Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4125 |
| ensemblid | ENSG00000104774.13 |
| hgncid | 6826 |
| symbol | MAN2B1 |
| name | mannosidase alpha class 2B member 1 |
| refseq_nuc | NM_000528.4 |
| refseq_prot | NP_000519.2 |
| ensembl_nuc | ENST00000456935.7 |
| ensembl_prot | ENSP00000395473.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 12646512 |
| end | 12666742 |
| strand | - |
| ver | v1.2 |
| region | chr19:12646512-12666742 |
| region5000 | chr19:12641512-12671742 |
| regionname0 | MAN2B1_chr19_12646512_12666742 |
| regionname5000 | MAN2B1_chr19_12641512_12671742 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1011 | 221 | 30 | 28 | 127 | 4 | 31 | 103 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0002 | 0/0 | 1011 | 28 | 1 | 12 | 7 | 4 | 4 | 6 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0003 | 0/0 | 1011 | 26 | 3 | 10 | 6 | 4 | 3 | 5 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0004 | 0/0 | 1011 | 19 | 17 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0005 | 0/0 | 1011 | 18 | 2 | 9 | 2 | 1 | 4 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0006 | 0/0 | 1011 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0007 | 0/0 | 1011 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0008 | 0/0 | 1011 | 8 | 0 | 3 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0009 | 0/0 | 1011 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0010 | 0/0 | 1011 | 6 | 0 | 4 | 2 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0011 | 0/0 | 1011 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0012 | 0/0 | 1011 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0013 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0014 | 0/0 | 1011 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0015 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0016 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0017 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0018 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0019 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0020 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0021 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0022 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| a0023 | 0/1 | 1011 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | MGAYA others(1006): Show |
chr19 | 12641512 | 12671742 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3033 | 207 | 20 | 27 | 127 | 4 | 28 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0001c0010 | 0/0 | 3033 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0001c0015 | 0/0 | 3033 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0001c0024 | 0/0 | 3033 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0001c0029 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0001c0030 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0002c0002 | 0/0 | 3033 | 24 | 1 | 10 | 5 | 4 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0002c0022 | 0/0 | 3033 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0002c0025 | 0/0 | 3033 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0003c0003 | 0/0 | 3033 | 22 | 3 | 8 | 5 | 4 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0003c0021 | 0/0 | 3033 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0003c0037 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0003c0038 | 0/0 | 3033 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0004c0005 | 0/0 | 3033 | 14 | 14 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0004c0019 | 0/0 | 3033 | 3 | 2 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0004c0023 | 0/0 | 3033 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0005c0004 | 0/0 | 3033 | 18 | 2 | 9 | 2 | 1 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0006c0006 | 0/0 | 3033 | 9 | 9 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0006c0014 | 0/0 | 3033 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0007c0008 | 0/0 | 3033 | 7 | 7 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0007c0018 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0008c0007 | 0/0 | 3033 | 8 | 0 | 3 | 0 | 5 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0009c0012 | 0/0 | 3033 | 5 | 4 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0009c0016 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0010c0009 | 0/0 | 3033 | 6 | 0 | 4 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0011c0011 | 0/0 | 3033 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0012c0013 | 0/0 | 3033 | 4 | 3 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0013c0017 | 0/0 | 3033 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0014c0020 | 0/0 | 3033 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0015c0027 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0016c0032 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0017c0028 | 0/0 | 3033 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0018c0034 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0019c0036 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0020c0033 | 0/0 | 3033 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0021c0026 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0022c0035 | 0/0 | 3033 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 | ||
| a0023c0031 | 0/1 | 3033 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | ATGGG others(3028): Show |
chr19 | 12641512 | 12671742 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3185 | 205 | 20 | 27 | 125 | 4 | 28 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0001c0001t0002 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0001c0010t0001 | 0/0 | 3185 | 6 | 6 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0001c0015t0001 | 0/0 | 3185 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0001c0024t0001 | 0/0 | 3185 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0001c0029t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0001c0030t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0002c0002t0001 | 0/0 | 3185 | 24 | 1 | 10 | 5 | 4 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0002c0022t0001 | 0/0 | 3185 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0002c0025t0001 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0003c0003t0001 | 0/0 | 3185 | 22 | 3 | 8 | 5 | 4 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0003c0021t0001 | 0/0 | 3185 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0003c0037t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0003c0038t0001 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0004c0005t0001 | 0/0 | 3185 | 14 | 14 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0004c0019t0001 | 0/0 | 3185 | 3 | 2 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0004c0023t0001 | 0/0 | 3185 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0005c0004t0001 | 0/0 | 3185 | 18 | 2 | 9 | 2 | 1 | 4 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0006c0006t0001 | 0/0 | 3185 | 9 | 9 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0006c0014t0001 | 0/0 | 3185 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0007c0008t0001 | 0/0 | 3185 | 7 | 7 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0007c0018t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0008c0007t0001 | 0/0 | 3185 | 8 | 0 | 3 | 0 | 5 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0009c0012t0001 | 0/0 | 3185 | 5 | 4 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0009c0016t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0010c0009t0001 | 0/0 | 3185 | 6 | 0 | 4 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0011c0011t0001 | 0/0 | 3185 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0012c0013t0001 | 0/0 | 3185 | 4 | 3 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0013c0017t0001 | 0/0 | 3185 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0014c0020t0001 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0015c0027t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0016c0032t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0017c0028t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0018c0034t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0019c0036t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0020c0033t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0021c0026t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0022c0035t0001 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| a0023c0031t0001 | 0/1 | 3185 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | CTTTC others(3180): Show |
chr19 | 12641512 | 12671742 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 3 | 9 | 0 | 3 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0010t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0010t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0010t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0010t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0015t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0015t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0015t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0015t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0024t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0024t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0029t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0001c0030t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0002 | 0/0 | 9 | 0 | 4 | 1 | 3 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0022t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0022t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0025t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0002c0025t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0003 | 0/0 | 8 | 0 | 4 | 1 | 1 