | A | 106 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(103): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.433+94C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 3/7 | chr5 | 177338394 | |||||||
| chr5:177338863 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.316-258C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177338863 | |||||||
| chr5:177338904 | A | C | 1 | a0001c0001t0002g0023 | 3 | HG02451.hp2 HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.316-299T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177338904 | |||||||
| chr5:177338988 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(100): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.316-383A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177338988 | |||||||
| chr5:177339103 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0001g0148 |
3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316-498C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339103 | |||||||
| chr5:177339176 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(127): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.316-571T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339176 | |||||||
| chr5:177339186 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0045 others(7): Show |
18 | HG02040.hp2 HG02071.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.316-581C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339186 | |||||||
| chr5:177339195 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.316-590T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339195 | |||||||
| chr5:177339456 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-851C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339456 | |||||||
| chr5:177339542 | A | T | 23 | a0001c0001t0001g0216 a0001c0001t0002g0007 a0001c0001t0002g0023 others(20): Show |
34 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.316-937T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339542 | |||||||
| chr5:177339545 | C | T | 6 | a0001c0001t0003g0004 a0001c0001t0003g0210 a0001c0001t0003g0232 others(3): Show |
14 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-940G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339545 | |||||||
| chr5:177339546 | G | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-941C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339546 | |||||||
| chr5:177339586 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.316-981A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339586 | |||||||
| chr5:177339865 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-1260A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339865 | |||||||
| chr5:177339868 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0116 a0001c0001t0001g0127 |
3 | HG01099.hp1 HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.316-1263C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177339868 | |||||||
| chr5:177340101 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.316-1496T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340101 | |||||||
| chr5:177340291 | A | C | 4 | a0001c0001t0003g0043 a0001c0001t0003g0211 a0001c0001t0003g0222 others(1): Show |
4 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-1686T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340291 | |||||||
| chr5:177340419 | A | G | 23 | a0001c0001t0001g0216 a0001c0001t0002g0007 a0001c0001t0002g0023 others(20): Show |
34 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.316-1814T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340419 | |||||||
| chr5:177340520 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.316-1915C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340520 | |||||||
| chr5:177340672 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0200 |
2 | HG02109.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.316-2067T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340672 | |||||||
| chr5:177340676 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.316-2071C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340676 | |||||||
| chr5:177340766 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-2161A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340766 | |||||||
| chr5:177340786 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.316-2181T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340786 | |||||||
| chr5:177340789 | C | CT | 2 | a0001c0001t0001g0022 a0001c0001t0001g0203 |
4 | HG00639.hp1 HG03654.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-2185dupA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340789 | |||||||
| chr5:177340816 | A | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-2211T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340816 | |||||||
| chr5:177340881 | A | T | 1 | a0001c0001t0003g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-2276T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340881 | |||||||
| chr5:177340916 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.316-2311C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340916 | |||||||
| chr5:177340975 | A | T | 1 | a0001c0001t0001g0015 | 3 | NA18948.hp2 NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.316-2370T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340975 | |||||||
| chr5:177340976 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-2371G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340976 | |||||||
| chr5:177340977 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.316-2372C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177340977 | |||||||
| chr5:177341002 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0067 others(6): Show |
14 | HG01256.hp1 HG01981.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.316-2397T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341002 | |||||||
| chr5:177341064 | C | CT | 13 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0073 others(10): Show |
15 | HG01109.hp1 HG01981.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.316-2460dupA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341064 | |||||||
| chr5:177341064 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.316-2459G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341064 | |||||||
| chr5:177341064 | CT | C | 99 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(96): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.316-2460delA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341064 | |||||||
| chr5:177341065 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.316-2460A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341065 | |||||||
| chr5:177341070 | T | C | 2 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.316-2465A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341070 | |||||||
| chr5:177341089 | A | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(103): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.316-2484T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341089 | |||||||