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0021t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0037t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0003c0038t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0019t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0019t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0023t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0004c0023t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0005c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0006t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0014t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0014t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0014t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0006c0014t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0008t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0018t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0018t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0007c0018t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0008c0007t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0012t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0012t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0012t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0012t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0016t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0016t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0009c0016t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0010c0009t0001g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0010c0009t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0010c0009t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0011c0011t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0011c0011t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0011c0011t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0011c0011t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0012c0013t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0012c0013t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0013c0017t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0013c0017t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0014c0020t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0014c0020t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0015c0027t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0016c0032t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0017c0028t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0018c0034t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0019c0036t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0020c0033t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0021c0026t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0022c0035t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| a0023c0031t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0182 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00280 | hp1 | a0008 | c0007 | t0001 | g0146 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0204 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00544 | hp2 | a0010 | c0009 | t0001 | g0007 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00558 | hp1 | a0015 | c0027 | t0001 | g0045 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00609 | hp2 | a0011 | c0011 | t0001 | g0217 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00621 | hp2 | a0014 | c0020 | t0001 | g0134 | EAS | CHS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0032 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00642 | hp1 | a0008 | c0007 | t0001 | g0148 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00733 | hp1 | a0008 | c0007 | t0001 | g0147 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0271 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01070 | hp1 | a0005 | c0004 | t0001 | g0189 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0167 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01074 | hp2 | a0008 | c0007 | t0001 | g0150 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01081 | hp1 | a0003 | c0021 | t0001 | g0033 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01099 | hp2 | a0005 | c0004 | t0001 | g0194 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01106 | hp1 | a0010 | c0009 | t0001 | g0144 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01109 | hp1 | a0012 | c0013 | t0001 | g0177 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01168 | hp2 | a0005 | c0004 | t0001 | g0024 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01243 | hp1 | a0003 | c0021 | t0001 | g0033 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01258 | hp2 | a0002 | c0022 | t0001 | g0272 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01261 | hp1 | a0005 | c0004 | t0001 | g0015 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01261 | hp2 | a0010 | c0009 | t0001 | g0007 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01346 | hp2 | a0016 | c0032 | t0001 | g0166 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01358 | hp2 | a0010 | c0009 | t0001 | g0007 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01361 | hp2 | a0005 | c0004 | t0001 | g0192 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01515 | hp2 | a0008 | c0007 | t0001 | g0098 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01516 | hp1 | a0008 | c0007 | t0001 | g0149 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0261 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0260 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01517 | hp2 | a0008 | c0007 | t0001 | g0099 | EUR | IBS | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01884 | hp1 | a0012 | c0013 | t0001 | g0014 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01884 | hp2 | a0007 | c0008 | t0001 | g0187 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01891 | hp1 | a0006 | c0006 | t0001 | g0023 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01928 | hp1 | a0005 | c0004 | t0001 | g0025 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01934 | hp2 | a0004 | c0023 | t0001 | g0049 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01943 | hp1 | a0005 | c0004 | t0001 | g0025 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01952 | hp2 | a0009 | c0012 | t0001 | g0232 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01975 | hp1 | a0001 | c0029 | t0001 | g0118 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01975 | hp2 | a0002 | c0022 | t0001 | g0275 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01993 | hp1 | a0010 | c0009 | t0001 | g0007 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02055 | hp2 | a0004 | c0005 | t0001 | g0216 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02080 | hp1 | a0002 | c0025 | t0001 | g0296 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02129 | hp2 | a0005 | c0004 | t0001 | g0265 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02145 | hp2 | a0009 | c0012 | t0001 | g0029 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0183 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02257 | hp2 | a0006 | c0006 | t0001 | g0280 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0205 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02273 | hp2 | a0005 | c0004 | t0001 | g0191 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02280 | hp1 | a0004 | c0005 | t0001 | g0211 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02280 | hp2 | a0006 | c0014 | t0001 | g0040 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02293 | hp2 | a0005 | c0004 | t0001 | g0190 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02300 | hp2 | a0017 | c0028 | t0001 | g0052 | AMR | PEL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02451 | hp1 | a0004 | c0023 | t0001 | g0048 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02451 | hp2 | a0004 | c0005 | t0001 | g0207 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02615 | hp1 | a0004 | c0019 | t0001 | g0030 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02615 | hp2 | a0018 | c0034 | t0001 | g0200 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02622 | hp2 | a0004 | c0005 | t0001 | g0212 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02630 | hp1 | a0009 | c0016 | t0001 | g0178 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02630 | hp2 | a0004 | c0005 | t0001 | g0208 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02647 | hp1 | a0019 | c0036 | t0001 | g0283 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02647 | hp2 | a0007 | c0008 | t0001 | g0039 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02717 | hp1 | a0006 | c0006 | t0001 | g0279 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02717 | hp2 | a0009 | c0012 | t0001 | g0231 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02809 | hp1 | a0009 | c0016 | t0001 | g0287 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02809 | hp2 | a0004 | c0005 | t0001 | g0027 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02818 | hp1 | a0004 | c0005 | t0001 | g0206 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02818 | hp2 | a0004 | c0005 | t0001 | g0215 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0047 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02886 | hp2 | a0007 | c0008 | t0001 | g0288 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02895 | hp1 | a0004 | c0005 | t0001 | g0213 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02895 | hp2 | a0012 | c0013 | t0001 | g0014 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02896 | hp1 | a0004 | c0005 | t0001 | g0209 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02896 | hp2 | a0001 | c0010 | t0001 | g0228 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02897 | hp1 | a0001 | c0010 | t0001 | g0224 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02897 | hp2 | a0004 | c0005 | t0001 | g0027 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02965 | hp1 | a0013 | c0017 | t0001 | g0026 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0292 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02970 | hp1 | a0020 | c0033 | t0001 | g0202 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02970 | hp2 | a0001 | c0015 | t0001 | g0221 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02976 | hp1 | a0005 | c0004 | t0001 | g0195 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02976 | hp2 | a0007 | c0018 | t0001 | g0233 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03041 | hp2 | a0001 | c0015 | t0001 | g0220 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03098 | hp1 | a0006 | c0006 | t0001 | g0282 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03098 | hp2 | a0009 | c0012 | t0001 | g0230 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0262 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03130 | hp2 | a0007 | c0018 | t0001 | g0235 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03139 | hp2 | a0006 | c0006 | t0001 | g0185 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03195 | hp2 | a0013 | c0017 | t0001 | g0026 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03209 | hp1 | a0006 | c0006 | t0001 | g0263 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03209 | hp2 | a0006 | c0006 | t0001 | g0281 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03453 | hp2 | a0001 | c0015 | t0001 | g0226 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03486 | hp1 | a0001 | c0010 | t0001 | g0227 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03492 | hp2 | a0001 | c0024 | t0001 | g0285 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03516 | hp1 | a0005 | c0004 | t0001 | g0196 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03516 | hp2 | a0004 | c0019 | t0001 | g0030 | AFR | ESN | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03540 | hp2 | a0001 | c0015 | t0001 | g0225 | AFR | GWD | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03579 | hp1 | a0006 | c0014 | t0001 | g0041 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03579 | hp2 | a0012 | c0013 | t0001 | g0014 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03654 | hp2 | a0005 | c0004 | t0001 | g0035 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03669 | hp2 | a0005 | c0004 | t0001 | g0193 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0270 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03704 | hp1 | a0001 | c0024 | t0001 | g0284 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03704 | hp2 | a0005 | c0004 | t0001 | g0035 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0237 | SAS | PJL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03831 | hp2 | a0001 | c0030 | t0001 | g0123 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03834 | hp1 | a0005 | c0004 | t0001 | g0015 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04228 | hp1 | a0003 | c0038 | t0001 | g0297 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18522 | hp1 | a0006 | c0014 | t0001 | g0043 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18522 | hp2 | a0013 | c0017 | t0001 | g0188 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18612 | hp1 | a0014 | c0020 | t0001 | g0117 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18906 | hp1 | a0007 | c0008 | t0001 | g0289 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18941 | hp2 | a0011 | c0011 | t0001 | g0219 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18948 | hp2 | a0005 | c0004 | t0001 | g0015 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18953 | hp2 | a0002 | c0025 | t0001 | g0295 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18966 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18970 | hp2 | a0011 | c0011 | t0001 | g0028 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18971 | hp1 | a0011 | c0011 | t0001 | g0218 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18977 | hp1 | a0021 | c0026 | t0001 | g0044 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18986 | hp2 | a0022 | c0035 | t0001 | g0276 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18991 | hp2 | a0003 | c0037 | t0001 | g0294 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19030 | hp2 | a0007 | c0008 | t0001 | g0199 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19043 | hp1 | a0007 | c0008 | t0001 | g0198 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19067 | hp1 | a0011 | c0011 | t0001 | g0028 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19067 | hp2 | a0010 | c0009 | t0001 | g0132 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19240 | hp1 | a0006 | c0006 | t0001 | g0023 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA19240 | hp2 | a0001 | c0010 | t0001 | g0222 | AFR | YRI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20129 | hp1 | a0009 | c0016 | t0001 | g0184 | AFR | ASW | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0214 | AFR | ASW | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20752 | hp1 | a0008 | c0007 | t0001 | g0093 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20752 | hp2 | a0005 | c0004 | t0001 | g0024 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | TSI | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01123 | hp1 | a0004 | c0019 | t0001 | g0236 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02109 | hp1 | a0007 | c0018 | t0001 | g0234 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02486 | hp1 | a0004 | c0005 | t0001 | g0210 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02486 | hp2 | a0001 | c0010 | t0001 | g0229 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG02559 | hp2 | a0009 | c0012 | t0001 | g0029 | AFR | ACB | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03471 | hp1 | a0001 | c0010 | t0001 | g0223 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| HG03471 | hp2 | a0007 | c0008 | t0001 | g0201 | AFR | MSL | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0197 | AFR | USA | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA21309 | hp1 | a0006 | c0006 | t0001 | g0264 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| NA21309 | hp2 | a0006 | c0014 | t0001 | g0042 | AFR | LWK | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| homoSapiens | chm13v2 | a0023 | c0031 | t0001 | g0254 | REF | REF | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0119 | REF | REF | MAN2B1_chr19_12641512_12671742 | MAN2B1 | chr19 | 12641512 | 12671742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:12646663 | C | T | 1 | a0014 | 2 | HG00621.hp2 NA18612.hp1 |
missense_variant | MODERATE | c.2993G>A | p.Arg998His | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 24/24 | 3034/3185 | 2993/3036 | 998/1011 | chr19 | 12646663 | |||
| chr19:12649959 | C | T | 2 | a0012 a0018 |
5 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
missense_variant | MODERATE | c.2221G>A | p.Gly741Arg | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/24 | 2262/3185 | 2221/3036 | 741/1011 | chr19 | 12649959 | |||
| chr19:12652193 | G | A | 1 | a0010 | 6 | HG00544.hp2 HG01106.hp1 HG01261.hp2 others(3): Show |
missense_variant | MODERATE | c.2006C>T | p.Pro669Leu | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/24 | 2047/3185 | 2006/3036 | 669/1011 | chr19 | 12652193 | |||
| chr19:12652385 | G | A | 1 | a0020 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1906C>T | p.Pro636Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 15/24 | 1947/3185 | 1906/3036 | 636/1011 | chr19 | 12652385 | |||
| chr19:12655780 | G | C | 1 | a0013 | 3 | HG02965.hp1 HG03195.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.1744C>G | p.Gln582Glu | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/24 | 1785/3185 | 1744/3036 | 582/1011 | chr19 | 12655780 | |||
| chr19:12657035 | C | A | 4 | a0007 a0009 a0012 others(1): Show |
23 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
missense_variant | MODERATE | c.1441G>T | p.Ala481Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 12/24 | 1482/3185 | 1441/3036 | 481/1011 | chr19 | 12657035 | |||
| chr19:12658134 | T | C | 1 | a0008 | 8 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(5): Show |
missense_variant | MODERATE | c.1238A>G | p.Asn413Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/24 | 1279/3185 | 1238/3036 | 413/1011 | chr19 | 12658134 | |||
| chr19:12661276 | C | T | 6 | a0002 a0003 a0007 others(3): Show |
77 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(74): Show |
missense_variant | MODERATE | c.1010G>A | p.Arg337Gln | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/24 | 1051/3185 | 1010/3036 | 337/1011 | chr19 | 12661276 | |||
| chr19:12661351 | G | A | 9 | a0002 a0003 a0004 others(6): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
missense_variant | MODERATE | c.935C>T | p.Thr312Ile | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/24 | 976/3185 | 935/3036 | 312/1011 | chr19 | 12661351 | |||
| chr19:12661364 | G | A | 1 | a0016 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.922C>T | p.Arg308Cys | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/24 | 963/3185 | 922/3036 | 308/1011 | chr19 | 12661364 | |||
| chr19:12663394 | G | C | 7 | a0002 a0004 a0005 others(4): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
missense_variant | MODERATE | c.832C>G | p.Leu278Val | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/24 | 873/3185 | 832/3036 | 278/1011 | chr19 | 12663394 | |||
| chr19:12663706 | T | C | 1 | a0022 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.760A>G | p.Thr254Ala | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 801/3185 | 760/3036 | 254/1011 | chr19 | 12663706 | |||
| chr19:12663718 | C | A | 1 | a0011 | 5 | HG00609.hp2 NA18941.hp2 NA18970.hp2 others(2): Show |
missense_variant | MODERATE | c.748G>T | p.Ala250Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 789/3185 | 748/3036 | 250/1011 | chr19 | 12663718 | |||
| chr19:12663780 | C | T | 1 | a0017 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.686G>A | p.Arg229Gln | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 727/3185 | 686/3036 | 229/1011 | chr19 | 12663780 | |||
| chr19:12664813 | C | A | 1 | a0019 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.609G>T | p.Glu203Asp | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/24 | 650/3185 | 609/3036 | 203/1011 | chr19 | 12664813 | |||
| chr19:12665433 | C | T | 1 | a0015 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.355G>A | p.Val119Met | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/24 | 396/3185 | 355/3036 | 119/1011 | chr19 | 12665433 | |||
| chr19:12665502 | C | T | 1 | a0021 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.286G>A | p.Gly96Ser | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/24 | 327/3185 | 286/3036 | 96/1011 | chr19 | 12665502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:12648277 | G | C | 1 | a0006c0014 | 4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
synonymous_variant | LOW | c.2562C>G | p.Ala854Ala | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/24 | 2603/3185 | 2562/3036 | 854/1011 | chr19 | 12648277 | |||
| chr19:12648352 | T | G | 1 | a0001c0030 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.2487A>C | p.Leu829Leu | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/24 | 2528/3185 | 2487/3036 | 829/1011 | chr19 | 12648352 | |||
| chr19:12649386 | G | A | 1 | a0006c0006 | 9 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.2310C>T | p.Pro770Pro | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 19/24 | 2351/3185 | 2310/3036 | 770/1011 | chr19 | 12649386 | |||
| chr19:12649413 | G | A | 1 | a0004c0023 | 2 | HG01934.hp2 HG02451.hp1 |
synonymous_variant | LOW | c.2283C>T | p.Pro761Pro | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 19/24 | 2324/3185 | 2283/3036 | 761/1011 | chr19 | 12649413 | |||