| chr5:177341109 | C | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(82): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-2504G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341109 | |||||||
| chr5:177341184 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-2579T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341184 | |||||||
| chr5:177341223 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0173 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.316-2618G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341223 | |||||||
| chr5:177341255 | G | A | 1 | a0001c0009t0006g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.316-2650C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341255 | |||||||
| chr5:177341346 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0104 |
2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.316-2741C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341346 | |||||||
| chr5:177341361 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.316-2756G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341361 | |||||||
| chr5:177341404 | G | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02145.hp1 HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.316-2799C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341404 | |||||||
| chr5:177341565 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.316-2960T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341565 | |||||||
| chr5:177341590 | G | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.316-2985C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341590 | |||||||
| chr5:177341894 | T | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0045 others(8): Show |
19 | HG02040.hp2 HG02071.hp2 HG02523.hp1 others(16): Show |
intron_variant | MODIFIER | c.316-3289A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341894 | |||||||
| chr5:177341997 | TA | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0087 |
4 | HG03704.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.316-3393delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177341997 | |||||||
| chr5:177342168 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.316-3563G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342168 | |||||||
| chr5:177342230 | G | A | 5 | a0001c0001t0003g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 others(2): Show |
5 | HG02572.hp1 HG03195.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.316-3625C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342230 | |||||||
| chr5:177342352 | T | A | 1 | a0001c0001t0001g0026 | 2 | NA18968.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.316-3747A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342352 | |||||||
| chr5:177342423 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0199 a0001c0001t0001g0207 others(1): Show |
4 | HG00423.hp2 NA18949.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-3818G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342423 | |||||||
| chr5:177342505 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.316-3900A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342505 | |||||||
| chr5:177342898 | C | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0069 a0001c0001t0001g0136 others(2): Show |
6 | HG00597.hp1 HG02132.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-4293G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177342898 | |||||||
| chr5:177343099 | A | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG02572.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-4494T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343099 | |||||||
| chr5:177343241 | G | C | 1 | a0001c0001t0001g0036 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.316-4636C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343241 | |||||||
| chr5:177343280 | T | C | 2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.316-4675A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343280 | |||||||
| chr5:177343323 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0225 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.316-4718A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343323 | |||||||
| chr5:177343406 | G | C | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-4801C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343406 | |||||||
| chr5:177343564 | G | GAC | 7 | a0001c0001t0001g0062 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG00733.hp2 HG02083.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.316-4961_316-4960d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343564 | |||||||
| chr5:177343564 | GAC | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0019 others(27): Show |
42 | HG00642.hp1 HG01123.hp1 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.316-4961_316-4960d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343564 | |||||||
| chr5:177343584 | C | CACACACA others(41): Show |
9 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0230 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(50): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACACA others(39): Show |
1 | a0001c0001t0001g0180 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.316-4980_316-4979i others(48): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACACA others(37): Show |
52 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(49): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(46): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACACA others(39): Show |
1 | a0001c0001t0001g0036 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(48): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACACA others(35): Show |
9 | a0001c0001t0001g0191 a0001c0001t0001g0216 a0001c0001t0002g0037 others(6): Show |
11 | HG01167.hp2 HG02647.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(44): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACACA others(33): Show |
15 | a0001c0001t0002g0007 a0001c0001t0002g0023 a0001c0001t0002g0039 others(12): Show |
24 | HG01109.hp2 HG01515.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(42): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACACG others(31): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(40): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACACGGA others(29): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0114 a0001c0001t0001g0148 |
3 | HG02572.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(38): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACATGGA others(29): Show |
3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-4980_316-4979i others(38): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343584 | C | CACGGAAT others(27): Show |
16 | a0001c0001t0001g0242 a0001c0001t0003g0004 a0001c0001t0003g0043 others(13): Show |
24 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.316-4980_316-4979i others(36): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343584 | |||||||
| chr5:177343686 | G | A | 10 | a0001c0001t0001g0242 a0001c0001t0003g0043 a0001c0001t0003g0211 others(7): Show |
10 | HG02258.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.316-5081C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343686 | |||||||
| chr5:177343695 | T | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-5090A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343695 | |||||||
| chr5:177343855 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.316-5250C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343855 | |||||||
| chr5:177343964 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.316-5359G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177343964 | |||||||
| chr5:177344144 | G | A | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.316-5539C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344144 | |||||||
| chr5:177344176 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.316-5571G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344176 | |||||||
| chr5:177344210 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-5605G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344210 | |||||||
| chr5:177344211 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.316-5606G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344211 | |||||||
| chr5:177344222 | TA | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0185 a0001c0001t0001g0204 others(5): Show |
8 | HG02572.hp1 HG02630.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.316-5618delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344222 | |||||||
| chr5:177344235 | A | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316-5630T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344235 | |||||||
| chr5:177344281 | C | CT | 16 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0096 others(13): Show |
16 | HG00597.hp1 HG01175.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.316-5677dupA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344281 | |||||||
| chr5:177344281 | CT | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(95): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.316-5677delA | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344281 | |||||||
| chr5:177344281 | CTT | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0212 a0001c0001t0001g0225 others(9): Show |
21 | HG01243.hp1 HG01516.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.316-5678_316-5677d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344281 | |||||||
| chr5:177344285 | T | C | 1 | a0001c0001t0003g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316-5680A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344285 | |||||||
| chr5:177344470 | C | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0169 a0001c0001t0001g0176 others(3): Show |
6 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.316-5865G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344470 | |||||||
| chr5:177344471 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.316-5866C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344471 | |||||||
| chr5:177344762 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.316-6157G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344762 | |||||||
| chr5:177344813 | GGAAAATC others(34): Show |
G | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.316-6249_316-6209d others(43): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344813 | |||||||
| chr5:177344897 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0225 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.315+6276G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344897 | |||||||
| chr5:177344931 | G | A | 7 | a0001c0001t0001g0242 a0001c0001t0003g0004 a0001c0001t0003g0210 others(4): Show |
15 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.315+6242C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344931 | |||||||
| chr5:177344935 | A | AAGAAGAG others(3): Show |
10 | a0001c0001t0001g0242 a0001c0001t0003g0043 a0001c0001t0003g0211 others(7): Show |
10 | HG02258.hp2 HG02572.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.315+6228_315+6237d others(12): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344935 | |||||||
| chr5:177344935 | A | AGAGAAAG others(8): Show |
6 | a0001c0001t0003g0004 a0001c0001t0003g0210 a0001c0001t0003g0232 others(3): Show |
14 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.315+6237_315+6238i others(17): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344935 | |||||||
| chr5:177344958 | GAAGA | G | 1 | a0001c0001t0001g0014 | 3 | HG01106.hp2 NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.315+6211_315+6214d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177344958 | |||||||
| chr5:177345026 | C | G | 16 | a0001c0001t0001g0242 a0001c0001t0003g0004 a0001c0001t0003g0043 others(13): Show |
24 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.315+6147G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345026 | |||||||
| chr5:177345177 | C | CA | 11 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0087 others(8): Show |
13 | HG00639.hp1 HG01192.hp2 HG03654.hp2 others(10): Show |
intron_variant | MODIFIER | c.315+5995dupT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345177 | |||||||
| chr5:177345177 | CA | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0114 a0001c0001t0001g0164 others(4): Show |
7 | HG01167.hp2 HG02897.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+5995delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345177 | |||||||
| chr5:177345339 | T | TA | 20 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0066 others(17): Show |
21 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.315+5833dupT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | |||||||
| chr5:177345339 | T | TAA | 66 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(63): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.315+5832_315+5833d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | |||||||
| chr5:177345339 | T | TAAA | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(6): Show |
9 | HG01192.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.315+5831_315+5833d others(5): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | |||||||
| chr5:177345339 | TA | T | 27 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0068 others(24): Show |
35 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(32): Show |
intron_variant | MODIFIER | c.315+5833delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345339 | |||||||
| chr5:177345646 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0111 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.315+5527C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345646 | |||||||
| chr5:177345730 | G | GGCAT | 4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0230 others(1): Show |
4 | HG01891.hp1 HG02723.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.315+5439_315+5442d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345730 | |||||||
| chr5:177345730 | GGCAT | G | 33 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0051 others(30): Show |
36 | HG00423.hp2 HG00733.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.315+5439_315+5442d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345730 | |||||||
| chr5:177345732 | C | CATTT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(8): Show |