| chr19:12652264 | G | A | 1 | a0001c0010 | 6 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.1935C>T | p.Asn645Asn | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/24 | 1976/3185 | 1935/3036 | 645/1011 | chr19 | 12652264 | |||
| chr19:12655742 | C | T | 1 | a0001c0029 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.1782G>A | p.Gln594Gln | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/24 | 1823/3185 | 1782/3036 | 594/1011 | chr19 | 12655742 | |||
| chr19:12658469 | G | C | 2 | a0002c0022 a0003c0021 |
4 | HG01081.hp1 HG01243.hp1 HG01258.hp2 others(1): Show |
synonymous_variant | LOW | c.1068C>G | p.Pro356Pro | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 8/24 | 1109/3185 | 1068/3036 | 356/1011 | chr19 | 12658469 | |||
| chr19:12663719 | G | A | 5 | a0001c0010 a0001c0015 a0004c0019 others(2): Show |
21 | HG01123.hp1 HG01952.hp2 HG02109.hp1 others(18): Show |
synonymous_variant | LOW | c.747C>T | p.Thr249Thr | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/24 | 788/3185 | 747/3036 | 249/1011 | chr19 | 12663719 | |||
| chr19:12664828 | G | A | 1 | a0001c0024 | 2 | HG03492.hp2 HG03704.hp1 |
synonymous_variant | LOW | c.594C>T | p.Phe198Phe | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/24 | 635/3185 | 594/3036 | 198/1011 | chr19 | 12664828 | |||
| chr19:12666567 | G | A | 2 | a0002c0025 a0003c0037 |
3 | HG02080.hp1 NA18953.hp2 NA18991.hp2 |
synonymous_variant | LOW | c.135C>T | p.Ala45Ala | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/24 | 176/3185 | 135/3036 | 45/1011 | chr19 | 12666567 | |||
| chr19:12666663 | G | C | 1 | a0003c0038 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.39C>G | p.Arg13Arg | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/24 | 80/3185 | 39/3036 | 13/1011 | chr19 | 12666663 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:12646529 | G | A | 1 | a0001c0001t0002 | 2 | NA18945.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*91C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 24/24 | 91 | chr19 | 12646529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:12646811 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2924-79C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12646811 | |||||||
| chr19:12646882 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2924-150C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12646882 | |||||||
| chr19:12646884 | C | T | 24 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0215 others(21): Show |
28 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.2924-152G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12646884 | |||||||
| chr19:12647136 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2923+97A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12647136 | |||||||
| chr19:12647140 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2923+93C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12647140 | |||||||
| chr19:12647183 | C | T | 4 | a0001c0015t0001g0220 a0001c0015t0001g0221 a0001c0015t0001g0225 others(1): Show |
4 | HG02970.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2923+50G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 23/23 | chr19 | 12647183 | |||||||
| chr19:12647629 | G | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2665-31C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647629 | |||||||
| chr19:12647672 | C | A | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2665-74G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647672 | |||||||
| chr19:12647717 | G | T | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2665-119C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647717 | |||||||
| chr19:12647843 | T | C | 1 | a0020c0033t0001g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2665-245A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647843 | |||||||
| chr19:12647909 | A | G | 33 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(30): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.2664+266T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12647909 | |||||||
| chr19:12648001 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0239 a0001c0001t0001g0240 |
8 | HG00438.hp2 NA18941.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.2664+174C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12648001 | |||||||
| chr19:12648025 | G | T | 1 | a0006c0006t0001g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2664+150C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12648025 | |||||||
| chr19:12648060 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0142 |
3 | HG03239.hp1 HG04115.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2664+115A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 21/23 | chr19 | 12648060 | |||||||
| chr19:12648505 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2437-103C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648505 | |||||||
| chr19:12648509 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2437-107C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648509 | |||||||
| chr19:12648766 | G | GC | 20 | a0003c0003t0001g0047 a0004c0005t0001g0197 a0004c0005t0001g0206 others(17): Show |
22 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2437-365_2437-364i others(3): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648766 | |||||||
| chr19:12648785 | A | C | 1 | a0008c0007t0001g0149 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2436+351T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648785 | |||||||
| chr19:12648803 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2436+333A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648803 | |||||||
| chr19:12648822 | C | G | 10 | a0007c0008t0001g0039 a0007c0008t0001g0198 a0007c0008t0001g0199 others(7): Show |
11 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2436+314G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648822 | |||||||
| chr19:12648893 | G | A | 8 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0215 others(5): Show |
9 | HG02055.hp2 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2436+243C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648893 | |||||||
| chr19:12648951 | T | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0124 |
2 | NA18950.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2436+185A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12648951 | |||||||
| chr19:12649017 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2436+119G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 20/23 | chr19 | 12649017 | |||||||
| chr19:12649291 | G | T | 1 | a0002c0002t0001g0277 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2355+50C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 19/23 | chr19 | 12649291 | |||||||
| chr19:12649473 | A | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(81): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.2268-45T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649473 | |||||||
| chr19:12649477 | C | CT | 22 | a0001c0001t0001g0082 a0001c0001t0001g0090 a0001c0001t0001g0094 others(19): Show |
22 | HG00621.hp2 HG01346.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.2268-50dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(2): Show |
26 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0089 others(23): Show |
30 | HG00733.hp2 HG01361.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.2268-58_2268-50dup others(9): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(3): Show |
43 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0037 others(40): Show |
51 | HG00423.hp1 HG00621.hp1 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.2268-59_2268-50dup others(10): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(4): Show |
12 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0092 others(9): Show |
12 | HG00438.hp1 HG02257.hp2 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.2268-60_2268-50dup others(11): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(5): Show |
4 | a0001c0001t0001g0159 a0001c0001t0001g0171 a0001c0001t0001g0248 others(1): Show |
4 | HG00558.hp1 HG02071.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2268-61_2268-50dup others(12): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0004c0005t0001g0027 |
4 | HG02809.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268-62_2268-50dup others(13): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(7): Show |
9 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0004c0005t0001g0213 others(6): Show |
9 | HG01884.hp2 HG02055.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2268-63_2268-50dup others(14): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(8): Show |
30 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0036 others(27): Show |
33 | HG00140.hp1 HG00323.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.2268-64_2268-50dup others(15): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(9): Show |
15 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0081 others(12): Show |
22 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.2268-65_2268-50dup others(16): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0001g0105 a0005c0004t0001g0189 a0005c0004t0001g0191 others(1): Show |
4 | HG00280.hp1 HG01070.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.2268-66_2268-50dup others(17): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0101 a0005c0004t0001g0190 |
2 | HG02293.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.2268-67_2268-50dup others(18): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | C | CTTTTTTT others(16): Show |
1 | a0008c0007t0001g0147 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2268-50_2268-49ins others(23): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | CT | C | 35 | a0001c0001t0001g0126 a0002c0002t0001g0002 a0002c0002t0001g0034 others(32): Show |
54 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.2268-50delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649477 | CTTTTT | C | 4 | a0001c0010t0001g0223 a0012c0013t0001g0014 a0012c0013t0001g0177 others(1): Show |
6 | HG01109.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2268-54_2268-50del others(5): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649477 | |||||||
| chr19:12649575 | G | A | 3 | a0001c0001t0001g0127 a0004c0023t0001g0048 a0004c0023t0001g0049 |
3 | HG01934.hp2 HG02451.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2268-147C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649575 | |||||||
| chr19:12649631 | G | A | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268-203C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649631 | |||||||