15 | HG00099.hp1 HG00642.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.315+5440_315+5441i others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345732 | |||||||
| chr5:177345735 | G | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(43): Show |
75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.315+5438C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345735 | |||||||
| chr5:177345736 | C | CATTCATT others(1): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0026 others(2): Show |
13 | HG01258.hp1 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.315+5436_315+5437i others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | |||||||
| chr5:177345736 | C | CATTT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(64): Show |
102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.315+5433_315+5436d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | |||||||
| chr5:177345736 | C | CATTTATT others(1): Show |
11 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0059 others(8): Show |
21 | HG00558.hp1 HG00597.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.315+5429_315+5436d others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | |||||||
| chr5:177345736 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(44): Show |
76 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.315+5437G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | |||||||
| chr5:177345736 | CATTT | C | 17 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
25 | HG01243.hp1 HG02071.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.315+5433_315+5436d others(6): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | |||||||
| chr5:177345736 | CATTTATT others(1): Show |
C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0045 others(9): Show |
20 | HG02040.hp2 HG02523.hp1 HG03098.hp1 others(17): Show |
intron_variant | MODIFIER | c.315+5429_315+5436d others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345736 | |||||||
| chr5:177345739 | T | G | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+5434A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345739 | |||||||
| chr5:177345740 | T | C | 2 | a0001c0001t0001g0036 a0004c0003t0001g0040 |
3 | HG02258.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.315+5433A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345740 | |||||||
| chr5:177345785 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.315+5388A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345785 | |||||||
| chr5:177345798 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0165 a0001c0001t0001g0173 others(1): Show |
5 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+5375G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345798 | |||||||
| chr5:177345870 | C | T | 1 | a0001c0008t0003g0240 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.315+5303G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345870 | |||||||
| chr5:177345979 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.315+5194C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345979 | |||||||
| chr5:177345987 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.315+5186G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177345987 | |||||||
| chr5:177346090 | T | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(104): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.315+5083A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346090 | |||||||
| chr5:177346224 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315+4949T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346224 | |||||||
| chr5:177346238 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.315+4935G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346238 | |||||||
| chr5:177346412 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+4761A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346412 | |||||||
| chr5:177346412 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.315+4761A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346412 | |||||||
| chr5:177346635 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.315+4538C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346635 | |||||||
| chr5:177346651 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.315+4522A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346651 | |||||||
| chr5:177346669 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.315+4504T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346669 | |||||||
| chr5:177346732 | A | G | 2 | a0001c0001t0003g0233 a0001c0001t0003g0234 |
2 | HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.315+4441T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177346732 | |||||||
| chr5:177347017 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(85): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.315+4156G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347017 | |||||||
| chr5:177347041 | T | G | 5 | a0001c0001t0001g0242 a0001c0001t0003g0043 a0001c0001t0003g0211 others(2): Show |
5 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+4132A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347041 | |||||||
| chr5:177347127 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18950.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.315+4046T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347127 | |||||||
| chr5:177347134 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.315+4039G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347134 | |||||||
| chr5:177347402 | G | A | 88 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(85): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.315+3771C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347402 | |||||||
| chr5:177347452 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315+3721A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347452 | |||||||
| chr5:177347973 | A | T | 1 | a0001c0001t0001g0025 | 2 | NA18946.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.315+3200T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347973 | |||||||
| chr5:177347981 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.315+3192G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177347981 | |||||||
| chr5:177348232 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0210 a0001c0001t0003g0232 |
11 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.315+2941T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348232 | |||||||
| chr5:177348292 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.315+2881G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348292 | |||||||
| chr5:177348384 | C | G | 23 | a0001c0001t0001g0216 a0001c0001t0002g0007 a0001c0001t0002g0023 others(20): Show |
34 | HG01109.hp2 HG01167.hp2 HG01515.hp2 others(31): Show |
intron_variant | MODIFIER | c.315+2789G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348384 | |||||||
| chr5:177348661 | C | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0225 |
3 | HG03098.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.315+2512G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348661 | |||||||
| chr5:177348687 | C | CA | 48 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(45): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.315+2485dupT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348687 | |||||||
| chr5:177348687 | CA | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(67): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.315+2485delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348687 | |||||||
| chr5:177348687 | CAA | C | 18 | a0001c0001t0001g0048 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
26 | HG01167.hp1 HG01243.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.315+2484_315+2485d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348687 | |||||||
| chr5:177348815 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.315+2358G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348815 | |||||||
| chr5:177348850 | C | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(51): Show |
69 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.315+2323G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348850 | |||||||
| chr5:177348878 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.315+2295G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348878 | |||||||
| chr5:177348883 | CA | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(84): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.315+2289delT | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348883 | |||||||
| chr5:177348883 | CAA | C | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG01069.hp2 HG01168.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+2288_315+2289d others(4): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177348883 | |||||||
| chr5:177349273 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.315+1900C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349273 | |||||||
| chr5:177349303 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0045 others(7): Show |
18 | HG02040.hp2 HG02071.hp2 HG02523.hp1 others(15): Show |
intron_variant | MODIFIER | c.315+1870C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349303 | |||||||
| chr5:177349363 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.315+1810A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349363 | |||||||
| chr5:177349533 | GATGAAGG others(7): Show |
G | 1 | a0001c0001t0001g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.315+1626_315+1639d others(16): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349533 | |||||||
| chr5:177349799 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.315+1374A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349799 | |||||||
| chr5:177349848 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.315+1325C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349848 | |||||||
| chr5:177349957 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.315+1216C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177349957 | |||||||
| chr5:177350021 | A | C | 106 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(103): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.315+1152T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350021 | |||||||
| chr5:177350234 | A | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+939T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350234 | |||||||
| chr5:177350249 | A | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+924T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350249 | |||||||
| chr5:177350250 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+923C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350250 | |||||||
| chr5:177350251 | A | G | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+922T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350251 | |||||||
| chr5:177350290 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+883A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350290 | |||||||
| chr5:177350292 | A | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+881T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350292 | |||||||
| chr5:177350294 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+879C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350294 | |||||||
| chr5:177350304 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+869C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350304 | |||||||
| chr5:177350324 | G | A | 5 | a0001c0001t0002g0039 a0001c0001t0002g0248 a0001c0001t0002g0249 others(2): Show |
6 | HG01515.hp2 HG01517.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+849C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350324 | |||||||
| chr5:177350341 | C | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+832G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350341 | |||||||
| chr5:177350399 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.315+774T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350399 | |||||||
| chr5:177350441 | C | G | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+732G>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350441 | |||||||
| chr5:177350442 | T | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+731A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350442 | |||||||
| chr5:177350443 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+730C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350443 | |||||||
| chr5:177350445 | T | G | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+728A>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350445 | |||||||
| chr5:177350450 | T | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+723A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350450 | |||||||
| chr5:177350492 | G | A | 105 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0031 others(102): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.315+681C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350492 | |||||||
| chr5:177350497 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.315+676C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350497 | |||||||
| chr5:177350559 | G | T | 1 | a0001c0001t0004g0024 | 2 | HG01496.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.315+614C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350559 | |||||||
| chr5:177350587 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+586C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350587 | |||||||
| chr5:177350588 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+585C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350588 | |||||||
| chr5:177350589 | T | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+584A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350589 | |||||||
| chr5:177350590 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+583C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350590 | |||||||
| chr5:177350595 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+578C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350595 | |||||||
| chr5:177350597 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+576C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350597 | |||||||