| chr19:12649697 | T | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(106): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.2267+216A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649697 | |||||||
| chr19:12649810 | G | A | 1 | a0022c0035t0001g0276 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2267+103C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649810 | |||||||
| chr19:12649850 | T | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(132): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2267+63A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649850 | |||||||
| chr19:12649910 | C | G | 10 | a0007c0008t0001g0039 a0007c0008t0001g0198 a0007c0008t0001g0199 others(7): Show |
11 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.2267+3G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | 12649910 | |||||||
| chr19:12650262 | G | C | 1 | a0002c0002t0001g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2047-40C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650262 | |||||||
| chr19:12650357 | C | CT | 9 | a0001c0001t0001g0057 a0001c0001t0001g0072 a0001c0001t0001g0087 others(6): Show |
9 | HG01515.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2047-136dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650357 | |||||||
| chr19:12650357 | CT | C | 54 | a0001c0001t0001g0155 a0001c0001t0001g0244 a0001c0001t0001g0248 others(51): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.2047-136delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650357 | |||||||
| chr19:12650361 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2047-139A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650361 | |||||||
| chr19:12650430 | C | T | 9 | a0004c0005t0001g0197 a0004c0005t0001g0206 a0004c0005t0001g0207 others(6): Show |
9 | HG01934.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2047-208G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650430 | |||||||
| chr19:12650519 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2047-297G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650519 | |||||||
| chr19:12650544 | G | A | 2 | a0006c0006t0001g0023 a0006c0006t0001g0185 |
3 | HG01891.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2047-322C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650544 | |||||||
| chr19:12650568 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2047-346T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650568 | |||||||
| chr19:12650604 | C | T | 1 | a0001c0030t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2047-382G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650604 | |||||||
| chr19:12650622 | T | G | 1 | a0002c0002t0001g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2047-400A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650622 | |||||||
| chr19:12650650 | G | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0053 others(18): Show |
28 | HG00423.hp1 HG00621.hp1 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.2047-428C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650650 | |||||||
| chr19:12650674 | C | CT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0104 a0001c0001t0001g0120 others(2): Show |
6 | HG03139.hp2 NA18945.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.2047-453dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650674 | |||||||
| chr19:12650869 | TCCATGTT others(2): Show |
T | 20 | a0003c0003t0001g0047 a0004c0005t0001g0197 a0004c0005t0001g0206 others(17): Show |
22 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.2047-656_2047-648d others(11): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650869 | |||||||
| chr19:12650952 | G | A | 1 | a0007c0008t0001g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2047-730C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650952 | |||||||
| chr19:12650973 | C | CT | 25 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0110 others(22): Show |
27 | HG00323.hp2 HG01167.hp1 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.2047-752dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650973 | |||||||
| chr19:12650973 | C | CTT | 12 | a0004c0005t0001g0197 a0004c0005t0001g0206 a0004c0005t0001g0207 others(9): Show |
13 | HG01891.hp1 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2047-753_2047-752d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650973 | |||||||
| chr19:12650973 | CT | C | 38 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0001t0001g0089 others(35): Show |
43 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.2047-752delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12650973 | |||||||
| chr19:12651109 | G | T | 2 | a0003c0003t0001g0260 a0003c0003t0001g0261 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2047-887C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651109 | |||||||
| chr19:12651156 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2047-934G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651156 | |||||||
| chr19:12651424 | A | G | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2046+729T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651424 | |||||||
| chr19:12651640 | TGA | T | 22 | a0001c0001t0001g0009 a0001c0001t0001g0076 a0001c0001t0001g0078 others(19): Show |
25 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.2046+511_2046+512d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651640 | |||||||
| chr19:12651740 | C | G | 1 | a0003c0003t0001g0047 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2046+413G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651740 | |||||||
| chr19:12651853 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0162 a0001c0001t0001g0250 |
3 | HG02080.hp2 NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2046+300A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651853 | |||||||
| chr19:12651881 | A | G | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2046+272T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651881 | |||||||
| chr19:12651959 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0156 a0001c0001t0001g0286 |
3 | HG00323.hp1 HG01978.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2046+194A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651959 | |||||||
| chr19:12651969 | T | C | 135 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(132): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.2046+184A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 16/23 | chr19 | 12651969 | |||||||
| chr19:12652477 | C | T | 1 | a0020c0033t0001g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1831-17G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652477 | |||||||
| chr19:12652536 | C | CT | 122 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(119): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1831-77dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652536 | |||||||
| chr19:12652536 | C | CTT | 9 | a0001c0001t0001g0083 a0001c0001t0001g0242 a0006c0014t0001g0040 others(6): Show |
9 | HG02280.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1831-78_1831-77dup others(2): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652536 | |||||||
| chr19:12652618 | A | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(81): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1831-158T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652618 | |||||||
| chr19:12652619 | C | G | 1 | a0003c0003t0001g0182 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1831-159G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652619 | |||||||
| chr19:12652625 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1831-165C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652625 | |||||||
| chr19:12652840 | A | AT | 6 | a0001c0001t0001g0120 a0004c0005t0001g0027 a0004c0005t0001g0213 others(3): Show |
7 | HG01361.hp2 HG02809.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1831-381dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652840 | |||||||
| chr19:12652840 | AT | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(123): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1831-381delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12652840 | |||||||
| chr19:12653035 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1831-575A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653035 | |||||||
| chr19:12653087 | GC | G | 10 | a0001c0010t0001g0222 a0001c0010t0001g0223 a0001c0010t0001g0224 others(7): Show |
10 | HG02486.hp2 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.1831-628delG | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653087 | |||||||
| chr19:12653144 | G | GT | 25 | a0001c0001t0001g0053 a0001c0001t0001g0078 a0001c0001t0001g0094 others(22): Show |
25 | HG00423.hp2 HG00733.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.1831-685dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653144 | |||||||
| chr19:12653144 | GT | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(93): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.1831-685delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653144 | |||||||
| chr19:12653149 | T | G | 1 | a0001c0001t0001g0090 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1831-689A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653149 | |||||||
| chr19:12653388 | A | AC | 49 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(46): Show |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1831-929dupG | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653388 | |||||||
| chr19:12653388 | AC | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(157): Show |
210 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.1831-929delG | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653388 | |||||||
| chr19:12653393 | C | CA | 33 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(30): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.1831-934_1831-933i others(3): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653393 | |||||||
| chr19:12653394 | C | G | 1 | a0006c0014t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1831-934G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653394 | |||||||
| chr19:12653395 | C | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0240 |
7 | NA18941.hp1 NA18943.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831-935G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653395 | |||||||
| chr19:12653496 | C | T | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1831-1036G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653496 | |||||||
| chr19:12653602 | A | T | 2 | a0009c0012t0001g0029 a0009c0012t0001g0232 |
3 | HG01952.hp2 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1831-1142T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653602 | |||||||
| chr19:12653615 | T | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1831-1155A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653615 | |||||||
| chr19:12653637 | G | A | 1 | a0003c0003t0001g0292 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1831-1177C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653637 | |||||||
| chr19:12653835 | C | T | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1831-1375G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653835 | |||||||
| chr19:12653950 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1831-1490G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12653950 | |||||||
| chr19:12654008 | C | T | 16 | a0007c0008t0001g0039 a0007c0008t0001g0187 a0007c0008t0001g0198 others(13): Show |
19 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1831-1548G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654008 | |||||||
| chr19:12654094 | A | G | 1 | a0003c0003t0001g0292 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1830+1600T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654094 | |||||||
| chr19:12654155 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0076 others(20): Show |
26 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.1830+1539C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654155 | |||||||
| chr19:12654260 | T | C | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+1434A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654260 | |||||||
| chr19:12654264 | C | G | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+1430G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654264 | |||||||
| chr19:12654338 | G | A | 1 | a0002c0002t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1830+1356C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654338 | |||||||
| chr19:12654409 | T | C | 2 | a0001c0001t0001g0290 a0021c0026t0001g0044 |
2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1830+1285A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654409 | |||||||
| chr19:12654470 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1830+1224T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654470 | |||||||
| chr19:12654998 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1830+696G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12654998 | |||||||
| chr19:12655121 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1830+573A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655121 | |||||||
| chr19:12655208 | C | T | 2 | a0006c0014t0001g0042 a0006c0014t0001g0043 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1830+486G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655208 | |||||||
| chr19:12655264 | G | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+430C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655264 | |||||||
| chr19:12655278 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1830+416G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655278 | |||||||
| chr19:12655296 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0291 |
2 | HG00423.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1830+398A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655296 | |||||||
| chr19:12655335 | C | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1830+359G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655335 | |||||||
| chr19:12655478 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1830+216A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655478 | |||||||
| chr19:12655556 | G | A | 83 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(80): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1830+138C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 14/23 | chr19 | 12655556 | |||||||
| chr19:12656074 | G | T | 10 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0114 others(7): Show |
10 | HG00621.hp2 NA18612.hp1 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.1645-195C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656074 | |||||||
| chr19:12656099 | G | A | 7 | a0004c0005t0001g0197 a0004c0005t0001g0206 a0004c0005t0001g0207 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1645-220C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656099 | |||||||
| chr19:12656142 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1645-263C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656142 | |||||||
| chr19:12656190 | G | A | 3 | a0002c0002t0001g0205 a0004c0023t0001g0048 a0004c0023t0001g0049 |
3 | HG01934.hp2 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1645-311C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656190 | |||||||
| chr19:12656215 | T | G | 20 | a0003c0003t0001g0047 a0004c0005t0001g0197 a0004c0005t0001g0206 others(17): Show |
22 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1645-336A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656215 | |||||||
| chr19:12656356 | C | CA | 15 | a0001c0001t0001g0018 a0001c0001t0001g0083 a0001c0001t0001g0109 others(12): Show |
17 | HG01123.hp1 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1644+214dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656356 | |||||||
| chr19:12656525 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1644+46G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 13/23 | chr19 | 12656525 | |||||||
| chr19:12657096 | C | G | 8 | a0006c0006t0001g0023 a0006c0006t0001g0185 a0006c0006t0001g0263 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1420-40G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657096 | |||||||
| chr19:12657298 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0158 |
3 | HG02132.hp2 HG02165.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1419+148A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657298 | |||||||
| chr19:12657336 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1419+110G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657336 | |||||||
| chr19:12657417 | C | T | 5 | a0007c0008t0001g0039 a0007c0008t0001g0288 a0007c0008t0001g0289 others(2): Show |
5 | HG02647.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+29G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657417 | |||||||
| chr19:12657430 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1419+16C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 11/23 | chr19 | 12657430 | |||||||
| chr19:12657577 | G | A | 81 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(78): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.1310-22C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657577 | |||||||
| chr19:12657611 | G | A | 9 | a0007c0008t0001g0198 a0007c0008t0001g0199 a0007c0018t0001g0233 others(6): Show |
10 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1310-56C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657611 | |||||||
| chr19:12657918 | G | A | 1 | a0010c0009t0001g0132 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1309+145C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657918 | |||||||
| chr19:12657954 | C | CA | 53 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0046 others(50): Show |
56 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1309+108dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | |||||||
| chr19:12657954 | CA | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0110 a0001c0001t0001g0111 others(23): Show |
31 | HG01123.hp1 HG01891.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.1309+108delT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | |||||||
| chr19:12657954 | CAA | C | 11 | a0001c0001t0001g0074 a0001c0001t0001g0083 a0001c0001t0001g0084 others(8): Show |
11 | HG00741.hp2 HG01981.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+107_1309+108d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | |||||||
| chr19:12657954 | CAAA | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0017 others(82): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.1309+106_1309+108d others(5): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | |||||||
| chr19:12657954 | CAAAA | C | 8 | a0001c0001t0001g0101 a0007c0008t0001g0198 a0007c0018t0001g0233 others(5): Show |
9 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309+105_1309+108d others(6): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12657954 | |||||||
| chr19:12658029 | G | T | 35 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(32): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.1309+34C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 10/23 | chr19 | 12658029 | |||||||
| chr19:12658215 | C | G | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1230+9G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 9/23 | chr19 | 12658215 | |||||||
| chr19:12658359 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0162 a0001c0001t0001g0250 |
3 | HG02080.hp2 NA18989.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1110-15C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 8/23 | chr19 | 12658359 | |||||||
| chr19:12658580 | T | C | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-70A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658580 | |||||||
| chr19:12658619 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1027-109T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658619 | |||||||
| chr19:12658662 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1027-152C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658662 | |||||||
| chr19:12658690 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1027-180G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658690 | |||||||
| chr19:12658850 | C | A | 19 | a0004c0005t0001g0197 a0004c0005t0001g0206 a0004c0005t0001g0207 others(16): Show |
21 | HG01123.hp1 HG01891.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1027-340G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658850 | |||||||
| chr19:12658872 | T | C | 1 | a0006c0006t0001g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1027-362A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658872 | |||||||
| chr19:12658874 | T | G | 1 | a0020c0033t0001g0202 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1027-364A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658874 | |||||||