| chr5:177350598 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+575A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350598 | |||||||
| chr5:177350602 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+571C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350602 | |||||||
| chr5:177350603 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+570A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350603 | |||||||
| chr5:177350606 | A | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+567T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350606 | |||||||
| chr5:177350609 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+564C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350609 | |||||||
| chr5:177350611 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+562C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350611 | |||||||
| chr5:177350612 | T | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+561A>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350612 | |||||||
| chr5:177350613 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+560C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350613 | |||||||
| chr5:177350615 | A | ACCCCCCA others(94): Show |
1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+557_315+558ins others(101): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350615 | |||||||
| chr5:177350617 | TGCTGGGC others(64): Show |
T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+485_315+555del others(71): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350617 | |||||||
| chr5:177350748 | A | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+425T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350748 | |||||||
| chr5:177350749 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+424A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350749 | |||||||
| chr5:177350750 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+423C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350750 | |||||||
| chr5:177350822 | A | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+351T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350822 | |||||||
| chr5:177350823 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+350C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350823 | |||||||
| chr5:177350826 | GGTTCAAG others(3): Show |
G | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+337_315+346del others(10): Show |
LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350826 | |||||||
| chr5:177350844 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+329A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350844 | |||||||
| chr5:177350861 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+312A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350861 | |||||||
| chr5:177350914 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.315+259T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350914 | |||||||
| chr5:177350963 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+210C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350963 | |||||||
| chr5:177350968 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+205C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177350968 | |||||||
| chr5:177351057 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+116C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351057 | |||||||
| chr5:177351082 | A | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+91T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351082 | |||||||
| chr5:177351101 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+72C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351101 | |||||||
| chr5:177351103 | C | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+70G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351103 | |||||||
| chr5:177351104 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+69A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351104 | |||||||
| chr5:177351105 | C | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+68G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351105 | |||||||
| chr5:177351107 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+66C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351107 | |||||||
| chr5:177351110 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+63C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351110 | |||||||
| chr5:177351113 | C | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+60G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351113 | |||||||
| chr5:177351114 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+59C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351114 | |||||||
| chr5:177351115 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+58C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351115 | |||||||
| chr5:177351116 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+57C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351116 | |||||||
| chr5:177351118 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+55C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351118 | |||||||
| chr5:177351119 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+54C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351119 | |||||||
| chr5:177351122 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+51C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351122 | |||||||
| chr5:177351123 | G | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+50C>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351123 | |||||||
| chr5:177351124 | G | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.315+49C>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351124 | |||||||
| chr5:177351167 | A | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.315+6T>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351167 | |||||||
| chr5:177351169 | T | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.315+4A>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 2/7 | chr5 | 177351169 | |||||||
| chr5:177351373 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.196+79T>C | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351373 | |||||||
| chr5:177351414 | C | A | 1 | a0001c0001t0001g0253 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.196+38G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351414 | |||||||
| chr5:177351445 | G | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.196+7C>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351445 | |||||||
| chr5:177351449 | C | T | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.196+3G>A | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351449 | |||||||
| chr5:177351450 | A | C | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | splice_donor_variant&intron_variant | HIGH | c.196+2T>G | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351450 | |||||||
| chr5:177351451 | C | A | 1 | a0004c0003t0001g0040 | 1 | NA18522.hp2 | splice_donor_variant&intron_variant | HIGH | c.196+1G>T | LMAN2 | ENSG00000169223.16 | transcript | ENST00000303127.12 | protein_coding | 1/7 | chr5 | 177351451 |