| chr19:12658888 | A | T | 1 | a0006c0006t0001g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1027-378T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12658888 | |||||||
| chr19:12659018 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1027-508C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659018 | |||||||
| chr19:12659020 | C | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0152 others(4): Show |
9 | HG02129.hp1 HG02135.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027-510G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659020 | |||||||
| chr19:12659171 | A | G | 2 | a0008c0007t0001g0098 a0008c0007t0001g0099 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1027-661T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659171 | |||||||
| chr19:12659268 | C | G | 9 | a0007c0008t0001g0198 a0007c0008t0001g0199 a0007c0018t0001g0233 others(6): Show |
10 | HG01952.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-758G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659268 | |||||||
| chr19:12659297 | C | CT | 9 | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0083 others(6): Show |
9 | HG01243.hp2 HG02135.hp2 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.1027-788dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | |||||||
| chr19:12659297 | CT | C | 23 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0060 others(20): Show |
28 | HG00323.hp1 HG00438.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1027-788delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | |||||||
| chr19:12659297 | CTT | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(56): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.1027-789_1027-788d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | |||||||
| chr19:12659297 | CTTT | C | 8 | a0002c0002t0001g0205 a0002c0002t0001g0266 a0003c0003t0001g0292 others(5): Show |
9 | HG01891.hp1 HG02258.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027-790_1027-788d others(5): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659297 | |||||||
| chr19:12659298 | T | A | 4 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(1): Show |
4 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-788A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659298 | |||||||
| chr19:12659328 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1027-818C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659328 | |||||||
| chr19:12659492 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1027-982T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659492 | |||||||
| chr19:12659745 | G | C | 9 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(6): Show |
10 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1027-1235C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659745 | |||||||
| chr19:12659812 | CT | C | 86 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(83): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027-1303delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659812 | |||||||
| chr19:12659849 | A | G | 5 | a0007c0008t0001g0039 a0007c0008t0001g0288 a0007c0008t0001g0289 others(2): Show |
5 | HG02647.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027-1339T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659849 | |||||||
| chr19:12659920 | G | T | 2 | a0001c0001t0001g0290 a0021c0026t0001g0044 |
2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1026+1340C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659920 | |||||||
| chr19:12659946 | T | C | 3 | a0007c0008t0001g0288 a0007c0008t0001g0289 a0009c0016t0001g0287 |
3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1026+1314A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12659946 | |||||||
| chr19:12660273 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1026+987T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660273 | |||||||
| chr19:12660276 | G | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1026+984C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660276 | |||||||
| chr19:12660301 | C | G | 2 | a0004c0005t0001g0206 a0004c0005t0001g0207 |
2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1026+959G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660301 | |||||||
| chr19:12660406 | A | G | 86 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(83): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.1026+854T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660406 | |||||||
| chr19:12660450 | C | G | 35 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(32): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.1026+810G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660450 | |||||||
| chr19:12660481 | G | A | 3 | a0002c0002t0001g0273 a0004c0023t0001g0048 a0004c0023t0001g0049 |
3 | HG01934.hp2 HG01981.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1026+779C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660481 | |||||||
| chr19:12660496 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1026+764G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660496 | |||||||
| chr19:12660752 | A | AT | 40 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0053 others(37): Show |
42 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1026+507dupA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | |||||||
| chr19:12660752 | A | ATTTTT | 6 | a0001c0001t0001g0050 a0004c0005t0001g0027 a0004c0005t0001g0213 others(3): Show |
7 | HG02280.hp2 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+503_1026+507d others(7): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | |||||||
| chr19:12660752 | AT | A | 72 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0069 others(69): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1026+507delA | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | |||||||
| chr19:12660752 | ATT | A | 9 | a0002c0002t0001g0205 a0002c0002t0001g0274 a0002c0022t0001g0275 others(6): Show |
10 | HG01081.hp2 HG01891.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1026+506_1026+507d others(4): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660752 | |||||||
| chr19:12660935 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0163 a0016c0032t0001g0166 |
4 | HG00323.hp2 HG01346.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+325A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660935 | |||||||
| chr19:12660978 | C | T | 5 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(2): Show |
6 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1026+282G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660978 | |||||||
| chr19:12660999 | T | C | 11 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(8): Show |
12 | HG01934.hp2 HG02055.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1026+261A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12660999 | |||||||
| chr19:12661009 | A | G | 87 | a0001c0001t0001g0082 a0002c0002t0001g0002 a0002c0002t0001g0034 others(84): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1026+251T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661009 | |||||||
| chr19:12661060 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1026+200A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661060 | |||||||
| chr19:12661152 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0081 |
2 | HG00642.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1026+108T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661152 | |||||||
| chr19:12661158 | C | A | 4 | a0005c0004t0001g0195 a0005c0004t0001g0196 a0013c0017t0001g0026 others(1): Show |
5 | HG02965.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+102G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661158 | |||||||
| chr19:12661176 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1026+84C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661176 | |||||||
| chr19:12661210 | G | A | 1 | a0002c0002t0001g0205 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026+50C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 7/23 | chr19 | 12661210 | |||||||
| chr19:12661449 | T | C | 75 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0203 others(72): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.910-73A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661449 | |||||||
| chr19:12661505 | C | A | 1 | a0002c0002t0001g0204 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.910-129G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661505 | |||||||
| chr19:12661550 | C | A | 9 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(6): Show |
10 | HG02055.hp2 HG02280.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.910-174G>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661550 | |||||||
| chr19:12661628 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.910-252T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661628 | |||||||
| chr19:12661760 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910-384C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661760 | |||||||
| chr19:12661824 | G | GA | 10 | a0001c0001t0001g0053 a0001c0001t0001g0169 a0006c0006t0001g0023 others(7): Show |
11 | HG01891.hp1 HG02257.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-449dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661824 | |||||||
| chr19:12661824 | GA | G | 9 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(6): Show |
9 | HG01070.hp1 HG02698.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.910-449delT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661824 | |||||||
| chr19:12661838 | A | G | 1 | a0007c0008t0001g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.910-462T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661838 | |||||||
| chr19:12661855 | T | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.910-479A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661855 | |||||||
| chr19:12661910 | T | TCTCGGCT others(6): Show |
1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.910-547_910-535dup others(13): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661910 | |||||||
| chr19:12661913 | C | T | 1 | a0001c0001t0001g0017 | 2 | NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.910-537G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12661913 | |||||||
| chr19:12662017 | G | A | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-641C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662017 | |||||||
| chr19:12662159 | A | G | 1 | a0005c0004t0001g0024 | 2 | HG01168.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.910-783T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662159 | |||||||
| chr19:12662293 | T | C | 2 | a0001c0001t0001g0290 a0021c0026t0001g0044 |
2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.910-917A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662293 | |||||||
| chr19:12662319 | A | G | 15 | a0007c0008t0001g0187 a0007c0008t0001g0198 a0007c0008t0001g0199 others(12): Show |
18 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.910-943T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662319 | |||||||
| chr19:12662357 | G | A | 7 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(4): Show |
8 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+960C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662357 | |||||||
| chr19:12662486 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0067 others(4): Show |
13 | HG00438.hp2 HG02155.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.909+831G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662486 | |||||||
| chr19:12662654 | A | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0053 others(14): Show |
24 | HG00423.hp1 HG00621.hp1 HG02004.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+663T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662654 | |||||||
| chr19:12662744 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.909+573T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662744 | |||||||
| chr19:12662855 | T | G | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.909+462A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662855 | |||||||
| chr19:12662863 | G | A | 18 | a0002c0002t0001g0205 a0004c0005t0001g0197 a0004c0005t0001g0206 others(15): Show |
20 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.909+454C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662863 | |||||||
| chr19:12662863 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.909+454C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662863 | |||||||
| chr19:12662937 | C | CA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0170 others(91): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.909+379dupT | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662937 | |||||||
| chr19:12662948 | A | T | 9 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0002g0061 others(6): Show |
10 | HG00609.hp2 NA18522.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.909+369T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662948 | |||||||
| chr19:12662949 | A | T | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.909+368T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662949 | |||||||
| chr19:12662951 | T | A | 12 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0004c0023t0001g0048 others(9): Show |
13 | HG01891.hp1 HG01934.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.909+366A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662951 | |||||||
| chr19:12662952 | A | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.909+365T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662952 | |||||||
| chr19:12662953 | A | T | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.909+364T>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662953 | |||||||
| chr19:12662954 | T | A | 2 | a0004c0023t0001g0048 a0004c0023t0001g0049 |
2 | HG01934.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.909+363A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662954 | |||||||
| chr19:12662966 | A | G | 1 | a0007c0008t0001g0187 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.909+351T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12662966 | |||||||
| chr19:12663151 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.909+166A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12663151 | |||||||
| chr19:12663169 | G | A | 5 | a0004c0005t0001g0027 a0004c0005t0001g0213 a0004c0005t0001g0214 others(2): Show |
6 | HG02055.hp2 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+148C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12663169 | |||||||
| chr19:12663235 | C | G | 7 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(4): Show |
7 | HG02109.hp2 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+82G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | 12663235 | |||||||
| chr19:12663484 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-22T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663484 | |||||||
| chr19:12663488 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-26C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663488 | |||||||
| chr19:12663495 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-33T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663495 | |||||||
| chr19:12663510 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-48G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663510 | |||||||
| chr19:12663512 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-50A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663512 | |||||||
| chr19:12663520 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-58T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663520 | |||||||
| chr19:12663566 | A | AGATGCAA others(15): Show |
1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-105_764-104ins others(22): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663566 | |||||||
| chr19:12663582 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.764-120G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663582 | |||||||
| chr19:12663583 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+120T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663583 | |||||||
| chr19:12663584 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+119C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663584 | |||||||
| chr19:12663587 | C | G | 1 | a0002c0002t0001g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.763+116G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663587 | |||||||
| chr19:12663606 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+97C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663606 | |||||||
| chr19:12663607 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+96C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663607 | |||||||
| chr19:12663608 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.763+95T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 5/23 | chr19 | 12663608 | |||||||
| chr19:12663929 | G | C | 5 | a0004c0023t0001g0048 a0004c0023t0001g0049 a0007c0008t0001g0288 others(2): Show |
5 | HG01934.hp2 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-94C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12663929 | |||||||
| chr19:12664018 | A | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.631-183T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664018 | |||||||
| chr19:12664035 | G | A | 1 | a0007c0008t0001g0289 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.631-200C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664035 | |||||||
| chr19:12664048 | G | A | 60 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0031 others(57): Show |
87 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.631-213C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664048 | |||||||
| chr19:12664087 | G | A | 1 | a0002c0002t0001g0277 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.631-252C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664087 | |||||||
| chr19:12664274 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.631-439A>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664274 | |||||||
| chr19:12664460 | C | T | 5 | a0004c0023t0001g0048 a0004c0023t0001g0049 a0007c0008t0001g0288 others(2): Show |
5 | HG01934.hp2 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.630+332G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664460 | |||||||
| chr19:12664471 | G | A | 4 | a0006c0006t0001g0279 a0006c0006t0001g0280 a0006c0006t0001g0281 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+321C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664471 | |||||||
| chr19:12664763 | G | A | 1 | a0005c0004t0001g0035 | 2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.630+29C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664763 | |||||||
| chr19:12664791 | C | G | 1 | a0003c0003t0001g0047 | 1 | HG02886.hp1 | splice_donor_variant&intron_variant | HIGH | c.630+1G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 4/23 | chr19 | 12664791 | |||||||
| chr19:12665022 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.437-37C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665022 | |||||||
| chr19:12665185 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.436+167C>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665185 | |||||||
| chr19:12665208 | G | C | 3 | a0007c0008t0001g0288 a0007c0008t0001g0289 a0009c0016t0001g0287 |
3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.436+144C>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665208 | |||||||
| chr19:12665318 | G | A | 2 | a0001c0001t0001g0290 a0021c0026t0001g0044 |
2 | NA18977.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.436+34C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 3/23 | chr19 | 12665318 | |||||||
| chr19:12665638 | C | G | 4 | a0006c0014t0001g0040 a0006c0014t0001g0041 a0006c0014t0001g0042 others(1): Show |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+65G>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 2/23 | chr19 | 12665638 | |||||||
| chr19:12665984 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.160-179A>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12665984 | |||||||
| chr19:12666040 | T | A | 1 | a0003c0003t0001g0292 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-235A>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666040 | |||||||
| chr19:12666082 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.160-277C>T | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666082 | |||||||
| chr19:12666177 | C | T | 1 | a0007c0008t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.159+366G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666177 | |||||||
| chr19:12666352 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.159+191T>G | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666352 | |||||||
| chr19:12666452 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.159+91T>C | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666452 | |||||||
| chr19:12666472 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.159+71G>A | MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 1/23 | chr19 | 12666472 |